5/2007 התשס"ז/י"א רשומות ISRAEL STATE RECORDS ט' באב התשס"ז July 24, 2007 יומן הפטנטים והמדגמים PATENTS AND DESIGNS JOURNAL PATENTS Applications filed Applications accepted Patents granted Patents renewed Patents not in force Patents renewed for 20 years Patents expired Extension orders renewed Notices Changes in particulars entered in register Corrigenda Country codes Indices of applications accepted DESIGNS Designs registered Designs renewed Designs void עמוד Page 1756 1898 2112 2113 2115 2116 2117 2118 2119 פטנטים 2123 2124 2125 i בקשות שהוגשו בקשות שקובלו פטנטים שניתנו פטנטים שחודשו פטנטים שתוקפם פקעו פטנטים שחודשו לעשרים שנה פטנטים שפג תוקפם צווי הארכה שחודשו הודעות שינויים בפרטים רשומים בפנקס תיקוני טעויות קודים למדינות מפתחות לבקשות שקובלו 2127 2141 2142 מדגמים מדגמים שנרשמו מדגמים שחודשו מדגמים שבוטלו ידיעות כלליות : וכו' בענייני פטנטים ומדגמים יש לשלוח אל, מסמכים,מכתבים ירושלים,4 רח' הסדנא,רשם הפטנטים והמדגמים ירושלים והיא פתוחה לציבור בימי חול, תלפיות,4 לשכת הפטנטים נמצאת ברח' הסדנא .12:30 - ו8:30 שאינם ערבי שבת או מועד בין השעות שקלים בעד כל2.50 לשכת הפטנטים מספקת תצלומים של פירוטים ושרטוטים במחיר של .עמוד או חלק ממנו 'אג רות ללשכת הפטנטים מתקבלות אך ורק על ידי תשלום לחשבון הלשכה בבנק הדואר מס יש להציג קבלת בנק הדואר ללשכה יחד עם הבקשה לפעולה שעבורה האגרה. 0-24145-2 .שולמה GENERAL INFORMATION Letters, documents, etc. concerning Patents and Designs should be addressed to: The Commissioner of Patents and Designs, 4 Hasadnah St., Jerusalem The Patent Office is located at 4 Hasadnah St., Talpiot, Jerusalem and is open to the public on weekdays, except on Fridays or on the eves of holydays, from 08:30 to 12:30 hrs. 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EP 04104997.4 12/10/2004 PCT/EP/2005/055156 WO/2006/040318 22/09/2005 July 24, 2007– ט' באב התשס"ז קינאז גמא לטיפול באנמיהP13 מעכבי 182112 USE OF TGF-? ANTAGONISTS OF LIMIT NEPHROTOXICITY OF IMMUNOSUPPRESSIVE AGENTS THE MCW RESEARCH FOUNDATION, INC. US 60/612187 22/09/2004 PCT/US/2005/033942 WO/2006/036729 C07D A61K TGF–? שימוש באנטגוניסטים של להגבלת רעילות כליתית של גורם מדכאי חיסון 1784 22/03/2007 182113 מערכת חלבונים ומוצרי מזון הכוללים אותה PROTEIN SYSTEM AND FOOD PRODUCTS INCLUDING SAME KRAFT FOODS HOLDINGS, INC. US 11/278210 31/03/2006 19/09/2005 182114 MAGNESIUM REMOVAL FROM MAGNESIUM REDUCED METAL POWDERS H.C. STARCK INC. US 10/953163 29/09/2004 PCT/US/2005/033291 WO/2006/039126 29/09/2005 182115 182117 STENT VERYAN MEDICAL LIMITED GB 0421085.2 22/09/2004 PCT/GB/2005/003665 WO/2006/032902 1785 B22F הסרת מגנזיום מאבקות מתכת המכילות כמות מחוזרת של מגנזיום STEROID ANALOGS AND CHARACTERIZATION AND TREATMENT METHODS HOLLIS-EDEN PHARMACEUTICALS, INC. 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IL 164260 23/09/2004 PCT/IL/2005/001016 WO/2006/033109 20/09/2005 A44B A61B מקטע מפרקי משופר מדיגוס בע"מ F16M שיטה ומערכת להתאמת מיקום של אוביקט July 24, 2007– ט' באב התשס"ז 27/09/2005 182134 PROCESS FOR PRODUCTION OF 2CHLORO-4-NITROIMIDAZOLE OTSUKA PHARMACEUTICAL CO., LTD. 2004JP 27/09/2004 278974 PCT/JP/2005/018230 WO/2006/035960 22/09/2005 –ניטרואימידזול4––כלורו2 תהליך ליצירת 182135 LIQUID ALLERGY VACCINE FORMULATION FOR ORMUCOSAL ADMINISTRATION ALK-ABELLO A/S DK PA200401468 27/09/2004 60/613892 27/09/2004 US PCT/DK/2005/000601 WO/2006/034707 10/09/2005 July 24, 2007– ט' באב התשס"ז A61K תכשיר חיסון נוזלי לאלרגיה למתן אורומוקסלי 182136 NOVEL PYRIMIDINE DERIVATIVES AND THEIR USE AS PPAR-ALPHA MODULATORS BAYER HEALTHCARE AG DE 102004046623.8 PCT/EP/2005/009734 WO/2006/032384 C07D C07D תולדות חדשות של פירימידין ושימוה בהן ALPHA – PPAR כמאפננות 25/09/2004 1790 28/09/2005 182137 ADDITIVE FOR LIQUID OR LIQUIFIED HYDROCARBON FUELED DIRECT FIRED BURNERS, OPEN FLAMES AND RELATED PROCESSES ENVIROFUELS, L.L.C. 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US 60/616010 04/10/2004 60/630528 22/11/2004 US PCT/US/2005/035868 WO/2006/041945 25/03/2007 182158 USING A WEB CAMERA ON A PC FOR DIAGNOSIS AND TREATMENT OF MENTAL DISORDERS DAVID WEXELMAN 25/03/2007 182159 182161 STABLE TABLET FORMULATION OF TETRAHYDROBIOPTERIN BIOMARIN PHARMACEUTICAL INC. US 60/629189 17/11/2004 PCT/US/2005/041252 WO/2006/055511 July 24, 2007– ט' באב התשס"ז קו ייצור אוטומטי לייצור שעוות בשביל תהליך יציקה בשעווה נעלמת מיכאל רסין C07K תהליך החלפת יון נגדי עבור פפטידים A61M סטימולאציה בדרך הראיה על ידי צילום אינטרנט במחשב עבור אבחנה ורפואה למחלת נפש דוד וקסלמן B29C מכשיר המחבר שיניים לפטין יפים COGGED CLUTCH DEVICE LAPATIN OLGA 16/11/2005 B65G A61K פורמולציה גלולה יציבה של טטראהידרוביופטרין 1796 28/09/2005 182162 שיטה לאומדן הגבהה ומערכת רדאר המשתמשת בשיטה זו ELEVATION ESTIMATION METHOD AND RADAR APPARATUS USING IT THALES NEDERLAND B.V. NL 1027151 30/09/2004 PCT/EP/2005/054870 WO/2006/035041 28/09/2005 182163 A METHOD FOR FINDING THE LOCATION OF A MOBILE TERMINAL IN A CELLULAR RADIO SYSTEM QUALCOMM INCORPORATED US 10/954847 29/09/2004 PCT/US/2005/035084 WO/2006/039434 28/09/2005 05/10/2005 H04L CDMA מכשיר ושיטה לזיהוי חוזרים לזמן פסבדולייט 182165 HIGH FLUX AND LOW FOULING FILTRATION MEDIA H04Q שיטה לאיתור מיקום מסוף נייד במערכת רדיו סלולרית 182164 APPARATUS AND METHOD FOR CDMA TIME PSEUDOLITE FOR REPEATER IDENTIFICATION QUALCOMM INCORPORATED US 10/955274 29/09/2004 PCT/US/2005/035085 WO/2006/039435 G01S B01D מדיה לסינון עם זרימה עם זרימה גבוהה וסתימה נמוכה THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK US 60/616592 06/10/2004 60/633987 07/12/2004 US PCT/US/2005/035738 WO/2007/001405 1797 July 24, 2007– ט' באב התשס"ז 23/09/2005 182166 BUSINESS PROCESS MANAGEMENT SYSTEM AND METHOD DATA QUALITY SOLUTIONS LLC US 60/612615 24/09/2004 11/141710 01/06/2005 US PCT/US/2005/033918 WO/2006/036720 25/03/2007 182167 REMOTE CONTROL BRAKING SYSTEM ZIV MAGUZ 25/03/2007 ENERGY PRODUCTION DAVID COHEN July 24, 2007– ט' באב התשס"ז B62H זיו מגוז 182169 A61K תכשיר דיאודורנט הפעיל לזמן ארוך חלאבין תעשיות בע"מ 182170 CMP COMPOSITION WITH A POLYMER ADDITIVE FOR POLISHING NOBLE METALS CABOT MICROELECTRONICS CORPORATION US US10/963108 12/10/2004 PCT/US/2005/036577 WO/2006/044417 25/03/2007 שיטה ומערכת לניהול עיבוד עסקי מערכת בלימה בשלט רחוק LONG ACTING DEODORANT COMPOSITION HLAVIN INDUSTRIES LTD. 11/10/2005 G06F 182171 C09G הרכב לליטוש כימי–מכני עם תוסף פולימר לליטוש מתכות אצילות F03B ייצור אנרגיה דוד כהן 1798 25/03/2007 182172 SYNTHETIC DERIVATIVES OF BETA GLYCOLIPIDS AND COMPOSITIONS THEREOF FOR THE TREATMENT OF PATHOLOGIC DISORDERS HADASIT MEDICAL RESEARCH SERVICES & DEVELOPMENT LTD 27/09/2005 ,נגזרות מלאכותיות של בתא–גליקוליפידים תכשירים המכילים אותם ושיטות לטיפול בהפרעות פתולוגיות הדסית שרותי מחקר רפואי ופיתוח בע"מ 182173 SHEET METAL LID FOR A BEVERAGE CAN, PROVIDED WITH A LARGE PERFORATION BALL PACKAGING EUROPE GMBH EP 04104724.2 28/09/2004 PCT/EP/2005/054858 WO/2006/035033 22/09/2005 182174 TARGET PROPERTY MAPS FOR SURVEILLANCE SYSTEMS OBJECTVIDEO INC. 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US 60/621669 26/10/2004 60/624547 04/11/2004 US 60/654937 23/02/2005 US 60/654941 23/02/2005 US 60/654938 23/02/2005 US PCT/CA/2005/001577 WO/2006/045177 July 24, 2007– ט' באב התשס"ז מלחים של חרדל של איזופוספוראמיד ואנלוגים שלהם כחומרים נגד גידולים 182753 METHOD FOR THE AUTOMATED PRODUCTION OF THREEDIMENSIONAL OBJECTS AND TEXTURED SUBSTRATES FROM TWO-DIMENSIONAL OR THREEDIMENSIONAL OBJECTS 2089275 ONTARIO LTD. US 60/621669 26/10/2004 60/624547 04/11/2004 US 60/654936 23/02/2005 US 60/654941 23/02/2005 US 60/654938 23/02/2005 US 60/654937 23/02/2005 US PCT/CA/2005/001579 WO/2006/045178 C07F G03H שיטה לייצור של מצע בעל מראה הולוגרפי 1892 04/11/2005 182755 METABOLITES OF CERTAIN [1,4]DIAZEPINO [6,7,1-IJ]QUINOLINE DERIVATIVES AND METHODS OF PREPARATION AND USE THEREOF WYETH US 60/625335 05/11/2004 PCT/US/2005/040289 WO/2006/052886 02/11/2005 182756 REVERSE MICELLE COMPOSITION FOR DELIVERY OF METAL CATIONS COMPRISING A DIGLYCERIDE AND A PHYTOSTEROL AND METHOD OF PREPARATION MEDESIS PHARMA S.A. EP 04025987.1 02/11/2004 PCT/IB/2005/003605 WO/2006/048773 18/10/2005 182757 MOBILE OR STATIONARY MODULAR SELF-CONTAINED DEHYDRATION TOILET, DEHYDRATION ENGINE, AND GRAY WATER RECOVERY SYSTEM LUMBERT STEVEN US 10/904234 29/10/2004 PCT/US/2005/037334 WO/2006/049856 1893 C07D מטבוליטים של תולדות של קרטין ] קווינולין ושיטותIJ–6,7,1[]דיאזפינו1,4[ להכנתן ושימוש בהם A61K תרכובת של מיצלות הפוכות למסירת המכילים דיגליצרידים,קטיוני מתכת ופיטוסטרול ושיטה להכנתה C02F נייד או נייח, מודולרי,מתקן שרותים יבש מנוע ייבוש ומערכת,בעל מיכל עצמי הבראה למים אפורים July 24, 2007– ט' באב התשס"ז 20/10/2005 182758 OPTICAL CORRELATION APPARATUS AND METHOD INSTRO PRECISION LTD. GB 0424432.3 04/11/2004 PCT/GB/2005/004051 WO/2006/048604 05/11/2004 182759 G01S מכשיר ושיטה למתאם אופטי H01M דלקים מוצקים לתאי דלק SOLID FUELS FOR FUEL CELLS UOP LLC PCT/US/2004/037099 WO/2006/052243 09/11/2005 182760 CONJUGATE MOLECULE COMPOUNDS WITH ENHANCED CELL UPTAKE ACTIVITY XIGEN S.A. 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US 60/624357 01/11/2004 PCT/US/2005/039686 WO/2006/052608 C07D C07D תכשירים ושיטות,תרכובות פירידאזין July 24, 2007– ט' באב התשס"ז 16/11/2005 182768 DRUG COMBINATION COMPRISING A SELECTIVE SEROTONIN REUPTAKE INHIBITOR AND GLUCOCORTICOID RECEPTOR ANTAGONIST FOR THE TREATMENT OF DEPRESSION N.V. ORGANON EP 04257199.2 19/11/2004 PCT/EP/2005/056023 WO/2006/053884 03/11/2005 צירוף תרופתי המכיל מעכב בררני של טעינה מחדש של סרטונין ואנטגוניסט של קולטן גלוקוקורטיקואיד לטיפול בדיכאון 182769 HUMIDITY CONTROL DEVICE MULTISORB TECHNOLOGIES, INC. US 10/984080 09/11/2004 PCT/US/2005/039999 WO/2006/052748 26/10/2005 182771 A THYMUS-SPECIFIC PROTEIN IMMUNE SYSTEM KEY LTD US 60/621086 25/10/2004 PCT/IL/2005/001113 WO/2006/046239 24/01/2005 MEDICAL CONNECTOR JR. ROWAN P. SMITH US 10/971906 PCT/US/2005/002259 WO/2006/046961 A61K 182772 C08K התקן לבקרת לחות C07K חלבון תימוס מסויים IMMUNE SYSTEM KEY LTD A61M מחבר רפואי 25/10/2004 July 24, 2007– ט' באב התשס"ז 1896 NOTICE UNDER SECTION 26 OF THE PATENTS LAW, 5727-1967 The applications, particulars of which are set out below, have been accepted pursuant to Section 17 of the Patents Law. Any person wishing to oppose the grant of a patent on any of the applications published here, may, within three months from the date of this journal, give to the Commissioner of Patents notice under Section 30 of the Patents Law, in the manner prescribed in regulations 57 et seq of the Patents Regulations, 5728-1968 Particulars of the applications, where applicable, are given in the following order: [11] [21] Number of application [54] Title of invention [22] Application date [31] [32] [33] Number and date of foreign application – convention country. *[51] Int.Cl. [61] Application for patent of addition [62] Divisional application [71] Applicant [72] Inventor [87] International Publication Number [74] Address for service [57] Abridgement of invention (in the language in which the specification is drawn up) *Note: As from Patents and Designs Journal No.1/06, patent applications are classified according to the Eighth Edition of the International Patent Classification (2006) 1897 - לחוק הפטנטים תשכ"ז26 הודעה לפי סעיף 1976 הבקשות שפרטיהן מתפרסמים להלן קובלו כל המעונין. לחוק הפטנטים17 לפי סעיף להתנגד למתן פטנט על פי בקשה מהבקשות תוך שלושה חדשים,המתפרסמות רשאי להגיש לרשם הפטנטים,מתאריך יומן זה לחוק30 הודעת התנגדות לפי סעיף ואילך57 הפטנטים בדרך הקבועה בתקנה .1968 – תשכ"ח,לתקנות הפטנטים פרטי הבקשות במידה ויישימים מובאים לפי :סדר זה מספר הבקשה שם האמצאה תאריך הבקשה מספר ותאריך של בקשות החוץ – מדינת האגוד *סיווג בינלאומי – מהדורה שביעית בקשה לפטנט מוסף בקשת חלוקה המבקש הממציא מס' פרסום של בקשה הבינלאומית מען למסירת מסמכים )תקציר האמצאה (בשפה בה ערוך הפירוט ' החל מיומן הפטנטים והמדגמים מס:*הערה ניתן ציון לבקשות פטנטים הסיווג לפי1/06 המהדורה השמינית של הסיווג הבינלאומי )2006 של פטנטים (משנה July 24, 2007– ט' באב התשס"ז ]11[]21[ 114668 ליגנד של קינאז טרנסממברנלי של גידול , תכשירים המכילים אותו,)Htk( כבד מולקולות של חומצות גרעין המקודדות וקטורים הכוללים מולקולות,ליגנדים כאלה תאי מאכסן,של חומצות גרעין כאלה שיטה להכנת,הכוללים וקטורים כאלה ליגנד כזה והשימוש בו להכנת תרופה Htk וכתרופה לשפעול רצפטור ]54[ HEPATOMA TRANSMEMBRANE KINASE (HTK) LIGAND, COMPOSITIONS COMPRISING THE SAME, NUCLEIC ACID MOLECULES ENCODING SUCH LIGANDS, HOST CELLS COMPRISING SUCH VECTORS, A METHOD FOR PREPARATION OF SUCH LIGAND AND USE THEREOF IN PREPARATION OF A MEDICAMENT AND AS A MEDICAMENT FOR ACTIVATING HTK RECEPTOR ]22[ ]31[ ]51[ ]71[ ]74[ 19.07.1995 08/277722 ]32[ 20.07.1994 ]33[ US Int. Cl.8 A61K 038/17, C07K 014/47, C12N 015/12 GENENTECH, INC., U.S.A. S. HOROWITZ & CO., ,' הורוביץ ושות.ש ZION HOUSE, תל,41-45 שדרות רוטשילד,בית ציון 41-45 ROTHSCHILD BLVD., אביב TEL AVIV 65784 [57] An isolated protein molecule which induces phosphorylation of the hepatoma transmembrane kinase (Htk) receptor and binds to the Htk receptor, and comprises an amino acid sequence selected from the group consisting of: (a) amino acids 25-333 of the amino acid sequence shown in figure 2 (SEQ ID NO:4); (b) the naturally occurring amino acid sequence for a mature Htk ligand from an animal species other than those sequences of (a); (c) allelic variants of the sequences (a) or (b) that phosphorylate and bind the Htk receptor; and (d) the sequences of (a), (b), (c) having a single conservative amino acid substitution as defined in Table 1 that phosphorylate and bind the Htk receptor, the figures and tables as shown in the specification. __________ July 24, 2007– ט' באב התשס"ז 1898 ]11[]21[ 122991 ושימושיהםP53 וריאנטים של חלבון הרפואיים ]54[ P53 PROTEIN VARIANTS AND THERAPEUTICAL USES THEREOF ]22[ ]31[ ]51[ 17.07.1996 95/08729 ]32[ 19.07.1995 ]33[ FR Int. Cl.8 A61K 038/16, 048/00, A61P 035/00, C07K 014/035, 014/82, 019/00, C12N 015/09, 015/12, 015/62, 015/86 AVENTIS PHARMA S.A, FRANCE LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו INDUSTRIAL PARK, OMER, באר שבע,5352 .ד. ת, עומר,גן תעשייה P.O.B. 5352, BEER-SHEVA 84152 ]71[ ]74[ [57] Variant of p53 protein in which a part of the oligomerisation domain as well as all of the regulation domain are deleted and replaced by an artificial leucine zipper characterized in that the deletion of the Cterminal part is made from the residue 326 or from the residue 337 and further characterized in that all or part of the transactivation domain is deleted and replaced by the viral protein 16 of the herpes simplex virus (VP16) transactivation domain. __________ 1899 July 24, 2007– ט' באב התשס"ז ]11[]21[ 123201 ) קאמפטותצין המותמריםS)20 תולדות הכנתן ותכשירי, והמסיסים במים5 בעמדה רוקחות המכילים אותן ]54[ WATER SOLUBLE 5SUBSTITUTED 20(S)CAMPTOTHECIN DERIVATIVES, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME ]22[ ]31[ 22.04.1997 08/655259 ]32[ 05.06.1996 ]33[ US 08/655258 05.06.1996 US 08/771391 19.12.1996 US Int. Cl.8 A61K 031/395, A61P 035/00, C07D 491/00, 491/22 REDDY-CHEMINOR, INC., U.S.A. DR. REDDY'S LABORATORIES LIMITED, INDIA WO/1997/046563 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]51[ ]71[ ]87[ ]74[ [57] A compound of the formula or its pharmaceutically acceptable salts, wherein R1, R2, R3 and R4 independently represent hydrogen or represent a group selected from hydroxy, (C1-C6) alkoxy, substituted amino wherein the amino group is mono or disubstituted and the substituents are selected from (C1-C6) alkyl or halo (C1-C6) alkyl; (C1-C6) alkyl or substituted (C1-C6) alkyl wherein the substituents are selected from hydroxy, (C1-C6) alkoxy, halo (C1-C6) alkyl, cyano, nitro, amino, or (C1-C6) alkylamino; R1, R2, R3 and R4 are not all the same except July 24, 2007– ט' באב התשס"ז where all of R1, R2, R3 and R4 are hydrogen; R5 represents hydrogen or (C1C6) alkyl; and R6 represents hydrogen, (C1C6) alkyl, benzyl where the phenyl group may be unsubstituted or mono, di or tri substituted with substituents selected from halogen, (C1-C6) alkoxy, cyano, nitro, (C1C6) alkyl, amino, or substituted amino wherein the amino group is mono or disubstituted with (C1-C6) alkyl groups; substituted benzoyl wherein the substituents are selected from (C1-C6) alkyl, halo (C1-C6) alkyl, halogen, (C1-C6) 1900 alkoxy, cyano, nitro, amino, or (C1-C6) alkylamino; substituted (C1-C6) alkyl, wherein the substituents are selected from halogen, hydroxy, (C1-C6) alkoxy, phenoxy, or amino in which the amino group can be unsubstituted, mono or disubstituted wherein the substituents are selected from hydroxy or (C1-C6) alkyl, when the amino group is disubstituted the substituents are independent or combined together to form a ring having 5 or 6 ring atoms the ring atoms being carbon, nitrogen, and optionally oxygen atoms; or a heterocyclic ring having 5 to 7 carbon atoms and one or two nitrogen atoms, with a proviso that (i) when R1 is methoxy, R6 is not hydrogen or unsubstituted (C1-C6) alkyl group; (ii) when R2 is hydroxyl, (C1-C6) alkoxy, alkylamino, R6 is not hydrogen or unsubstituted (C1-C6) alkyl group; (iii) when R5 is (C1-C6) alkyl, R6 is not hydrogen or unsubstituted (C1-C6) alkyl group; (iv) when R1 through R5 represent hydrogen, R6 is not hydrogen or unsubstituted (C1-C6) alkyl. __________ ]11[]21[ 123248 HCV NS3 תכשירים המכילים מקטע של הליקז ]54[ COMPOSITIONS COMPRISING AN HCV NS3 HELICASE FRAGMENT ]22[ ]31[ ]51[ 12.09.1996 08/529169 ]32[ 15.09.1995 ]33[ US Int. Cl.8 A61K 038/43, 048/00, C07K 014/18, 019/00, C12N 009/14, 015/51, 015/55, 015/62, G01N 033/50 CHIRON CORPORATION, U.S.A. WO/1997/012043 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]71[ ]87[ ]74[ [57] Composition comprising an HCV NS3 helicase fragment having the same amino acid sequence as shown in SEQ ID NO:2 or having, when optimally aligned, The applications for division from this application have not yet been published at least 70% homology with the amino acid sequence shown in SEQ ID NO:2 and having essentially the same biological activity. ,171901,171900,171896 בקשות חלוקה מבקשה זו .שטרם פורסמו ___________ 1901 July 24, 2007– ט' באב התשס"ז ]11[]21[ ]54[ OSTEOTOME FOR RHINOPLASTY ]22[ ]51[ ]71[ ]74[ 03.05.1998 Int. Cl.8 A61B 001/00, 017/16 EFRON ROZAN EFRON ROZAN, MOSHE KOL 8 APP.16 TEL AVIV 69626 124301 אוסטאוטום לרינופלסטי אביב- תל,אפרון רוזן ,אפרון רוזן אביב- תל,8/16רחוב משה קול [57] An osteotome for rhinoplasty comprising a handle (1), a carrying part (2) linked rigidly with the handle and two cutting elements (3) secured on the carrying part, each of them being bounded by the inner surface and outer surface which cross each other and form a cutting edge (6) at the point of intersection, in which case, both cutting elements present each other their inner surfaces, are located symmetrically relative to each other and have a gap in between for the nasal septum. __________ July 24, 2007– ט' באב התשס"ז 1902 ]11[]21[ 126835 נוגדנים לקולטן של אינטרפרון ALPHA/BETA ]54[ ANTIBODIES AGAINST INTERFERON ALPHA/BETA RECEPTOR ]22[ ]31[ ]51[ 29.04.1997 118096 ]32[ 01.05.1996 ]33[ IL Int. Cl.8 A61K 039/395, A61P 037/02, 043/00, C07K 016/28, C12N 005/10, 005/12, 015/13, 015/63, G01N 033/53, 033/577 YEDA RESEARCH AND רחובות,ידע חברה למחקר ופיתוח בע"מ DEVELOPMENT CO. LTD. WO/1997/041229 INTERLAB LTD., ,אינטר לאב בע"מ KIRYAT WEIZMANN נס ציונה,קרית ויצמן NES ZIONA 76110 ]71[ ]87[ ]74[ [57] An antibody wherein said antibody binds to the IFN α/β receptor or its IFNAB-BPI and IFNAB-BPII soluble forms and said antibody selectively blocks the biological activity of IFN- α. __________ ]11[]21[ 127162 מולקולות הקשורות עם פגיעה בכליות ]54[ KIDNEY INJURY RELATED MOLECULES ]22[ ]31[ 23.05.1997 60/018228 ]32[ 24.05.1996 ]33[ US 60/023442 23.08.1996 US Int. Cl.8 A61K 038/17, 039/395, 048/00, 051/10, A61P 013/12, C07K 014/435, 014/47, 016/18, 019/00, C12N 005/10, 005/12, 015/12, 015/63 BIOGEN IDEC MA INC., U.S.A. THE GENERAL HOSPITAL CORPORATION, U.S.A. WO/1997/044460 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]51[ ]71[ ]87[ ]74[ [57] A polypeptide comprising an amino acid sequence that is at least 90% identical to the sequence of SEQ ID NO:3, SEQ ID NO:5 or SEQ ID NO:7, and which is a kidney injury molecule (KIM), said KIM being a cell surface protein selectively expressed in post-ischemic mammalian kidney tissue. __________ 1903 July 24, 2007– ט' באב התשס"ז ]11[]21[ 128407 ליגאנד הקשור בגורם נמק של גידול ]54[ TUMOR NECROSIS FACTOR RELATED LIGAND ]22[ ]31[ 07.08.1997 023541 ]32[ 07.08.1996 ]33[ US 028515 18.10.1996 US 040820 18.03.1997 US Int. Cl.8 A61K 038/19, 039/395, 048/00, A61P 035/00, 037/00, 043/00, C07K 014/525, 016/24, C12N 001/15, 001/19, 001/21, 005/10, 015/12, 015/28, 015/63 BIOGEN IDEC MA INC., U.S.A. THE FACULTY OF MEDICINE OF THE UNIVERSITY OF GENEVA, SWITZERLAND WO/1998/005783 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]51[ ]71[ ]87[ ]74[ [57] A DNA sequence selected from the group consisting of: (a) a DNA sequence comprising a nucleotide sequence shown in SEQ ID NO:1 or 3; (b) a DNA sequence which encodes a polypeptide having the amino acid sequence shown in SEQ ID NO:2 or 4; (c) a DNA sequence which encodes a fragment of the polypeptide of (b), wherein said fragment has the capability of regulating cell death; (d) a DNA sequence which is 60% homologous to the DNA sequence of (a) and which encodes a polypeptide which is capable of regulating cell death; (e) a DNA sequence being degenerate to a DNA sequence of any one of (a) to (c); and (f) a DNA sequence encoding a soluble form of the polypeptide encoded by the DNA sequence of any one of (a) or (e) which retains the capability of regulating cell death; or the complementary strand thereof. _________ July 24, 2007– ט' באב התשס"ז 1904 ]11[]21[ 128691 תולדות באנזאמידין המותמרות על ידי חומצת אמינו טבעתית ותולדות חומצלה הידרוקסית טבעתית ושימושם נגד קרישה ]54[ BENZAMIDINE DERIVATIVES SUBSTITUTED BY CYCLIC AMINO ACID AND CYCLIC HYDROXY ACID DERIVATIVES AND THEIR USE AS ANTICOAGULANTS ]22[ ]31[ 11.09.1997 08/713066 ]32[ 12.09.1996 ]33[ US 08/920319 27.08.1997 US Int. Cl.8 A61K 031/00, 031/395, A61P 007/00, C07C 043/263, 211/43, 217/54, 229/52, 275/28, 279/18, 323/07, C07D 213/64, 251/26, 401/12, 403/12 SCHERING AKTIENGESELLSCHAFT, GERMANY WO/1998/011094 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]51[ ]71[ ]87[ ]74[ [57] A compound of the formulae: 1905 July 24, 2007– ט' באב התשס"ז wherein: A is –C(R8) = or –N=; Z1 and Z2 are independently –O-, -N(R9)-, -S-, -S(O)-, -S(O)2-, or –OCH2-; R1 and R4 are each independently hydrogen, halo, alkyl, nitro –OR9, C(O)OR9, -C(O)N(R9)R10, -N(R9)R10, N(R9)C(O)R9 or N(H)S(O)2R12; R2 is –C(NH)NH2 –C(NH)N(H)OR9, C(NH)N(H)C(O)OR12, C(NH)N(H)C(O)R9, -C(NH)N(H)S(O)2R12 or –C(NH)N(H)C(O)N(H)R9; R3 is hydrogen, halo, alkyl, haloalkyl, nitro, ureido, guanidine, -OR9, C(NH)NH2, -C(NH)N(H)OR9, C(O)N(R9)R10, -R11-C(O)N(R9)R10, CH(OH)C(O)N(R9)R10, -N(R9)R10, R11N(R9)R10, -C(O)OR9, -R11-C(O)OR9, N(R9)C(O)R9, (1,2)-tetrahydropyrimidinyl (optionally substituted by alkyl), (1,2)imidazolyl (optionally substituted by alkyl), or (1,2)-imidazolinyl (optionally substituted by alkyl); R5 and R6 are independently hydrogen, halo, alkyl, haloalkyl, nitro, N-(R9)R10, C(O)OR9, -C(O)N(R9)R10, C(O)N(R9)CH2C(O)N(R9)R10, N(R9)C(O)N(R9)R10, -N(R9)C(O)R10, or – N(R9)S(O)2R12; R7 is –N(R9)-(C(R9)(R10))n-R13 (where n is 0 to 4), -O-(C(R9)(R10))n-R13 (where n is o to 4), or –N(R14)R15; R8 is hydrogen, alkyl or halo; each R9 and R10 is independently hydrogen, alkyl, aryl (optionally substituted by halo, alkyl, hydroxy, alkoxy, aralkoxy, amino, dialkylamino, monoalkylamino, nitro, carboxy, alkoxycarbonyl, aminocarbonyl, monoalkylaminocarbonyl, or dialkylaminocarbonyl), or aralkyl (optionally substituted by halo, alkyl, aryl, hydroxy, alkoxy, aralkyl, amino, dialkylamino, monoalkylamino, nitro, carboxy, alkoxycarbonyl, aminocarbonyl, monoalkylaminocarbonyl, or dialkylaminocarbonyl); July 24, 2007– ט' באב התשס"ז R11 is a straight or branched alkylene chain; R12 is alkyl, aryl (optionally substituted by halo, alkyl, hydroxy, alkoxy, aralkoxy, amino, dialkylamino, monoalkylamino, nitro, carboxy, alkoxycarbonyl, aminocarbonyl, monoalkylaminocarbonyl, or dialkylaminocarbonyl), or aralkyl (optionally substituted by halo, alkyl, aryl, hydroxy, alkoxy, aralkyl, amino, dialkylamino, monoalkylamino, nitro, carboxy, alkoxcyarbonyl, aminocarbonyl, monoalkylaminocarbonyl, or dialkylaminocarbonyl); R13 is a mono- bi- or tri-cyclic carbocyclic ring system containing from 3 to 15 carbon atoms which may be partially or fully saturated or aromatic, wherein the carbon atoms may be optionally oxidized and wherein the carbocyclic ring system is substituted by –C(R9)(R10))m-R16 (where m is 0 to 4), and is optionally substituted by alkyl, aryl, aralkyl, alkoxy, aryloxy, aralkoxy, halo, haloalkyl, haloalkoxy, hydroxy, -N(R9)R10, -C(O)OR9, or – C(O)N(R9)R10; Or R13 is a mono-, bi- or tri-cyclic heterocyclic ring system containing from 3 to 15 ring members including carbon and 1 to 4 hetero atoms selected from nitrogen, oxygen and sulfur atoms, wherein the carbon, nitrogen and sulfur atoms may be optionally oxidized and wherein the heterocyclic ring system may be partially or fully saturated or aromatic and is substituted by –(C(R9)(R10))m-R16 (where m is 0 to 4), and is optionally substituted by alkyl, aryl, aralkyl, alkoxy, aryloxy, aralkoxy, halo, haloalkyl, haloalkoxy, hydroxy, -N(R9)R10, -C(O)OR9, or – C(O)N(R9)R10; R14 and R15, together with the nitrogen atom, form a mono- bi- or tri-cyclic heterocyclic ring system containing from 3 to 15 ring members including carbon and 1 to 3 additional hetero atoms selected from 1906 nitrogen, oxygen and sulfur atoms, wherein the carbon, nitrogen, or sulfur atoms may be optionally oxidized and wherein the heterocyclic ring system may be partially or fully saturated or aromatic and is substituted by –C(R9)(R10)m-R16 (where m is 0 to 4), and is optionally substituted by alkyl, aryl, aralkyl, alkoxy, aryloxy, aralkoxy, halo, haloalkyl, haloalkoxy, hydroxy, -N(R9)R10, C(O)OR9, or –C(O)N(R9)R10; and R16 is –C(O)OR9 or –C(O)N(R9)R10; provided that when R7 is –N(R9)(C(R9)(R10)n-R13 (where n is 0), R13 can not be phenyl, naphthyl or piperidinyl substituted by –C(O)OR9; when R7 is –O(C(R9)(R10))n-R13 (where n is 0), R13 can not be phenyl, naphthyl, piperidinyl or pyrrolidinyl substituted by –C(O)OR9; and when R7 is –N(R14)R15, R14 and R15, together with the nitrogen atom, can not be piperazinyl or piperidinyl substituted by – C(O)OR9; as a single stereoisomer or a mixture thereof; or a pharmaceutically acceptable salt thereof. _________ ]11[]21[ 128765 תכשירי רוקחות המכילים איזופלאבונים ]54[ PHARMACEUTICAL COMPOSITIONS CONTAINING ISOFLAVONES ]22[ ]31[ ]51[ 29.08.1997 PO2039 ]32[ 30.08.1996 ]33[ AU Int. Cl.8 A61K 000/833000 000/840000 031/12, 031/16, 031/215, 031/353, 031/404, 031/473, A61P 001/00, 009/00, 013/00, 015/00, 017/10, 017/14, 019/00, 025/00, 025/28, 029/00, 035/00, C07C 049/24, 049/82, 069/035, 069/30, 229/00, 235/12, C07D 209/08, 209/32, 311/38, 471/06 NOVOGEN RESEARCH PTY LTD., AUSTRALIA WO/1998/008503 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]71[ ]87[ ]74[ [57] Use of a compound for the manufacture of a medicament for the treatment, amelioration, defence against, and/or prevention of menopausal syndrome including hot flushes, anxiety and depression, mood swings, night sweats, headaches, and urinary incontinence; osteoporosis; premenstrual syndrome including fluid retention and cyclical mastalgia, and dysmenorrhoea; Reynaud's Syndrome; Reynaud's 1907 Phenomenon; Buergers Disease; coronary artery spasm; migraine headaches; hypertension; benign prostatic hypertrophy; breast cancer; uterine cancer; ovarian cancer; testicular cancer; large bowel cancer; endometrial cancer; prostatic cancer; uterine cancer; atherosclerosis; Alzheimers disease; inflammatory diseases including inflammatory bowel disease, ulcerative colitis, and Crohns disease; rheumatic July 24, 2007– ט' באב התשס"ז diseases including rheumatoid arthritis; acne; baldness including male pattern baldness (alopecia hereditaria); psoriasis and/or diseases associated with oxidant stress including cancer, myocardial infarction, stroke, arthirits, sunlight induced skin damage or cataracts whereby the compound is selected from the group consisting of R1 is H, or RACO where RA is C1-10 alkyl or an amino acid, R8 is CORD where RD is H, OH, C1-10 alkyl or an amino acid, R9 is CO2RC or CORE where RC is C1-10 alkyl and RE is H, C1-10 alkyl or an amino acid, R10 is CORc or CORcORE where RC and RE are as previously defined, R11 is H or OH, R12 is H, COOH, CO2RC where RC and is as previously defined, or CONHRE where RE is as previously defined, R13 is H or RB where RB is an amino acid or CORA where RA is as previously defined, R14 is H, or CORA where RA is as previously defined, R15 is CORA where RA is as previously defined, R16 is H, CORB or CO2RC where RB and RC are as previously defined, R17 is H or hydroxy C1-10 alkyl, R18 is H or C1-10 alkyl, and "----" represents either a single bond or a double bond; provided that where the use is a use for the manufacture of a medicament for the treatment or prophylaxis of menopausal syndrome or premenstrual tension syndrome compounds of the formulae July 24, 2007– ט' באב התשס"ז 1908 where R2 is OH; or where the compound is are specifically excluded; and provided that where the use is a use for the manufacture of a medicament for the treatment of a form of cancer, autoimmune diseases including rheumatoid arthritis or osteoporosis compounds of the formula where R2 is OH, and R4 is CO2H or CO2CH2CH3 are specifically excluded. The applications for division from this application have not yet been published ,181059 בקשות חלוקה מבקשה זו .שטרם פורסמו ________ 1909 July 24, 2007– ט' באב התשס"ז ]11[]21[ 130123 הביטוי, LAG–3 מוטנטים של החלבון השימוש בהם ושיטה לייצורם,שלהם ]54[ MUTANTS OF THE LAG-3 PROTEIN, THEIR EXPRESSION AND USE AND METHOD FOR THEIR PRODUCTION ]22[ ]31[ ]51[ 25.11.1997 96/14608 ]32[ 28.11.1996 ]33[ FR Int. Cl.8 A61K 038/17, 045/00, 051/00, A61P 035/00, 037/02, 037/06, C07K 014/435, 014/705, 019/00, C12N 001/21, 005/10, 015/12, 015/62, 015/63 INSTITUT GUSTAVE ROUSSY, FRANCE INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM), FRANCE APPLIED RESEARCH SYSTEMS ARS HOLDING N.V., NETHERLANDS ANTILLES WO/1998/023741 REINHOLD COHN AND ,ריינהולד כהן ושותפיו PARTNERS, תל אביב,4060 .ד. ת, 21 רחוב אחד העם 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]71[ ]87[ ]74[ [57] Purified polypeptide corresponding to a mutated form of the soluble LAG-3 protein or of one of its fragments comprising the extracellular domain D1 and D2, consisting in an amino acid substitution at one of the positions selected from the group consisting of: position 30 where aspartic acid is replaced by alanine (D30A), position 56 where histidine is replaced by alanine (H56A), position 77 where tyrosine is replaced by phenylalanine (Y77F), position 88 where arginine is replaced by alanine (R88A), position 103 where arginine is replaced by alanine (R103A), position 109 where aspartic acid is replaced by glutamic acid (D109E), position 115 where arginine is replaced by alanine (R115A); or a deletion of the region between position 54 (P) and position 66(A). _________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 130405 1910 ]54[ USE OF COMPLEXES BETWEEN CATIONIC LIPOSOMES AND POLYDEOXYRIBONUCLEOTIDES FOR PREPARATION OF MEDICAMENTS ]22[ ]51[ ]71[ ]74[ 10.06.1999 Int. Cl.8 A61K 009/127, 031/00, 047/48 GENTIUM SPA, ITALY REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] Complexes formed by cationic liposomes and by polydeoxyribonucleotides having a molecular weight in the range 7,00060,000 Da, preferably 10,000-60,000 Da, שימוש בקומפלכסים הנוצרים בין ליפוזומים קטיונים ופולידאוקסיריבונוקליאוטידים להכנת תרופות ,ריינהולד כהן ושותפיו תל,4060 .ד. ת, 21 רחוב אחד העם אביב obtainable by depolymerization of nucleic acids, wherein the polydeoxyribonucleotides are located on the outer surface of the liposome, for use as a medicament. _________ ]11[]21[ ]54[ OPTICAL RESONATORS WITH DISCONTINUOUS PHASE ELEMENTS ]22[ ]31[ ]51[ ]71[ 29.04.1998 120754 ]32[ 01.05.1997 Int. Cl.8 H01S 003/08 YEDA RESEARCH AND DEVELOPMENT CO. LTD. WO/1998/050986 IP – PARTNERSHIP, P.O.BOX 669 RAANANA 43350 ]87[ ]74[ [57] An optical resonator comprising reflector elements (20, 23) and at least one static discontinuous phase element (86) disposed between said reflector elements, said at least one discontinuous phase element having planar regions (90) and at least one sharp discontinuity defining a boundary (95) between said planar regions, said at least one discontinuous phase element being aligned such that said planar regions introduce a discontinuous phase 1911 132455 מהודים אופטיים עם אלמנטים של פאזה לא מתמשכת ]33[ IL רחובות,ידע חברה למחקר ופיתוח בע"מ ,הנרי סיני רעננה,669 .ד. ת, change to separate regions of field distributions in at least one desired mode propagating in said resonator, such that said separate regions of said field distributions of said at least one desired mode, after traversing said element, are generally in phase, and said at least one sharp discontinuity being operative to produce a change in the phase of at least one undesired mode of said resonator, and being disposed at a location corresponding July 24, 2007– ט' באב התשס"ז to an area of significant intensity of said at least one undesired mode, whereby the divergence of said at least one undesired mode is greater than the divergence naturally arising from the cavity of said at least one desired mode and propagation of said at least one undesired mode is suppressed. __________ ]11[]21[ 132666 תכשירי רוקחות פיטואסטרוגניים ]54[ PHYTOESTROGENIC PHARMACEUTICAL PREPARATIONS ]22[ ]51[ ]71[ 01.11.1999 Int. Cl.8 A61K 003/600000 045/00, 045/06, C07D 311/02 MIGAL GALILEE ראש פינה,מיג"ל מרכז ידע גליל עליון TECHNOLOGICAL CENTER LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו INDUSTRIAL PARK, OMER, באר שבע,5352 .ד. ת, עומר,גן תעשייה P.O.B. 5352, BEER-SHEVA 84152 ]74[ [57] Phytoestrogenic pharmaceutical composition comprising as active July 24, 2007– ט' באב התשס"ז ingredient at least one isoflavan having estrogen-like activity, optionally also 1912 carrier, adjuvant, excipient or diluent. comprising a pharmaceutically acceptable __________ 132700 חוט מאריך בעל שקע ותקע מאובטחים יראל יאירוב ,ירושלים יראל יאירוב, רח' שבתאי הנגבי ,75\19ירושלים [ ]57מערכת לאבטחה של מחבר זכר-נקבה, המערכת כוללת: (א) שני מעטים חיצוניים ( )1,2דמויי קונוס חלול, כל אחד מיועד להכלה של חלק זכרי או חלק נקבי ,כל מעטה חיצוני כולל :שתי קליפות ()4ת כל אחת מהווה מחצית מעטפת קונוס המתחברות זו לזו ,כל קליפה כוללת בשוליה, סמוך לאזור החיבור עם הקליפה השניה ,שני מבנים דמויי כנף ( ,)12כך שבחיבור הקליפות זו לזו ,המבנים דמויי הכנף מתחברים ויוצרים משני צידי הקונוס החלול – שני חללים מאורכים []11[]21 EXTENSION CORD WITH FASTENED PLUG AND SOCKET []54 02.11.1999 Int. Cl.8 H01R 004/00 YAREL YAIROV YAREL YAIROV, SHABTAY HANEGBI ST 75/19 JERUSALEM []22 []51 []71 []74 (12א); בדופן הפנימית של המבנים דמויי הכנף, לאורך השוליים נמצאות מגרעות ארוכות; (ב) שתי שיני אבטחה ( )16נפרדות הכוללות: מבנה מאורך שקצה אחד שלו מיועד לאחיזה באחד מהחללים המאורכים הנוצרים מחיבור שני מבנים דמויי כנף ,והקצה השני של שן האבטחה כולל בליטה ( )14המתאימה למגרעת במבנה דמוי הכנף; כך שבזמן ששני מעטים חיצוניים דמויי קונוס מתחברים זה לזה ,שתי שיני אבטחה מצמידות את החללים המאורכים שנוצרו ע"י המבנים דמויי הכנף בקירבה אלו לאלו. ________ 133195 ט' באב התשס"ז –July 24, 2007 []11[]21 1913 אצילאנלידים שאינם סטרואידים המותמרים בקבוצת (הטרו) ציקליות עם פעילות מעורבת של גאסטגן ואנדרוגן ותהליכים להכנתם ]54[ NONSTEROIDAL (HETERO) CYCLICALLY SUBSTITUTED ACYLANILIDES WITH MIXED GESTAGEN AND ANDROGEN ACTIVITY AND PROCESSES FOR THEIR PRODUCTION ]22[ ]31[ ]51[ 02.06.1998 197 23 722.3 ]32[ 30.05.1997 ]33[ DE Int. Cl.8 A61K 031/16, 031/365, 031/38, 031/41, 031/50, 031/535, A61P 005/26, 005/34, C07C 235/26, C07D 237/32, 249/18, 265/02, 271/12, 285/10, 307/00, 307/88, 311/76, 333/72 SCHERING AKTIENGESELLSCHAFT, GERMANY WO/1998/054159 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]71[ ]87[ ]74[ [57] Compounds of the formula where R1 and R2 are the same or different and are each a hydrogen atom, a C1-C5alkyl group or a halogen atom, or else, together with the carbon atom of the chain, are a ring having a total of 3-7 members, R3 is a C1-C5-alkyl group or a partly or fully fluorinated C1-C5-alkyl group, A is a mono- or bicyclic, carbocyclic or heterocyclic, aromatic ring which is optionally substituted by one or more radicals selected from halogen atoms, C1C5-alkyl groups, C2-C5-alkenyl groups, CR5=CR6R7 where R5, R6 and R7 are the same or different and are each independently hydrogen atoms or C1-C5alkyl groups, hydroxyl groups, hydroxyl July 24, 2007– ט' באב התשס"ז groups which bear a C1-C10-acyl group, a C3-C10-carbalkoxyalkyl group, a C2-C5cyanoalkyl group, a C3-C10 unsubstituted or substituted allyl group, a C3-C10 unsubstituted or substituted propargyl group, a C2-C5-alkoxyalkyl group or a C1C5-alkyl group substituted fully or partly by fluorine atoms, or is selected from the cyano or nitro group, C1-C5-alkoxy groups, C1-C5-alkylthio groups, mono- or disubstituted C1-C10 amino groups or partly or fully fluorinated C1-C5-alkyl groups, B is a carbonyl or a CH2 group and Ar is a ring system selected from the group of the subformulae 1914 where the X3a, X4, X6, X7 radicals (in the subformula 2), the X4, X6, X7 radicals (in the subformulae 3 and 4), the X3a, X3b, X4, X6, X7 radicals (in the subformulae 5, 6 and 7) or the Y4, Y5, Y7, Y8 radicals (in the subformulae 8, 9, 10 and 11) are the same or different and are selected from hydrogen atoms, C1-C5-alkyl groups which may additionally contain a hydroxyl group optionally etherified with a C1-C5-alkyl group or esterified with a C1-C5-alkanoyl group, partly or fully fluorinated C1-C5alkyl groups, C2-C5-alkenyl groups, CR5=CR6R7 where R5, R6 and R7 are each as defined above, alkynyl groups -C≡CR5 where R5 is as defined above, the X3a and X3b radicals, together with the carbon atoms of the benzofused ring system 5, 6 or 7, may also form a ring having a total of 3-7 members, and additionally the X4, X6, X7 radicals (in the subformulae 2, 3, 4, 5, 6 and 7) or the Y4, Y5, Y7, Y8 radicals (in the subformulae 8, 9, 10 and 11) are selected from halogen atoms, hydroxyl groups, C1-C5-alkoxy groups or C1-C5-alkanoyl groups, and also, in the case that B is a CH2 group, the physiologically tolerated salts of the compounds of the general formula I with acids. ________ 1915 July 24, 2007– ט' באב התשס"ז ]11[]21[ 133686 ,אנלוגים של גליקופרוטאין הורמונים הכנתם והשימוש בהם ]54[ GLYCOPROTEIN HORMONE ANALOGS, THEIR PREPARATION AND THEIR USE ]22[ ]31[ ]51[ ]71[ 25.06.1998 60/050784 ]32[ 25.06.1997 ]33[ US Int. Cl.8 A61K 038/22, 038/24, C07K 014/575, 014/59, C12N 015/16 APPLIED RESEARCH SYSTEMS ARS HOLDING N.V., NETHERLANDS ANTILLES WO/1998/058957 INTERPHARM LABORATORIES ,אינטרפארם מעבדות בע"מ LTD., , פארק לתעשיות עתירות ידע,קרית ויצמן KIRYAT WEIZMANN ציונה-נס NES ZIONA 76110 ]87[ ]74[ [57] An analog of glycoprotein hormone, wherein said glycoprotein hormone is selected from the group consisting of human chronic gonadotropin (hCG), human luteinizing hormone (hLH), human folicile stimulating hormone (hFSH), human thyroid stimulating hormone (hTSH) and functional muteins thereof, wherein functional muteins are modified forms of the glycoprotein hormones, wherein the modifications do not create inter-subunit disulphide bonds, and wherein at least 80% of the functional biological activity of the original hormone is retained, having an α- subunit and a β- subunit, wherein the amino acid sequences of said glycoprotein hormone subunit are modified so as to create an intersubunit disulfide bond between an α- subunit cysteine and a β-subunit cysteine, which cysteines are disposed within two residues of native cysteine residue positions of said glycoprotein hormone and not outside of the outermost cysteine units of the corresponding native subunit, for improved stability, said analog retaining at least 25% of the affinity of the corresponding hormone for its native glycoprotein hormone receptor. __________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 133799 1916 מקדימים עצבים מגבילי גדילה ]54[ LINEAGE-RESTRICTED NEURONAL PRECURSORS ]22[ ]31[ 03.07.1998 08/909435 ]32[ 04.07.1997 ]33[ US 09/109858 02.07.1998 US Int. Cl.8 A61K 048/00, C12N 005/06, 005/08 UNIVERSITY OF UTAH RESEARCH FOUNDATION, U.S.A. WO/1999/001159 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]51[ ]71[ ]87[ ]74[ [57] A method of isolating a pure population of mammalian CNS neuronrestricted precursor cells comprising the steps of: (a) isolating a population of mammalian multipotent CNS stem cells capable of generating both neurons and glia; (b) incubating the multipotent CNS stem cells in a medium configured for inducing said cells to begin differentiating; (c) removing A2B5 + cells from the differentiating cells via specific antibody capture with an antibody that specifically recognizes A2B5; (d) purifying from the differentiating cells a subpopulation of cells expressing embryonic neural cell adhesion molecule; and (e) incubating the purified subpopulation of cells in a medium configured for supporting adherent growth thereof, wherein the cells are derived from (i) spinal cords of approximately 13.5 day embryos of rats or equivalent embryonic stages of other mammals, or (ii) cells equivalent to (i) developed by proliferation and differentiation from early embryonic spinal cord tissue or embryonic stem cells, and wherein the isolated cells are capable of self-renewal in the presence of FGF. _________ ]11[]21[ 1917 134371 July 24, 2007– ט' באב התשס"ז ]54[ תכשיר לבקרת ריבוי ומוות של תאים COMPOSITION FOR REGULATING CELL PROLIFERATION AND CELL DEATH ]22[ ]31[ 05.08.1998 60/054777 ]32[ 05.08.1997 ]33[ US 60/075067 18.02.1998 US 60/075111 18.02.1998 US 60/086317 21.05.1998 US ]51[ Int. Cl.8 A61K 048/00, C12N 015/19, 015/31 ]71[ BIONICHE LIFE SCIENCES INC., CANADA ]87[ WO/1999/007383 ]74[ EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688, HERZLIYA 46733 [57] A composition comprising: (b) a pharmaceutically acceptable carrier, (a) Mycobacterium phlei-DNA (M-DNA), wherein the M-DNA has anti-cancer and activity. The applications for division from this application have not yet been published ,180924 בקשות חלוקה מבקשה זו .שטרם פורסמו ____________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 134494 1918 –13 תהליכים להכנת נגזרות דאוקסיאנטראציקלין ותכשירים רפואיים המכילים אותן ]54[ PROCESSES FOR PREPARING 13DEOXYANTHRACYCLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ]22[ ]31[ ]51[ ]71[ 13.08.1998 08/910218 ]32[ 13.08.1997 ]33[ US Int. Cl.8 A61K 031/704, A61P 035/00, C07H 015/252, C12P 019/56 GEM PHARMACEUTICALS, INC., U.S.A. WO/1999/008687 EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688, HERZLIYA 46733 ]87[ ]74[ [57] A pharmaceutical composition for treating a mammalian host in need of an anticancer treatment, comprising an effective anticancer amount without limitation on total cumulative dosage of at least one compound of the formula wherein R1 is H or OH: R2 is H, OH, or OMe; R3 is H or OH: R4 is H or OH: and R5 is a carbohydrate or substituted carbohydrate, and wherein the total cumulative dosage is at least 825 mg/m2. __________ ]11[]21[ 1919 134926 July 24, 2007– ט' באב התשס"ז ]54[ VACUUM PLASMA PROCESSOR HAVING COIL WITH ADDED CONDUCTING SEGMENTS TO ITS PERIPHERAL PART ]22[ ]31[ ]51[ ]71[ 16.09.1998 08/931504 ]32[ 16.09.1997 Int. Cl.8 H01J 037/00 LAM RESEARCH CORPORATION, U.S.A. WO/1999/014784 WOLFF, BREGMAN AND GOLLER, 19B KEREN HAYESOD ST., P.O.B. 1352, JERUSALEM 91013 ]87[ ]74[ [57] A vacuum plasma processor for treating a workpiece with a plasma comprising a vacuum chamber where the workpiece is adapted to be located, the chamber having an inlet for introducing into the chamber a gas which can be converted into the plasma for treating the workpiece, a coil (100) positioned to couple an RF field to the gas for exciting the gas to the plasma state, the RF field derived from a main part of the coil interacting with an electromagnetic shield, the electromagnetic shield substantially confining the coil RF field to structure associated with the processor and interacting with the RF field derived from the main coil part in such a manner as to tend to reduce (a) the RF field derived from the main coil part in a part of the July 24, 2007– ט' באב התשס"ז מעבד פלסמה בואקום בעל סליל עם קטעים מוליכים שהוספו להיקפו ]33[ US , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד plasma generally aligned with a peripheral portion of the main coil part and (b) plasma flux density in the part of the plasma generally aligned with the main coil part peripheral portion relative to flux density of a portion of the plasma generally inside the part of the plasma generally aligned with the main coil part peripheral portion, the main coil part peripheral portion including an additional coil structure (161-168) for supplying an additional amount of RF field to the portion of the plasma generally aligned with the main coil part peripheral portion, the additional amount of RF field supplied increasing the plasma flux density in the part of the plasma generally aligned with the main coil part peripheral portion. 1920 _________ ]11[]21[ 135520 -8-בנז(ו)איל-8-מותמרות-N תולדות ,מטאנמין-3- ]אוקטן1.2.3[ אזאביציקלו ותכשירים פרמצבטיים המכילים אותן ]54[ N-SUBSTITUTED 8-BENZ(O)YL-8AZABICYCLO [3.2.1.] OCTANE-3METHANAMINE DERIVATIVES, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ]22[ ]31[ 07.10.1998 97/12580 ]32[ 09.10.1997 ]33[ FR 97/12583 09.10.1997 FR Int. Cl.8 A61K 031/46, A61P 025/00, C07D 451/02 SANOFI AVENTIS, FRANCE WO/1999/019325 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]51[ ]71[ ]87[ ]74[ [57] Compound in the form of a pure geometrical isomer or a mixture of such isomers of the formula 1921 July 24, 2007– ט' באב התשס"ז in which U represents (A) either a 2, 3dihydro-1H-inden-2-yl group of the formula or (B) a heterocylic group of the formula in which V represents a hydrogen or halogen atom, a (C1-C3) alkyl group or one or two (C1-C3) alkoxy groups, W and X each represent, respectively, either two oxygen atoms, or an oxygen atom and a CH2 group, or a CH2 group and an oxygen atom, or an oxygen atom and a CO group, n represents the number 0 or 1, R represents either a propyl group when U represents a 2,3-dihydro-1H-inden-2-yl group of general formula (A) or a hydrogen atom or a (C1-C3) alkyl group when U represents a heterocyclic group of general formula (B), Y represents one or more atoms or groups chosen from the following: hydrogen, halogen, (C1-C3) alkyl and (C1-C3) alkoxy, and Z represents two hydrogen atoms or an oxygen atom. __________ ]11[]21[ 136544 תרבות אנושית של נוגדני עכבר ]54[ HUMANIZATION OF MURINE ANTIBODY ]22[ ]31[ ]51[ ]71[ 04.12.1998 08/986016 ]32[ 05.12.1997 ]33[ US Int. Cl.8 C12P 021/08, C40B 004/01000 THE SCRIPPS RESEARCH INSTITUTE, U.S.A. WO/1999/029888 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]87[ ]74[ July 24, 2007– ט' באב התשס"ז 1922 [57] A method of producing a humanized mouse monoclonal antibody which consists of the steps: (a) constructing a first human antibody heavy or light chain library consisting of antibody heavy chains or antibody light chains in which each chain in the first human antibody light or heavy chain library has three complementarity determining region (CDR) loops in which the complementarity determining region three (CDR3) loop in each light or heavy chain has the amino acid sequence of a corresponding mouse antibody heavy or light chain CDR3 loop and is flanked by unaltered human framework residues; (b) constructing a second human antibody heavy or light chain library consisting of antibody heavy chains or antibody light chains, in which each chain in the second human antibody heavy or light chain library has three complementarity determining region (CDR) loops in which the complementarity determining region three (CDR3) loop in each light or heavy chain has the amino acid sequence of a corresponding mouse antibody heavy or light chain CDR3 loop and is flanked by unaltered human framework residues; wherein the chains of said second human antibody heavy or light chain library are the complementary heavy or light chain of said first human antibody heavy or light chain library chains, such that one library is a light chain library and the other library is a heavy chain library; (c) creating a library of heavy and light chain pairs by combining chains from said first human antibody heavy or light chain library of step (a) with a complementary chain from an antibody which binds a preselected antigen forming a library of heavy and light chain pairs; (d) isolating antigen binding chains of step (a) by selecting from the library of step (c), a heavy and light chain pair which binds to said preselected antigen, isolating from the antigen binding heavy and light chain pair, the antigen binding chains of step (a); (e) creating a humanized pair library by combining isolated antigen binding chains of step (d), with chains of said library of step (b), so that a first isolated chain of step (d), together with a complementary second chain in said library of step (b) combine to form a heavy and light chain humanized pair library; (f) selecting from the humanized pair library of step (e) a humanized heavy and light chain pair that binds to said preselected antigen; and (g) combining two of said selected humanized heavy and light chain pair of step (f) to form a whole antibody; wherein said humanized mouse monoclonal antibody binds the same antigen as the mouse monoclonal antibody. __________ ]11[]21[ 1923 136566 July 24, 2007– ט' באב התשס"ז ]54[ METHOD FOR TRANSFER ALIGNMENT OF AN INERTIAL MEASUREMENT UNIT IN THE PRESENCE OF UNKNOWN AIRCRAFT MEASUREMENTS DELAYS ]22[ ]51[ ]71[ 05.06.2000 Int. Cl.8 F41G 007/36 RAFAEL-ARMAMENT DEVELOPMENT AUTHORITY LTD. JOSEPH BEN-YAAKOV, JACOB REINER DR. MARK FRIEDMAN LTD., MOSHE AVIV TOWER, 54TH FLOOR 7 JABOTINSKY STREET 52520 RAMAT GAN ]72[ ]74[ [57] A method for velocity match transfer alignment between a carrier vehicle and a carried vehicle comprised of: (a) repeatedly measuring a velocity difference between the carrier vehicle and the carried vehicle; (b) subsequent to each said measurement, updating a state vector that include a predicted value of said velocity difference; (c) between said measurements, propagating said state vector forward in time; and (d) moving the carrier vehicle and the carried vehicle along a trajectory that July 24, 2007– ט' באב התשס"ז שיטה לכיוונון של יחידת מדידה אינרציאלית בנוכחות עיכובי מדידות מטוסים בלתי ידועים ,רשות לפיתוח אמצעי לחימה בע"מ-רפא"ל חיפה יעקב ריינר,יוסף בן יעקב ,ד"ר מרק פרידמן בע"מ ,77 ז'בוטינסקי54 קומה,מגדל משה אביב גן-רמת includes a first segment, a second segment and a third segment, said moving along said first segment being effected at a first substantially constant velocity, said moving along second segment including an acceleration, said moving along said third segment being effected at a second substantially constant velocity different from said first velocity, said measuring, said updating, and said propagating being effected during said moving along said first and third segments, only said propagating being effected while moving along said second segment. 1924 __________ ]11[]21[ 136767 שימוש באוריאות פניליות והטרוציקליות RAF מותמרות ליצור תרופות לעיכוב קינאז ומספר תרכובות חדשות כאלה ]54[ USE OF SUBSTITUED PHENYL AND HETEROCYCLIC UREAS FOR THE MANUFACTURE OF MEDICAMENTS FOR THE INHIBITION OF RAF KINASE AND SOME SUCH NEW COMPOUNDS ]22[ ]31[ ]51[ 22.12.1998 08/996343 ]32[ 22.12.1997 ]33[ US Int. Cl.8 A61K 031/33, A61P 035/00, C07D 231/38, 257/06, 261/14, 263/38, 271/10, 277/38, 285/12, 307/66, 333/36, 401/12, 403/12, 409/12, 413/12, 417/12 BAYER PHARMACEUTICALS CORPORATION, U.S.A. WO/1999/032106 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]71[ ]87[ ]74[ [57] Use of a compound of the formula 1925 July 24, 2007– ט' באב התשס"ז wherein B is phenyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, naphthyl, quinolinyl, isoquinolinyl, phthalimidinyl, furyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, benzofuryl, benzothienyl, indolyl, benzopyrazolyl, benzoxazolyl, benzisoxazolyl, benzothiazolyl or benzisothiazolyl, substituted by one or more substituents independently selected from the group consisting of halogen, up to per-halosubstitution, and Xn, wherein n is 0-3 and each X is independently selected from the group consisting of –CN, -CO2R5, -C(O)NR5R5', -C(O)R5, -NO2, -OR5, -SR5, -NR5R5'-NR5C(O)OR5', -NR5C(O)R5', C1C10 alkyl, C2-C10 alkenyl, C1-C10 alkoxy, C3-C10 cycloalkyl, C6-C14 aryl, C3-C13 heteroaryl, up to per halo-substituted C1C10 alkyl, up to per halo-substituted C2-C10 alkenyl, up to per halo-substituted C1-C10 alkoxy, up to per halo-substituted C3-C10 cycloalkyl and –Y-Ar; wherein R5 and R5' are independently selected from H, C1-C10 alkyl, C2-C10 alkenyl, C3-C10 cycloalkyl, up to perhalosubstituted C1-C10 alkyl, up to per- halosubstituted C2-C10 alkenyl and up to per-halosubstituted C3-C10 cycloalkyl, wherein Y is –O-, -S-, -N(R5)-, -(CH2)m-, C(O)-, -CH(OH)-, (CH2)mO-, NR5C(O)NR5 NR5'-, NR5C(O)-, C(O)NR5-, (CH2)mS-, -(CH2)mN(R5)-, O(CH2)m-, -CHXa, -CXa2-, -S-(CH2)m- and –N(R5)(CH2)m-, m=1-3, and Xa is halogen; and Ar is a 5-10 member aromatic structure containing 0-4 members of the group consiting of nitrogen, oxygen and sulfur optionally substituted by halogen up to per-halosubstitution and optionally substituted by Zn1, wherein n1 is 0 to 3 and each Z is independently selected from the group consisting of –CN, =O, -CO2R5, C(O)NR5R5', -C(O)-NR5, -NO2, -OR5, SR5, -NR5R5', -NR5C(O)OR5', -C(O)R5, NR5C(O)R5', -SO2R5, SO2NR5R5', C1-C10 alkyl, C1-C10 alkoxy, C3-C10 cycloalkyl, up to per halo-substituted C1-C10 alkyl; and up to per halo substituted C3-C10 cycloalkyl, and A is a heteroaryl moiety selected from the group consisting of wherein R1 is selected from the group consisting of halogen, C3-C10 alkyl, C3-C10 cycloalkyl, C1-C13 heteroaryl, C6-C14 aryl, C7-24 alkaryl, up to per-halosubstituted C1C10 alkyl, up to per-halosubstituted C3-C10 cycloalkyl, up to per-halosubstituted C1- C13 heteroaryl, up to per-halosubstitued C6-14 aryl, and up to per-halosubstituted C714 alkaryl; R2 is selected from the group consisting of H, -C(O)R4, -C(O)NR3R3', C1-C10 alkyl, C3-C10 cycloalkyl, C7-C24 alkaryl, C4-C23 July 24, 2007– ט' באב התשס"ז 1926 alkheteroaryl, substituted C1-C10 alkyl, substituted C3-C10 cycloalkyl, substituted C7-C24 alkaryl and substituted C4-C23 alkheteroaryl, where if R2 is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of –CN, -CO2R4, -C(O)-NR3R3', -NO2, -OR4, -SR4, and halogen up to perhalosubstitution, wherein R3 and R3' are independently selected from the group consisting of H, -OR4, -SR4, -NR4R4', C(O)R4, -CO2R4, -C(O)NR4R4', C1-C10 alkyl, C3-C10 cycloalkyl, C6-C14 aryl, C3C13 heteroaryl up to per halosubstituted C1C10 alkyl, up to per-halosubstituted C3-C10 cycloalkyl, and up to per-halosubstituted, C6-C14 aryl or C3-C13 heteroaryl; and wherein R4 and R4' are independently selected from the group consisting of H, C1-C10 alkyl, C3-C10 cycloalkyl, C6-C14 aryl, C3-C13 heteroaryl, up to perhalosubstituted C1-C10 alkyl, up to perhalosubstituted C3-C10 cycloalkyl, and up to per-halosubstituted, C6-C14 aryl or C3C13 heteroaryl, Ra is C1-C10 alkyl, C3-C10 cycloalkyl, up to per-halosubstituted C1-C10 alkyl and up to per-halosubstituted C3-C10 cycloalkyl; and Rb is hydrogen or halogen, Rc is hydrogen, halogen, C1-C10 alkyl, up to per-halosubstituted C1-C10 alkyl or combines with R1 and the ring carbon atoms to which R1 and Rc are bound to form a 5- or 6- membered cycloalkyl, aryl or hetaryl ring with 0-2 members selected from O, N and S; subject to the proviso that where A is B is not wherein n=2-4, for the manufacture of a medicament for the treatment of cancerous cell growth mediated by raf kinase. 1927 Claimed as novel are compounds of the formula July 24, 2007– ט' באב התשס"ז wherein R2 is selected from the group consisting of H, -C(O)R4, -CO2R4, C(O)NR3R3', C1-C10 alkyl, C3-C10 cycloalkyl, substituted C1-C10 alkyl, substituted C3-C10 cycloalkyl, where if R2 is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of –CN, -CO2R4, -C(O)NR3R3', -NO2, -OR4, -SR4, and halogen up to per-halosubstitution, wherein R3 and R3' are independently selected from the group consisting of H, C1-C10 alkyl, C3-C10 cycloalkyl, up to perhalosubstituted C1-C10 alkyl, and up to perhalosubstituted C3-C10 cycloalkyl, and wherein R4 and R4' are independently selected from the group consisting of H, C1-C10 alkyl, C3-C10 cycloalkyl, up to perhalosubstituted C1-C10 alkyl, and up to perhalosubstituted C3-C10 cycloalkyl, wherein R1 is selected from the group consisting of C3-C6 alkyl, C3-C6 cycloalkyl, up to perhalosubstituted C3-C6 alkyl and up to perhalosubstituted C3-C6 cycloalkyl, B is phenyl, pyridinyl, indolinyl, isoquinolinyl, quinolinyl, or naphthyl; substituted by C6-C14 aryl, C3-C13 heteroaryl, or –Y-Ar, wherein the cyclic structures of B are optionally substituted by halogen, up to per halo, and optionally substituted by X1n and wherein n=0-2; each X1 is independently selected from the group of –CN, -CO2R5, -C(O)R5, C(O)NR5R5', -OR5, -NO2, -NR5R5', C1-C10 alkyl, C2-10-alkenyl, C1-C10-alkoxy, C3-C10 cycloalkyl, -SR5, -NR5C(O)OR5', NR5C(O)R5', substituted C1-C10 alkyl, substituted C2-10 alkenyl, substituted C1- July 24, 2007– ט' באב התשס"ז C10-alkoxy, substituted C3-C10 cycloalkyl, wherein if X1 is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of –CN, -CO2R5, -C(O)R5, C(O)NR5R5', -OR5, -SR5, -NR5R5', NO2, NR5C(O)R5', -NR5C(O)OR5' and halogen up to per-halosubstitution; wherein R5 and R5' are independently selected from H, C1-C10 alkyl, C2-10alkenyl, C3-C10 cycloalkyl, C6-C14 aryl, C3C13 heteroaryl, C7-C24 alkaryl, C4-C23 alkheteroaryl, up to per-halosubstituted C1C10 alkyl; up to per-halosubstituted C2-10alkenyl, and up to per-halosubstituted C3C10 cycloalkyl, wherein Y is –O-, -S-, N(R5)-, -(CH2)-m, -C(O)-, -CH(OH)-, (CH2)mO-, -NR5C(O)NR5R5'-, -NR5C(O)-, -C(O)NR5-, -(CH2)mS-, (CH2)mN(R5)-, O(CH2)m-, -CHXa, -CXa2-, -S-(CH2)m- and –N(R5)(CH2)m-, m=1-3, and Xa is halogen; and Ar is a 5-10 member aromatic structure containing 0-4 members of the group consisting of nitrogen, oxygen and sulfur which is optionally substituted by halogen up to per-halo and optionally substituted by Znl, wherein nl is 0 to 3 and each Z is independently selected from the group consisting of –CN, -CO2R5, =O, C(O)NR5R5', -C(O)R5, -NO2, -OR5, -SR5, NR5R5', -NR5C(O)OR5', NR5C(O)R5', SO2R5, -SO2R5 R5' C1-C10 alkyl, C1-C10 alkoxy, C3-C10 cycloalkyl, substituted C1C10 alkyl, and substituted C3-C10 cycloalkyl, wherein if Z is a substituted group, it is substituted by one or more substituents independently selected from 1928 the group consisting of –CN, -CO2R5, C(O)NR5R5', =O, -OR5, -SR5, -NO2, NR5R5', -NR5C(O)R5', -NR5C(O)OR5', C1- wherein R1 is selected from the group consisting of C3-C10 alkyl, C3-C10 cycloalkyl, up to per-halosubstituted C3C10 alkyl and up to per-halosubstituted C3C10 cycloalkyl, B is phenyl, pyridinyl, indolinyl, isoquinolinyl, quinolinyl or naphthyl which is substituted by phenyl, pyridinyl or Y-Ar, wherein the cyclic structures of B are optionally substituted by halogen, up to per-halosubstitution, and optionally substituted by X1n wherein n=0-2; each X1 is independently selected from the group consisting of –CN, -CO2R5, C(O)R5, -C(O)NR5R5', -OR5, -NO2, NR5R5', C1-C10 alkyl, C2-10-alkenyl, C1-10alkoxy, C3-C10 cycloalkyl, and C6-C14 aryl, -SR5, -NR5C(O)OR5', -C3-C10 heteroaryl, substituted C1-C10 alkyl, substituted C2-10alkenyl, substituted C1-10-alkoxy, substituted C3-C10 cycloalkyl, substituted C6-C14 aryl, substituted C3-C13 heteroaryl, and independently selected from the group consisting of –CN, -CO2R5, -C(O)R5, C(O)NR5R5', -OR5, -SR5, -NR5R5', NO2, NR5C(O)R5', -NR5C(O)OR5', NR5C(O)OR5' and halogen up to perhalosubstitution; wherein R5 and R5' are independently selected from H, C1-C10 alkyl, C2-10-alkenyl, C3-C10 cycloalkyl, C6C4 aryl, C3-C13 heteroaryl, C7-C24 alkaryl, 1929 C10 alkyl, C1-C10 alkoxyl, and C3-C10 cycloalkyl; or of the formula C4-C23 alkheteroaryl, up to perhalosubstituted C1-C10 cycloalkyl wherein Y is –O-, -S-, -N(R5)-, -(CH2)-m, -C(O)-, CH(OH)-, (CH2)mO-, -NR5C(O)OR5', NR5C(O)-, -C(O)NR5-, -(CH2)mS-, (CH2)mN(R5)-, -O(CH2)m-, -CHXa, -CXa2-, -S-(CH2)m- and –N(R5)(CH2)m-, m = 1-3, and Xa is halogen; and Ar is a 5-10 member aromatic structure containing 0-4 members of the group consisting of nitrogen, oxygen and sulfur which is unsubstituted or substituted by halogen up to per-halo and optionally substituted by Zn1, wherein n1 is 0 to 3 and each Z is independently selected from the group consisting of CN, -CO2R5, -C(O)R5, =O, -C(O)NR5R5', -C(O)R5, -NO2, -OR5, SR5, -NR5R5', -NR5C(O)OR5', NR5C(O)R5', -SO2R5, -SO2R5R5', C1-C10 alkyl, C1-C10 alkoxy, C3-C10 cycloalkyl, substituted C1-C10 alkyl, and substituted C3-C10 cycloalkyl, wherein if Z is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of CN, -CO2R5, -C(O)R5, =O, -OR5, -SR5, -NO2, NR5R5', -NR5C(O)R5', -NR5C(O)OR5', C1C10 alkyl, C1-C10 alkoxy, and C3-C10 cycloalkyl, subject to the proviso that where R1 is t-butyl, B is not July 24, 2007– ט' באב התשס"ז wherein R6 is –NHC(O)-O-t-butyl, -O-npentyl, -O-n-butyl, -O-propyl-, C(O)NH- (CH3)2, -OCH2CH(CH3)2, or or of the formula wherein R1 is selected from the group consisting of C3-C10 alkyl, C3-C10 cycloalkyl, up to per-halosubstituted C3C10 alkyl and up to per-halosubstituted C3C10 cycloalkyl, Rb is hydrogen or halogen and B is phenyl, pyridinyl, indolinyl, isoquinolinyl, quinolinyl, or naphthyl substituted by phenyl, pyridinyl or –Y-Ar, wherein the cyclic structures of B are optionally substituted by halogen, up to per halo, and optionally substituted by X1n and wherein n=0-2; each X1 is independently selected from the group consisting of CN, -OR5, -NR5R5', C1-C10 alkyl; -CO2R5, -C(O)NR5R5', -C(O)R5, -NO2, SR5, -NR5C(O)OR5', -NR5C(O)R5', C3-C10 cycloalkyl, substituted C1-C10 alkyl, substituted C2-C10-alkenyl, substituted C1C10-alkoxy, and substituted C3-C10 cycloalkyl, wherein if X1 is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of –CN, -CO2R5, C(O)R5, -C(O)NR5R5', -OR5, -NR5R5', NO2, -NR5C(O)R5', -NR5C(O)OR5' and halogen up to per-halo substitution; July 24, 2007– ט' באב התשס"ז wherein R5 and R5' are independently selected from H, C1-C10 alkyl, C2-10alkenyl, C3-C10 cycloalkyl, up to perhalosubstituted C1-C10 alkyl, up to perhalosubstituted C2-10-alkenyl, and up to per-halosubstituted C3-C10 cycloalkyl, wherein Y is –O-, -S-, -N(R5)-, -(CH2)m-, C(O)-, -CH(OH)-, -(CH2)mO-, -CHXa, CXa2-, -S-(CH2)m- and –N(R5)(CH2)m-, m = 1-3, and Xa is halogen; and Ar is a 5-10 member aromatic structure containing 0-4 members of the group consisting of nitrogen, oxygen and sulfur which is unsubstituted or substituted by halogen up to per-halosubstitution and optionally substituted by Zn1, wherein n1 is 0 to 3 and each Z is independently selected from the group consiting of –CN, -CO2R5, -C(O)R5, =O, -C(O)NR5R5', -C(O)-, NR5, NO2, -OR5, -SR5, -NR5R5', -NR5C(O)OR5', -NR5C(O)R5', -SO2R5, -SO2R5R5', C1-C10 alkyl, C1-C10 alkoxy, C3-C10 cycloalkyl, substituted C1-C10 alkyl, and substituted C3-C10 cycloalkyl, wherein if Z is a substituted group, it is substituted by the one or more substituents independently selected from the group consisting of –CN, -CO2R5, -C(O)NR5R5', =O, -OR5, -SR5, - 1930 NO2, -NR5R5', -NR5C(O)R5', NR5C(O)OR5', C1-C10 alkyl, C1-C10 alkoxyl, and C3-C10 cycloalkyl, subject to the proviso that where R1 is t-butyl and Rb is H, B is not of the formula or a compound of the formula wherein Ra is C1-C10 alkyl, C3-C10 cycloalkyl, up to per-halosubstituted, C1C10 alkyl and up to per-halosubstituted C3C10 cycloalkyl; and B is phenyl, pyridinyl, indolinyl, isoquinolinyl, quinolinyl, or naphthyl; substituted by phenyl, pyridinyl or –Y-Ar; wherein the cyclic structures of B are optionally substituted by halogen, up to per halo, and optionally substituted by X1n wherein n=0-2, each X1 is independently selected from the group consisting of –CN, -NO2, -OR5 and C1-C10 alkyl, -SR5, -CO2R5, -C(O)R5, C(O)NR5R5', -NR5C(O)OR5', -NR5C(O)R5', -C3-C10 cycloalkyl, substituted C1-C10 alkyl, substituted C2C10-alkenyl, substituted C1-C10-alkoxy, and substituted C3-C10 cycloalkyl, wherein if X1 is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of –CN, -CO2R5, -C(O)R5, -C(O)NR5R5', -OR5 – SR5, -NR5R5', -NO2, NR5C(O)R5', NR5C(O)OR5' and halogen up to perhalosubstitution; wherein R5 and R5' are independently selected from H, C1-C10 alkyl, -C2-C10alkenyl, C3-C10 cycloalkyl, up to perhalosubstituted C1-C10 alkyl, up to per- 1931 halosubstituted C2-C10-alkenyl, and up to per-halosubstituted C3-C10 cycloalkyl wherein Y is –O-, -S-, -N(R5)-, -(CH2)m-, C(O)-, -CH(OH)-, -(CH2)mO-, NR5C(O)NR5R5'-, -NR5C(O)-, -C(O)NR5-, -(CH2)mS-, -(CH2)mN(R5)-, -O(CH2)m-, CHXa, -CXa2-, -S-(CH2)m- and N(R5)(CH2)m-, m=1-3, and Xa is halogen; and Ar is a 5-10 aromatic structure containing 0-4 members of the group consisting of nitrogen, oxygen and sulfur which is unsubstituted or substituted by halogen up to per-halo and optionally substituted by Zn1, wherein n1 is 0 to 3 and each Z is independently selected from the group consisting of –CN, -CO2R5, C(O)R5, =O, -C(O)NR5R5', -C(O)R5, -NO2, -OR5, -SR5, -NR5R5', -NR5C(O)OR5', NR5C(O)R5', -SO2R5, -SO2R5R5', C1-C10 alkyl, C1-C10 alkoxy, C3-C10 cycloalkyl, substituted C1-C10 alkyl, substituted C3-C10 cycloalkyl, wherein if Z is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of –CN, -CO2R5, C(O)NR5R5', =O, -OR5, -SR5, -SR5, -NO2, NR5R5', -NR5C(O)R5' and –NR5C(O)OR5', C1-C10 alkyl, C1-C10 alkoxyl, and C3-C10 cycloalkyl; or of the formula July 24, 2007– ט' באב התשס"ז R1 is selected from the group consisting of halogen, C3-C10 alkyl, C3-13-heteroaryl, C614 aryl, C7-24-alkaryl, C3-C10 cycloalkyl, up to per-halosubstituted C1-C10 alkyl, up to per-halosubstituted C3-C10 cycloalkyl, up to per-halosubstituted C1-13-heteroaryl, up to per-halosubstituted C6-14-aryl, and up to per-halosubstituted C7-24-alkaryl; B is phenyl, pyridinyl, indolinyl, isoquinolinyl, quinolinyl, or naphthyl substituted by phenyl, pyridinyl or –Y-Ar, wherein the cyclic structures of B are optionally substituted by halogen, up to per halo, and optionally substituted by X1n, wherein n = 0-2 each X1 is independently selected from the group consisting of –CN, -OR5, -NR5R5', C1-C10 alkyl; -CO2R5, C(O)NR5R5', -C(O)R5, =O, -NO2, -SR5, NR5C(O)OR5', -NR5C(O)R5', C3-C10 cycloalkyl, substituted C2-10-alkenyl, substituted C1-10-alkoxy, substituted C3-C10 cycloalkyl, wherein if X1 is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of –CN, -CO2R5, C(O)R5, -C(O)NR5R5', -OR5, -NR5R5', NO2, -NR5C(O)R5', -NR5C(O)OR5' and halogen up to per-halo substitution; wherein R5 and R5' are independently selected from H, C1-C10 alkyl, C2-10alkenyl, C3-C10 cycloalkyl, up to per- July 24, 2007– ט' באב התשס"ז halosubstituted C1-C10 alkyl, up to perhalosubstituted C2-10-alkenyl, and up to per-halosubstituted C3-C10 cycloalkyl, wherein Y is –O-, -S-, -N(R5)-, -(CH2)m-, C(O)-, -CH(OH)-, -(CH2)mO-, NR5C(O)NR5R5'-, -NR5C(O)-, -C(O)NR5-, -(CH2)mS-, -(CH2)mN(R5)-, -O(CH2)m-, CHXa, -CXa2-, -S-(CH2)m- and – N(R5)(CH2)m-, m=1-3, and Xa is halogen; and Ar is a 5-10 member aromatic structure containing 0-4 members of the group consisting of nitrogen, oxygen and sulfur which is unsubstituted or substituted by halogen up to per-halosubstitution and optionally substituted by Zn1, wherein n1 is 0 to 3 and each Z is independently selected from the group consisting of –CN, -CO2R5, =O, -C(O)R5, -C(O)NR5R5', -C(O)-, NR5, NO2, -OR5, -SR5, -NR5R5', -NR5C(O)OR5', -NR5C(O)R5', -SO2R5, -SO2R5R5', C1-C10 alkyl, C1-C10 alkoxy, C3-C10 cycloalkyl, substituted C1-C10 alkyl, substituted C3-C10 cycloalkyl, wherein if Z is a substituted group, it is substituted by the one or more substituents independently selected from the group consisting of –CN, -CO2R5, C(O)NR5R5', =O, -OR5, -SR5, -NO2, NR5R5', -NR5C(O)R5', -NR5C(O)OR5', C1C10 alkyl, C1-C10 alkoxyl and C3-C10 cycloalkyl; or of the formula 1932 wherein R1 is selected from the group consisting of C3-C10 alkyl, C3-C10 cycloalkyl, up to per-halosubstituted C3C10 alkyl and up to per-halosubstituted C3C0 cycloalkyl, Rb is hydrogen or halogen, and wherein B is phenyl, pyridinyl, indolinyl, isoquinolinyl, quinolinyl, or naphthyl substituted by phenyl, pyridinyl or –Y-Ar, wherein the cyclic structures of B are optionally substituted by halogen, up to per halo, and optionally substituted by X1n, n=0-3 and each X1 is independently selected from the group consisting of –CN, -CO2R5, -C(O)NR5R5', -C(O)R5, -NO2, OR5, -SR5, -NR5R5' –NR5C(O)OR5', NR5C(O)R5', C1-C10 alkyl, C2-C10-alkenyl, substituted C1-C10-alkoxy, and substituted C3-C10 cycloalkyl, wherein if X1 is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of –CN, -CO2R5, -C(O)R5, C(O)NR5R5', -OR5, -SR5, -NR5R5', -NO2, NR5C(O)R5', -NR5C(O)OR5' and halogen up to per-halosubstitution; wherein R5 and R5' are independently selected from H, C1-C10 alkyl, C2-10alkenyl, C3-C10 cycloalkyl, up to perhalosubstituted C1-C10 alkyl, up to per- halosubstituted C2-10-alkenyl, and up to per-halosubstituted C3-C10 cycloalkyl, wherein Y is –O-, -S-, -N(R5)-, -(CH2)m-, C(O)-, -CH(OH)-, -(CH2)mO-, NR5C(O)NR5R5'-, NR5C(O)-, -C(O)NR5-, (CH2)mS-, -(CH2)mN(R5)-, -O(CH2)m-, CHXa, -CXa2-, -S-(CH2)m- and – N(R5)(CH2)m-, m = 1-3 and Xa is halogen; and Ar is a 5-10 member aromatic structure containing 0-4 members of the group consisting of nitrogen, oxygen and sulfur which is unsubstituted or substituted by halogen up to per-halo and optionally substituted by Zn1, wherein n1 is 0 to 3 and each Z is independently selected from the group consisting of –CN, -CO2R5, C(O)R5, =O, -C(O)NR5R5', -C(O)R5, -NO2, -OR5, -SR5, -NR5R5', -NR5C(O)OR5', NR5C(O)R5', -SO2R5, -SO2 R5R5', C1-C10 alkyl, C3-C10 cycloalkyl, substituted C1-C10 alkyl, substituted C3-C10 cycloalkyl, wherein if Z is a substituted group, it is substituted by one or more substituents independently selected from the group consisting of –CN, -CO2R5, -C(O)NR5R5', =O, -OR5, -SR5, -NO2, -NR5R5', NR5C(O)R5', -NR5C(O)OR5', C1-C10 alkyl, C1-C10 alkoxyl, and C3-C10 cycloalkyl. __________ ]11[]21[ 1933 136855 July 24, 2007– ט' באב התשס"ז IFNAR2/IFN קומפלקס ]54[ IFNAR2/IFN COMPLEX ]22[ ]31[ ]51[ 18.12.1998 60/068295 ]32[ 19.12.1997 ]33[ US Int. Cl.8 A61K 038/19, 038/21, C07K 014/555, 014/715, 019/00, C12N 015/12, 015/62 APPLIED RESEARCH SYSTEMS ARS HOLDING N.V., NETHERLANDS ANTILLES WO/1999/032141 INTERPHARM LABORATORIES ,אינטרפארם מעבדות בע"מ LTD., , פארק לתעשיות עתירות ידע,קרית ויצמן KIRYAT WEIZMANN ציונה-נס NES ZIONA 76110 ]71[ ]87[ ]74[ [57] A complex comprising a Type I interferon (IFN) and a subunit of the human interferon α/β receptor (INFAR) which is capable of binding to the Type I IFN of the complex, wherein said Type I IFN is: (a) a native Type I IFN; (b) a fragment of (a) which has Type I IFN biological activity; (c) a variant of (a) or (b) which has at least 70% sequence identity with (a) or (b) and which has Type I IFN biological activity; (d) a variant of (a) or (b) which is encoded by a DNA sequence which hybridizes to the complement of the native DNA sequence encoding (a) or (b) under moderately stringent conditions and which has Type-I IFN biological activity; or (e) a salt or functional derivative of (a), (b), (c) or (d) which has Type I IFN . biological activity; and wherein said IFNAR is: (f) a native human IFNAR polypeptide chain; (g) a fragment of (f) which has IFNAR biological activity; (h) a variant of (f) or (g) which has at least 70% sequence identity with (f) or (g) and which has IFNAR biological activity; (i) a variant of (f) or (g) which is encoded by a DNA sequence which hybridizes to the complement of the native DNA sequence encoding (f) or (g) under moderately stringent conditions and which has IFNAR biological activity; or (j) a salt or functional derivative of (f), (g), (h), or (i) which has IFNAR biological activity. __________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 137403 1934 – ) – ציסR4,S1( תכשירי רוקחות המכילים – ) – (ציקלופרופילאמינו6 – – אמינו2[– 4 1 – – ציקלופנטן2 – ] – איל9 – – פוריןH9 – מתאנול ]54[ PHARMACEUTICAL COMPOSITIONS COMPRISING (1S,4R) – CIS – 4 – [2 – AMINO – 6 – (CYCLOPROPYLAMINO) – 9H – PURIN – 9 – YL] – 2 – CYCLOPENTENE – 1 – METHANOL ]22[ ]31[ ]51[ ]71[ 04.02.1999 9802472.2 ]32[ 06.02.1998 ]33[ GB Int. Cl.8 A61K 031/52, A61P 031/18, C07D 473/16, C12P 017/18 GLAXO GROUP LIMITED, UNITED KINGDOM WO/1999/039691 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A pharmaceutical composition comprising (1S, 4R)-cis-4-[2-amino-6cyclopropylamino)-9H-purin-9-yl)-2cyclopentene-1-methanol, or a pharmaceutically acceptable derivative thereof, a metal chelator, and at least one sweetening agent selected from the group consisting of sorbitol, saccharin, acesulfame, fructose, sucralose, and aspartame, at a pH range of 2.0 to 4.5. __________ ]11[]21[ ]54[ ERYTHROPOIETIN LIPOSOMAL DISPERSION ]22[ ]31[ ]51[ ]71[ 12.02.1999 98103111.5 ]32[ 23.02.1998 Int. Cl.8 A61K 009/00, 009/127, 038/18 CILAG GMBH INTERNATIONAL, SWITZERLAND WO/1999/042085 DR. SHLOMO COHEN & CO., 124 IBN GABIROL ST., P.O.B. 11490, TEL AVIV 62038 ]87[ ]74[ 137808 פיזור של אריתרופויאטין כלפוזומים ]33[ EP ,'ד"ר שלמה כהן ושות תל אביב,11490 .ד. ת, 124 אבן גבירול [57] A liposome-based parenteral composition comprising: (a) an effective amount of an active ingredient comprising erythropoietin or its pharmaceutically acceptable derivatives 1935 July 24, 2007– ט' באב התשס"ז having the biological properties of causing bone marrow cells to increase production of reticulocytes and red blood cells; (b) a lipidic phase comprising: (i) lecithin or hydrogenated lecithin; (ii) a charged electropositive or electronegative lipid compound and (iii) cholesterol or a derivative thereof selected from cholesterol esters, polyethylene glycol derivatives of cholesterol (PEG-cholesterols), and organic acid derivatives of cholesterols; and (c) a phosphate buffer. __________ ]11[]21[ 138453 תכשירים והרכבים של פפטידים והשימוש בהם ]54[ PEPTIDE COMPOSITIONS AND FORMULATIONS AND USE OF SAME ]22[ ]31[ ]51[ ]71[ 12.03.1999 09/039308 ]32[ 13.03.1998 ]33[ US Int. Cl.8 A61K 038/00, 038/06, 038/07, 038/17, C07K 014/435 CONNECTIVE TISSUE IMAGINEERING LLC, U.S.A. LAWRENCE B SANDBERG, PHILIP J ROOS, THOMAS F MITTS WO/1999/045941 EDWARD LANGER, ,אדוארד לנגר 44-46 MONTEFIORE STREET תל אביב,44-46מונטיפיורי TEL AVIV 65201 ]72[ ]87[ ]74[ [57] A composition useful in treating mammalian tissue, said composition being comprised of a peptide selected from the group consisting of SEQ ID NO:17 (Valine-Valine-Proline-Glutamine), SEQ ID NO:18 (Valine-Alanine-Alanine- Arginine-Proline-Glycine), SEQ ID NO:19 (Leucine-Glycine-Alanine-GlycineGlycine-Alanine-Glycine), and SEQ ID NO: 23 (Valine-Glycine-ValineHydroxyproline-Glycine). __________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 138831 1936 מערכת מידע מופעלת ע"י מבט ]54[ GAZE-ACTUATED INFORMATION SYSTEM ]22[ ]51[ ]71[ 03.10.2000 Int. Cl.8 G01C 021/00 RAFAEL-ARMAMENT DEVELOPMENT AUTHORITY LTD. DR. MARK FRIEDMAN LTD., MOSHE AVIV TOWER, 54TH FLOOR 7 JABOTINSKY STREET 52520 RAMAT GAN ]74[ [57] A method for providing a pilot with information associated with at least one region of a field of view visible to the pilot from within a cockpit without requiring a visual display, the method comprising the steps of: (i) determining an eye gaze direction relative to a given frame of reference for at least one eye of the pilot by: (a) employing a helmet-mounted system to derive direction information related to a relative eye gaze direction for at least one eye of the pilot relative to a helmet worn by the pilot, (b) deriving position information related to a position of said helmet within a cockpit, and ,רפא"ל רשות לפיתוח אמצעי לחימה בע"מ חיפה ,ד"ר מרק פרידמן בע"מ ,77 ז'בוטינסקי54 קומה,מגדל משה אביב גן-רמת (c) processing said direction information and said position information to derive said eye gaze direction relative to a frame of reference associated with said cockpit; (ii) determining a reference direction relative to said given frame of reference; (iii) comparing said eye gaze direction with said reference direction; and (iv) if said eye gaze direction and said reference direction are equal to within a given degree of accuracy, generating audio output audible to the pilot and indicative of information associated with said reference direction. __________ ]11[]21[ 1937 138856 July 24, 2007– ט' באב התשס"ז אקטינסידינים סמי–סינטטיים ותכשירי רוקחות המכילים אותם ]54[ SEMI-SYNTHETIC ECTEINASCIDINS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ]22[ ]31[ ]51[ ]71[ 05.04.1999 60/080802 ]32[ 06.04.1998 ]33[ US Int. Cl.8 A61K 031/4995, 035/00, A61P 035/00, C07D 515/00 THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS, U.S.A. WO/1999/051238 EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688, HERZLIYA 46733 ]87[ ]74[ [57] The compound Et 757, of the formula __________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 138911 1938 תוצר ביניים גיפפטיד בהכנת חומרים הגורמים להפרשה מוגברת של הורמון הגדילה ]54[ DIPEPTIDE INTERMEDIATE COMPOUND IN THE SYNTHESIS OF GROWTH-HORMONE SECRETAGOGUES ]22[ ]31[ ]51[ ]62[ ]71[ ]87[ ]74[ 04.12.1996 60/009469 ]32[ 28.12.1995 ]33[ US Int. Cl.8 A61K 038/05, A61P 005/06, 019/10, C07D 417/04, C07K 005/02, 005/06 DIVISION FROM 124449 PFIZER INC., U.S.A. WO/1997/024369 LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו INDUSTRIAL PARK, OMER, באר שבע,5352 .ד. ת, עומר,גן תעשייה P.O.B. 5352, BEER-SHEVA 84152 [57] Compounds of the formula the racemic-diastereomeric mixtures and optical isomers of said compounds, wherein Z200 is T-BOC, CBZ, CF3C(O)-, FMOC, TROC, trityl, or tosyl; e is 0 or 1; n and w are each independently 0, 1 or 2, provided that w and n cannot both be 0 at the same time; Y is oxygen or sulfur; R1 is hydrogen, -CN, (CH2)qN(X6)C(O)X6, (CH2)qN(X6)C(O)(CH2)t-A1, -(CH2)qN(X6)SO2-(CH2)t-A1, (CH2)qN(X6)SO2X6, (CH2)qN(X6)C(O)N(X6)(CH2)t-A1, -(CH2)qN(X6)C(O)N(X6)(X6), (CH2)qC(O)N(X6)(X6), (CH2)qC(O)N(X6)(CH2)t-A1; -(CH2)qC(O)OX6, -(CH2)qC(O)O(CH2)tA1, -(CH2)qOX6, -(CH2)qOC(O)X6, -(CH2)qOC(O)(CH2)t-A1, (CH2)qOC(O)N(X6)(CH2)t-A1, - 1939 (CH2)qOC(O)N(X6)(X6), -(CH2)qC(O)X6, -(CH2)qC(O)(CH2)t-A1, (CH2)qN(X6)C(O)OX6, -(CH2)qN(X6)SO2N(X6)(X6), (CH2)qS(O)mX6, -(CH2)qS(O)m(CH2)t-A1; -(C1-C10) alkyl, -(CH2)t-A1, -(CH2)q-(C3C7) cycloalkyl, -(CH2)q-Y1-(C1-C6) alkyl, -(CH2)q-Y1-(CH2)t-A1 or -(CH2)q-Y1(CH2)t-(C3-C7) cycloalkyl; where the alkyl and cycloalkyl groups in the definition of R1 are optionally substituted with (C1-C4) alkyl, hydroxyl, (C1-C4) alkyl, hydroxyl, carboxyl, CONH2, -S(O)m(C1-C6) alkyl, -CO2(C1-C4) alkyl ester, 1H-tetrazol-5-yl or 1, 2 or 3 fluoro; Y1 is O, S(O)m, -C(O)NR6-, -CH=CH-, C=C-, -N(X6)C(O)-, -C(O)NX6-, -C(O)O-, -OC(O)N(X6)- or –OC(O)-; q is 0, 1, 2, 3 or 4; t is 0, 1, 2 or 3; July 24, 2007– ט' באב התשס"ז said (CH2)q group and (CH2)t group may each be optionally substituted with hydroxyl, (C1-C4) alkoxy, carboxyl, CONH2, -S(O)m(C1-C6) alkyl, -CO2(C1-C4) alkyl, 1H-tetrazol-5-yl, 1 to 3 fluoro or 1 or 2 (C1-C4) alkyl; R2 is hydrogen (C1-C8) alkyl, -(C0-C3) alkyl-(C3-C8) cycloalkyl, -(C1-C4) alkyl-A1 or A1; where the alkyl groups and the cycloalkyl groups in the definition of R2 are optionally substituted with hydroxyl, C(O)OX6. –C(O)N(X6)(X6), -N(X6)(X6), -S(O)m(C1-C6) alkyl, -C(O)A1, -C(O)(X6), CF3, CN or 1, 2 or 3 halogen; R3 is A1, (C1-C10) alkyl, (C1-C6) alkyl-A1, (C1-C6) alkyl-(C3-C7) cycloalkyl; -(C1-C5) alkyl-X1-(C1-C5) alkyl-(C3-C7) cycloalkyl; where the alkyl groups in the definition of R3 are optionally substituted with S(O)m(C1-C6) alkyl, -C(O)OX3, 1, 2, 3, 4 or 5 halogens, or 1, 2, or 3 OX3; X1 is S(O)m –N(X2)C(O)-, -C(O)N(X2)-, OC(O)-, -C(O)O-, -CX2=CX2-; N(X2)C(O)O-, =OC(O)N(X2)- or –C=C-; R4 is hydrogen, (C1-C6) alkyl or (C3-C7) cycloalkyl, or R4 is taken together with R3 and the carbon atom to which they are attached and form (C5-C7) cycloalkyl, (C5C7) cycloalkenyl, a partially saturated or fully saturated 4- to 8-membered ring having 1 to 4 heteroatoms independently selected from the group consisting of oxygen, sulfur and nitrogen, or is a bicyclic ring system consisting of a partially saturated or fully saturated 5- or 6-membered ring, fused to a partially saturated, fully unsaturated or fully saturated 5- or 6-membered ring, optionally having 1 to 4 heteroatoms independently selected from the group consisting of nitrogen, sulfur and oxygen; X4 is hydrogen or (C1-C6) alkyl or X4 is taken together with R4 and the nitrogen atom to which X4 is attached and the carbon atom to which R4 is attached and form a five to seven membered ring; R6 is a bond or is where a and b are independently 0, 1, 2 or 3; X5 and X5a are each independently selected from the group consisting of hydrogen, trifluoromethyl, A1 and optionally substituted (C1-C6) alkyl; the optionally substituted (C1-C6) alkyl in the definition X5 and X5a is optionally substituted with a substituent selected from the group consisting of A1, -OX2, -S(O)m(C1-C6) alkyl, -C(O)OX2, (C3-C7) cycloalkyl, N(X2)(X2) and –C(O)N(X2)(X2); or the carbon bearing X5 and X5a forms an alkylene bridge with the nitrogen atom bearing Z200 and R8 where the alkylene bridge contains 1 to 5 carbon atoms provided that X5 or X5a but not both may be on the carbon atom and Z200 or R8 but not both may be on the nitrogen atom; or X5 is taken together with X5a and the carbon atom to which they are attached and form a partially saturated or fully saturated 3- to 7-membered ring, or a partially saturated or fully saturated 4- to 8-membered ring having 1 to 4 heteroatoms independently selected from the group consisting of oxygen, sulfur and nitrogen; or X5 is taken together with X5a and the carbon atom to which they are attached and form a bicyclic ring system consisting of a partially saturated or fully saturated 5or 8-membered ring, optionally having 1 or 2 heteroatoms independently July 24, 2007– ט' באב התשס"ז 1940 selected from the group consisting of nitrogen, sulfur and oxygen, fused to a partially saturated, fully saturated or fully unsaturated 5- or 6-membered ring, optionally having 1 to 4 heteroatoms independently selected from the group consisting of nitrogen, sulfur and oxygen; Z1 is bond, O or N-X2, provided that when a and b are both 0 then Z1 is not N-X2 or O-; R8 is hydrogen or optionally substituted (C1-C6) alkyl; where the optionally substituted (C1-C6) alkyl in the definition of R8 is optionally independently substituted with A1, C(O)O-(C1-C6) alkyl, -S(O)m(C1-C6) alkyl, 1 to 5 halogens, 1 to 3 hydroxy, 1 to 3 –OC(O) (C1-C10) alkyl or 1 to 3 (C1-C6) alkoxy; A1 for each occurrence is independently (C5-C7) cycloalkenyl, phenyl or a partially saturated, fully saturated or fully unsaturated 4- to 8-membered ring optionally having 1 to 4 heteroatoms independently selected from the group consisting of oxygen, sulfur and nitrogen, or a bicylic ring system consisting of a partially saturated, fully unsaturated or fully saturated 5- or 6-membered ring, optionally having 1 to 4 heteroatoms independently selected from the group consisting of nitrogen, sulfur and oxygen, fused to a partially saturated, fully saturated or fully unsaturated 5- or 6membered ring, optionally having 1 to 4 heteroatoms independently selected from the group consisting of nitrogen, sulfur and oxygen; A1 for each occurrence is independently optionally substituted, in one or optionally both rings if A1 is a bicyclic ring system, with up to three substituents, each substituent independently selected from the group consisting of F, Cl, Br, I, OCF3, OCF2H, CF3, CH3, OCH3, -OX6, C(O)N(X6)(X6), -C(O)OX6, oxo, (C1-C6) alkyl, nitro, cyano, benzyl, -S(O)m(C1-C6) alkyl, 1H-tetrazol-5-yl, phenyl, phenoxy, 1941 phenylalkyloxy, halophenyl, methylenedioxy, -N(X6)(X6), -N(X6)(X6), N(X6)C(O)(X6), -SO2N(X6)(X6), N(X6)SO2X6, -CONX11X12, -SO2NX11X12, -NX6SO2X12, -NX6CONX11X12, NX6SO2NX11X12, -NX6C(O)X12, imidazolyl, thiazolyl and tetrazolyl, provided that if A1 is optionally substituted with methylenedioxy then it can only be substituted with one methylenedioxy; where X11 is hydrogen or optionally substituted (C1-C6) alkyl; the optionally substituted (C1-C6) alkyl defined for X11 is optionally independently substituted with phenyl, phenoxy, (C1-C6) alkoxycarbonyl, -S(O)m(C1-C6) alkyl, 1 to 5 halogens, 1 to 3 hydroxy, 1 to 3 (C1-C10) alkanoyloxy or 1 to 3 (C1-C6) alkoxy; X12 is hydrogen, (C1-C6) alkyl, phenyl, thiazolyl, imidazolyl, furyl or thienyl, provided that when X12 is not hydrogen, X12 is optionally substituted with one to three substituents independently selected from the group consisting of Cl, F, CH3 OCH3, OFC3 and CF3; or X11 and X12 are taken together to form – (CH2)r-L1-(CH2)r; L1 is C(X2)(X2), O, S(O)m or N(X2); R for each occurrence is independently 1, 2 or 3; X2 for each occurrence is independently hydrogen, optionally substituted (C1-C6) alkyl, or optionally substituted (C3-C7) cycloalkyl, where the optionally substituted (C1-C6) alkyl and optionally substituted (C3-C7) cycloalkyl in the definition of X2 are optionally independently substituted with –S(O)m(C1C6) alkyl, -C(O)OX3, 1 to 5 halogens or 1 to 3 –OX3; X3 for each occurrence is independently hydrogen or (C1-C6) alkyl; X6 for each occurrence is independently hydrogen, optionally substituted (C1-C6) alkyl, (C2-C6) halogenated alkyl, optionally substituted (C3-C7) cycloalkyl, (C3-C7)-halogenated cycloalkyl, where optionally substituted (C1-C6) alkyl and July 24, 2007– ט' באב התשס"ז optionally substituted (C3-C7) cycloalkyl in the definition of X6 is optionally independently substituted with hydroxyl, (C1-C4) alkoxy, carboxyl, CONH2, S(O)m(C1-C6) alkyl, -CO2(C1-C4) alkyl, 1H-tetrazol-5-yl or 1 or 2 (C1-C4) alkyl; or when there are two X6 groups on one atom and both X6 are (C1-C6) alkyl, the two (C1C6) alkyl groups may be optionally joined and, together with the atom to which the two X6 groups are attached, form a 4- to 9membered ring optionally having oxygen, sulfur or NX7; X7 is hydrogen or (C1-C6) alkyl optionally substituted by hydroxyl; and m for each occurrence is independently 0, 1 or 2; with the proviso that: X6 and X12 cannot be hydrogen when it is attached to C(O) or SO2 in the form C(O)X6, C(O)X12, SO2X12; and when R is a bond then L is N(X2) and each r in the definition –(CH2)r-L-(CH2)r- is 2 or 3. __________ ]11[]21[ ]54[ PREPARATIONS FOR THE APPLICATION OF ANTI INFLAMMATORY, ESPECIALLY ANTISEPTIC AGENTS AND/OR AGENTS PROMOTING THE HEALING OF WOUNDS, TO THE UPPER RESPIRATORY TRACT AND/OR THE EAR ]22[ ]31[ ]51[ ]71[ 27.05.1999 60/086895 ]32[ 27.05.1998 Int. Cl.8 A61K 045/00 EURO – CELTIQUE S.A., LUXEMBOURG WO/1999/060998 DR. YITZHAK HESS & PARTNERS, 279 HAYARKON ST., P.O.B. 6451, TEL AVIV 61063 ]87[ ]74[ [57] The use of povidone iodine combined with a liposome preparation, in the manufacture of a pharmaceutical preparation for the prevention or the treatment of infections, the treatment of 139230 ,תכשירים עבור היישום של אנטי– זיהומים במיוחד גורמים מחטאים ו\או גורמים המסייעים לריפוי של פצעים לשטח הנשימתי העליון ו\או האוזן ]33[ US ,ד"ר יצחק הס ושותפיו תל אביב,6451 .ד. ת, 279 רחוב הירקון wounds and/or for functional tissue remodeling and repair, in the ciliary epithelial tissue of the upper respiratory tract and the ear. _________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 139360 1942 כימרות נגיפיות המורכבות מיחידות HIV–1– וCAEV–גנטיוות מ ]54[ VIRAL CHIMERAS COMPRISED OF CAEV AND HIV-1 GENETIC ELEMENTS ]22[ ]31[ 30.04.1999 60/083652 ]32[ 30.04.1998 ]33[ US 09/302171 29.04.1999 US Int. Cl.8 A61K 039/21, A61P 031/18, 037/04, C07K 014/005, 014/15, C12N 007/01, 015/62, 015/867 UNIVERSITY OF SOUTHERN CALIFORNIA, U.S.A. WO/1999/056774 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]51[ ]71[ ]87[ ]74[ [57] A polynucleotide comprising a chimeric retroviral genome (CHIV), wherein the chimeric retroviral genome comprises expression control segments that direct its expression in a mammalian host cell, and wherein the retroviral particle produced by expressing the retroviral genome in a host cell generates an immune response against HIV-1 but is not pathogenic to a primate, characterized in that the chimeric retroviral genome consists of a caprine arthirits encephalitis virus (CAEV) viral genome, wherein the HIV-1 envelope gene has been substituted for the CAEV envelope gene. _________ ]11[]21[ 139612 תרכובות מ–מורקסלה קטרהליס ]54[ COMPOUNDS FROM MORAXELLA CATARRHALIS ]22[ ]31[ ]51[ ]71[ 07.05.1999 9810285.8 ]32[ 13.05.1998 ]33[ GB Int. Cl.8 A61K 039/02, 039/395, C07K 014/195, 016/12, C12N 015/31 SMITHKLINE BEECHAM BIOLOGICALS S.A., BELGIUM WO/1999/058684 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] An isolated polypeptide useful in a vaccine against Moraxella catarrhalis infection comprising an amino acid sequence which has at least 85% identity 1943 July 24, 2007– ט' באב התשס"ז to the amino acid sequence selected from the group consisting of: SEQ ID NO:4 and SEQ ID NO:6 over the entire length of SEQ ID NO:4 or SEQ ID NO:6 respectively. _________ ]11[]21[ ]54[ CONTINUOUS POLYAMIDATION PROCESS ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 26.05.1999 60/087316 ]32[ 29.05.1998 Int. Cl.8 C08G 069/28 SOLUTIA INC., U.S.A. WO/1999/061511 EITAN, MEHULAL, PAPPO, KUGLER, 11 HAMENOFIM ST. HERZLIYA 46120 [57] A process for producing a polyamide from dicarboxylic acid monomer and diamine monomer, comprising: mixing molten dicarboxylic acid monomer and molten diamine monomer in equimolar amounts, thereby producing a molten reaction mixture; flowing the reaction mixture through at least one unvented reaction vessel, the residence time of the reaction mixture in the at least one 139816 תהליך פוליאמידציה מתמשך ]33[ US , קוגלר, פאפו, מהולל,איתן הרצליה,11המנופים unvented reaction vessel being between 0.01 minutes and 30 minutes, thereby forming a first product stream that comprises polyamide and water of polymerization; and flowing the first product stream through at lest one vented vessel, whereby water of polymerization is removed, thereby forming a second product stream that comprises polyamide. ________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 139995 1944 ]54[ SYSTEM AND METHOD FOR SPHERICAL STEREOSCOPIC PHOTOGRAPHING ]22[ ]51[ ]71[ ]74[ 29.11.2000 Int. Cl.8 G03B 035/00 RVC LLC, U.S.A. NAOMI ASSIA & CO. LAW OFFICES, 32 HABARZEL ST. RAMAT HACHAYAL TEL AVIV 69710 מערכת ושיטה לצילום סטריאוסקופי ספירי ,נעמי אסיא ושות' משרד עורכי דין אביב- תל, רמת החייל32 רח' הברזל [57] A photographing system for capturing a full stereoscopic spherical image, or a continuous part thereof, said system comprising a three dimensional array of cameras (5, 5', 5''), positioned at an equal distance from a common center and pointing out from said common centre, such that the lenses of all said cameras are lying on a spherical surface, wherein the collective field of view (11, 12, 13) captured by all said lenses covers the whole visual environment surrounding said photographing system, or a continuous part thereof, and wherein any point in said collective field of view is captured by at least two of said lenses. _________ ]11[]21[ 1945 140141 July 24, 2007– ט' באב התשס"ז העברת קידוד בתקשורת נתונים ]54[ TRANSCODING IN DATA COMMUNICATIONS ]22[ ]31[ ]51[ 07.12.2000 99811158.7 ]32[ 14.12.1999 ]33[ EP Int. Cl.8 G06F 017/00, G06Q 002/000000 H03M 007/00, 007/14, H04L 009/00, 009/32, H04N 007/26 IBM CORPORATION, U.S.A. SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]71[ ]74[ [57] A method of transcoding a data message, comprising a plurality of data fields and an authentication code, to produce a transcoded message for transmission to a destination device, the data message being received from a source device wherein said data fields have been coded in accordance with a first coding system, whereby respective data field codes are generated for said data fields and a message code is derived from said data field codes, and wherein said message code has been coded in accordance with a second coding system to generate said authentication code, the method comprising; determining for each data field of the received data message whether to maintain, modify or omit that field; for a July 24, 2007– ט' באב התשס"ז field to be maintained, maintaining that field in said transcoded message; for a field to be omitted, coding the field in accordance with said first coding system to generate an omitted field code dependent upon the data field code for that field, and replacing that field by said omitted field code in the transcoded message; for a field to be modified, coding that field in accordance with said first coding system to generate modified field code dependent upon the data field code for that field, and replacing that field by a modified field, comprising modified data and said modified field code, in the transcoded message; and including said authentication code in the transcoded message. 1946 _________ ט' באב התשס"ז –July 24, 2007 1947 ]11[]21[ ]54[ PROCESSES TO GENERATE SUSPENSIONS OF WATERINSOLUBLE BIOLOGICALLY ACTIVE COMPOUNDS CONTAINING PARTICLES OF SIZES OF UP TO TWO MICRONS ]22[ ]31[ ]51[ ]71[ ]72[ 18.06.1999 60/089852 ]32[ 19.06.1998 Int. Cl.8 A61K 009/00, 009/16, 009/51 RTP PHARMA INC., U.S.A. GARY W. PACE, G. MICHAEL VACHON, K. AWADHESH MISHRA, INGE B. HENRIKSEN, VAL KRUKONIS, ANTHONY GODINAS WO/1999/065469 JEREMY M. BEN-DAVID & CO. LTD., HAR HOTZVIM HI-TECH PARK, P.O.B. 45087, JERUSALEM 91450 ]87[ ]74[ [57] A process for preparing a suspension of particles of a water-insoluble or substantially water-insoluble biologically active compound of up to 2000 nm in size comprising the steps of: (a) dissolving a water-insoluble or substantially water-insoluble biologically active compound and a first surface modifier in a liquefied compressed gas 140276 תהליכים להכנת תרחיפים של תרכובות שאינן נמסות במים בעלות פעילות ביולוגית המכילים חלקיקים בגודל עד שני מיקרונים ]33[ US ,דוד ושות' בע"מ- בן.ירמיהו מ ,45087 .ד. ת, הר חוצבים,רחוב המרפא ירושלים solvent therefor and forming a solution; and (b) expanding the compressed fluid solution prepared in step (a) into water or an aqueous solution or dispersion comprising a second surface modifier and optional further water-soluble agents thereby producing a suspension of microparticles, wherein the first and second surface modifiers are different. __________ July 24, 2007– ט' באב התשס"ז 1948 ]11[]21[ ]54[ TRAY OF A THERMOPLASTIC MATERIAL FOR THE PACKAGING OF FOODSTUFFS WHICH TEND TO RELEASE BAD SMELLING VOLATILE SUBSTANCES ]22[ ]31[ ]51[ ]71[ ]72[ 02.01.2001 00830018.8 ]32[ 18.01.2000 Int. Cl.8 B65D 081/26 SIRAP-GEMA S.P.A., ITALY PIERGIOVANNI LUCIANO, FEDERICO LANZANI, RENATO MAURI, MATTEO BRAZZOLI, PATRIZIA FAVA DR. MARK FRIEDMAN LTD., MOSHE AVIV TOWER, 54TH FLOOR 7 JABOTINSKY STREET 52520 RAMAT GAN ]74[ [57] A tray for packaging food products which may release smelly volatile substances, produced from a sheet of substantially open-cell expanded 140677 מגש מחומר טרמופלסטי לאריזת דברי מזון הנוטים לשחרר חומרים המדיפים ריח רע ]33[ EP ,ד"ר מרק פרידמן בע"מ ,77 ז'בוטינסקי54 קומה,מגדל משה אביב גן-רמת thermoplastic material characterized in that said sheet contains a finely divided solid material provided with adsorbing properties towards said substances. ____________ ]11[]21[ ]54[ ACID-TRIGGERED RELEASE MICROCAPSULES ]22[ ]31[ ]51[ ]71[ 28.07.1999 126333 ]32[ 30.07.1998 Int. Cl.8 A01N 025/00, B01J 013/00 SYNGENTA LIMITED, UNITED KINGDOM WO/2000/005952 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ 1949 141066 מיקרוקפסולות המשחררות את חומר הפעיל בנוכחות חומצה ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם July 24, 2007– ט' באב התשס"ז [57] A microcapsule formed of a polyurea shell wall and an encapsulated ingredient or ingredients enclosed within the shell wall, the wall comprising at least one oligomeric acetal moiety. _________ ]11[]21[ ]54[ BENZAZOLES: BENZOXAZOLE, BENZTHIAZOLE AND BENZIMIDAZOLE DERIVATIVES ]22[ ]31[ ]51[ ]71[ 21.07.1999 9816654.9 ]32[ 30.07.1998 Int. Cl.8 A01N 043/78, C07D 417/00 SYNGENTA LIMITED, UNITED KINGDOM WO/2000/006566 S. HOROWITZ & CO., ZION HOUSE, 41-45 ROTHSCHILD BLVD., TEL AVIV 65784 ]87[ ]74[ 141109 בנזיתיאזול, נגזרות בנזוקסאזול:בנזאזולים ובנזימידאזול ]33[ GB ,' הורוביץ ושות.ש תל,41-45 שדרות רוטשילד,בית ציון אביב [57] A compound of the formula wherein X is O or S; n is 0 or 1; Y is O, S or NR7; R1 is hydrogen, halogen, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 haloalkoxy, C1-6 alkylthio, C1-6 haloalkylthio, C3-6 cycloalkyl, C1-6alkoxy (C1-6) alkyl or SF5; R2 is hydrogen, halogen, C1-6 alkyl, C1-6 alkoxy, C1-6 haloalkoxy, C1-6 alkylthio, C1-6 haloalkylthio, C1-6 alkylsulfinyl, C1-6 haloalkylsulfinyl, C1-6 alkylsulfonyl, C1-6 haloalkylsulfonyl, C1-6 haloalkyl, cyano, nitro, CHO, CH=NOR5, C1-6 alkylcarbonyl, C1-6 alkoxycarbonyl or SF5; or together R1 and R2 form a five or six membered saturated or unsaturated carbocyclic ring, July 24, 2007– ט' באב התשס"ז optionally substituted by one or two C1-6 alkyl groups; R3 is hydrogen, C1-6 alkyl, CH2 (C1-4 haloalkyl), C1-6 cyanoalkyl, C3-6 alkenyl, C3-6 alkynyl, C1-6 alkoxy (C1-6) alkyl, C1-6 alkylthio (C1-6) alkyl, C1-6 alkoxy (C1-6) alkyl, C1-6 alkylcarbonyl, C1-6 alkoxycarbonyl, formyl, C1-6 alkylcarbonyl (C1-6) alkyl, C1-6 alkoxycarbonyl (C1-6) alkyl, C1-6 alkylaminocarbonyl, di(C1-6) alkylaminocarbonyl, optionally substituted phenoxycarbonyl, optionally substituted phenyl (C1-4) alkyl or S(O)qR6; R4 is hydrogen, halogen, cyano, C1-8 alkyl, C1-6 haloalkyl, C1-6 cyanoalkyl, C2-6 alkenyl, C26 alkynyl, C3-7 cycloalkyl, C3-7 1950 halocycloalkyl, C3-7 cyanocycloalkyl, C1-3 alkyl (C3-7) cycloalkyl, C1-3 alkyl (C3-7) halocycloalkyl, C3-6 cycloalkyl (C1-6) alkyl, C5-6 cycloalkenyl, C5-6 cycloalkenyl (C1-6) alkyl, C2-6 haloalkenyl, C1-6 cyanoalkenyl, C1-6 alkoxy (C1-6) alkyl, formyl, C1-6 carboxyalkyl, C1-6 alkylcarbonyl, (C1-6) alkyl, C1-6 alkoxycarbonyl (C1-6) alkyl, C1-6 alkylthio (C1-6) alkyl, C1-6 alkylsulfinyl (C1-6) alkyl, C1-6 alkylsulfonyl (C1-6) alkyl, aminocarbonyl (C1-6) alkyl, C1-6 alkylaminocarbonyl (C1-6) alkyl, di (C1-6) alkylaminocarbonyl (C1-6) alkyl, C1-6 alkoxycarbonyl, di(C1-6) alkylaminocarbonyl, optionally substituted phenyl, optionally substituted phenyl (C1-4) alkyl, optionally substituted phenyl (C2-4) alkenyl, optionally substituted heteroaryl, optionally substituted heteroaryl (C1-4) alkyl, optionally substituted heterocyclyl, optionally substituted heterocyclyl (C1-4) alkyl, a group OR8, a group SH, a group S(O)pR9, a group NR10R11 or a group C(R12)=NOR13; R5 is hydrogen, C1-6 alkyl, optionally substituted phenyl or optionally substituted phenyl (C1-4) alkyl; R6 is C1-6 alkyl, C1-6 haloalkyl or optionally substituted phenyl; R7 is hydrogen, cyano, C1-8 alkyl, C1-6 haloalkyl, C1-6 cyanoalkyl, C2-6 alkenyl, C2-6 alkynyl, C3-7 cycloalkyl, C2-6 haloalkenyl, C3-6 cycloalkyl (C1-6) alkyl, C1-6 alkoxy (C1-6) alkyl, C1-6 alkoxycarbonyl, C1-6 alkylcarbonyl, C1-6 alkylaminocarbonyl, di(C1-6) alkylaminocarbonyl, optionally substituted phenyl or optionally substituted heteroaryl; R8 is hydrogen, C1-6 alkyl, C1-6 haloalkyl, C3-6 alkenyl, C1-4 cyanoalkyl, C1-6 alkoxycarbonyl (C1-6) alkyl, optionally substituted phenyl, optionally substituted phenyl (C1-4) alkyl, optionally substituted heteroaryl, N=C(CH3)2; R9 is C1-6 alkyl, C1-6 haloalkyl, C3-6 alkenyl, cyano, C1-4 cyanoalkyl, C1-6 alkoxycarbonyl (C1-6) alkyl, optionally substituted phenyl, optionally substituted phenyl (C1-4) alkyl or optionally substituted heteroaryl; R10 and R11 are, independently, hydrogen, C1-8 alkyl, C3-7 cycloalkyl, C3-6 alkenyl, C3-6 alkynyl, C2-6 haloalkyl, C1-6 alkoxy (C1-6) alkyl, C1-6 alkoxycarbonyl, optionally substituted phenoxycarbonyl, formyl, C1-6 alkylcarbonyl, C1-6 alkylSO2, optionally substituted phenylSO2 or optionally substituted phenyl (C1-4) alkyl; R12 is C1-3 alkyl; R13 is C1-6 alkyl, optionally substituted phenyl (C1-2) alkyl; and p and q are, independently 0, 1 or 2. ________ ]11[]21[ ]54[ PURINE ACYCLIC NUCLEOSIDE DERIVATIVES AND THEIR PREPARATION ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 05.08.1999 09/130214 ]32[ 06.08.1998 Int. Cl.8 C07D 473/18, C12P 017/18 MEDIVIR AB, SWEDEN WO/2000/008025 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 1951 141161 תולדות של פיורין נוקלאוסיד אציקלי והכנתן ]33[ US ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה July 24, 2007– ט' באב התשס"ז [57] A compound of the formula wherein R6 and R7 are lower alkyl or benzyl or R6 and R7 taken together are -CH2CH2-, -CH2CH2CH2- or -CH2CH2CH2CH2-, R8 is C1-C21 saturated or monounsaturated, optionally substituted alkyl, R25 is hydrogen or –C(O)NR27R28 wherein R27 and R28 are independently selected from lower alkyl, phenyl and benzyl or R27 and R28, taken together with the nitrogen to which they are attached, form a pyrrolidinyl group or a piperidinyl group and R26 is lower alkyl, phenyl or benzyl, wherein the term "lower alkyl" stands for straight or branched chain alkyl radicals containing from 1 to 7 carbon atoms. They are intermediates for antiviral compounds. _________ ]11[]21[ 141370 ,חומצות גרעין המבקרות את הביטוי של בעגבניות ושימוש בהןB ומקודדת לגן לשינוי ביוסינטיזה של קרטנואידים ]54[ POLYNUCLEOTIDES CONTROLLING THE EXPRESSION OF AND CODING FOR GENE B IN TOMATO AND USE OF SAME FOR ALTERING CAROTENOID BIOSYNTHESIS ]22[ ]31[ ]51[ 12.08.1999 09/134607 ]32[ 14.08.1998 ]33[ US Int. Cl.8 A01K 067/00, C07K 014/415, C12N 009/12, 015/29, 015/52, 015/55, 015/70, 015/82 YISSUM RESEARCH יישום חברה לפיתוח המחקר של DEVELOPMENT COMPANY OF ירושלים,האוניברסיטה העברית בירושלים THE HEBREW UNIVERSITY OF JERUSALEM WO/2000/008920 G.E. EHRLICH (1995) LTD., ,) בע"מ1995( ארליך.אי.ג'י AYALON TOWER, 15TH FLOOR, ,11 רחוב מנחם בגין, 15 קומה,מגדל אילון 11 MENACHEM BEGIN STREET, רמת גן 52521 RAMAT GAN ]71[ ]87[ ]74[ [57] An isolated polynucleotide encoding a polypeptide having an amino acid sequence at least 95% similar to SEQ ID July 24, 2007– ט' באב התשס"ז NO:17, SEQ ID NO:18 or SEQ ID NO:19, wherein said polypeptide has a major lycopene cyclase activity, said major 1952 lcopene cyclase activity comprising production of at least a few percent βcarotene when said polynucleotide is introduced into lycopene-accumulating E. coli cells. ________ ]11[]21[ 141562 תכשירים עם חלקיקים לנתינה דרך הריאות ותהליכים להכנתם ]54[ PARTICULATE COMPOSITIONS FOR PULMONARY DELIVERY AND METHODS FOR THE PREPARATION THEREOF ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 13.09.1999 60/100163 ]32[ 14.09.1998 ]33[ US Int. Cl.8 A61K 009/00, 009/72, 047/36, 047/38 NEKTAR THERAPEUTICS, U.S.A. WO/2000/015262 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 [57] Particles for delivery of an active agent to the alveoli of a human patient, said particles comprising the active agent and at least about 40% by weight of a hygroscopic growth inhibitor selected from the group consisting of β-cyclodextrin, hydroxypropyl-β-cyclodextrin, sulfobutylether β-cyclodextrin, hydroxyethylstarch, dextranomer, and maltodextrins, wherein the hygroscopic growth inhibitor is incorporated within the particles, and wherein the particles exhibit a drop in emitted dose under simulated lung conditions of not more than about 25%. _________ 1953 July 24, 2007– ט' באב התשס"ז ]11[]21[ 141990 תאים המציגים אנטיגנים עם בטוי ציטוקין המוגבר באופן גנטי ]54[ ANTIGEN-PRESENTING CELLS WITH GENETICALLY ENHANCED CYTOKINE EXPRESSION ]22[ ]31[ ]51[ 14.09.1999 60/100468 ]32[ 15.09.1998 ]33[ US Int. Cl.8 A61K 038/20, 048/00, C07K 014/54, C12N 005/08, 015/24, 015/86, G01N 033/574 UNIVERSITY OF PITTSBURGH OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION, U.S.A. WO/2000/015264 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]71[ ]87[ ]74[ [57] Use of an effective amount of genetically modified dendritic cells which have not been pre-loaded with tumor associated antigen, for the manufacture of an injectable medicament for treating an individual having a tumor wherein said dendritic cells have been genetically modified to enhance expression of IL-12 by transduction with a vector encoding IL12, and whereby the injection of said dendritic cells results in the treatment of said tumor. __________ July 24, 2007– ט' באב התשס"ז 1954 ]11[]21[ 142172 תכשיר תרופתי לטיפול ברסטנוזיס ]54[ PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF RESTENOSIS ]22[ ]31[ ]51[ 14.07.1999 125336 ]32[ 14.07.1998 ]33[ IL Int. Cl.8 A61K 009/127, 031/66, 031/663, A61P 009/00, 009/14, C07F 009/38, 009/58 YISSUM RESEARCH יישום חברה לפיתוח המחקר של DEVELOPMENT COMPANY OF ירושלים,האוניברסיטה העברית בירושלים THE HEBREW UNIVERSITY OF ,הדסית שרותי מחקר רפואי ופתוח בע"מ JERUSALEM ירושלים HADASIT MEDICAL RESEARCH SERVICES AND DEVELOPMENT LTD. WO/2000/003677 EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688, HERZLIYA 46733 ]71[ ]87[ ]74[ [57] Use of an active ingredient being particulate bisphosphonate (BP), or a particulate complex or salt of BP, or particulate polymer of BP, being in a micronized particulate form having a diameter within the range of 0.01-10 μm, for the preparation of a pharmaceutical composition for the prevention or treatment of vascular restenosis. A pharmaceutical composition wherein said BP has the formula R1 is H, OH or halogen group; and R2 is halogen; linear or branched C1-C10 alkyl or C2-C10 alkenyl optionally substituted by heteroaryl or heterocyclyl C1-C10 alkylamino or C3-C8 cycloalkyl- amino where the amino may be a primary, secondary or tertiary; -NHY where Y is hydrogen, C3-C8 cycloalkyl, aryl or heteroaryl; or –SZ where Z is chlorosubstituted phenyl or pyridinyl. __________ 1955 July 24, 2007– ט' באב התשס"ז ]11[]21[ ]54[ METHOD AND APPARATUS FOR COVERING A STENT ]22[ ]31[ ]51[ ]71[ ]74[ 21.03.2001 09/532653 ]32[ 22.03.2000 Int. Cl.8 A61F 002/06, A61M 029/00 MEDINOL LTD. EITAN, MEHULAL, PAPPO, KUGLER, 11 HAMENOFIM ST. HERZLIYA 46120 [57] A covered stent comprising: an expandable stent with a longitudinal axis, the stent being expandable from a first diameter to a second diameter; a covering affixed to the stent, the cover being formed of linear fibers of pericardium, wherein in 142176 התקן ושיטה לכיסוי מרחיב\תומך כלי דם ]33[ US אביב- תל,מדינול בע"מ , קוגלר, פאפו, מהולל,איתן הרצליה,11המנופים the first diameter, the pericardium fibers form a first angle with respect to the longitudinal axis of the stent, and in the second diameter, the pericardium fibers form a second angle with respect to the longitudinal axis of the stent. __________ ]11[]21[ ]54[ DEVICE FOR THE DELIVERY OF AN AEROSOLIZED ACTIVE AGENT ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 07.10.1999 60/103702 ]32[ 09.10.1998 Int. Cl.8 A61M 015/00 NEKTAR THERAPEUTICS, U.S.A. WO/2000/021594 WOLFF, BREGMAN AND GOLLER, 19B KEREN HAYESOD ST., P.O.B. 1352, JERUSALEM 91013 [57] A device for controlling the delivery of an aerosolized active agent to the lungs of a human patient, said device comprising a flow resistance modulator adapted to change the flow resistance during delivery over one inhalation of an aerosolized 142215 התקן לנתינת חומר פעיל כתרסיס ]33[ US , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד active agent to the lungs of a human patient from a first flow resistance during an initial time period to a second flow resistance following the initial time period wherein the second flow resistance is less than the first flow resistance. __________ July 24, 2007– ט' באב התשס"ז 1956 ]11[]21[ 142391 תולדות של איזוסורביד מונוניטראט והשימוש בהן כאמצעים מרחיבי כלי דם בעלי סבילות משופרת ]54[ DERIVATIVES OF ISOSORBID MONONITRATE AND THEIR UTILIZATION AS VASODILATOR AGENTS WITH REDUCED TOLERANCE ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 04.10.1999 P9802076 ]32[ 07.10.1998 ]33[ ES Int. Cl.8 A61K 031/34, A61P 009/00, C07D 493/04 LACER, S.A., SPAIN WO/2000/020420 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 [57] A derivative of isosorbide mononitrate, or a pharmaceutically acceptable salt thereof, of the formula wherein one of A and B represents –ONO2 and the other represents wherein: either (i) Z is a sulphur atom and R is an optionally substituted C1-C4 alkyl group, 1957 an optionally substituted aryl group or an optionally substituted aralkyl group; or (ii) Z is an oxygen atom and R is the group July 24, 2007– ט' באב התשס"ז wherein R1 is hydrogen or an optionally substituted C1-C4 alkyl group, an optionally substituted aryl group or an optionally substituted aralkyl group. ___________ ]11[]21[ ]54[ USE OF VALSARTAN OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF FOR PRODUCING A PHARMACEUTICAL PREPARATION FOR THE TREATMENT OF INVASIVE LUNG AND INVASIVE BREAST CANCER ]22[ ]31[ 22.12.1999 98811257.9 ]32[ 23.12.1998 98811258.7 23.12.1998 Int. Cl.8 A61K 031/41 NOVARTIS AG, SWITZERLAND WO/2000/038676 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]51[ ]71[ ]87[ ]74[ [57] Use of valsartan or a pharmaceutically acceptable salt thereof for producing a pharmaceutical preparation The applications for division from this application have not yet been published 143233 שימוש בוולסרטן או במלח רוקחי מקובל שלו להכנת תכשיר רפואי לטיפול בסרטן ריאות ובסרטן שד פולשיים ]33[ EP EP ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה for the treatment of invasive lung and invasive breast cancer. ,179017,179016,179015 בקשות חלוקה מבקשה זו .שטרם פורסמו ____________ July 24, 2007– ט' באב התשס"ז 1958 ]11[]21[ 143830 – בנזיסוקסאזולילפנטיל2 תולדות a2 – בנזואילפנטילפירידואינדול2 –ו – אדרנוספטור אנטגוניסטים הכנתן ותכשירי,ואנלוגים שלהן רוקחות המכילים אותן ]54[ A2- ADRENOCEPTOR ANTAGONIST 2 BENZISOXAZOLYLPENTYL AND 2 BENZOYLPENTYLPYRIDOINDOLE DERIVATIVES AND ANALOGS THEREOF, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ]22[ ]31[ ]51[ 14.12.1999 98204358.0 ]32[ 21.12.1998 ]33[ EP Int. Cl.8 A61K 031/395, A61P 003/10, 015/00, 025/00, C07D 471/04, 491/048, 495/04 JANSSEN PHARMACEUTICA N.V., BELGIUM WO/2000/037466 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, אביב TEL AVIV 61040 ]71[ ]87[ ]74[ [57] A compound of the formula a N-oxide form, a pharmaceutically acceptable addition salt or a stereochemically isomeric form thereof, wherein: Alk is 1,5-pentanediyl; n is 1 or 2; p is 1 and q is 2; or p is 2 and q is 1; X is –O-, -S-, or NH; each R1 is independently hydrogen, halogen, C1-6 alkyl, nitro, hydroxyl or C1-4 alkyloxy; D is a radical of the formula wherein m is 1 or 2; each R3 independently is hydrogen, C1-4 alkyl, C1-4 alkyloxy or halo. _________ 1959 July 24, 2007– ט' באב התשס"ז ]11[]21[ 144040 תת מערכת לאספקת אנרגיה חשמלית ליחידת קצה המחוברת בכבלי תקשורת ]54[ POWER SUPPLY SUBSYSTEM FOR POWERING A NODE OVER COMMUNICATION CABLING ]22[ ]31[ 19.12.1999 60/115628 ]32[ 12.01.1999 ]33[ US 09/293343 16.04.1999 US 09/365584 02.08.1999 US Int. Cl.8 G06F 001/26, H02G 003/00, H04L 012/10, 012/44, 029/06, 029/08, H04Q 007/00 POWERDSINE LTD. הוד השרון,פאורדסיין בע"מ WO/2000/041496 SIMON KAHN C/O POWERDSINE ,)סיימון קאהן (פאורדסיין בע"מ LTD., השרון- הוד,7220 .ד. ת, 1רח' הנגר 1 HANAGAR ST. P.O.BOX 7220 HOD HASHARON 45421 ]51[ ]71[ ]87[ ]74[ [57] A power supply subsystem for providing electrical power to at least node over communication cabling, the power supply subsystem comprising: a management and control unit; a power supply interface for distributing power into the communication cabling substantially without interfering with data communication; and current limiting circuitry controlling current of said power distributed into said communication cabling via said power supply interface; wherein said current limiting circuitry is July 24, 2007– ט' באב התשס"ז operative to provide a first current limit level which is never exceeded, and a second current limit level which is not exceeded for more than a predetermined period of time, and wherein said management and control unit is operative to interrogate the at least one node to which it is intended to transmit power over the communication cabling in order to determine whether the node's characteristics allow it to receive power over the communication cabling. 1960 The applications for division from this application have not yet been published ,157292 בקשות חלוקה מבקשה זו .שטרם פורסמו __________ ]11[]21[ 144055 5 – ) – (היטרוציקלילסולפונאמידו4 ) – מתוקסיפנוקס2( –6 –– מתוקסי –פניל – פירידלפרימידנים2 – ]54[ 4 - (HETEROCYCLYLSULFONAMIDO)- 5 - METHOXY - 6 - (2 METHOXYPHENOXY ) - 2 - PHENYLPYRIDYLPYRIMIDINES ]22[ ]31[ ]51[ ]71[ 10.01.2000 99100784.0 ]32[ 18.01.1999 ]33[ EP Int. Cl.8 A61K 031/505, A61P 043/00, C07D 401/12, 403/12, 413/12, 417/12 F. HOFFMANN-LA ROCHE AG, SWITZERLAND WO/2000/042035 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., ,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, תל אביב TEL AVIV 61040 ]87[ ]74[ [57] A compound of the formula 1961 July 24, 2007– ט' באב התשס"ז wherein R1 is pyridyl, pyridyl substituted with halogen, lower alkyl, hydroxy-lower alkyl or lower alkenyl, pyrrolyl, pyrrolyl substituted with halogen, lower alkyl, hydroxy-lower alkyl or lower alkenyl, imidazolyl, imidazolyl substituted with halogen, lower alkyl, hydroxy-lower alkyl or lower alkenyl, thiazolyl, thiazolyl substituted with halogen, lower alkyl, hydroxy-lower alkyl or lower alkenyl, thiazolinyl, thiazolinyl substituted with halogen, lower alkyl, hydroxy-lower alkyl or lower alkenyl, oxazolyl, or oxazolyl substituted with halogen, lower alkyl, hydroxy-lower alkyl or lower alkenyl; R2 is (i) R21, (ii) –Y-R22, (iii) heterocyclyl selected from the group consisting of pyrimidinyl, imidazolyl, oxadizolyl, oxazolyl and thiazolyl, or (iv) heterocyclyl selected from the group consisting of pyrimidinyl, imidazolyl, oxadiazolyl, oxazolyl and thiazolyl, which is mono-, di- or tri-substituted, independently, with hydroxy, lower alkenyl, amino, lower alkanoylamino, lower alkoxycarbonylamino, lower alkyl or hydroxyl-lower alkyl; R21 is cyano, hydroxy-lower alkyl, carboxy, -C(O)NRaRb, -(CH2)1-4NHRc, (CH2)1-4 NHC(O)NH(CH2)0-3CH3, amidino, hydroxyamidino, lower alkoxycarbonyl or hydroxy-lower alkoxycarbonyl; R22 is hydrogen, lower alkanoyl, carboxylower alkyl, lower alkoxycarbonyl, lower alkoxycarbonyl-lower alkyl, carbamoyllower alkyl, di-lower alkylcarbamoyllower alkyl, allyl, lower alkyl or hydroxylower alkyl; Ra is hydrogen, lower alkyl, or lower alkyl substituted with hydroxy or lower alkoxy; Rb is hydrogen or lower alkyl; Rc is hydrogen, acetyl or lower alkylsulfonyl; X is –CH- or –N; and Y is –O-, -NH-; or a pharmaceutically acceptable salt or ester thereof. __________ July 24, 2007– ט' באב התשס"ז 1962 ]11[]21[ ]54[ MEDICAL SYSTEM CALIBRATION WITH STATIC METAL COMPENSATION ]22[ ]31[ ]51[ ]71[ ]74[ 11.07.2001 09/621322 ]32[ 20.07.2000 Int. Cl.8 A61B 005/00, 005/06 BIOSENSE, INC., U.S.A. DR. SHLOMO COHEN & CO., 124 IBN GABIROL ST., P.O.B. 11490, TEL AVIV 62038 [57] A method for calibrating a medical system capable of generating a magnetic field for tracking a position of a medical device, the method comprising the steps of: (a) defining a mapping volume within the generated magnetic field; (b) placing a metallic object within the mapping volume; (c) aligning a sensor at a first point within the mapping volume and measuring the magnetic field at the first point the sensor to establish a first coordinate position (Xi, Yi, Zi)); (d) moving the sensor to a next point (Xi + dx, Yi + dy, Zi + dz) along one coordinate axis by an added distance component (dx, dy, dz) and measuring the magnetic field at the next point to establish a next coordinate position; (e) interpolating the magnetic field at an intermediate point between the first 144271 כיול של מערכת רפואית באמצעות פיצוי סטטי מתכתי ]33[ US ,'ד"ר שלמה כהן ושות תל אביב,11490 .ד. ת, 124 אבן גבירול position and the next coordinate position to establish an interpolated intermediate coordinate position; (f) determining the position difference between the interpolated intermediate coordinate position and an actual intermediate coordinate position; (g) comparing the position difference to an error limit; (h) setting (Xi, Yi, Zi) of the next point as (Xi=Xi+dx, Yi=Yi+dy, Zi=Zi+dz) if the position difference is within the error limit and repeating steps (d)-(g) along another coordinate axis; and (i) setting the added distance component (dx, dy, dz) by decreasing the value of the added distance component if the position difference is not within the error limit and repeating steps (d)-(g) along the same coordinate axis. _________ 1963 July 24, 2007– ט' באב התשס"ז ]11[]21[ ]54[ METHOD OF ENHANCING NEEDLELESS TRANSDERMAL POWDERED DRUG DELIVERY ]22[ ]31[ 21.01.2000 60/116907 ]32[ 22.01.1999 09/235944 22.01.1999 Int. Cl.8 A61M 005/30 POWDERJECT RESEARCH LIMITED, UNITED KINGDOM WO/2000/043058 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]51[ ]71[ ]87[ ]74[ [57] Use of a therapeutic agent in the manufacture of a medicament for administering the therapeutic agent to a predetermined area of skin or mucosa of a vertebrate subject by a method comprising: (a) accelerating particles into, across or both into and across the area of skin or mucosa, and 144380 שיטה להגברת שיחרור תת–עורי של ללא מחט,תרופה בצורת אבקה ]33[ US US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם (b) topically positioning a first transdermal drug delivery device or a first occlusive dressing over the area of skin or mucosa, wherein the particles or the first transdermal drug delivery device or the first occlusive dressing, or a combination thereof, comprise the therapeutic agent. __________ ]11[]21[ 144757 צורה גבישית של אפלרנון ]54[ EPLERENONE CRYSTALLINE FORM ]22[ ]31[ 04.12.2000 60/169639 ]32[ 08.12.1999 ]33[ US 60/169556 08.12.1999 US 60/169683 08.12.1999 US 60/169807 08.12.1999 US 60/169707 08.12.1999 US 60/169608 08.12.1999 US Int. Cl.8 A61K 031/58, A61P 009/00, 013/06, C07J 071/00 PHARMACIA CORPORATION, U.S.A. WO/2001/041535 LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו INDUSTRIAL PARK, OMER, באר שבע,5352 .ד. ת, עומר,גן תעשייה P.O.B. 5352, BEER-SHEVA 84152 ]51[ ]71[ ]87[ ]74[ July 24, 2007– ט' באב התשס"ז 1964 [57] A pharmaceutical composition in an oral dosage form comprising from about 0.5 mg to about 500 mg eplerenone, and at least one pharmaceutically acceptable excipient, wherein: (a) the eplerenone present in the composition has a phase purity of from about 90% to about 100% Form L crystalline eplerenone, and (b) the Form L crystalline eplerenone is characterized by an X-ray powder diffraction pattern at a wavelength of 1.54056Å comprising one or more peaks that are selected from the group consisting of 8.0±0.2 degrees 2θ, 12.4±0.2 degrees 2θ, 12.8±0.2 degrees 2θ, and 13.3±0.2 degrees 2θ. ____________ ]11[]21[ 144761 צורת מצב מוצק של סלקוקסיב בעל יכולת חיים מוגברת ]54[ SOLID-STATE FORM OF CELECOXIB HAVING ENHANCED BIOAVAILABILITY ]22[ ]31[ 06.12.2000 60/169856 ]32[ 08.12.1999 ]33[ US 09/730663 06.12.2000 US Int. Cl.8 A61K 009/14, 031/42, C07D 261/00, 261/08 PHARMACIA CORPORATION, U.S.A. WO/2001/042221 LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו INDUSTRIAL PARK, OMER, באר שבע,5352 .ד. ת, עומר,גן תעשייה P.O.B. 5352, BEER-SHEVA 84152 ]51[ ]71[ ]87[ ]74[ [57] Amorphous celecoxib, wherein said amorphous celecoxib exhibits a glass transition measurable by differential scanning calorimetry. ___________ 1965 July 24, 2007– ט' באב התשס"ז ]11[]21[ ]54[ SYSTEM AND METHOD FOR PROCESSING FINANCIAL TRANSACTIONS ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 18.02.2000 60/120760 ]32[ 19.02.1999 Int. Cl.8 G06Q 002/000000 003/00000 MOBIL OIL CORPORATION, U.S.A. WO/2000/049551 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] A method for processing transactions comprising the steps of: transmitting a signal to one of a plurality of point-of-sale devices, said signal comprising customer identification data; transmitting an authorization request from one of said plurality of point-of-sale devices to a transaction processing system, said authorization request comprising a merchant identifier, transaction data, and 144846 מערכת ושיטה לניהול העברות פיננסיות ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם said customer identification data; determining, from said customer identification data, a payment processor that corresponds to said merchant identifier; transmitting said authorization request to said payment processor; and transmitting to one of said plurality of point-of-sale devices, said payment processor's response to said authorization request. __________ July 24, 2007– ט' באב התשס"ז 1966 ]11[]21[ 144910 תרכובות ציקליות ותכשירי רוקחות המכילים אותן ]54[ CYCLIC COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME ]22[ ]31[ ]51[ 12.04.2000 60/129510 ]32[ 15.04.1999 ]33[ US Int. Cl.8 A61K 031/426, A61P 011/06, C07C 237/40, C07D 213/81, 231/38, 233/90, 239/42, 263/48, 277/00, 277/56, 409/12, 417/12 BRISTOL-MYERS SQUIBB COMPANY, U.S.A. WO/2000/062778 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]71[ ]87[ ]74[ [57] A compound or a salt thereof of the formula as described in the specification. ____________ 1967 July 24, 2007– ט' באב התשס"ז ]11[]21[ 145052 פרו–תרופות המכילות זרחן ]54[ PHOSPHORUS-CONTAINING PRODRUGS ]22[ ]31[ 03.03.2000 60/123013 ]32[ 05.03.1999 ]33[ US 60/153127 08.09.1999 US Int. Cl.8 A61K 031/66, A61P 003/10, 009/00, 031/12, 033/00, 035/00, C07F 009/00, 009/02, 009/6584 METABASIS THERAPEUTICS, INC., U.S.A. WO/2000/052015 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]51[ ]71[ ]87[ ]74[ [57] A compound of the formula wherein: V, W, and W' are independently selected from the group consisting of –H, alkyl, aralkyl, alicyclic, aryl, substituted aryl, heteroaryl, substituted heteroaryl, 1alkenyl, and 1-alkynyl; or together V and Z are connected via an additional 3-5 atoms to form a cyclic group containing 57 ring atoms, optionally 1 heteroatom, substituted with hydroxy, acyloxy, alkoxycarbonyloxy, or aryloxycarbonyloxy attached to a carbon atom that is three atoms from both Y groups attached to the phosphorus; or together V and Z are connected via an additional 3-5 atoms to form a cyclic group, optionally containing 1 heteroatom, said cyclic group is fused to an aryl group at the beta and gamma position to the Y adjacent to V; together V July 24, 2007– ט' באב התשס"ז and W are connected via an additional 3 carbon atoms to form an optionally substituted cyclic group containing 6 carbon atoms and substituted with one substituent selected from the group consisting of hydroxy, acyloxy, alkoxycarbonyloxy, alkylthiocarbonyloxy, and aryloxycarbonyloxy, attached to one of said additional carbon atoms that is three atoms from a Y attached to the phosphorus; together Z and W are connected via an additional 3-5 atoms to form a cyclic group, optionally containing one heteroatom, and V must be aryl, substituted aryl, heteroaryl, or substituted heteroaryl; together W and W' are connected via an additional 2-5 atoms to form a cyclic group, optionally containing 1968 0-2 heteroatoms, and V must be aryl, substituted aryl, heteroaryl, or substituted heteroaryl; Z is selected from the group consisting of –CHR2OH, -CHR2OC(O)R3, CHR2OC(S)R3, -CHR2OC(S)OR3, CHR2OC(O)SR3, -CHR2OCO2R3, -OR2, SR2, -CHR2N3, -CH2aryl, -CH(aryl)OH, CH(CH=CR22)OH, -CH(C≡CR2)OH, -R2, NR22, -OCOR3, -OCO2R3, -SCOR3, SCO2R2, -NHCOR2, -NHCO2R3, CH2NHaryl, -(CH2)p-OR12, and –(CH2)pSR12; p is an integer 2 or 3; with the provisos that: (a) V, Z, W, W' are not all –H; (b) when Z is –R2, then at least one of V, W, and W' is not –H, alkyl, aralkyl, or alicyclic; R2 is selected from the group consisting of R3 and –H; R3 is selected from the group consisting of alkyl, aryl, alicyclic, and aralkyl; R6 is selected from the group consisting of –H, and lower alkyl, acyloxycarbonyl, alkoxycarbonyloxy alkyl and lower acyl; R12 is selected from the group cosnsiting of –H, and lower acyl; each Y is independently selected from the group consisting of –O-, -NR6- with the proviso that at least one Y is –NR6-; M is selected from the group that when attached to PO2-3, P2O3-6, P3O94- or P(O)(NHR6)O- is a biologically active agent but is not an FBPase inhibitor, and is attached to the phosphorus in formula I via a carbon, oxygen, sulfur or nitrogen atom; with the proviso that: (1) M is not –NH(lower alkyl), -N(lower alkyl)2, -NH(lower alkylhalide), -N(lower alkylhalide)2, or –N(lower alkyl) (lower alkylhalide); and (2) R6 is not lower alkylhalide; and pharmaceutically acceptable prodrugs and salts thereof. _________ ]11[]21[ ]54[ METHOD FOR THE IDENTIFICATION, ISOLATION, OR SEPARATION OF IDENTICAL NUCLEIC ACID FRAGMENTS FROM A MIXTURE OF AT LEAST TWO NUCLEIC ACID POPULATIONS ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 09.03.2000 19911130.8 ]32[ 12.03.1999 Int. Cl.8 C12Q 001/68 INTEGRAGEN, S.A.S., FRANCE WO/2000/053802 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 1969 145141 של קטעי, או הפרדה, בידוד,שיטה לזיהוי חומצות גרעין זהות מתוך תערובת של לפחות שתי אוכלוסיות של חומצות גרעין ]33[ DE ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה July 24, 2007– ט' באב התשס"ז [57] A method for the identification (or isolation or separation) of identical nucleic acid fragments from a mixture of at least two nucleic acid populations, comprising: (a) separate digestion of the nucleic acids of said at least two populations with at least one restriction enzyme; (b) ligation of an adaptor sequence to the restriction fragments; (c) amplification of the adaptor-ligated restriction fragments generated in (a) and . (b) using differently labeled adaptorspecific primers; (d) hybridization of the amplification products from the different nucleic acid populations with each other; (e) elimination of homohybrids based on labeling of primers; and (f) identification (or isolation or separation) of the identical, fully matched, heterohybrid fragments __________ ]11[]21[ 145299 גליצרופוספאטים ציקליים ואנלוגיים שלהם ]54[ CYLIC GLYCEROPHOSPHATES AND ANALOGS THEREOF ]22[ ]31[ ]51[ ]71[ 24.03.2000 129179 ]32[ 25.03.1999 ]33[ IL Int. Cl.8 A61K 031/66, A61P 005/00, 035/00, 035/02, C07F 009/00, 009/02 YEDA RESEARCH AND רחובות,ידע חברה למחקר ופיתוח בע"מ DEVELOPMENT CO. LTD. WO/2000/057864 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A pharmaceutical composition comprising a pharmaceutically acceptable July 24, 2007– ט' באב התשס"ז carrier and, as an active ingredient, a compound of the formula 1970 wherein Y is –(CH2)m-, -CH(OH)- or – C(=O)-, and m is 1-3; X is H, alkyl, -CH2OH-, CH2Oacyl or – CH2acyl; and R is H, a cation, alkyl or optionally substituted aryl; provided that: said compound is not one of: phenyl 1,3-cyclic propanediol phosphate; cyclic dihydroxyacetone phosphate; 1,3-cyclic propanediol phosphate; 1,3-cyclic glycerophosphate. __________ ]11[]21[ 145357 תכשירי, תהליך להכנתם,מעכבי אמיד רוקחות המכילים אותם והשימוש בהם לייצור תרופות לטיפול במחלות המתווכות על ידי ציטוקין ]54[ AMIDE INHIBITORS, PROCESS FOR THEIR PREPARATION, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND THEIR USE IN THE MANUFACTURE OF MEDICAMENTS FOR THE TREATMENT OF CYTOKINE MEDIATED DISEASES ]22[ ]31[ 13.03.2000 9906279.6 ]32[ 17.03.1999 ]33[ GB 9926667.8 11.11.1999 GB Int. Cl.8 A61K 031/505, A61P 043/00, C07D 239/88, 401/12, 403/12, 405/12, 409/12 ASTRAZENECA AB, SWEDEN WO/2000/055153 S. HOROWITZ & CO., ,' הורוביץ ושות.ש ZION HOUSE, תל,41-45 שדרות רוטשילד,בית ציון 41-45 ROTHSCHILD BLVD., אביב TEL AVIV 65784 ]51[ ]71[ ]87[ ]74[ [57] An amide derivative of the formula wherein X is –NHCO- or –CONH; m is 0, 1, 2 or 3; R1 is hydroxy, halogeno, trifluoromethyl, cyano, mercapto, nitro, amino, carboxy, carbamoyl, formyl, (1-6C) alkyl, (2-6C) alkenyl, (2-6C) alkynyl, (1-6C) alkoxy, (16C) alkylthio, (1-6C) alkylsuphinyl, (1-6C) alkylsulfphonyl, (1-6C) alkylamino, di-[(1- 1971 6C) alkyl] amino, (1-6C) alkoxycarbonyl, N-(1-6C) alkylcarbamoyl, N,N-di[(16C)alkyl] carbamoyl, (2-6C) alkanoyl, (26C) alkanoyloxy, (1-6C) alkanoylamino, N-(1-6C) alkyl-(1-6C) alkanoylamino, N(1-6C) alkylsulphamoyl, N,N-di[(16C)alkyl) sulphamoyl, (1-6C) alkanesulphonylamino, N-(1-6C)alkyl-(1- July 24, 2007– ט' באב התשס"ז 6C) alkanesulphonylamino, halogeno-(16C) alkyl, hydroxyl-(1-6C) alkyl, (1-6C) alkoxy-(1-6C) alkyl, cyano-(1-6C) alkyl, amino-(1-6C) alkyl, (1-6C) alkylamino-(16C) alkyl, di[[(1-6C) alkyl] amino-(1-6C) alkyl, carboxy-(1-6C) alkyl, (1-6C) alkoxycarbonyl-(1-6C) alkyl, carbamoyl(1-6C) alkyl, N-(1-6C) alkylcarbamoyl-(16C) alkyl, N,N-di[(1-6C) alkyl] carbamoyl-(1-6C) alkyl, halogeno-(2-6C) alkoxy, hydroxy-(2-6C) alkoxy, (1-6C) alkoxy-(2-6C) alkoxy, cyano-(1-6C) alkoxy, carboxy-(1-6C) alkoxy, (1-6C) alkoxycarbonyl-(1-6C) alkoxy, carbamoyl(1-6C) alkoxy, N-(1-6C) alkylcarbamoyl(1-6C) alkoxy, N,N-di-[(1-6C) alkyl] carbamoyl-(1-6C) alkoxy, amino-(2-6C) alkoxy, (1-6C) alkylamino-(2-6C) alkoxy, di-[(1-6C) alkyl] amino-(2-6C) alkoxy, halogeno-(2-6C) alkylamino, hydroxy-(26C) alkylamino, (1-6C) alkoxy-(2-6C) alkylamino, cyano-(1-6C) alkylamino, carboxy-(1-6C) alkylamino, (1-6C) alkoxycarbonyl-(1-6C) alkylamino, carbamoyl-(1-6C) alkylamino, N-(1-6C) alkylcarbamoyl-(1-6C) alkylamino, N,Ndi-[(1-6C) alkyl] carbamoyl-(1-6C) alkylamino, amino-(2-6C) alkylamino, (16C) alkylamino-(2-6C) alkylamino, di-[(16C) alkyl] amino-(2-6C) alkylamino, N-(16C) alkyl-halogeno-(1-6C) alkylamino, N(1-6C) alkyl-hydroxy-(2-6C) alkylamino, N-(1-6C) alkyl-(1-6C) alkoxy-(2-6) alkylamino, N-(1-6C) alkyl-cyano-(1-6C) alkylamino, N-(1-6C)alkyl-carboxy-(1-6C) alkylamino, N-(1-6C) alkyl-(1-6C) alkoxycarbonyl-(1-6C) alkylamino, N-(16C) alkyl-carbamoyl-(1-6C) alkylamino, N-(1-6C) alkyl-N-(1-6C) alkylcarbamoyl(1-6C) alkylamino-N-(1-6C) alkyl-N,Ndi[(1-6C) alkyl] carbamoyl-(1-6C) alkylamino, N-(1-6C) alkylamino-(2-6C) alkylamino, N-(1-6C) alkyl-(1-6C) alkylamino-(2-6C) alkylamino, N-(1-6C) alkyl-di-[(1-6C) alkyl] amino-(2-6C) alkylamino, halogeno-(2-6C) alkanoylamino, hydroxyl-(2-6C) alkanoylamino, (1-6C) alkoxy-(2-6C) July 24, 2007– ט' באב התשס"ז alkanoylamino, cyano-(2-6C) alkyanoylamino, carboxy-(2-6C) alkanoylamino, (1-6C) alkoxycarbonyl-(26C) alkanoylamino, carbamoyl-(2-6C) alkanoylamino, N-(1-6C) alkylcarbamoyl(2-6C) alkanoylamino, N,N-di[(1-6C) alkyl] carbamoyl-(2-6C) alkanoylamino, amino-(2-6C) alkanoylamino, (1-6C) alkylamino-(2-6C) alkanoylamino or di[(1-6C) alkyl] amino-(2-6C) alkanoylamino, or R1 is aryl, aryl-(1-6C) alkyl, aryl-(16C) alkoxy, aryloxy, arylamino, N-(1-6C) alkyl-arylamino, aryl-(1-6C) alkylamino, N-(1-6C) alkyl-aryl-(1-6C) alkylamino, aroylamino, arylsulphonylamino, Narylsulphamoyl, aryl-(2-6C) alkanoylamino, heteroaryl, heteroaryl-(16C) alkyl, heteroaryloxy, heteroaryl-(16C) alkoxy, heteroarylamino, N-(1-6C) alkyl-heteroarylamino, heteroaryl-(1-6C) alkylamino, N-(1-6C) alkyl-heteroaryl-(16C) alkylamino, heteroarylcarbonylamino, heteroarylsulphonylamino, Nheteroarylsulphamoyl, heteroaryl-(2-6C) alkanoylamino, heteroaryl-(1-6C) alkoxy(1-6C) alkyl, heteroaryl-(1-6C) alkylamino-(1-6C) alkyl, N-(1-6C) alkylheteroaryl-(1-6C) alkylamino-(1-6C) alkyl, heterocyclyl, heterocyclyl-(1-6C) alkyl, heterocyclyloxy, heterocyclyl-(1-6C) alkoxy, heterocyclamino, N-(1-6C) alkylheterocyclylamino, heterocyclyl-(1-6C) alkylamino, N-(1-6C) alkyl-heterocyclyl(1-6C) alkylamino, heterocyclylcarbonylamino, heterocyclcylsulphonylamino, Nheterocyclcylsulphamoyl, heterocyclyl-(26C) alkanoylamino, heterocyclyl-(1-6C) alkoxy-(1-6C) alkyl, heterocyclyl-(1-6C) alkylamino-(1-6C) alkyl or N-(1-6C) alkyl-heterocyclyl-(1-6C) alkylamino-(16C) alkyl, or (R1)m is a (1-3C) alkylenedioxy group, and wherein any of the R1 substituents defined hereinbefore which comprises a CH2 group which is attached to 2 carbon atoms or a CH3 group which is attached to 1972 a carbon atom may optionally bear on each said CH2 or CH3 group a substituent selected from hydroxy, amino, (1-6C) alkoxy, (1-6C) alkylkamino, di-[(1-6C) alkyl] amino and heterocyclyl, and wherein any aryl, heteroaryl or heterocyclyl group in a R1 substituent may optionally bear 1 or 2 substituents selected from hydroxy, halogeno, (1-6C) alkyl, (16C) alkoxy, carboxy, (1-6C) alkoxycarbonyl, N-(1-6C) alkylcarbamoyl, N,N-di-[(1-6C) alkyl] carbamoyl, (2-6C) alkanoyl, amino, (1-6C) alkylamino, di[(1-6C) alkyl] amino, halogeno-(1-6C) alkyl, hydroxy-(1-6C) alkyl, (1-6C) alkoxy-(1-6C) alkyl, cyano-(1-6C) alkyl, amino-(1-6C) alkyl, (1-6C) alkylamino-(16C) alkyl, di-[(1-6C) alkyl, di-[(1-6C) alkyl] amino-(1-6C) alkyl, aryl and aryl(1-6C) alkyl, and wherein any heterocyclyl group in a R1 substituent may optionally bear 1 or 2 oxo or thioxo substituents; n is 0, 1 or 2; R2 is hydroxy, halogeno, trifluoromethyl, cyano, mercapto, nitro, amino, carboxy, (1-6C) alkoxycarbonyl, (1-6C) alkyl, (26C) alkenyl, (2-6C) alkynyl, (1-6C) alkoxy, (1-6C) alkylamino or di-[(1-6C) alkyl] amino; R3 is hydrogen, halogeno, (1-6C) alkyl or (1-6C) alkoxy; q is 0, 1, 2 3 or 4; and Q is aryl, aryloxy, aryl-(1-6C) alkoxy, arylamino, N-(1-6C) alkyl-arylamino, aryl(1-6C) alkylamino, N-(1-6C) alkyl-aryl-(16C) alkylamino, aroylamino, arylsulphonylamino, N-arylcarbamoyl, Narylsulphamoyl, aryl-(2-6C) alkanoylamino, (3-7C) cycloalkyl, heteroaryl, heteroaryloxy, heteroaryl-(16C) alkoxy, heteroarylamino, N-(1-6C) alkyl-heteroarylamino, heteroaryl-(1-6C) alkylamino, N-(1-6C) alkyl-heteroaryl-(16C) alkylamino, heteroarylcarbonylamino, heteroarylsulphonylamino, Nheteroarylcarbamoyl, Nheteroarylsulphamoyl, heteroaryl-(2-6C) alkanoylamino, heterocyclyl, 1973 heterocyclcyloxy, heterocyclyl-(1-6C) alkoxy, heterocyclylamino, N-(1-6C) alkyl-heterocyclylamino, heterocyclyl-(16C) alkylamino, N-(1-6C) alkylheterocyclyl-(1-6C) alkylamino, heterocyclcarbonylamino, heterocyclylsulphonylamino, Nheterocyclcarbamoyl, Nheterocyclylsulphamoyl or heterocyclyl(2-6C) alkanoylamino, and Q is optionally substituted with 1, 2 or 3 substituents selected from hydroxy, halogeno, trifluoromethyl, cyano, mercapto, nitro, amino, carboxy, carbamoyl, formyl, (1-6C) alkyl, (2-6C) alkenyl, (2-6C) alkynyl, (16C) alkoxy, (1-6C) alkylthio, (1-6C) alkylsulphinyl, (1-6C) alkylsulphonyl, (16C) alkylamino, di-[(1-6C) alkyl] amino, (1-6C) alkoxycarbonyl, N-(1-6C) alkylcarbamoyl, N,N-di[(1-6C) alkyl] carbamoyl, (2-6C) alkanoyl, (2-6C) alkanoyloxy, (1-6C) alkanoylamino, N-(16C) alkyl-(1-6C) alkanoylamino, N-(1-6C) alkylsulphamoyl, N,N-di-[(1-6C) sulphamoyl, (1-6C) alkanesulphonylamino, N-(1-6C) alkyl-(16C) alkanesulphonylamino, halogeno-(16C) alkyl, hydroxy-(1-6C) alkyl, (1-6C) alkoxy-(1-6C) alkyl, cyano-(1-6C) alkyl, amino-(1-6C) alkyl, (1-6C) alkylamino(1-6C) alkyl, di-[(1-6C) alkyl] amino-(16C) alkyl, carboxy-(1-6C) alkyl, (1-6C) alkoxycarbonyl-(1-6C) alkyl, carbamoyl(1-6C) alkyl, N-(1-6C) alkylcarbamoyl-(16C) alkyl, N-N-di-[(1-6C) alkyl] carbamoyl-(1-6C) alkyl, halogeno-(2-6C) alkoxy, hydroxy-(2-6C) alkoxy (1-6C) alkoxy-(2-6C) alkoxy, cyano-(1-6C) alkoxy, carboxy-(1-6C) alkoxy, (1-6C) alkoxycarbonyl-(1-6C) alkoxy, carbamoyl(1-6C) alkoxy, N-(1-6C) alkylcarbamoyl(1-6C) alkoxy, N,N-di-[(1-6C) alkyl] carbamoyl-(1-6C) alkoxy, amino-(2-6C) alkoxy, halogeno-(2-6C) alkylamino, hydroxy-(2-6C) alkylamino, (1-6C) alkoxy-(2-6C) alkylamino, cyano-(1-6C) alkylamino, carboxy-(1-6C) alkylamino, (1-6C) alkoxycarbonyl-(1-6C) alkylamino, July 24, 2007– ט' באב התשס"ז carbamoyl-(1-6C) alkylamino, N-(1-6C) alkylcarbamoyl-(1-6C) alkylamino, N,Ndi-[(1-6C) alkyl] carbamoyl-(1-6C) alkylamino, amino-(2-6C) alkylamino, (16C) alkylamino-(2-6C) alkylamino, di-[(16C) alkyl] amino-(2-6C) alkylamino, N-(16C) alkyl-halogeno-(1-6C) alkylamino, N(1-6C) alkyl-hydroxy-(2-6C) alkylamino, N-(1-6C) alkyl-(1-6C) alkoxy-(2-6C) alkylamino, N-(1-6C) alkyl-cyano-(1-6C) alkylamino, N-(1-6C) alkyl-carboxy-(16C)-alkylamino, N-(1-6C) alkyl-(1-6C) alkoxycarbonyl-(1-6C) alkyamino, N-(16C) alkyl-carbamoyl-(1-6C) alkylamino, N-(1-6C) alkyl-N-(1-6C) alkylcarbamoyl(1-6C) alkylamino, N-(1-6C) alkyl-N,N-di[(1-6C) alkyl] carbamoyl-(1-6C) alkylamino, N-(1-6C) alkylamino-(2-6C) alkylamino, N-(1-6C) alkyl-(1-6C) alkylamino-(2-6C) alkylamino, N-(1-6C) alkyl-di-[(1-6C) alkyl] amino-(2-6C) alkylamino, halogeno-(2-6C) alkanoylamino, hydroxy-(2-6C) alkanoylamino, (1-6C) alkoxy-(2-6C) alkanoylamino, cyano-(2-6C) alkanoylamino, carboxy-(2-6C) alkanoylamino, (1-6C) alkoxycarbonyl-(26C) alkanoylamino, carboxy-(2-6C) alkanoylamino, (1-6C) alkoxycarbonyl-(26C) alkanoylamino, carboxy-(2-6C) alkanoylamino, (1-6C) alkoxycarbonyl-(26C) alkanoylamino, carbamoyl-(2-6C) alkanoylamino, N-(1-6C) alkylcarbamoyl(2-6C) alkanoylamino, N,N-di-[(1-6C) alkyl] carbamoyl-(2-6C) alkanoylamino, amino-(2-6C) alkanoylamino, (1-6C) alkylamino-(2-6C) alkanoylamino, di-[(16C) alkyl] amino-(2-6C) alkanoylamino, aryl, aryl-(1-6C) alkyl, aryl-(1-6C) alkoxy, aryloxy, arylamino, N-(1-6C) alkylarylamino, aryl-(1-6C) alkylamino, N-(16C) alkyl-aryl-(1-6C) alkylamino, aroylamino, arylsulphonylamino, Narylsulphamoyl, aryl-(2-6C) alkanoylamino, heteroaryl, heteroaryl-(16C) alkyl, heteroaryloxy, heteroaryl-(1-6C) alkoxy, heteroarylamino, N-(1-6C) alkylheteroarylamino, heteroaryl-(1-6C) July 24, 2007– ט' באב התשס"ז alkylamino, N-(1-6C) alkyl-heteroaryl-(16C) alkylamino, heteroarylcarbonylamino, heteroarylsulphonylamino, Nheteroarylsulphamoyl, heteroaryl-(2-6C) alkanoylamino, heteroaryl-(1-6C) alkoxy(1-6C) alkyl, heteroaryl-(1-6C) alkylamino-(1-6C) alkyl, N-(1-6C) alkylheteroaryl-(1-6C) alkylamino-(1-6C) alkyl, heterocyclyl, heterocyclyl-(1-6C) alkyl, heterocyclyloxy, heterocyclyl-(1-6C) alkoxy, heterocyclylamino, N-(1-6C) alkyl-heterocyclylamino, heterocyclyl-(16C) alkylamino, N-(1-6C) alkylheterocyclyl-(1-6C) alkylamino, heterocyclylcarbonylamino, heterocyclylsulphonylamino, Nheterocyclylsulphamoyl, heterocyclyl-(26C) alkanoylamino, heterocyclyl-((1-6C) alkoxy-(1-6C) alkyl, heterocyclyl-(1-6C) alkylamino-(1-6C) alkyl and N-(1-6C) alkyl-heterocyclyl-(1-6C) alkylamino-(16C) alkyl, or Q is substituted with a (1-3C) alkylenedioxy group, and wherein any of the substituents on Q defined hereinbefore which comprises a CH2 group which is attached to 2 carbon atoms or a CH3 group which is attached to a carbon atom may optionally bear on each said CH2 or CH3 group a substituent selected from hydroxy, amino, (1-6C) alkoxy, (1-6C) alkylamino, di-[(1-6C) alkyl] amino and heterocyclyl, and wherein any aryl, heteroaryl or heterocyclyl group in a substituent on Q may optionally bear 1 or 2 substituents selected from hydroxy, halogeno, (1-6C) alkyl, (1-6C) alkoxy, carboxy (1-6C) alkoxycarbonyl, N-(1-6C) alkylcarbamoyl, N,N-di-[(1-6C) alkyl] carbamoyl, (2-6C) alkanoyl, amino, (1-6C) alkylamino, di[(1-6C) alkyl] amino, halogeno-(1-6C) alkyl, hydroxy(1-6C) alkyl, (1-6C) alkoxy(1-6C) alkyl, cyano-(1-6C) alkyl, amino(1-6C) alkyl, (1-6C) alkylamino-(1-6C) alkyl, di-[(1-6C) alkyl] amino-(1-6C) alkyl, aryl and aryl-(1-6C) alkyl, and wherein Q when it is a heterocyclyl group or it contains a heterocyclyl group or any 1974 heterocyclyl group in a substituent on Q may optionally bear 1 or 2 oxo or thioxo substituents; or a pharmaceuticallyacceptable salt or in-vivo-cleavable ester thereof; wherein an in-vivo-cleavable ester of a compound of the formula Ia is a pharmaceutically-acceptable ester of a compound of the formula Ia containing a carboxy group selected from a (1-6C) alkanoyloxymethyl ester, a (3-8C) cycloalkoxycarbonyloxy (1-6C) alkyl ester, a 1,3-dioxolan-2-ylmethyl ester and a (1-6C) alkoxycarbonyloxyethyl ester; and wherein R1 or Q when it is aryl, a substituent on Q when it is aryl or the aryl group within a R1 substituent or a Q group or within a substituent on Q is phenyl, indenyl, indanyl, naphthyl, tetrahydronaphthyl or fluorenyl; and wherein R1 or Q when it is heteroaryl, the heteroaryl group within a R1 substituent or a Q group, a substituent on Q when it is heteroaryl or the heteroaryl group within a substituent on Q is an aromatic 5- or 6membered monocyclic ring, a 9- or 10membered bicyclic ring or a 13- or 14membered tricyclic ring each with up to five ring heteroatoms selected from oxygen, nitrogen and sulphur; and wherein R1 or Q when it is heterocyclyl, a substituent on Q when it is heterocyclyl or the heterocyclyl group within a R1 substituent or a Q group or within a substituent on Q is a non-aromatic saturated or partially saturated 3- to 10membered monocyclic or bicyclic ring with up to five heteroatoms selected from oxygen, nitrogen and sulphur; except that 3-(5-benzamido-2-methylphenyl)-2methyl-3,4-dihydroquinazolin-4-one, 3-[5(4-methylbenzamido)-2-methylphenyl]-2methyl-3,4-dihydroquinazolin-4-one and 3-[5-(4-methoxybenzamido)-2methylphenyl]-2-methyl-3,4dihydroquinazolin-4-one are excluded. __________ ]11[]21[ 145401 תכשריי רוקחות,תרכובות הטרוציקליות המכילים אותן והשימוש בהן בטיפול באי סדרים הקשורים בקולטן הכמוקין ]54[ HETEROCYCLIC COMPOUNDS, PHARMACEUTICAL COMPOSITIONS COMPRISING THEM AND THEIR USE FOR TREATING DISORDERS INVOLVING A CHEMOKINE RECEPTOR ]22[ ]31[ ]51[ 24.03.2000 60/125823 ]32[ 24.03.1999 ]33[ US Int. Cl.8 A61K 031/395, A61P 043/00, C07D 213/00, 213/36, 215/16, 401/12, 405/12, 409/12, 413/12, 417/12 ANORMED, INC., CANADA WO/2000/056729 REINHOLD COHN AND ,ריינהולד כהן ושותפיו PARTNERS, תל אביב,4060 .ד. ת, 21 רחוב אחד העם 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]71[ ]87[ ]74[ 1975 July 24, 2007– ט' באב התשס"ז [57] A compound of the formula and the salts thereof, wherein, W is a nitrogen atom and Y is void or, W is a carbon atom and Y=H; R1 to R7 may be the same or different and are independently hydrogen or an unsubstituted straight, branched or cyclic C1-6 alkyl, or R1 and R2 together represent =O R8 is an unsubstituted heterocyclic group or an aromatic group; Ar is an aromatic or heteroaromatic ring; n and n' are independently, 0-2; X is a group of the formula wherein, Ring A is a saturated or unsaturated 5 or 6-memberd ring, and P is C, N, S or O, optionally substituted with halogen, lower alkyl or alkoxy, or hydroxy; wherein Ring B is a 5 to 7membered ring; wherein Ring A or Ring B is bound to group W from any position through group V; wherein V is a chemical bond or V is a (CH2)n'- group (where n''=0-2), or V is a C=O group, and wherein Z is hydrogen; a C0-6 alkyl group substituted with a fused or unfused aromatic or heterocyclic group; a C2-6 alkyl group; a C0-6 alkylamino or C3-7 cycloalkylamino group wherein one or more carbons in said C0-6 alkyl, C2-6 alkyl, or C0-6 alkylamino are optionally replaced with one or more heteroatoms, are substituted with =O, or both; or Z is a carbonyl or a sulfonyl, each optionally substituted with a C1-7 alkyl, amino, aryl, C1-6 alkaryl or a heterocyclic ring; each Z is optionally substituted with one or more halogen; nitro, cyano, carbonyl, carboxyl, alkyl, alkenyl, cycloalkyl, hydroxyl, thiol, amino, acyl, carboxylate, sulfonate, carboxamide, sulfonamide, C1-4 alkoxy optionally substituted with halogen, C2-4 alkanoyl, C1-4 alkylsulfonyl, aryl, aryloxy or heterocyclyl; and the pharmaceutically acceptable acid addition salts thereof; and any stereoisonteric forms and mixtures of stereoisomeric forms thereof. __________ July 24, 2007– ט' באב התשס"ז 1976 ]11[]21[ ]54[ FORWARD LINK POWER CONTROL OF MULTIPLE DATA STREAMS TRANSMITTED TO A MOBILE STATION USING A COMMON POWER CONTROL CHANNEL 145652 בקרת כוח בקישור קידמי של אפיקי מידע מרובים המשודרים לתחנה ניידת בשימוש בערוץ בקרת כוח משותף ]22[ ]31[ ]51[ ]71[ 06.04.2000 09/288262 ]32[ 08.04.1999 ]33[ US Int. Cl.8 H04B 007/005, 007/26, H04J 013/00 QUALCOMM INCORPORATED, U.S.A. ]87[ WO/2000/062443 ]74[ SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT [57] In a mobile radio telephone (e) transmitting the power control signal communication system, a method for from the mobile station to the at least one controlling transmit power levels of a base station; plurality of different data streams (f) receiving the power control signal at the transmitted from at least one base station at least one base station; to a mobile station, comprising the steps (g) forming a first received stream of of: power control commands from the (a) transmitting a first data stream from the received power control signal at the at least at least one base station to the mobile one base station; and station, and transmitting a second data (h) controlling a transmit power level of stream from the at least one base station to the first data stream from the at least base the mobile station; station in accordance with the first (b) receiving the first and second data received stream of power control streams at the mobile station; commands, and controlling a transmit (c) forming a first stream of power control power level of the second data stream from commands at the mobile station in the at least one base station in accordance accordance with either the first or second with the first received stream of power received data stream; control commands. (d) forming a power control signal at the mobile station from the first stream of power control commands; 1977 July 24, 2007– ט' באב התשס"ז ,178966 The applications for division from this application have not yet been published בקשות חלוקה מבקשה זו .שטרם פורסמו _________ ]11[]21[ ]54[ ANTAGONIST OF THE INTEGRIN ALPHA-4 SUBUNIT FOR THE TREATMENT OF FIBROSIS ]22[ ]31[ 21.04.2000 60/130847 ]32[ 22.04.1999 60/137214 01.06.1999 Int. Cl.8 A61K 039/395 BIOGEN IDEC MA INC., U.S.A. WO/2000/064474 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]51[ ]71[ ]87[ ]74[ [57] Use of a composition comprising an antibody homolog which is an antagonist of an interaction between an alpha4 subunit-bearing integrin and a ligand for The applications for division from this application have not yet been published 145898 – של4 אנטגוניסט של תת–יחידת אלפא אינטגרין לטיפול בלייפת ]33[ US US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם an alpha4 subunit-bearing integrin for the preparation of a pharmaceutical composition for the treatment of fibrosis in a subject. ,182908 בקשות חלוקה מבקשה זו .שטרם פורסמו _____________ July 24, 2007– ט' באב התשס"ז 1978 ]11[]21[ ]54[ METHOD FOR THE PREPARATION OF CITALOPRAM ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 22.11.1999 PA199900920 ]32[ 25.06.1999 Int. Cl.8 C07D 307/00, 307/87 H. LUNDBECK A/S, DENMARK WO/2000/013648 DR. SHLOMO COHEN & CO., 124 IBN GABIROL ST., P.O.B. 11490, TEL AVIV 62038 145959 שיטה להכנה של ציטאלופרם ]33[ DK ,'ד"ר שלמה כהן ושות תל אביב,11490 .ד. ת, 124 אבן גבירול [57] A method for the preparation of citalopram comprising reaction of a compound of the formula where R is halogen, or CF3-(CF2)n-SO2-Owherein n is an integer in the range 0-8, incl., with a cyanide source in a stoichiometric amount or in excess in the presence of a palladium catalyst and a catalytic amount of Cu+ or Zn2+, or with Zn(CN)2 in the presence a palladium catalyst, and isolation of the corresponding 5-cyano compound, i.e. citalopram as the base or a pharmaceutically acceptabls salt thereof. The compound of the formula 1979 July 24, 2007– ט' באב התשס"ז wherein R is CF3-(CF2)n-SO2-O- wherein n is an integer in the range 0-8 or R is iodo is claimed as novel. . ___________ ]11[]21[ 145962 נגזרות אינדאזול או בנזוטריאזול להדברת תכשריים, תהליך להכנתן,מזיקים המכילים נגזרות כאלה ושיטות לשימוש בהן ]54[ PESTICIDAL INDAZOLE OR BENZOTRIAZOLE DERIVATIVES, A PROCESS FOR THEIR PREPARATION, COMPOSITIONS CONTAINING SUCH DERIVATIVES AND METHODS FOR THE USE THEREOF ]22[ ]31[ 04.04.2000 9909062.3 ]32[ 20.04.1999 ]33[ GB 0002039.6 28.01.2000 GB Int. Cl.8 A01N 043/64, 043/72, C07D 401/12, 413/12, 417/12 SYNGENTA LIMITED, UNITED KINGDOM WO/2000/063207 S. HOROWITZ & CO., ,' הורוביץ ושות.ש ZION HOUSE, תל,41-45 שדרות רוטשילד,בית ציון 41-45 ROTHSCHILD BLVD., אביב TEL AVIV 65784 ]51[ ]71[ ]87[ ]74[ [57] A compound of the formula wherein G is either July 24, 2007– ט' באב התשס"ז 1980 wherein A, R1, R3, R4, R5, R6, J, E, D, M1, M2 are as defined in the specification. ___________ ]11[]21[ ]54[ ANTI-CD20 ANTIBODY FOR USE IN TREATMENT OF RHEUMATOID ARTHRITIS ]22[ ]31[ 04.05.2000 60/133018 ]32[ 07.05.1999 60/139621 17.06.1999 Int. Cl.8 A61K 039/395, A61P 037/00 GENENTECH, INC., U.S.A. BIOGEN IDEC INC., U.S.A. ]51[ ]71[ ]87[ ]74[ WO/2000/067796 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 146005 לטיפול בדלקת מפרקיםCD20 נוגדן כנגד ראומטואידית ]33[ US US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם [57] Use of an anti-CD20 antibody in the manufacture of a medicament for treatment of rheumatoid arthiritis in a mammal. ___________ 1981 July 24, 2007– ט' באב התשס"ז ]11[]21[ ]54[ PROCESS FOR PREPARING IMIDACHLOPRID ]22[ ]31[ ]51[ ]71[ 18.10.2001 09/752416 ]32[ 29.12.2000 Int. Cl.8 C07D 401/06 SINON CORPORATION, TAIWAN R.O.C. G.E. EHRLICH (1995) LTD., AYALON TOWER, 15TH FLOOR, 11 MENACHEM BEGIN STREET, 52521 RAMAT GAN ]74[ [57] A process for preparing imidachloprid, comprising: reacting 2nitroiminoimidazolidine with 2-chloro-5chloromethyl pyridine in the presence of an alkali carbonate in an organic solvent, wherein a stoichiometric amount of the 2- 146027 תהליך להכנת אימידאכלופריד ]33[ US ,) בע"מ1995( ארליך.אי.ג'י ,11 רחוב מנחם בגין, 15 קומה,מגדל אילון רמת גן chloro-5-chloromethyl pyridine is gradually added into mixture of a corresponding stoichiometric amount of the 2-nitroiminoimidazolidine and the organic solvent under reflux condition. __________ ]11[]21[ ]54[ EL TYPE PULVERIZERS ]22[ ]31[ ]51[ ]71[ 25.10.2001 09/698558 ]32[ 27.10.2000 Int. Cl.8 B02C 015/12 THE BABCOCK & WILCOX COMPANY, U.S.A. WOLFF, BREGMAN AND GOLLER, 19B KEREN HAYESOD ST., P.O.B. 1352, JERUSALEM 91013 ]74[ [57] An EL type pulveriser (10), comprising: a housing (12), a top grinding ring (18) having a continuous arcuate grinding track formed on a bottom surface of the top grinding ring and adapted to receive a plurality of pulveriser balls (14) each having an OD and circumference, and at least one integral snubber casted as part July 24, 2007– ט' באב התשס"ז 146157 EL כותשים מסוג ]33[ US , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד of the parent material of the top grinding ring and formed on an outer edge of the top grinding ring, snubber attachment means attached to the housing for securing the integral snubber to the housing, and a plurality of equally spaced apart flutes (26) extending downwardly from the outer edge of the top grinding ring. 1982 ____________ ]11[]21[ 146228 שיטה מחוץ לגוף לסינון תרכובות ]54[ IN-VITRO METHOD OF SCREENING COMPOUNDS ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 27.06.2000 60/141563 ]32[ 29.06.1999 ]33[ US Int. Cl.8 C12N 009/02, C12Q 001/26, G01N 033/50, 033/68 NEW YORK UNIVERSITY, U.S.A. WO/2001/001131 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 [57] An in-vitro method of screening for compounds that inhibit melanogenesis, the method comprising: treating cells expressing a tyrosinase-encoding gene with a test compound, and determining the cellular localization of tyrosinase in the presence of the test compound; wherein a change in the cellular localization of tyrosinase in the presence of the test compound as compared to in the absence of the test compound indicates that the test compound is a candidate for a compound that inhibits melanogenesis. ___________ 1983 July 24, 2007– ט' באב התשס"ז ]11[]21[ ]54[ EXTRUDED AERATED COMPOSITIONS AND PROCESS AND APPARATUS FOR PREPARING SUCH COMPOSITIONS ]22[ ]31[ ]51[ ]71[ 06.11.2001 00310835.4 ]32[ 06.12.2000 Int. Cl.8 A23G 000/93200 UNILEVER PLC, UNITED KINGDOM REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]74[ [57] A cold extruded composition comprising a fat phase and having an overrun of at least 90%, characterized in 146357 הרכבים אווריריים ותהליך והתקן לייצורם ]33[ EP ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם that at least 45% w/w of the fat phase is liquid at -5˚C. _____________ ]11[]21[ 146731 VIIa מעכבי פקטור ]54[ FACTOR VIIA INHIBITORS ]22[ ]31[ ]51[ ]71[ 27.05.2000 99111109.7 ]32[ 08.06.1999 ]33[ EP Int. Cl.8 A61K 038/05, A61P 007/02, C07K 005/068 SANOFI-AVENTIS DEUTSCHLAND GMBH, GERMANY WO/2000/075172 EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688, HERZLIYA 46733 ]87[ ]74[ [57] A compound of the formula July 24, 2007– ט' באב התשס"ז 1984 wherein r is 0, 1, 2 or 3; s is 0, 1, 2, 3 or 4; t is 0, 1 or 2; R1 is selected from the series consisting of hydrogen, R11-CO- and R12-SO2-; R11 is selected from the series consisting of hydrogen, (C1-C8)-alkyl, (C6-C14)-aryl, (C6-C14)-aryl-(C1-C4)-alkyl-, Het-, Het(C1-C4)-alkyl-,(C1-C8)-alkyloxy-(C6-C14)aryloxy-, (C6-C14)-aryl-(C1-C4)-alkyloxyamino, (C1-C8)-alkylamino-, (C6-C14)arylamino- and (C8-C14)-aryl-(C1-C4)alkylamino-, where all these groups are unsubstituted or substituted by one or more identical or different substituents R40; R12 is selected from the series consisting of (C1-C8)-alkyl, (C6-C14)-aryl, (C6-C14)-aryl(C1-C4)-alkyl-, Het-, Het-(C1-C4)-alkyl-, di((C1-C8(-alkyl)amino- and di((C6-C14)aryl-(C1-C4)-alkyl) amino-, where all these groups are unsubstituted or substituted by one or more identical or different substituents R40; R2 is hydrogen, R21(R22)CH-, R23-Het(CH2)k-, R23(R24)N-(CH2)m-D-(CH2)n- or R25(R26)N-CO-(CH2)p-D-(CH2)q-, where D is a divalent residue –C(R31)(R32)-, a divalent (C6-C14)-arylene residue or a divalent residue derived from an aromatic group Het containing 5 to 10 ring atoms of which 1, 2, 3 or 4 are identical or different ring heteroatoms selected from the series consisting of nitrogen, oxygen and sulfur, and the numbers k, m, n, p and q which are independent of each other and can be 1985 identical or different are 0, 1, 2, 3, 4 or 5, with the proviso that in case D is – C(R31)(R32)- the sum m+n cannot be 0 and the sum p+q cannot be 0; R21 and R22 which are independent of each other and can be identical or different are selected from the series consisting of hydrogen, (C1-C12)-alkyl, (C6-C14)-aryl, (C6-C14)-aryl-(C1-C4)-alkyl-, Het- and Het(C1-C4)-alkyl-, where all these groups are unsubstituted or substituted by one or more identical or different substituents from the series consisting of R40, (C1-C8)alkylamino-, di-((C1-C8)-alkyl)-amino-, (C6-C14)-aryl-(C1-C4)-alkylamino, (C6C14)-arylamino-, aminocarbonyl- and aminocarbonyl-(C1-C8)-alkyl-, or R21 and R22 together with the carbon atom to which they are bonded form a saturated or unsaturated 3-membered to 8membered carbocyclic ring which can be condensed to one or two ring systems which are heteroaromatic rings containing 5 to 10 ring atoms of which 1, 2 or 3 are identical or different heteroatoms selected from the series consisting of nitrogen, oxygen and sulfur, and/or (C6-C10) carbocyclic aromatic rings, where the resulting group R21(R22)CH- is unsubstituted or substituted by one or more identical or different substituents from the series consisting of R40, ((C1-C8)alkylamino-, di-((C1-C8)-alkyl)-amino-, (C6-C14)-aryl-(C1-C4)-alkylamino-, (C6C14)-arylamino-, aminocarbonyl- and aminocarbonyl-(C1-C8)-alkyl-; July 24, 2007– ט' באב התשס"ז R23 is hydrogen, R27-SO2- or R28-CO-; R24 is selected from the series consisting of hydrogen, (C1-C8)-alkyl, (C6-C14)-aryl and (C6-C14)-aryl-(C1-C4)-alkyl; R25 and R26 which are independent of each other and can be identical or different are selected from the series consisting of hydrogen, (C1-C8)-alkyl, (C6-C14)-aryl, (C6-C14)-aryl-(C1-C4)-alkyl-, Het- and Het(C1-C4)-alkyl-, where all these groups are unsubstituted or substituted by one or more identical or different substituents R40; R27 is selected from the series consisting of (C1-C8)-alkyl, (C6-C14)-aryl, (C6-C14)-aryl(C1-C4)-alkyl-, Het-, Het-(C1-C4)-alkyl-, amino, (C1-C8)-alkylamino-, di-((C1-C8)alkyl)amino-, (C6-C14)-arylamino- and (C6C14)-aryl-(C1-C4)-alkylamino-, where all these groups are unsubstituted or substituted by one or more identical or different substituents R40; R24 is selected from the series consisting of R27, (C1-C8)-alkyloxy- (C6-C14)-aryloxyand (C6-C14)-aryl-(C1-C4)-alkyloxy-, where all these groups are unsubstituted or substituted by one or more identical or different substituents R40; R31 and R32 which are independent of each other and can be identical or different are selected from the series consisting of hydrogen, (C1-C12)-alkyl, (C6-C14)-aryl, (C6-C14)-aryl-(C1-C4)-alkyl-, Het- and Het(C1-C4)-alkyl- where all these groups are unsubstituted or substituted by one or more identical or different substituents R40; R40 is selected from the series consisting of halogen, hydroxy, (C1-C8)-alkyloxy-, (C6C14)-aryl-(C1-C8)-alkyloxy-, (C6-C14)aryloxy-, (C1-C8)-alkyl, (C6-C14)-aryl, (C6C14)-aryl-(C1-C8)-alkyl-, (C1-C8)- alkylsulfonyl, trifluoromethyl, acetylamino-, amino, amidino, guanidine, oxo, nitro and cyano, where the groups R40 are independent of each other and can be identical or different; R91, R92 and R93 which are independent of each other and can be identical or different are selected from the series consisting of hydrogen, (C1-C8)-alkyl, (C6-C14)-aryl, (C6-C14)-aryl-(C1-C4)-alkyl-, Het- and Het(C1-C4)-alkyl-; R94 is selected from the series consisting of (C1-C4)-alkyl, (C6-C14)-aryl, amino, nitro, halogen, trifluoromethyl, hydroxy, (C1C4)-alkyloxy-, where the groups R94 are independent of each other and can be identical or different; R95 is selected from the series consisting of amidino, guanidine, ((C1-C4)-alkyl) oxycarbonylamidino-, ((C1-C4)-alkyl) oxycarbonylguanidino- and hydroxyamidino-; R96 is hydrogen; R97 is R99 –(C1-C8)-alkyl-; R99 is selected from the series consisting of hydroxycarbonyl-, (C1-C8)alkoxycarbonyl, -(C6-C14)-aryl-(C1-C4)alkyloxycarbonyl-, aminocarbonyl- and (C1-C8)-alkylaminocarbonyl-; Het is a saturated, partially unsaturated or aromatic monocyclic or bicyclic heterocyclic ring system containing 3 to 10 ring atoms of which 1, 2, 3 or 4 are identical or different heteroatoms selected from the series consisting of nitrogen, oxygen and sulfur; in all its stereoisomeric forms and mixtures thereof in any ratio, and its physiologically tolerable salts. ___________ July 24, 2007– ט' באב התשס"ז 1986 ]11[]21[ ]54[ METHOD AND INSTALLATION FOR TAPPING FRESH WATER AND DETECTING FRESH WATER SOURCE AT SEA ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 15.05.2000 99/07991 ]32[ 18.06.1999 Int. Cl.8 G01V 009/02 NYMPHEA WATER, FRANCE WO/2000/079309 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] A method of collecting fresh water that is resurgent at sea, the method being characterized in that: an installation is used which comprises an immersed reservoir, with its open concave side facing downwards and suitable for trapping fresh water, the circumference of the bottom end of said reservoir surrounding said fresh water resurgence, and fitting closely to the outline of the relief of the bottom of the sea so as to provide leakproofing between said circumference and the bottom of the 146846 שיטה והתקן לאגירת מיים מתוקים ולגילוי מקור מים מתוקים במי ים ]33[ FR ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם sea, said reservoir being constituted by a double-walled envelope into which there is injected a slurry of concrete of specific gravity close to 1, so as to enable the double-walled envelope to retain a shape of spherical cap after it has been filled with concrete; and fresh water is collected by means of a pipe with its first end opening out inside the reservoir, preferably into the top portion thereof and its second end opening out into a zone on land situated below sea level. __________ 1987 July 24, 2007– ט' באב התשס"ז ]11[]21[ 146979 מיכל ]54[ CONTAINER ]22[ ]31[ ]51[ ]71[ 07.06.2000 336144 ]32[ 08.06.1999 ]33[ NZ Int. Cl.8 B65D 081/18, 088/74, F25D 017/04 QPOD SYSTEMS LIMITED, NEW ZEALAND WO/2000/075041 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]87[ ]74[ [57] A container comprising a base (4), four side walls (5) and a top (14), the side walls having ducts therein through which gas can flow, wherein the gas moves up an adjacent pair of said side walls and down an opposing adjacent pair of side walls to form a pair of pathways, the pair of pathways crossing each other at the top without intersection of the pathways. ___________ July 24, 2007– ט' באב התשס"ז 1988 ]11[]21[ ]54[ APPARATUS AND METHOD FOR MEASURING INCLINATION ]22[ ]31[ ]51[ ]71[ 06.12.2001 140206 ]32[ 10.12.2000 Int. Cl.8 G01C 009/12 YUVAL SINGER FEDERICO SINGER, U.S.A. ]74[ YUVAL SINGER, 86 HATISHBI ST, HAIFA 34522 [57] Inclination measurement apparatus for mounting on a surface for measuring its inclination with respect to a desired measurement axis, the apparatus comprising: (a) a reference clinometer for issuing inclination measurement Vref responsive to the inclination of the surface with respect to the desired measurement axis; (b) an indexable turntable bearing a clinometer and rotatable between a pair of precisely reproducible diametrically opposite orientations with respect to the 1989 146981 התקן ושיטה למדידת שיפוע ]33[ IL חיפה,יובל זינגר ,יובל זינגר חיפה,86התישבי desired measurement axis for respectively issuing inclination measurements V0 and V180 responsive to the inclination of the surface with respect to the desired measurement axis; and (c) a controller for calculating a bias corrected inclination measurement Vreal of the inclination of the surface with respect to the desired measurement axis from an inclination measurement Vref at least during a periodic bias correction procedure for updating at least one of said clinometers' transient bias values. July 24, 2007– ט' באב התשס"ז ____________ ]11[]21[ ]54[ METHOD FOR DATA CARE IN A NETWORK OF PARTIALLY REPLICATED DATABASE SYSTEMS ]22[ ]31[ 13.05.2000 19928035.5 ]32[ 18.06.1999 99120009.8 14.10.1999 Int. Cl.8 G06F 017/00 SAP AG, GERMANY WO/2000/079408 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]51[ ]71[ ]87[ ]74[ [57] Method for data maintenance in an offline-distributed database network system (DBNS) which comprises a central system (CS) having a central database (CD), and a number of node systems (NS) having local databases (LD), wherein the local databases (LD) at least in some cases contain different subsets of the data from July 24, 2007– ט' באב התשס"ז 147105 שיטה לטיפול בנתונים ברשת של מערכות בסיס נתונים משוכפלות חלקית ]33[ DE EP ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה the central database (CD), change information relating to the data stored in the database (CD, LD) in the database network system (DBNS) is recorded in a plurality of node systems (NS), the change information is transmitted, when an online connection exists, as replication objects which are structured in a plurality of 1990 different types and contain an identification key, from the node systems to the central system or from the central system to the node systems, if there is no online connection, the replication objects are queued, in an outbound queue, for subsequent transmission, characterized in that the replication objects are, in a replication algorithm in the central system (CS), allocated by means of at least one lookup table (LUT) together with the change information to the node systems (NS) as responsibles to which they are intended to be transmitted, and the at least one lookup table is updated, in a realignment algorithm, taking account of the change information. ___________ ]11[]21[ ]54[ SYSTEM AND METHOD FOR MIGRATION OF SUBSCRIBER DATA ]22[ ]31[ ]51[ ]71[ ]74[ 17.12.2001 09/739745 ]32[ 20.12.2000 Int. Cl.8 G06F 017/30, H04Q 007/38 COMVERSE, INC., U.S.A. G.E. EHRLICH (1995) LTD., AYALON TOWER, 15TH FLOOR, 11 MENACHEM BEGIN STREET, 52521 RAMAT GAN [57] A method of relocating data in a communication system having at least one central management server and information servers geographically distributed to provide access to subscribers, said method comprising: 1991 147137 מערכת ושיטה לשינוע נתוני מנוי ]33[ US ,) בע"מ1995( ארליך.אי.ג'י ,11 רחוב מנחם בגין, 15 קומה,מגדל אילון רמת גן generating at the information servers an activity log file including location data and identifiers, the location data indicating which of the information servers provided access by the subscribers to information locally accessible by the information July 24, 2007– ט' באב התשס"ז servers and each identifier being associated with one of a communication device and a person using the communication system; initially storing the activity log file at the information servers; transferring log data derived from the activity log file from each of the information servers to the central management server; automatically performing pattern analysis at the central management server based on the location data and the identifiers; and relocating private data, associated with one of the identifiers, from a first location to a second location within the communication system when the pattern analysis indicates that service can be provided more efficiently from the second location. ___________ ]11[]21[ פורמולציות של הורמון הגדילה ]54[ GROWTH HORMONE FORMULATIONS ]22[ ]31[ 11.07.2000 9916252.1 ]32[ 12.07.1999 9918902.9 12.08.1999 Int. Cl.8 A61K 038/27, 047/26 SANDOZ AG, SWITZERLAND WO/2001/003741 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]51[ ]71[ ]87[ ]74[ 147253 [57] A multi-dosage, storage stable liquid human growth hormone formulation consisting essentially of growth hormone in isotonic phosphate buffered solution, a preservative and a non-ionic surfactant, ]33[ GB GB ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה wherein isotonicity of the phosphate buffered solution is provided by a neutral salt, a monosaccharide, a disaccharide or a sugar alcohol, the formulation having a pH in the range of 6.15 to 6.5. ____________ July 24, 2007– ט' באב התשס"ז 1992 ]11[]21[ ]54[ TELEPHONE NETWORK-BASED METHOD AND SYSTEM FOR AUTOMATIC INSERTION OF ENHANCED PERSONAL ADDRESS BOOK CONTACT DATA ]22[ ]31[ ]51[ ]71[ ]74[ 24.12.2001 09/774088 ]32[ 31.01.2001 Int. Cl.8 G10L 015/00, H04M 003/42 COMVERSE LTD. G.E. EHRLICH (1995) LTD., AYALON TOWER, 15TH FLOOR, 11 MENACHEM BEGIN STREET, 52521 RAMAT GAN [57] A telephone network-based system for automatic insertion of web-enhanced contact data into a personal address book associated with a user that has access to an electronic communications network, said system comprising: a first application unit operable to host the telephone networkbased system; a second application unit programmed to present the user with contact data obtained via the electronic communications network and assist the user in selecting at least a portion of the contact data for entry into the personal address book, said second application unit comprising: a voice response unit operable to route a user-initiated call into the system, to said second application unit; a recognition server comprising an automatic speech recognizer operable to convert a verbalized form of a new contact 1993 147276 שיטה ומערכת מבוססות רשת טלפון להחדרה אוטומטית של מידע משופר של תוכן ספר כתובות ]33[ US רמת החייל,קומברס בע"מ ,) בע"מ1995( ארליך.אי.ג'י ,11 רחוב מנחם בגין, 15 קומה,מגדל אילון רמת גן name to a text form, wherein the text form of the new contact name forms part of the user-initiated call; a storage unit operable to store at least one textual directory for loading into said recognition server; a comparison unit operable to compare the converted text form of the new contact name with a plurality of text entries in the at least one stored textual directory; and a textual directory unit for searching the electronic communications network to locate and select the contact data based on a telephone number corresponding to the new contact name, wherein the selected contact data is inserted into the personal address book associated with the user and wherein further, the selected contact data is data other than the new contact name and the telephone number corresponding to the new contact name. July 24, 2007– ט' באב התשס"ז __________ ]11[]21[ 147370 שיטה ומערכת להכוונת רכב מרוחק באמצעות ערוץ תקשורת מפגר ]54[ METHOD AND SYSTEM FOR GUIDING A REMOTE VEHICLE VIA LAGGED COMMUNICATION CHANNEL ]22[ ]51[ ]71[ 27.12.2001 Int. Cl.8 F41G 003/00, 007/00, G01S 005/00, 013/00, G05D 001/00, H04N 007/26 RAFAEL ARMAMENT ,רפא"ל רשות לפיתוח אמצעי לחימה בע"מ DEVELOPMENT AUTHORITY חיפה LTD. ITZAK FLORENTIN, LIAT אמיר קליסמן, ליאת ברגר,יצחק פלורנטין BERGER, AMIR KALISMAN LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו INDUSTRIAL PARK, OMER, באר שבע,5352 .ד. ת, עומר,גן תעשייה P.O.B. 5352, BEER-SHEVA 84152 ]72[ ]74[ [57] A method for guiding from a remote control center a vehicle towards a target object, said remote control center communicating with the vehicle by means of a lagged communication channel, comprising: at the vehicle: July 24, 2007– ט' באב התשס"ז (i) periodically capturing frame images by a camera, assigning to each of said captured frames an associated unique time stamp, and saving within a storage at the vehicle full frame data or partial frame data of captured frames and their associated time stamps; 1994 (ii) for a plurality of saved frames, sending to the control center via the lagged communication channel full frame data, partial frame data or a combination thereof with the corresponding associated time stamp for each sent frame so that approximate or exact version of the sent frames can be reconstructed and displayed at the control center; at the control center: (iii) receiving said frame data and associated time stamps, sequentially reconstructing frame images from each said sent full and/or partial frame data, and displaying the reconstructed images on a display; (iv) upon marking by an operator at the control center a point on a specific displayed frame, sending coordinates indication relating to said marked point as appearing on said specific frame or on a reference frame available at the control center, and the time stamp associated with said specific or reference frame, as is the case, to the vehicle; at the vehicle: (v) receiving said coordinates indication as marked and the sent frame time stamp; (vi) given the coordinates indication and frame time stamp as received, fast forward tracing said point or object coordinates from the said frame towards the most recently available captured frame, thereby finding the coordinates of the same point or object as appearing in the most recently available captured frame; and (vii) providing the coordinates of the target point or object within the most recently available captured frame, as found, to an inner guidance sub-system of the vehicle, for enabling it to track said object. _____________ 1995 July 24, 2007– ט' באב התשס"ז ]11[]21[ 147495 – און מותמרות2 – תרכובות פיפראזין ]54[ SUBSTITUTED PIPERAZINE - 2 ONE COMPOUNDS ]22[ ]31[ ]51[ ]71[ 26.07.2000 09/363196 ]32[ 28.07.1999 ]33[ US Int. Cl.8 A61K 031/395, A61P 007/00, C07D 403/14, 409/14, 471/02, 495/02 AVENTIS PHARMACEUTICALS INC., U.S.A. WO/2001/007436 EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688, HERZLIYA 46733 ]87[ ]74[ [57] A compound of the formula or a pharmaceutically acceptable salt thereof, an N-oxide thereof, a hydrate thereof or a solvate thereof, wherein L1 and L2 are independently methylene or ethylene; Cy1 is thiophen-isoxazol, thiophenoxadiazol, thiophen-thiadiazol, thiophentriazol, thiophen-pyridin or phenyl-triazol; wherein Cy2 is unsubstituted or substituted with one or more groups selected from amino, halo, which is selected from the group consisting of fluoro, chloro, bromo or iodo, hydroxyl, aryl, which is selected from the group consisting of phenyl or naphthyl, amidino, which is a group of formula alkyl, which is selected from the group consisting of methyl, ethyl or propyl, acylamino, which is selected from the group consisting of formylamino, acetylamino, propanoylamino, 2- July 24, 2007– ט' באב התשס"ז methylpropanoylamino, butanoylamino or palmitoylamino, carbamoyl, which is selected from the group consisting of carbamoyl or dimethylaminocarbamoyl, cyano, alkoxy, which is selected from the 1996 group consisting of methoxy, ethoxy, npropoxy, i-propoxy, n-butoxy or heptoxy, nitro, carbamate, which is selected from the group consisting of methylcarbamate, ethylcarbamate, t-butylcarbamate, benzylcarbamate or phenylcarbamate, or sulfamoyl; Cy2 is amino-quinazolin or pyrrolopyridin; wherein Cy2 is unsubstituted or substituted with one or more groups selected from amino, carbamoyl, which is as defined above, acylamino, which is as defined above, alkyl, which is as defined above, amidino, which is as defined above, alkyloxycarbonyl, which is selected from the group consisting of methoxycarbonyl, ethoxycarbonyl, or t-butyloxycarbonyl, hydroxyl, alkoxy, which is as defined above, aryl, which is selected from the group consisting of phenyl or naphthyl, isourea, which is a group of the formula guanidino, which is a group of the formula acylhydrazino, which is a group of the formula H2N-NHC(O)-, acyl, which is selected from the group consisting of formyl, acetyl, propanoyl, 2methylpropanoyl, butanoyl and palmitoyl, cyano, carboxyl, sulfamoyl, or halo, which is as defined above; and R1, R1a, R2, R2a, R4 and R4a are independently selected from hydrogen or alkyl, which is selected from the group consisting of methyl, ethyl or propyl. . ___________ 1997 July 24, 2007– ט' באב התשס"ז ]11[]21[ ]54[ EXPANDING PARALLEL JAW DEVICE FOR USE WITH AN ELECTROMECHANICAL DRIVER DEVICE ]22[ ]31[ ]51[ ]71[ 11.07.2000 351534 ]32[ 12.07.1999 Int. Cl.8 A61B 017/04 POWER MEDICAL INTERVENTIONS, INC., U.S.A. WO/2001/003587 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A fastening and cutting device for cutting and fastening a section of tissue, comprising: a first jaw (80); a second jaw (50) disposed in parallel and opposed correspondence with the first jaw; a vertical driver means coupled to said first jaw, which driver means causes the first jaw to linearly travel along an axis perpendicular to the axis of parallel correspondence of the first and second jaws, such that the first jaw separates from the second jaw when the driver means is biased for opening of the jaws and closes towards the second jaw when the driver means is biased for closing of the jaws; 147511 שימוש בהתקן בעל זרועות מקבילים יחד עם רכיב אלקטרומכני דוחף ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם and a cutting and stapling means (230, 232) disposed within the second jaw and coupled with a horizontal driver means for cutting and stapling a section of tissue disposed between the first and second jaws once the first jaw has been closed onto the second jaw; wherein the vertical driver means further includes a pair of threaded turning shafts and a horizontal threaded gearing shaft (130) disposed in turning and gearing relationship with said pair of threaded turning shafts, the rotation of the horizontal gearing shaft thereby causing the first jaw to translate. ____________ July 24, 2007– ט' באב התשס"ז 1998 ]11[]21[ 147630 מערכת עורך המביטה פנימה ושיטה לתרגום תוכנה ]54[ INTROSPECTIVE EDITOR SYSTEM, PROGRAM AND METHOD FOR SOFTWARE TRANSLATION ]22[ ]31[ ]51[ ]71[ 13.07.2000 09/362615 ]32[ 28.07.1999 ]33[ US Int. Cl.8 G06F 003/00, 009/44, 009/45, 009/46, 017/20 INTERNATIONAL BUSINESS MACHINES CORPORATION, U.S.A. WO/2001/008006 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]87[ ]74[ [57] A method for editing textual data for a software program, comprising: displaying a user interface containing a first textual data within a non-data, user interaction portion of the user interface; responsive to selection of the first textual data within the displayed user interface by a user for editing, introspecting source code for generating the user interface to identify a software object that includes the first textual data; receiving a second textual data which the user desires to replace the first textual data from a user input while the user interface is being displayed; storing the second textual data in a machine-readable form within the software object in place of the first textual data; and during execution of the source code for generating the user interface display after storing the second textual string within the software object, displaying the second textual data in place of the first textual data within the user interface. ____________ 1999 July 24, 2007– ט' באב התשס"ז ]11[]21[ 147719 שיטה והתקן לעיבוד בו זמני של מספר שיחות במערכת תקשורות פורשת טווח תדר ]54[ METHOD AND APPARATUS FOR CONCURRENTLY PROCESSING MULTIPLE CALLS IN A SPREAD SPECTRUM COMMUNICATIONS SYSTEM ]22[ ]31[ 11.08.2000 60/148790 ]32[ 13.08.1999 ]33[ US 09/519003 03.03.2000 US Int. Cl.8 H04J 013/02, 013/04, H04Q 007/22, 007/32, 007/38 QUALCOMM INCORPORATED, U.S.A. WO/2001/013669 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]51[ ]71[ ]87[ ]74[ [57] A method for processing one or more calls concurrently in a spread spectrum communications system, the method comprising: receiving an indication of a particular call to be processed; instantiating a type of a call control state machine in accordance with the type of the particular call, wherein the instantiated call control state machine is identified with and used to control processing of the particular call; and exchanging one or more data transmissions related to the particular call. __________ July 24, 2007– ט' באב התשס"ז 2000 ]11[]21[ 147799 שיטה להחלפת מידע בין טלפונים ניידים ]54[ METHOD OF EXCHANGING DATA BETWEEN MOBILE PHONES ]22[ ]31[ ]51[ ]71[ 23.01.2002 2001-5795 ]32[ 07.02.2001 ]33[ KR Int. Cl.8 H04B 001/38, H04M 001/274, 001/725, H04Q 007/20 SK TELETECH CO., LTD., REPUBLIC OF KOREA REINHOLD COHN AND ,ריינהולד כהן ושותפיו PARTNERS, תל אביב,4060 .ד. ת, 21 רחוב אחד העם 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]74[ [57] A method of exchanging data between mobile phones through an interworking function in an IS-95A/B network, comprising: a first step in which a receiving mobile phone enters data reception mode as a receiving user selects data call receiving mode; a second step in which a transmitting mobile phone initiates a data call to the receiving mobile phone; a third step in which as the receiving mobile phone answers the call, data exchange between the mobile phones proceeds; and a fourth step in which data transmission from the transmitting mobile phone to the receiving mobile phone is completed. ___________ ]11[]21[ 2001 147954 July 24, 2007– ט' באב התשס"ז ]54[ METHOD AND APPARATUS FOR MODELING OF THE INTRA-AND EXTRAVASCULAR OPERATIONS ON THE DIFFERENT SECTIONS OF THE CIRCULATION SYSTEM AND FOR TESTING OF THE INTRAVASCULAR DEVICES THEREFOR ]22[ ]51[ ]71[ ]72[ 03.02.2002 Int. Cl.8 A61B 005/021, G09B 023/28 EDWARD G.SHIFRIN EDWARD G. SHIFRIN, GENNADY S. NICKELSHPUR, ARKADY S. NICKELSHPUR, NACHMAN KUDLIK, WESLY S. MOORE, PETER RF BELL WOLFF, BREGMAN AND GOLLER, 19B KEREN HAYESOD ST., P.O.B. 1352, JERUSALEM 91013 ]74[ [57] A stand (1) for modeling intravascular and extravascular operation on circulation system sections and for testing intravascular devices for these operations, including a supporting structure, peristaltic pump (12) with a working head, reservoir (16) with fluid imitating blood, models (18, 20) of internal organs or some circulation system section, as well as tubing (22) to connect the peristaltic pump with the reservoir and with models of internal organs or of circulation system sections, wherein the improvement comprises: (a) a supporting structure with a bearing surface, and at least one peristaltic pump serving for providing circulation of liquid imitating blood and it is provided with a system for adjusting fluid circulation rate and direction of circulation; (b) a tubing passing through the working head of at least one peristaltic pump and including at least one closed tube (26) made substantially of transparent material, and at least a part of the closed tube July 24, 2007– ט' באב התשס"ז שיטה והתקן להדגמה של ניתונים תוך כלי הדם ומחוץ לכלי הדם בחלקים שונים של מערכת מחזור הדם לבדיקת התקנים לשימוש תוך כלי הדם שיפרין.אדוארד ג , ניקלשפור. גנאדי ס, שיפרין.אדוארד ג . וסלי ס, נחמן קודלין, ניקלשפור.ארכדי ס פיטר רפ בל,מור , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד disposed in the area of the working head of peristaltic pump is made of flexible material; (c) a hermetically sealed chamber (30) of transparent material mounted on the bearing surface of supporting structure, at least a part of said closed tube being disposed within said hermetically sealed chamber and detachable; (d) at least one model (32, 34) of a circulation system section mounted within the hermetically sealed chamber, between detachable ends of said closed tube, in such a way that said model forms, together with the closed tube, a single unit for circulation system imitation, the model being provided with an axial passage for introducing medical instrument therein, and said axial passage has an input port, disposed outside the hermetically sealed chamber and provided with a back valve; (e) means for filling the unit for circulation system imitation with a fluid imitating blood and taken from said reservoir; (f) means for filling the hermetically 2002 sealed chamber with transparent fluid under pressure to imitate the density of tissues surrounding outside the circulation system section; (g) means (50) for detecting leakages of fluid imitating blood from the circulation system section in modeling a surgical operation within said section; (h) means for removing air from the fluid circulating over the unit for imitation of blood circulation system, whereby there are modeled intravascular and extravascular surgical operations performed by minimally invasive surgery techniques inside circulation system sections, such as operation for placing within the aorta with an aneurysm a stentgraft and fixating it from inside to the aorta walls by means of special staplers, as well there are tested the performance and efficacy of new intravascular instruments developed for application in minimally invasive surgery techniques. __________ ]11[]21[ 148002 על ידי הטבעת,שיטה להגנה מהעתקה סימני–מים בוידאו ]54[ SCALING INDEPENDENT COPY PROTECTION TECHNIQUE FOR WATERMARKING IMAGES ]22[ ]31[ ]51[ ]71[ 01.08.2000 09/369642 ]32[ 06.08.1999 ]33[ US Int. Cl.8 G06T 001/00, G11B 020/10, H04N 005/91, 005/92, 007/26 MACROVISION CORPORATION, U.S.A. WO/2001/011890 EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688, HERZLIYA 46733 ]87[ ]74[ [57] A method to prevent illicit copying of video information comprising: 2003 (a) embedding a watermark having a first scale selected from the range of scales in July 24, 2007– ט' באב התשס"ז the video information for a first time period; (b) during or at the end of the first predetermined period, embedding a watermark having another scale selected from the range of scales in the content of the video information for a second time period; and (c) repeating step (b) using a different scale until a N number of scales is reached. ____________ ]11[]21[ ]54[ TOOLHOLDER ASSEMBLY ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 23.08.2000 09/388258 ]32[ 01.09.1999 Int. Cl.8 B23B 029/04 KENNAMETAL INC., U.S.A. WO/2001/015841 WOLFF, BREGMAN AND GOLLER, 19B KEREN HAYESOD ST., P.O.B. 1352, JERUSALEM 91013 [57] An apparatus for releasably holding a toolholder (25) with a shank (30) having lockable surfaces (90, 95) and a releasable surface (185), the apparatus comprising: (a) a tool support member (15) having a forwardly facing surface (35) and a bore (40) along a longitudinal axis (L), wherein the bore intersects the forwardly facing surface and extends rearwardly therefrom for receiving the shank of the toolholder; (b) a rotatable actuating bolt (20) positioned within the tool support member along a radial axis (R1) relative to the longitudinal axis and having a first end with a bolt locking segment having a bolt locking surface, wherein the actuating bolt further includes a releasing segment July 24, 2007– ט' באב התשס"ז 148284 מכלל מחזיק כלים ]33[ US , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד having a releasing surface for abutting and urging forwardly the releasable surface of the shank to eject the toolholder shank from the tool support member; (c) an actuating nut (75) rotatably fixed within the tool support member, threadably secured to a second end of the actuating bolt and having a nut locking segment having a nut locking surface, and (d) wherein rotation of the actuating bolt in a locking direction causes the actuating nut to be drawn to the bolt first end thereby drawing together the nut locking surface and the bolt locking surface such that they engage the toolholder lockable surfaces and lock the toolholder within the tool support member. 2004 __________ ]11[]21[ 148775 מערכת ושיטה לבדיקת הרשאה עבור העברת תוכן מוגן ]54[ SYSTEM AND METHOD OF VERIFYING AUTHORIZATION FOR COMMUNICATING PROTECTED CONTENT ]22[ ]31[ ]51[ ]71[ 19.10.2000 60/160355 ]32[ 19.10.1999 ]33[ US Int. Cl.8 H04L 009/32, H04N 005/00, 007/16 THOMSON LICENSING S.A., FRANCE WO/2001/030083 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A method for authenticating at least one security key and at least one identifier used to access protected content, said method comprising: receiving at a first device a plurality of security keys with said content; receiving said identifier at said first device to be 2005 used to provide said content to a second device, said identifier being associated with said second device; selecting one of said plurality of security keys using said first device; and, providing said content to said second device using said first device and selected security key. July 24, 2007– ט' באב התשס"ז ___________ ]11[]21[ 148926 מערכת ושיטה למתן שירותים סלולרים ברשתות שונות ]54[ SYSTEM AND METHOD FOR SHARING CELLULAR COMMUNICATION SERVICES AMONG MOBILE STATIONS OF DIFFERENT NETWORKS ]22[ ]51[ ]71[ ]74[ 27.03.2002 Int. Cl.8 H04L 029/06, H04Q 003/00, 007/20, 007/24, 007/38 CELLCOM ISRAEL LIMITED נתניה,סלקום ישראל בע"מ REINHOLD COHN AND ,ריינהולד כהן ושותפיו PARTNERS, תל אביב,4060 .ד. ת, 21 רחוב אחד העם 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] A wireless multi-protocol communications system for use by a subscriber, the system comprising: (a) a plurality of incompatible wireless single-protocol networks; (b) a plurality of single-protocol mobile stations, such that for each of said wireless single-protocol networks there is at least one of said single-protocol mobile stations operative to communicating thereover; and (c) a common telephone number which is shared among at least two of said mobile stations which are operative to communicating over incompatible wireless July 24, 2007– ט' באב התשס"ז single-protocol networks; wherein at least a first of said at least two mobile stations is operative over a first network having a Home Location Register (HLR) accommodating a configuration that includes a Calling Line Identity (CLI) associated with the first mobile station; said HLR is configured to comprise a new CLI, said CLI is associated with said common telephone number, thereby allowing the subscriber to utilize any of said at least two mobile stations to conduct communications according to said common telephone number. 2006 ,182840 The applications for division from this application have not yet been published בקשות חלוקה מבקשה זו .שטרם פורסמו ___________ ]11[]21[ ]54[ CUTTING TISSUE WITH ELECTROSURGICALLY DEPLOYED ELECTRODES ]22[ ]31[ ]51[ ]71[ 10.10.2000 09/418923 ]32[ 15.10.1999 Int. Cl.8 A61B 018/18 NEOTHERMIA CORPORATION, U.S.A. WO/2001/028445 G.E. EHRLICH (1995) LTD., AYALON TOWER, 15TH FLOOR, 11 MENACHEM BEGIN STREET, 52521 RAMAT GAN ]87[ ]74[ [57] Apparatus for electrosurgically cutting a targeted region of tissue, utilizing the output, including a return, of an electrosurgical generator, comprising: a support member extending between a tip and a base region, having a forward end region extending along a longitudinal axis from said tip and positionable in an insertion mode into adjacency with said 2007 148989 –חיתוך רקמה עם אלקטרודות חשמל ניתוחיות נפרשות ]33[ US ,) בע"מ1995( ארליך.אי.ג'י ,11 רחוב מנחם בגין, 15 קומה,מגדל אילון רמת גן targeted region of tissue, and having a deployment portion at said forward end region adjacent said tip; said support member forward end region being substantially cylindrical and said deployment portion including an outwardly open slot extending along said longitudinal axis from a securement region adjacent said tip to a forward location, July 24, 2007– ט' באב התשס"ז thence along a deployment slot region to a rearward location, having a slot width defined between oppositely disposed slot sides extending a slot depth to a slot bottom, including an electrically insulative surface located at said slot sides and bottom, said support member forward end region slot depth exhibiting a first dimensional extent from said securement region to an output location, and exhibiting a second dimensional extent greater than said first dimensional extent therefrom rearwardly toward said base region, said support member including a barrier fluid delivery channel having a fluid input in the vicinity of said base region and extending within said slot beneath said electrode to said output location, a thin, resilient electrode extending within said deployment portion during said insertion mode and deployable to move outwardly from two spaced apart support locations to define an electrode cutting portion and retractable to move toward said deployment portion; said electrode having a distal end positioned within said slot securement region and extending an arch defining distance beyond said rearward location; an actuator and electrical circuit assembly extending along said support member from said base region, mechanically connected with said electrode for effecting said deployment and retraction thereof, and having a terminal assembly electrically connectable with said generator for coupling a first said applied output to said electrode providing, in operative association with said return, electrosurgical cutting of said tissue by said electrode along said cutting portion when deployed; including a forward retainer component positioned over said electrode within said slot securement region and retaining it within said slot, and a rearward retainer component positioned within said slot over said electrode, said electrode being slidably mounted therebeneath; and said actuator assembly being configured to deploy said electrode by urging it fowardly in compression to effect outward movement thereof generally transversely to said longitudinal axis to an extent curving it into an outwardly depending arch formation, and effecting retraction of said electrode by urging it rearwardly to effect inward movement thereof toward said slot. ___________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 149049 2008 N – [R1)) – 2 – ] – – אמינו2 – N', N', N( – 3 – () – בנזיל3R )טרימתילהידראזינוקרבוניל – H1( – 1 – ] – איל1 – פיפרידין – 2 – ) – אילמתיל3 – אינדול תכשירי,מתילפרופיאונאמיד רוקחות המכילים אותו והשימוש בו להכנת תרופות לשחרור הורמון גדילה ]54[ 2 – AMINO – N – [(1R) – 2 – [(3R) – 3 BENZYL – 3 – (BENZYL – 3 – (N', N', N – TRIMETHYLHYDRAZINOCARBONYL) PIPERIDIN – 1 – YL] – 1 – (1H – INDOL – 3 – YLMETHYL) – 2 OXOETHYL] – 2 – METHYLPROPIONAMIDE, PHARMACEUTICAL COMPOSITION COMPRISING IT AND ITS USE FOR THE MANUFACTURING OF MEDICAMENTS FOR RELEASING GROWTH HORMONE ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 10.11.2000 PA199901618 ]32[ 10.11.1999 ]33[ DK Int. Cl.8 A61K 031/395, A61P 005/00, C07D 401/06 NOVO NORDISK A/S, DENMARK WO/2001/034593 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., ,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, תל אביב TEL AVIV 61040 [57] 2-Amino-N[(1R)-2-[(3R)-3-benzyl-3(N, N', N'-trimethylhydrazinocarbonyl) piperidin-1-yl)-1- (1 H-indol-3-ylmethyl)2-oxoethyl]-2-methylpropionamide or a pharmaceutically acceptable salt thereof. ____________ ]11[]21[ 2009 149177 July 24, 2007– ט' באב התשס"ז תרכובות הטרוציקליות ושימוש בהן כתרופות ]54[ HETEROCYCLIC COMPOUNDS AND THEIR USE AS MEDICINES ]22[ ]31[ 03.11.2000 99/13858 ]32[ 05.11.1999 ]33[ FR 00/06535 23.05.2000 FR Int. Cl.8 A61K 031/34, 031/35, 031/40, A61P 039/06, C07D 207/00, 263/02, 263/24, 307/00, 307/24, 317/00, 405/12, 407/12, 413/12, 521/00 SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.), FRANCE WO/2001/032654 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]51[ ]71[ ]87[ ]74[ [57] Compounds of the formula in racemic, enantiomeric, diastereoisomeric form or all combinations of these forms, in which R1 represents a hydrogen atom, an –OR3, SR3, oxo or cyclic acetal radical, in which R3 represents a hydrogen atom, an alkyl, arylalkyl, heterocycloalkycarbonyl, alkylcarbonyl, arylcarbonyl or aralkylcarbonyl radical, in which the alkyl, aryl or heterocycloalkyl radicals are optionally substituted by one or more identical or different substituents chosen from: alkyl, OH, alkoxy, nitro, cyano, halogen, or –NR4R5; R4 and R5 represent, independently, a hydrogen atom or an alkyl radical, or R4 July 24, 2007– ט' באב התשס"ז and R5 together with the nitrogen atom to which they are attached form an optionally substituted heterocycle, R2 represents a hydrogen atom, an alkyl, aryl, or aralkyl radical, the aryl group being optionally substituted by one or more identical or different radicals chosen from: -OR6,-NR7R8, halogen, cyano, nitro or alkyl, in which R6, R7 and R8 represent, independently, a hydrogen atom, an alkyl, aryl, aralkyl, alkylcarbonyl, arylcarbonyl or aralkylcarbonyl radical; A represents a radical 2010 in which R9, R10, R11, R12, R13 represent, independently, a hydrogen atom, a halogen, the OH group, an alkyl, alkoxy, cyano, nitro or –NR15R16 radical, R15 and R16 represent, independently, a hydrogen atom, an alkyl radial or a – COR17 group, or R15 and R16 together with the nitrogen atom to which they are attached form an optionally substituted heterocycle, R17 represents a hydrogen atom, an alkyl, alkoxy or –NR18R19 radical, R18 and R19 represent, independently, a hydrogen atom or an alkyl radical, or R18 and R19 together with the nitrogen atom to which they are attached form an optionally substituted heteroycle, R14 represents a hydrogen atom, an alkyl radical or a –COR20 group, R20 represents a hydrogen atom, an alkyl, alkoxy, aryl, aralkyl, hetrocycloalkyl or – NR21R22 radical, in which the alkyl, aryl or heterocycloalkyl radicals are optionally substituted by one or more identical or different substituents chosen from: alkyl, OH, alkoxy, nitro, cyano, halogen or –NR4R5; R21 and R22 represent, independently, a hydrogen atom or an alkyl radical, or R21 and R22 together with the nitrogen atom to which they are attached form an optionally substituted heterocycle, W represents S; X represents –(CH2)n-, -(CH2)n-CO-, N(R45)-CO-(CH2)n-CO-, -N(R45)-CO-DCO-, -CO-N(R45)-D-CO-, -CO-D-CO-, CH=CH-(CH2)n-CO-, -N(R45)-(CH2)n-CO-, 2011 -N(R45)-CO-C(R46R47)-CO-, -O-(CH2)nCO-, -N(R45)-CO-NH-C(R46R47)-CO-, -CO-N(R45)-C(R46R47)-CO-, -S(CH2)n-COor –Z-CO-; D represents a phenylene radical optionally substituted by one or more identical or different radicals chosen from alkyl, alkoxy, OH, nitro, halogen, cyano, or carboxyl optionally esterified by an alkyl radical; Z represents a heterocycle, R45 represents a hydrogen atom or an alkyl radical, R46 and R47 represent, independently, a hydrogen atom, an alkyl, aryl or aralkyl radical, the alkyl and aryl groups of which are optionally substituted by one or more identical or different substituents chosen from: the OH, -SH, halogen, nitro, alkyl, alkoxy, alkylthio, aralkoxy, aryl-alkylthio, -NR48R49 and carboxyl group optionally esterified by an alkyl radical; R48 and R49 represent, independently, a hydrogen atom, an alkyl radical or a – COR50 group, or R48 and R49 together with the nitrogen atom to which they are attached form an optionally substituted heterocycle, R50 represents a hydrogen atom, an alkyl, alkoxy or –NR51R52 radical, R51 and R52 represent, independently, a hydrogen atom or an alkyl radical, or R51 and R52 together with the nitrogen atom to which they are attached, form an optionally substituted heterocycle; n being an integer comprised between 0 and 6; Y represents –(CH2)p-, -C(R53R54)-(CH2)p-, July 24, 2007– ט' באב התשס"ז p being an integer comprised between 0 and 6; Het represents a heterocycle, as well as the addition salts with mineral and organic acids or with mineral and organic bases of said compound of formula (I), with the exception of the compounds of formula (I) in which when Het represents tetrahydrofuran or tetrahydropyran, R1 represents the OR3 radical with R3 representing a hydrogen atom, an alkyl, arylalkyl, heterocycloalkylcarbonyl radical the heterocycloalkyl radical of which is connected by a carbon atom, alkylcarbonyl, aralcarbonyl or aralkylcarbonyl radical, R2 represents a hydrogen and Y represents the –(CH2)pradical with p=0, then X represents –CON(R45)-C(R46R47)-CO- with R45 = R46 = H. -C(R53R54)-CO-; R53 and R54 represent, independently, a hydrogen atom, an alkyl radical, an aralkyl radical the aryl group of which is optionally substituted by one or more identical or different substituents chosen from: the OH, halogen, nitro, alkyl, alkoxy, -NR55R56 group, R55 and R56 represent, independently, a hydrogen atom, an alkyl radical or a –COR57 group, or R55 and R56 together with the nitrogen atom to which they are attached, form an optionally substituted heterocycle, R57 represents a hydrogen atom, an alkyl, alkoxy or –NR58R59 radical, R58 and R59 represent, independently, a hydrogen atom or an alkyl radical, or R58 and R59 together with the nitrogen atom to which they are attached form an optionally substituted heterocycle; ,173429 The applications for division from this application have not yet been published בקשות חלוקה מבקשה זו .שטרם פורסמו ___________ ]11[]21[ 149180 מערכת תקשורת אישית מיידית ]54[ PERSONAL INSTANT COMMUNICATION SYSTEM ]22[ ]31[ 20.10.2000 60/161135 ]32[ 22.10.1999 ]33[ US 09/472999 28.12.1999 US Int. Cl.8 H04M 003/00, 003/42, 003/487, 003/493, 003/56 COMVERSE LTD. קומברס בע"מ WO/2001/030057 G.E. EHRLICH (1995) LTD., ,) בע"מ1995( ארליך.אי.ג'י AYALON TOWER, 15TH FLOOR, ,11 רחוב מנחם בגין, 15 קומה,מגדל אילון 11 MENACHEM BEGIN STREET, רמת גן 52521 RAMAT GAN ]51[ ]71[ ]87[ ]74[ [57] Method for carrying out telephone conversations between two or more users (110), characterized by the following steps: July 24, 2007– ט' באב התשס"ז (a) each user registers and communicates his personal profile and preferences to a system (100) and assigns a weight to each 2012 preference according to its importance; (b) said system receives from the users said profiles and said weighted preferences and stores them; (c) said system matches between said users according to their profiles and weighted preferences; (d) said system presents to users a list of candidates for conversations according to the results of said match; (e) users select one or more said candidates from said results; and (f) said system creates a telephone connection between users and selected candidates. ____________ ]11[]21[ ]54[ ZWITTERIONIC SILOXANE POLYMERS AND IONICALLY CROSS-LINKED POLYMERS FORMED THEREFROM ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 26.10.2000 09/427216 ]32[ 26.10.1999 Int. Cl.8 C08G 077/38 MONA INDUSTRIES, INC., U.S.A. WO/2001/030886 S. HOROWITZ & CO., ZION HOUSE, 41-45 ROTHSCHILD BLVD., TEL AVIV 65784 2013 149196 פולימרים סילוקסן זוויטריוניים ופולימרים מחוברי יינון בהצלבה הנוצרים מהם ]33[ US ,' הורוביץ ושות.ש תל,41-45 שדרות רוטשילד,בית ציון אביב July 24, 2007– ט' באב התשס"ז [57] A method of preparing an ionically cross-linked composition of a thickened gel-like consistency comprising reacting (A) a diamino containing polysiloxane of the formula: wherein: R, which can be the same or different, is selected from substituted or unsubstituted alkyl or –OR9, wherein R9 is hydrogen or alkyl; R1 can be the same or different and is selected from R, R2 and a diamino containing radical of the formula –F1-NR5F—NH2; with the proviso that at least one R1 group is a diamino containing radical wherein: F1 is linear or branched alkylene of 1-12 carbon atoms; F is linear or branched alkylene of 1-10 carbon atoms; and R5 is hydrogen or lower alkyl; R2 can be the same or different and is selected from substituted or unsubstituted alkyl or –OR9, wherein R9 is hydrogen or alkyl, aryl and olefinic (vinyl); R3 and R4, which can be the same or different, are selected from substituted or unsubstituted alkyl, aryl, capped or uncapped polyoxyalkylene, alkarylene, aralkylene or alkenyl; a is an integer from 0 to 10,000; and b is an integer from 10 to 1000; with the proviso that when a pendant R1 group is a diamino containing radical a can be 0 or a and b are present in the ratio of a:b of least 1:1 to about 200:1; with (B), an acid containing reactant selected from itaconic acid and/or the trialkylsilyl ester derivatives thereof; substituted or unsubstituted cyclic acid anhydride; substituted or unsubstituted conjugated olefinic acid and mixtures of the same at an elevated temperature in the presence of (C) a low molecular weight silicone oil or other solvent for a time sufficient to form ionically cross-linked zwitterionic siloxane polymer of a gel-like consistency containing both carboxylic acid and secondary and/or tertiary amino radicals. __________ July 24, 2007– ט' באב התשס"ז 2014 ]11[]21[ 149205 או סימנים ושירות/שיטה לייצור תווים ו מידע מתקשורת הקשורים בכך ]54[ METHOD FOR GENERATING CHARACTERS AND/OR SYMBOLS AND THE INFORMATION AND COMMUNICATION SERVICE METHOD USING THEM ]22[ ]31[ ]51[ ]71[ 21.10.2000 1999/45925 ]32[ 21.10.1999 ]33[ KR Int. Cl.8 G06F 003/00, 003/023, G09G 005/00, 005/22 HEE-SUNG CHUNG, REPUBLIC OF KOREA WO/2001/029976 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A method for generating characters or symbols, comprising the steps of:defining and 'O' as basic strokes; compounding at least one basic stoke in sequence to define a composition rule for generating each language character or symbol; processing basic stroke input from keys to which the basic strokes are assigned, according to the composition rule to generate the corresponding character or symbol. 2015 July 24, 2007– ט' באב התשס"ז __________ ]11[]21[ 149206 VIH שיטה והתקן להבטל ]54[ METHOD AND DEVICE FOR INACTIVATION OF HIV ]22[ ]51[ ]71[ 18.04.2002 Int. Cl.8 A01N 059/20, B01J 020/02, C12N 007/00 THE CUPRON CORPORATION, U.S.A. WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]74[ [57] A device for inactivation of airborne epidemial viruses said device being provided with a virus-inactivating fibrous material, said material having incorporated therein copper oxide molecules which release ions of copper selected from the The applications for division from this application have not yet been published group consisting of Cu+ and Cu++ ions and combinations thereof from the copper oxide molecules which are bound to the fibers in said material, wherein said device is a face mask. ,174247 בקשות חלוקה מבקשה זו .שטרם פורסמו ___________ July 24, 2007– ט' באב התשס"ז 2016 ]11[]21[ 149308 –אמינואינדן לצורך1 שימוש בנגזרות של –יצור תרופה לטיפול בהפרעה במניה ביפולרת ]54[ USE OF 1-AMINOINDAN DERIVATIVES FOR THE MANUFACTURE OF A MEDICAMENT FOR THE TREATMENT OF MANIA IN BIPOLAR DISORDER ]22[ ]31[ ]51[ ]71[ 27.10.2000 60/161817 ]32[ 27.10.1999 ]33[ US Int. Cl.8 A61K 031/135, A61P 025/00, C07C 211/00, 211/42 TEVA PHARMACEUTICAL פתח,טבע תעשיות פרמצבטיות בע"מ INDUSTRIES LTD. תקווה WO/2001/030339 TEVA PHARMACEUTICAL ,טבע תעשיות פרמצבטיות בע"מ INDUSTRIES LTD., פתח תקוה,3190 .ד. ת, 5בזל 5 BASEL ST., P.O.BOX 3190, PETAH TIQVA 49131 ]87[ ]74[ [57] Use of a therapeutically effective amount of a compound of the formula wherein n is 0 or 1; each of R1 and R2 are hydrogen, C1-C4 alkyl, or halogen; R3 is hydrogen, C1-C4 alkyl, hydroxy, or C1-C4 alkoxy; R4 is hydrogen, or C1-C4 alkyl; R6 is hydrogen, substituted or unsubstituted C1-C12 alkyl, C6-C12 aryl, C7C12 aralkyl or A-N- R9R10, provided that R6 is not methyl when R1, R2, R3 and R4 are hydrogen atoms, wherein A is substituted or unsubstituted C1-C12 alkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted C7-C12 aralkyl, and each of R9 and R10 are independently hydrogen, C1-C12 alkyl, C6C12 aryl, C7-C12 aralkyl, COOtBu, or indanyl; or a racemic mixture, enantiomer, or salt thereof for the manufacture of a medicament for the treatment of mania in bipolar disorder in a subject. ____________ 2017 July 24, 2007– ט' באב התשס"ז ]11[]21[ 149412 – מתילן סטרואיד3 נגזרות של ]54[ 3-METHYLENE STEROID DERIVATIVES ]22[ ]31[ ]51[ ]71[ 23.11.2000 99204000.6 ]32[ 29.11.1999 ]33[ EP Int. Cl.8 A61K 031/56, A61P 019/02, 037/00, C07J 001/00, 071/00 N.V. ORGANON, THE NETHERLANDS WO/2001/040253 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A 3-methylene steroid derivative of the formula wherein R1 is H or together with R3 forms a βepoxide or R1 is absent if there is a 5-10 or 4-5 double bond; R2 is (C1-C5) alkyl or CF3; R3 is βH, βCH3 or together with R1 forms a β-epoxide or R3 is absent if there is a 510 double bond; R4 is H, (C1-C6) alkyl; Y is [H, H] [OH, H], =O, (C1-C6) alkyl], [OH, (C2-C5) alkenyl], [OH, (C2-C5) alkynyl] or (C1-C6) alkylidene, whereby said alkyl, alkenyl, alkynyl and alkylidene is optionally halogenated; or =NOR5, whereby R5 is H, (C1-C6) alkyl; dotted lines represent an optional double bond; or esters or ethers at 17-OH thereof, with the proviso that the 3-methylene steroid derivative is not any one from the list (7α, 17β)-7α-methyl-3-methylene-4estren-17-ol, (7α, 17α)-7-methyl-3methylene-19-norpregn-4-ene-17-ol, (7α, 17α)-7-methyl-3-methylene-19, 21dinorpregn-4-ene-17-ol, (7α)-17-keto-7methyl-3-methylene-4-estrene, (7α, 17α)7-methyl-3-methylene-19-norpregn-4-en20-yn-17-ol, 17β-hydroxy-7α-methyl-3methylene-17α-(2-propenyl)-4-estrene, and 17β-hydroxy-7α-(2-methyl-2-propenyl)-4estrene. _________ July 24, 2007– ט' באב התשס"ז 2018 ]11[]21[ ]54[ PHARMACEUTICAL COMPOSITIONS CONTAINING FED MODE INDUCING AGENTS ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 30.10.2000 09/432881 ]32[ 02.11.1999 Int. Cl.8 A61K 047/00 DEPOMED, INC., U.S.A. WO/2001/032217 WOLFF, BREGMAN AND GOLLER, 19B KEREN HAYESOD ST., P.O.B. 1352, JERUSALEM 91013 149421 תכשירי רוקחות המכילים גורמים המעוררים את דרכי ההזנה ]33[ US , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד [57] A pharmaceutical composition comprising: a drug retained in a solid matrix in a manner causing release of said drug from said solid matrix when said solid matrix is in the stomach, said solid matrix when in the stomach being of a size large enough to promote retention of said solid matrix in the stomach during the fed mode, and a fed mode inducing agent selected from the group consisting of: (a) glycylglycine and salts thereof, (b) alkali and alkaline earth metal docusates, (c) β-casomorphins, (d) dithioorganic acids of the formula in which n is 3 to 13, (e) arginine and arginine salts, (f) 3, 4-dihydro-1,2,3,-oxathiazin-4-ones of the formula 2019 July 24, 2007– ט' באב התשס"ז in which R1 and R2 are independently selected from the group consisting of H and C1-C10 alkyl, and salts thereof; in an amount that causes onset of the fed mode. __________ ]11[]21[ 149433 SMS-מענה וטיפול אטומטיים ל ]54[ SMS AUTOMATIC REPLY AND AUTOMATIC HANDLING ]22[ ]31[ ]51[ ]71[ ]72[ 01.05.2002 09/848339 ]32[ 04.05.2001 ]33[ US Int. Cl.8 H04M 003/50, 003/53, 003/533, H04Q 007/22 COMVERSE LTD. רמת החייל,קומברס בע"מ GIDEON FOSTICK, YUVAL יובל שמואלביץ,גדעון פוסטיק SHMUELEVITZ G.E. EHRLICH (1995) LTD., ,) בע"מ1995( ארליך.אי.ג'י AYALON TOWER, 15TH FLOOR, ,11 רחוב מנחם בגין, 15 קומה,מגדל אילון 11 MENACHEM BEGIN STREET, רמת גן 52521 RAMAT GAN ]74[ [57] A method of managing Short Message Service (SMS) messages including the steps of identifying an SMS message for a Message Recipient (MR) (12), determining whether the MR has set up at least one alternative handling instruction for SMS messages; and if it is determined that the MR has set up an alternative handling instruction for SMS messages, then executing the alternative handling instruction, the method characterized in that the at least one alternative handling instruction includes a saving instruction for saving SMS messages in a personalized folder for the MR. __________ July 24, 2007– ט' באב התשס"ז 2020 ]11[]21[ ]54[ BI-CORTICAL DENTAL IMPLANT ]22[ ]31[ ]51[ ]71[ 09.08.2001 138457 ]32[ 13.09.2000 Int. Cl.8 A61C 008/00 ADVANCED DENTAL ENGINEERING LTD. ZVI LASTER, SIMON GIRSHOVICH, DANIEL BARUC WO/2002/022037 JEREMY M. BEN-DAVID & CO. LTD., HAR HOTZVIM HI-TECH PARK, P.O.B. 45087, JERUSALEM 91450 ]72[ ]87[ ]74[ [57] A complementary system, which includes: an implant member (16), having: a portion which protrudes from the jawbone, when said implant member is installed in the jawbone; and a through conduit (46) at a far portion with respect to an operator, invisible to the operator, when said implant member is installed in the jawbone; and a template (60), having: a distal vertical section, running generally along a distal cortical plate of the jawbone, 2021 149563 שתל דנטלי דו–קורטיקלי ]33[ IL הנדסה דנטלית מתקדמת בע''מ דניאל ברוך, שמעון גרשוביץ,צבי לסטר ,דוד ושות' בע"מ- בן.ירמיהו מ ,45087 .ד. ת, הר חוצבים,רחוב המרפא ירושלים operative to press against the distal cortical plate; a proximal vertical section, running generally along a proximal cortical plate of the jawbone, which includes: a drill-bitchannel housing; and a drill-bit guide channel, located within said drill-bitchannel housing; and a lateral section (66), arranged to mesh with said portion of said implant member which protrudes from the jawbone, thus aligning said drill-bit guide channel with said through conduit of said implant member. July 24, 2007– ט' באב התשס"ז לתקנות35 פירוט זה נבחן בהתאם לתקנה 1968 – תשכ"ח,הפטנטים This specification was examined in accordance with regulation 35 of the Patent Regulations, 5728 - 1968 __________ ]11[]21[ ]54[ IMAGE SEARCHING DEFECT DETECTOR ]22[ ]31[ ]51[ ]71[ ]74[ 10.05.2002 60/290010 ]32[ 11.05.2001 Int. Cl.8 G01B 009/08, G06F 019/00 ORBOTECH LTD. ORBOTECH LTD., P.O.B. 215 , YAVNE 81102 [57] A method for detecting defects in electrical circuits, comprising: generating an acquired image corresponding to a part of an electrical circuit to be inspected; making a comparison of said acquired image with least two reference images, at least one of said reference images 149588 מערכת לגילוי תקלות באמצעות חיפוש בתמונות ]33[ US יבנה,אורבוטק בע"מ ,אורבוטק בע"מ יבנה,215 .ד. ת, representing a defect and at least one of said reference images representing an absence of a defect; and based on said comparison, providing an indication of a correspondence of said acquired image to a defect or to an absence of a defect. __________ July 24, 2007– ט' באב התשס"ז 2022 ]11[]21[ 149594 שיטה לאיתור ולהסרה אוטומטית של חדירה לרשת ]54[ METHOD FOR AUTOMATIC INTRUSION DETECTION AND DEFLECTION IN A NETWORK ]22[ ]31[ ]51[ ]71[ 29.11.2000 09/449531 ]32[ 29.11.1999 ]33[ US Int. Cl.8 G06F 002/120000 013/00, H04L 012/24 FORESCOUT TECHNOLOGIES INC., U.S.A. ODED COMAY, DORON SHIKMONI, YEHEZKEL YESHURUN, ODED AMIR WO/2001/039379 DR. MARK FRIEDMAN LTD., ,ד"ר מרק פרידמן בע"מ MOSHE AVIV TOWER, 54TH ,77 ז'בוטינסקי54 קומה,מגדל משה אביב FLOOR גן-רמת 7 JABOTINSKY STREET 52520 RAMAT GAN ]72[ ]87[ ]74[ [57] A method for detecting and handling a communication from an unauthorized source on a network, the method comprising the steps of: (a) receiving the communication from the unauthorized source; (b) analyzing the communication for detecting an information gathering procedure; (c) if said information-gathering procedure is detected, indicating a source address of the communication as an intruder source address; 2023 (d) returning an earmark to the unauthorized source of the communications; (e) analyzing each subsequent communication for a presence of said earmark; (f) if said earmark is present, indicating said source address of the communication as said intruder source address; and (g) if said source address is said intruder source address, handling the communication from said intruder source address. July 24, 2007– ט' באב התשס"ז ____________ ]11[]21[ ]54[ INHALER ]22[ ]31[ ]51[ ]71[ 01.12.2000 9928265.9 ]32[ 01.12.1999 Int. Cl.8 A61M 015/00 INNOVATA BIOMED LIMITED, UNITED KINGDOM WO/2001/039823 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]87[ ]74[ [57] A delivery device which comprises a reservoir (14, 15), a delivery passage for the delivery of material and a frusto conical metering member (18) characterised in that the delivery device (13) is provided with a plurality of July 24, 2007– ט' באב התשס"ז 149623 משאף ]33[ GB ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה reservoirs and that the metering member is provided with a plurality of measuring cups (22) adapted to transfer a plurality of measured doses of material from a plurality of the reservoirs to the delivery passage. 2024 __________ ]11[]21[ 149656 התקן ושיטה להקצאה ערוץ פקט משותף CDMA במערכת תקשורת ]54[ APPARATUS AND METHOD FOR ASSIGNING A COMMON PACKET CHANNEL IN A CDMA COMMUNICATION NETWORK ]22[ ]31[ 29.11.2000 1999/53630 ]32[ 29.11.1999 ]33[ KR 2000/8316 21.02.2000 KR 2000/10823 29.02.2000 KR 2000/11184 02.03.2000 KR 2000/17743 04.04.2000 KR Int. Cl.8 H04B 001/707, 007/216, 007/26, H04J 011/00, H04L 012/56, H04Q 007/36, 007/38 SAMSUNG ELECTRONICS CO., LTD., REPUBLIC OF KOREA WO/2001/039386 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]51[ ]71[ ]87[ ]74[ [57] A method of base station operation in a CDMA (Code Division Multiple access) communication system, comprising the steps of: transmitting use state formation of each physical packet channel and maximum available data rate information of the physical packet channel on a channel state indication channel; receiving, in the base station, information indicating that a mobile station has data to transmit and selecting an unused physical packet channel, using an access preamble; and transmitting an acquisition indicator signal for indicating an allowance of usage of the selected physical packet channel to the mobile station when the base station allows usage of the currently unused selected physical packet channel. ___________ 2025 July 24, 2007– ט' באב התשס"ז ]11[]21[ ]54[ SYSTEM AND METHOD PROTECTING THE IDENTITY OF TARGET TELEPHONE NUMBERS FROM UNAUTHORIZED ACCESS ]22[ ]31[ ]51[ ]71[ ]74[ 16.05.2002 09/903859 ]32[ 13.07.2001 Int. Cl.8 H04M 001/667, 003/22 COMVERSE, INC., U.S.A. G.E. EHRLICH (1995) LTD., AYALON TOWER, 15TH FLOOR, 11 MENACHEM BEGIN STREET, 52521 RAMAT GAN [57] A system to protect a target telephone number from unauthorized access, comprising: a first one-way encoding unit encoding a target telephone number using non-reversible encoding; a storage unit storing the encoded target telephone number; a second one-way encoding unit encoding a calling telephone number and a receiving telephone number using the nonreversible encoding; a monitoring unit; and a comparing unit determining whether the 149697 מערכת ושיטה להגנה על הזהות של מספרי טלפון מטרה מגישה לא מאושרת ]33[ US ,) בע"מ1995( ארליך.אי.ג'י ,11 רחוב מנחם בגין, 15 קומה,מגדל אילון רמת גן stored encoded target telephone number matches the encoded calling telephone number and/or the receiving telephone number and routing a call between the calling telephone number and the receiving telephone number matching the target telephone number to the monitoring unit, wherein the monitoring unit monitors and/or records the call and connects the calling telephone number to the receiving telephone number. __________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 149981 2026 ]54[ CONNECTING ASSEMBLY FOR SPINAL OSTEOSYNTHESIS ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 01.12.2000 99/15295 ]32[ 03.12.1999 Int. Cl.8 A61B 017/70 SPINEVISION S.A., FRANCE WO/2001/039677 SANFORD T.COLB & CO., P.O.B. 2273, REHOVOT [57] Connection assembly for spinal osteosynthesis comprising an osseous means including a connection area designed to cooperate with a connection means, characterised in that the bottom part of the connection means comprises a spherical shape (20) so that a connection means can be freely positioned in a הרכבה מחברת עבור אוסטיוסינטיזה שדרתית ]33[ FR ,' קולב ושות.סנפורד ט רחובות,2273 .ד. ת, מרמורק,4 שער הגיא connector (8) or in a connection element said spherical shape forming a longitudinal positioning stop with the connector or with the connection element, characterised in that the said connector or connection element has a complementary shaped cavity. ___________ ]11[]21[ 2027 149994 July 24, 2007– ט' באב התשס"ז ]54[ USE OF A COMBINATION OF A COMPOUND WHICH IS A SEROTONIN REUPTAKE INHIBITOR, AND DERAMCICLANE, FOR THE PREPARATION OF A PHARMACEUTICAL COMPOSITION USEFUL FOR THE TREATMENT OF DEPRESSION, ANXIETY DISORDERS AND OTHER AFFECTIVE DISORDERS ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 06.12.2000 60/169245 ]32[ 06.12.1999 Int. Cl.8 A61K 045/00 H. LUNDBECK A/S, DENMARK WO/2001/041701 DR. YITZHAK HESS & PARTNERS, 279 HAYARKON ST., P.O.B. 6451, TEL AVIV 61063 [57] The use of a combination of a compound , which is a serotonin reuptake inhibitor, and deramciclane, for the preparation of a pharmaceutical composition useful for the treatment of depression, anxiety disorders and other affective disorders, such as generalized anxiety disorder, panic anxiety, obsessive compulsive disorder, acute stress disorder, השימוש של שילוב של תרכובת של מעכב סירוטונין ודראמאסיסלין עבור ההכנה של,רפיוטייק תרכובת ,רוקחות המועילה עבור טיפול בדיכאון הפרעות חרדה והפרעות רגש אחרות ]33[ US ,ד"ר יצחק הס ושותפיו תל אביב,6451 .ד. ת, 279 רחוב הירקון post traumatic stress disorder and social anxiety disorder, eating disorders such as bulimia, anorexia and obesity, phobias, dysthymia, premenstrual syndrome, cognitive disorders, impulse control disorders, attention deficit hyperactivity disorder, drug abuse or any other disorder responsive to serotonin reuptake inhibitors. __________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 150390 2028 תכשירי רוקחות המכילים דיאסארין לטיפול בספחת ]54[ PHARMACEUTICAL COMPOSITIONS CONTAINING DIACEREIN FOR TREATING PSORIASIS ]22[ ]31[ ]51[ ]71[ 08.01.2001 0053/00 ]32[ 12.01.2000 ]33[ CH Int. Cl.8 A61K 031/192, 031/222, A61P 017/06, C07C 069/00, 069/157 LABORATOIRE MEDIDOM S.A., SWITZERLAND WO/2001/051044 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]87[ ]74[ [57] Use of diacerein or a pharmaceutically acceptable derivative thereof for the manufacture of a pharmaceutical composition for the treatment of psoriasis and diseases associated therewith. __________ ]11[]21[ 150474 שיטה ומערכת לאספקת רשימת מדיה המתואמת למשתמש ]54[ METHOD AND SYSTEM FOR PROVIDING A CUSTOMIZED MEDIA LIST ]22[ ]31[ ]51[ ]71[ 11.01.2001 09/487120 ]32[ 19.01.2000 ]33[ US Int. Cl.8 G06Q 003/000000 H04N 005/445, 007/16, 007/173 INDIVIDUAL NETWORK, LLC, U.S.A. WO/2001/054403 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]87[ ]74[ [57] A method for providing customized video media to a user over an electronic network comprising: receiving data from a user, directly or through an intermediary, which data identifies the user; generating a customized media list by a computer system, based on a personal preference of the user, wherein said list comprises a program or advertisement including at least one entertainment or information program or 2029 advertisement, or any combination of such programs or advertisements, which program or advertisement is selected from media options available independent of a broadcast schedule; sending said customized media list, directly or through an intermediary to said user of an electronic network; and transmitting customized video media from said customized media list, wherein said customized video media is transmitted July 24, 2007– ט' באב התשס"ז independent of a broadcast schedule; wherein the user is able to watch the customized video media at the user's The applications for division from this application have not yet been published leisure rather than according to said broadcast schedule. ,182204 בקשות חלוקה מבקשה זו .שטרם פורסמו __________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 150617 2030 ]54[ SOLID OXIDE FUEL CELL AND A PROCESS FOR PRODUCING ENERGY UTILIZING THE SAME ]22[ ]31[ 09.11.2001 60/247444 ]32[ 09.11.2000 60/269525 19.02.2001 60/289462 08.05.2001 60/308313 27.07.2001 Int. Cl.8 H01M 004/86, 008/04, 008/12 TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA, U.S.A. WO/2002/058169 WOLFF, BREGMAN AND GOLLER, 19B KEREN HAYESOD ST., P.O.B. 1352, JERUSALEM 91013 ]51[ ]71[ ]87[ ]74[ [57] A process of producing electrical energy, comprising: (a) providing a solid oxide fuel cell comprising a solid oxide electrolyte that is an electronic insulator which allows transfer of anions, a ceramic metal composite anode containing at least ceria and/or copper, and a cathode, at least the solid electrolyte and anode being prepared by forming at least two layers to form a תא סוללה עם תחמוצת מוצקה ושיטה להפקת אנרגיה המשתמשת בו ]33[ US US US US , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד porous anode layer and a dense solid electrolyte layer, and then impregnating the porous anode layer with at least ceria and/or copper; (b) contacting said cathode with an oxygen source; and (c) contacting said anode with a fuel comprising a sulfur-containing hydrocarbon having a sulfur content of from about 1 ppm to about 5000 ppm. __________ ]11[]21[ 2031 150728 July 24, 2007– ט' באב התשס"ז , איחסון,שיטה ומערכת לרישום מאובטח ניהול וקישור של מידע אישי אמין מאומת במערכת תקשורת נתונים ]54[ METHOD AND SYSTEM FOR SECURE REGISTRATION, STORAGE, MANAGEMENT AND LINKAGE OF PERSONAL AUTHENTICATION CREDENTIALS DATA OVER A NETWORK ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 16.01.2001 60/176020 ]32[ 14.01.2000 ]33[ US Int. Cl.8 G06F 002/120000 G06Q 003/000000 H04L 009/32 CATAVAULT, U.S.A. WO/2001/052023 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 [57] A method of managing and linking a user's personal authentication credentials over a network, comprising the steps of: registering the user with a secure network based system; inputting the user's user profile; creating a personal homepage and personal database for the user that resides on the system; inputting the user's authentication credentials for a plurality of third parties into the personal database; July 24, 2007– ט' באב התשס"ז linking to one of the plurality of third parties by the user via the personal homepage and/or personal database; retrieving and securely transmitting appropriate authentication credentials from the personal database on the system for the one of the plurality of third parties; and logging the user onto the one of the plurality of third party sites. 2032 __________ ]11[]21[ ]54[ ACOUSTIC METHOD FOR DISCRIMINATING BETWEEN PAPER AND PLASTIC ENVELOPES ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 02.04.2001 00/04443 ]32[ 07.04.2000 Int. Cl.8 B07C 005/00, 005/34 SOLYSTIC, FRANCE WO/2001/076775 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] In a machine for processing mail articles, a method of distinguishing between mail articles (P1, P2, P3) contained in envelopes made out of paper and mail articles contained in envelopes made out of plastics material, the method 2033 150792 שיטה אקוסטית להפרדת מעטפות נייר ופלסטיק ]33[ FR ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם being characterized in that it consists in displacing each mail article in front of a pressure member (5) so as to produce an acoustic signal that results from a suction effect of the pressure member on one face of said article while it moves in front of July 24, 2007– ט' באב התשס"ז said pressure member, and in comparing said acoustic signal with a reference signal in order to detect whether the envelope of said article is made out of paper or out of plastics material. ____________ ]11[]21[ ]54[ METAL MATERIAL WITH MODIFIED SURFACE, PREPARATION METHOD AND USE OF SAME ]22[ ]31[ ]51[ ]71[ 09.02.2001 00/01716 ]32[ 11.02.2000 Int. Cl.8 C23C 022/02, C25D 011/00 UNIVERSITE PARIS 7-DENIS DIDEROT, FRANCE WO/2001/059178 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A metallic material, the surface of which is modified by bonding aromatic groups to the said surface, optionally substituted by functional groups, the nature of the bond between the surface and the 150839 ,חומר מתכתי בעל פני שטח שעברו שינוי שיטת הכנה והשימוש בו ]33[ FR ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם aromatic groups that modify it being a carbon-metal bond of covalent type, and in particular being such that it withstands ultrasonic cleaning. __________ July 24, 2007– ט' באב התשס"ז 2034 ]11[]21[ ]54[ METHOD OF LINKING STEEL TUBES TO ALUMINUM RIBS ]22[ ]31[ 18.01.2001 10003874.3 ]32[ 28.01.2000 10057180.8 17.11.2000 Int. Cl.8 B23K 031/02 GEA ENERGIETECHNIK GMBH, GERMANY BENEDICT KORISCHEM, HORIA DINULESCU, RAIMUND WITTE, ECKARD VOLKMER WO/2001/054840 EDWARD LANGER, 44-46 MONTEFIORE STREET TEL AVIV 65201 ]51[ ]71[ ]72[ ]87[ ]74[ [57] A method of connecting aluminum rib strips folded so as to be corrugated, to the flat sides of flat steel tubes, characterized in that a layer of soldering agent consisting of a zinc-aluminum alloy with an aluminum content of 0.5% to 20% is applied to the flat sides to the flat tubes and a fluxing agent in the form of cesiumaluminum tetrafluoride is applied to the 150875 תהליך לחיבור צינורות פלדה לחוליות אלומיניום ]33[ DE DE ,אדוארד לנגר תל אביב,44-46מונטיפיורי contact zones of the rib strips with the flat sides, the application being carried out at room temperature, whereupon the rib strips are brought into mechanical contact with the flat sides and then, in that configuration, are heated in a furnace to a soldering temperature between 370oC and 470oC, and are finally exposed to room temperature for cooling. ____________ ]11[]21[ ]54[ AUTO-TORQUE, TAMPERPROOF SCREWS ]22[ ]51[ ]71[ ]74[ 04.08.2002 Int. Cl.8 F16B 023/00 MEIR AVGANIM DANIEL FREIMANN & CO., 5 DROYANOV ST. ,10TH FLOOR , TEL AVIV 63143 [57] A screw (10) having a screwthreaded shank (14) and a circular head (12), the head being provided with at least one radially extending screwdriver tip receiving portion defined between a first 2035 151060 ברגים חסיני חבלה ומותאמי פיתול מעצמם נחל שורק.נ. ד,מאיר אבגנים ,'דניאל פריימן ושות תל אביב,10 בית כלל קומה5דרויאנוב integrally formed projection (16a) of a generally right-angled triangle crosssection seen in a plane parallel to the axis of the screw head wherein the hypotenuse (16b) of the right angled triangle slopes July 24, 2007– ט' באב התשס"ז from the bottom of the first projections to the top thereof such that it is designed to become shaved-off the screw head by a pre-set shear force applied during tightening of the screw, and a second integrally formed projection designed to withstand a shear force greater than the said said pre-set force applied during slackening of the screw. ___________ ]11[]21[ ]54[ SYSTEM AND METHOD FOR ONLINE MONITORING AND BILLING OF POWER CONSUMPTION ]22[ ]31[ ]51[ ]71[ 28.02.2001 60/185832 ]32[ 29.02.2000 Int. Cl.8 G01D 004/00, G01R 022/00 QUADLOGIC CONTROLS CORPORATION, U.S.A. WO/2001/065823 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A system for monitoring energy usage on a power line, comprising: (a) an electronic microprocessor-controlled digital electricity metering device coupled to a power line and including a non- July 24, 2007– ט' באב התשס"ז 151406 מערכת ושיטה לניטור וחיוב צריכת אנרגיה ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם volatile, non-battery-powered data-storage device, wherein said metering device is operable to perform interval metering, store data acquired by said interval metering in said data-storage device, 2036 receive a data request, and transmit data in response to said request over said power line; and (b) a data collector coupled to said metering device via said power line, said data collector operable to: (i) receive data from and transmit data to said metering device over said power line, (ii) store data received from said metering device over said power line, and (iii) receive data from and transmit data to a remotely located computer. ,180435 The applications for division from this application have not yet been published בקשות חלוקה מבקשה זו .שטרם פורסמו ____________ ]11[]21[ ]54[ TELEMATICS METHOD FOR HELICOPTERS ]22[ ]31[ ]51[ ]71[ 28.02.2001 10010134.8 ]32[ 03.03.2000 Int. Cl.8 G01S 005/00, 005/14, 007/00 EADS DEUTSCHLAND GMBH, GERMANY WO/2001/065273 DR. YITZHAK HESS & PARTNERS, 279 HAYARKON ST., P.O.B. 6451, TEL AVIV 61063 ]87[ ]74[ 2037 151466 שיטה טלמטית עבור מסוקים ]33[ DE ,ד"ר יצחק הס ושותפיו תל אביב,6451 .ד. ת, 279 רחוב הירקון July 24, 2007– ט' באב התשס"ז [57] Telematics method for helicopters with an all-weather flight command and hazard warning system, which uses ground-based or satellite-supported mobile radio networks for mobile communication, characterized in that the system is connected with a satellite-supported and/or ground-based positioning system, whereby: (a) a completely or partially computerized transmission of positioning and deployment information takes place between the helicopters and a center, based on the connection of a positioning system with mobile voice and/or data transmission, to build up a formation and fleet management; (b) automatic, semi-automatic or manually controlled communication with databases takes place, in order, on one hand, to retrieve relevant data for the purposes of missions and/or flight safety, and, on the other hand, to transfer accurate data concerning the environment of the helicopter – such as weather, hazard settings, images, – to databases; (c) a direct or indirect mobile radio connection to existing ground-based systems for emergency and breakdown assistance, traffic and control systems of all kinds, is established and maintained; (d) transmission of patient diagnosis data takes place, for the purpose of determining the most appropriate hospital, which thus prepares for the primary treatment as well as to make available specialists for the emergency doctors aboard the helicopter; and (e) data on the status of the helicopter and/or crew are transmitted for the purpose of effective deployment planning, maintenance and spare parts supply. ___________ ]11[]21[ 151611 משק יעודי מודולי לטלפונים סלולריים ]54[ MODULE SPECIFIC INTERFACE FOR CELLULAR PHONES ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 04.02.2002 09/775500 ]32[ 05.02.2001 ]33[ US Int. Cl.8 H04M 001/06, 001/21, 001/725 MOSHE SHEALTIEL משה שאלתיאל WO/2002/063902 DR. MARK FRIEDMAN LTD., ,ד"ר מרק פרידמן בע"מ MOSHE AVIV TOWER, 54TH ,77 ז'בוטינסקי54 קומה,מגדל משה אביב FLOOR גן-רמת 7 JABOTINSKY STREET 52520 RAMAT GAN [57] A system for routing a call between at least one radio communication transceiver and at least one of a plurality of conventional telephones, the system comprising: (a) at least one detachable adaptor, each said adaptor operative for connecting to July 24, 2007– ט' באב התשס"ז the at least one radio communication transceiver, each said adaptor having: (i) a transceiver docking connector, said connector operative for connecting to the radio communication transceiver, and (ii) an interface module operatively connected to said docking connector, said 2038 module designed and configured for enabling information transfer between the at least one of a plurality of conventional telephones and the at least one transceiver; (b) a transceiver docking station for the at least one transceiver; (c) a system controller unit, operatively connected to said plurality of conventional telephones, for controlling operation of the system so as to route the call between the at least one radio communication transceiver and at least one of said plurality of conventional telephones, via said adaptor and said docking station. ___________ ]11[]21[ ]54[ SECURITY BAR TRANSFER MECHANISM ASSEMBLY ]22[ ]31[ ]51[ ]71[ 13.03.2001 524089 ]32[ 13.03.2000 Int. Cl.8 E04F 010/08 RAVCO INNOVATIONS INC., CANADA WO/2001/069029 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ 151668 מכלול למנגנון של מחיצת בטחון הניתנת להעברה ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם [57] A security bar assembly for an opening comprising: a plurality of security bars driven by a bar drive chain and a 2039 July 24, 2007– ט' באב התשס"ז storage drive chain; and a transfer mechanism comprising a transfer arm for moving bars between the bar drive chain and the storage drive chain. ____________ ]11[]21[ ]54[ SCANNING NEAR-FIELD OPTICAL MICROSCOPE ]22[ ]31[ 06.02.2002 0102953.7 ]32[ 06.02.2001 0124948.1 17.10.2001 Int. Cl.8 G02B 021/00 THE UNIVERSITY OF BRISTOL, UNITED KINGDOM WO/2002/063368 WOLFF, BREGMAN AND GOLLER, 19B KEREN HAYESOD ST., P.O.B. 1352, JERUSALEM 91013 ]51[ ]71[ ]87[ ]74[ [57] A scanning near-field optical microscope comprising: a probe (20) which is moveable into a near-field region (22) surrounding a surface of an illuminated sample (14); driving means arranged to provide relative motion between the probe and the sample July 24, 2007– ט' באב התשס"ז 151949 מיקרוסקופ אופטי לתירת שדה ליד גוף קורן ]33[ GB GB , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד surface; means for oscillating the probe across the surface, and a detector (24) arranged to detect electromagnetic radiation affected by an interaction between probe, field and sample in the near-field region; characterised in that, the microscope is arranged, in operation, to 2040 carry out a scan of the sample surface wherein scan area is covered by an arrangement of scan lines, each scan line being collected by oscillating the probe at or near its resonant frequency such that oscillation amplitude determines scan line length and their arrangement is provided by operation of the driving means. __________ ]11[]21[ ]54[ MILK SAMPLING APPARATUS AND METHOD ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 28.03.2001 0001196-5 ]32[ 03.04.2000 Int. Cl.8 A01J 005/04 DELAVAL HOLDING AB, SWEDEN WO/2001/074149 EITAN, PEARL, LATZER AND COHEN ZEDEK, P.O.B. 12688, HERZLIYA 46733 [57] A milk sampling apparatus for use with an automated milking system, said apparatus comprising a cassette (7) wherein milk sample collecting elements (9) are placed, and at least one filling member (27) capable of being placed above a selected one of said milk sample collecting elements by means of a positioning system, and capable of bringing a milk sample. representatively 2041 151990 מכשיר ושיטה לדגימת חלב ]33[ SE , לצר וכהן צדק, פרל,איתן הרצליה,12688 .ד. ת, 7 רחוב שנקר taken from milk yielded during a milking of an animal by means of said automated milking system, into said selected one of said milk sample collecting elements, wherein said positioning system comprises an arm (34) extending in a first direction (Y) in a plane (XY) above said milk sample collecting elements (9) and being movable in a second direction (X) in said plane, said first and second directions July 24, 2007– ט' באב התשס"ז being orthogonal; a first runner (32) holding said filling member and being movable along said arm; and characterized in that first (29) and second (31) drive means, wherein said first drive means is effective to move said arm in said second direction (X) in response to a first provided signal value or a first provided number of pulses and said second drive means is effective to move said first runner along said arm (Y direction) in response to a second provided signal value or a second provided number of pulses to position said filling member above said selected one of said milk sample collecting elements. __________ ]11[]21[ ]54[ HAND TOOL FOR INSERTING A VARIETY OF CONNECTORS INTO NARROW PLASTIC IRRIGATION PIPING ]22[ ]51[ ]71[ ]74[ 02.10.2002 Int. Cl.8 B25B 021/00, 023/14 MORDECHAI ELDAR MORDECHAI ELDAR, ODEM 12 NEVE SAVYON OR YEHUDA [57] A hand tool for inserting a selected connector into plastic piping, said tool comprising: a body (1) onto which a handle (2) is connected, said handle is capable of pivoting between an upward position and a downward position with respect to the body in response to pressure exerted on the handle, an axle mounted within the body with possibility for reciprocate movement in response to the July 24, 2007– ט' באב התשס"ז 152089 מכשיר ידני לנעיצת מגוון מחברים לצינוריות השקייה פלסטיות אור יהודה,מרדכי אלדר ,מרדכי אלדר אור יהודה, נוה סביון12 אודם pivoting of the handle, said reciprocate movement is respectively associated with fixation of the piping vis-à-vis the selected connector (22), bringing the piping (14) in proximity to the selected connector, inserting the selected connector into the piping and releasing the piping thereafter, grips (3), capable to be activated when said axle reciprocates to ensure fixation of the piping, bringing it towards the selected 2042 connector, inserting the selected connector and releasing the piping after the insertion is commenced, a spring means (6), cooperating with said handle and with said grips, said spring means is capable of resisting the pressure exerted on the handle and to return the handle into its upward position when the pressure is released, a drum (4), which is rotatably mounted on the axle, the one side of said drum is provided with at least two holes suitable for deployment therein of connectors having different size and shape, the opposite side of the drum is provided with a means for securing the drum in a position in which the selected connector is vis-à-vis the piping. __________ ]11[]21[ 152092 מערכת ושיטה לשידור מאובטח של נתונים ]54[ SECURE DATA TRANSMISSION SYSTEM AND METHOD ]22[ ]31[ 11.04.2001 00810331.9 ]32[ 17.04.2000 ]33[ EP 1179/00 15.06.2000 CH Int. Cl.8 H04L 009/00, 009/32, H04N 007/16 NAGRAVISION S.A., SWITZERLAND WO/2001/080563 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]51[ ]71[ ]87[ ]74[ [57] A management system of the rights of an audio/video data content encrypted 2043 by at least one control word accompanied by an encrypted file containing the control July 24, 2007– ט' באב התשס"ז word(s) and first conditions of using of the encrypted content defined by the provider of the content, characterised in that this system comprises means for decrypting the file, means for verifying if the first conditions are completed and if so, for reencrypting this file by associating to it second conditions of using defined by the distributor. ____________ ]11[]21[ ]54[ HAEMOSTATICALLY ACTIVE PREPARATION CONTAINING VWF AND METHOD FOR THE PRODUCTION THEREOF ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 04.04.2001 00108430.0 ]32[ 18.04.2001 Int. Cl.8 C07K 001/16, 014/745 OCTAPHARMA AG, SWITZERLAND WO/2001/079260 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] A process for preparing a hemostatically active preparation containing von Willebrand factor (vWF) from a fraction of human plasma by (I) chromatographic purification of a vWFcontaining plasma fraction on an anionexchange material which has the anionexchanging groups on grafted polymeric structures (tentacle materials), collecting a 152173 VWF תכשיר המוסטטי פעיל המכיל ושיטה להכנתו ]33[ EP ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם vWF-containing fraction, characterized in that (II) a purification of said fraction by sizeexclusion chromatography to prepare a purified thermally stable vWF-containing preparation follows; and (III) the preparation in a lyophilized state is heated to a temperature of more than 80oC for inactivating viruses. ____________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 152320 2044 ]54[ STORAGE CONTAINER FOR AT LEAST ONE HYPODERMIC NEEDLE ]22[ ]31[ ]51[ ]71[ 14.05.2001 00810415.0 ]32[ 15.05.2000 Int. Cl.8 A61M 005/32 ARES TRADING S.A., SWITZERLAND WO/2001/087388 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A storage container (1) for a hypodermic needle (2), the hypodermic needle having a connecting end which has connectors that are complementary with connectors on the tip of an injection instrument, one of the connectors having radial elasticity and devices for converting an axial force exerted between the needle and the injection instrument into at least one radial component capable of deforming the elastic connectors, the container having a housing designed for holding the needle entirely therein and in a determined position, and an opening giving access to the housing; wherein an exterior wall (1e) bounding the housing has a cylindrical guiding surface coaxial with a longitudinal axis of the housing and designed to engage with a 2045 מיכל אחסון עבור לפחות מחט תת–עורית אחת ]33[ EP ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם complementary guiding surface of the instrument so that the engagement of these guiding surfaces with each other allows the complementary connectors to be put in the assembling position, following the exertion on the devices for converting an axial force into least one radial component of a pressure coaxial with the longitudinal axis of the housing, wherein the housing holding the hypodermic needle in a determined position has two coaxial openings at a distance from each other, the first of these openings having a fixed diameter approximately equal to the diameter of the connecting end, while the second opening is delimited by elastically radial devices so as to allow its diameter to vary between a minimum diameter and maximum diameter. July 24, 2007– ט' באב התשס"ז __________ ]11[]21[ ]54[ APPARATUS FOR NONPENETRATING FILTRATION SURGERY ]22[ ]51[ ]71[ ]87[ ]74[ 08.05.2000 Int. Cl.8 A61B 018/20 I OPTIMA LTD WO/2001/085044 FENSTER & COMPANY, INTELLECTUAL PROPERTY LTD, 12 BASEL STREET ENTRANCE 1 P.O.BOX 10256 PETACH TIKVA [57] Apparatus for ophthalmic surgery comprising: a laser source (52) that generates a laser beam (54); a scanner (56) comprising an input for said laser beam and an output of a spatially scanned laser beam; and controlling circuitry configured to drive said laser beam over an eye (40) in order to July 24, 2007– ט' באב התשס"ז 152343 התקן לניתוח סינון לא חודר ר"ג,איי אופטימה בע"מ ,קניין רוחני בע"מ,'פנסטר ושות ,10256 .ד. ת, קרית אריה,1 כניסה12 בזל פתח תקוה remove tissue, in a pattern suitable for achieving percolation for non-penetrating filtration of the eye, in which sufficient tissue is removed to allow percolation of fluid out of the eye and provide a reduction in an elevated intra-ocular pressure, without penetrating into the eye. 2046 _________ ]11[]21[ ]54[ MOTION-TRACKING ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 20.04.2001 556135 ]32[ 21.04.2000 Int. Cl.8 A61B 005/103 INTERSENSE, INC., U.S.A. WO/2001/080736 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] A system for tracking the motion of an object relative to a moving reference frame, comprising: a first in inertial sensor mounted on the tracked object; a second inertial sensor mounted on the moving reference frame; and an element coupled to said first and second inertial sensors; characterized in that said element is 2047 152359 מעקב אחר תנועה ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם configured to determine an orientation of the object relative to the moving reference frame based on the signals from the first and second inertial sensors by integrating a relative angular rate signal determined from angular rate signals measured by the first and second inertial sensors. July 24, 2007– ט' באב התשס"ז ___________ ]11[]21[ ]54[ SECURING SHELL ASSEMBLIES TO PIPELINES ]22[ ]31[ ]51[ ]71[ 24.04.2001 0010329.1 ]32[ 28.04.2000 Int. Cl.8 F16L 041/06, 055/16, 055/175 LATTICE INTELLECTUAL PROPERTY LIMITED, UNITED KINGDOM WO/2001/084038 EITAN, PEARL, LATZER AND COHEN ZEDEK, P.O.B. 12688, HERZLIYA 46733 ]87[ ]74[ [57] A method for securing a shell assembly (1) to a pipeline (6), wherein the shell assembly includes a first part (2) for locating on a first side of the pipeline removed from a second side that is damaged or from which a branch is to extend, and a second part (3), optionally incorporating a branch (13), for locating on the second side that is damaged or from which the branch is to extend, the method comprising: positioning a containment ring (16) on the pipeline at a required position on the pipeline and surrounding the damaged area or the area from which the branch is to extend; positioning an annular seal (17) on the pipeline so that the annular July 24, 2007– ט' באב התשס"ז 152499 חיבור אבזרי מעטפת לצינורות ]33[ GB , לצר וכהן צדק, פרל,איתן הרצליה,12688 .ד. ת, 7 רחוב שנקר seal is wholly radially within the containment ring; positioning the second part of the shell assembly onto the annular seal; positioning the first part of the shell assembly on the pipeline and securing the first and second parts together to compress the annular seal and leave an annular space between the first and second parts and an external surface of the pipeline; providing a sealing device substantially preventing fluid from escaping from the annular space, wherein upper and lower sides of the containment ring are provided with an upper and lower groove, respectively, with the upper and lower annular grooves being 2048 connected to each other by a plurality of passages extending through the containment ring between the upper and lower grooves; and introducing sealant by a hole in a wall of the shell assembly, into the upper groove to fill the lower groove, the plurality of passages and the upper groove to provide sealing between the containment ring and the pipeline, and between the containment ring and the shell assembly. __________ ]11[]21[ ]54[ AXIAL EXTERNAL FIXATOR ]22[ ]31[ ]51[ ]71[ ]72[ 01.03.2001 00830381.0 ]32[ 26.05.2000 Int. Cl.8 A61B 017/64 ORTHOFIX S.R.L., ITALY DANIELE VENTURINI, MICHELE COATI, LUIGI ROSSI WO/2001/091654 MILLER-SIERADZKI, P.O.B. 6145, HAIFA 31061 ]87[ ]74[ [57] An axial unilateral external fixator for stabilizing bone fractures, comprising an extendible rod-like middle body (2) and oppositely located bone screw clamps (5, 6) which are articulated to respective ends (3, 4) of the rod-like middle body by 2049 152563 מקבע חיצוני אקסיאלי ]33[ EP ,שרצקי-מילר חיפה,6145 .ד. ת, 18מחניים means of ball joints, characterized in that a ball-and-socket joint (16) is mounted to each clamp, within a main body (20) with which a clamping arrangement (25, 26, 21, 22, 23) of said bone screws is associated or co-operates. July 24, 2007– ט' באב התשס"ז __________ ]11[]21[ 152648 שיטה לאספקת שירות קריאת קול בחבילת נתונים ברשת תקשורת אלחוטית ומבנה רשת עבורה ]54[ METHOD OF PROVIDING PACKET VOICE CALL SERVICE IN WIRELESS COMMUNICATION NETWORK AND NETWORK ARCHITECTURE THEREFOR ]22[ ]31[ ]51[ ]71[ 11.01.2002 12459/2001 ]32[ 10.03.2001 ]33[ KR Int. Cl.8 H04L 012/56, 012/66, H04M 007/00 SAMSUNG ELECTRONICS CO., LTD., REPUBLIC OF KOREA WO/2002/073896 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]87[ ]74[ [57] A network architecture for providing a packet voice call over a packet-based network to a circuit network terminal supporting wireless communication over a circuit-based network, comprising: a radio access network (RAN) (210) for providing a call service to the circuit network terminal; a mediation gateway (230) connected to the RAN via a predetermined signaling interface of the circuit-based network, for performing location registration, authorization, and mobility management to provide a packet voice call service to the circuit network terminal and July 24, 2007– ט' באב התשס"ז making the circuit network terminal recognized as a packet network terminal in the packet-based network by performing IP registration for the circuit network terminal; and an access gateway (250) connected to the mediation gateway via a predetermined signaling interface, for providing predetermined traffic interfacing upon request from the mediation gateway, and connected to the RAN, for transmitting voice traffic from the circuit network terminal to a terminal of a called party via the packet-based network. 2050 __________ ]11[]21[ ]54[ DYNAMICALLY CONTROLLING VIDEO AND DATA TRANSMISSIONS ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 10.04.2001 09/574877 ]32[ 19.05.2000 Int. Cl.8 H04N 007/173 INTEL CORPORATION, U.S.A. WO/2001/091474 WOLFF, BREGMAN AND GOLLER, 19B KEREN HAYESOD ST., P.O.B. 1352, JERUSALEM 91013 [57] A method comprising: broadcasting selected content, including broadcast programming together with viewer selectable ancillary data, to a plurality of viewers; receiving real time feedback from those viewers indicative of the demographics of the audience for the 2051 152798 בקרה דינמית של שידורי וידאו ונתונים ]33[ US , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד selected broadcast programming and ancillary data, and automatically and automatically and selectively modifying the content being broadcast based on the dynamic broadcast demographics and the broadcast programming selected together with the ancillary data. July 24, 2007– ט' באב התשס"ז __________ ]11[]21[ 153229 – 1 – – (אימידזול2 – הידרוקסי1 –שימוש ב , – חומצה דו–פוספונית1 ,1 – ייל) אתאן בהכנת תרופה לטיפול למצבים של עלייה לא–נורמלית של שינוי עצם ]54[ USE OF 1 – HYDROXY – 2 – (IMIDAZOL – 1 – YL) ETHANE – 1, 1 – DIPHOSPHONIC ACID IN THE PREPARATION OF A MEDICAMENT FOR THE TREATMENT OF CONDITIONS OF ABNORMALLY INCREASED BONE TURNOVER ]22[ ]31[ 18.06.2001 09/597135 ]32[ 20.06.2000 ]33[ US 60/267689 09.02.2001 US Int. Cl.8 A61K 031/663, A61P 019/08, 019/10, C07F 009/00, 009/6503 NOVARTIS AG, SWITZERLAND WO/2001/097788 LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו INDUSTRIAL PARK, OMER, באר שבע,5352 .ד. ת, עומר,גן תעשייה P.O.B. 5352, BEER-SHEVA 84152 ]51[ ]71[ ]87[ ]74[ [57] Use of 1-hydroxy-2-(imidazol-l-yl) ethane-1, 1-diphosphonic acid, or a pharmaceutically acceptable salt thereof, or any hydrate thereof in the preparation of a medicament for the treatment of conditions of abnormally increased bone turnover in which the 1-hydroxy-2- (imidazol-1-yl) ethane-1, 1-diphosphonic acid, or a pharmaceutically acceptable salt thereof, or any hydrate thereof is administered intermittently and in which the period between administrations is at least about 6 months. ___________ July 24, 2007– ט' באב התשס"ז 2052 ]11[]21[ ]54[ COMPOSITIONS AND METHODS FOR COATING MEDICAL DEVICES ]22[ ]31[ ]51[ ]62[ ]71[ 11.06.1997 08/662341 ]32[ 12.06.1996 Int. Cl.8 A61F 002/54, A61L 027/00 DIVISION FROM 127446 THE REGENTS OF THE UNIVERSITY OF MICHIGAN, U.S.A. REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]74[ [57] An in vivo medical treatment device coated with a polymeric matrix, said polymeric matrix comprising at least one 153374 תכשירים ושיטות לציפוי התקנים רפואיים ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם biocompatible biodegradable polymer and a pharmceutially effective amount of at least one nucleic acid. _________ ]11[]21[ 153439 –6,1––אוקסאדיאזוליל3 תרופות המכילות – נאפטירידין )–אונים עבור המניעה וטיפולH1(2 בסכיזופרניות ]54[ MEDICINES COMPRISING 3OXADIAZOLYL-1,6 NAPHTHYRIDIN- ...P 2(1H)-ONES FOR THE PREVENTION AND TREATMENT OF SCHIZOPHRENIAS ]22[ ]31[ ]51[ ]71[ 12.06.2001 2000-185814 ]32[ 21.06.2000 ]33[ JP Int. Cl.8 A61K 031/4375, A61P 025/18, C07D 471/04 DAINIPPON SUMITOMO PHARMA CO., LTD., JAPAN WO/2001/098300 DR. YITZHAK HESS & PARTNERS, ,ד"ר יצחק הס ושותפיו 279 HAYARKON ST., תל אביב,6451 .ד. ת, 279 רחוב הירקון P.O.B. 6451, TEL AVIV 61063 ]87[ ]74[ [57] A medicine for prevention and treatment of schizophrenias comprising a 5-substituted-3-oxadiazolyl-1, 6- 2053 naphthyridin-2(1H)-one derivative of the formula July 24, 2007– ט' באב התשס"ז wherein: Het is an oxadiazolyl group; R1 is a hydrogen atom, a lower alkyl group, a cyclolower alkyl group, a trifluoromethyl group, a lower alkenyl group, a lower alkynyl group, a lower alkoxy group, a lower alkoxy-lower alkyl group, a hydroxy-lower alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group; and R2 is a hydrogen atom, a lower alkyl group, a cyclolower alkyl group, a cyclo-lower alkylmethyl group, a lower alkenyl group, a cyclo-lower alkenyl group, a lower alkynyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group, or a physiologically acceptable acid addition salt thereof. __________ ]11[]21[ ]54[ SYSTEM FOR MONITORING HEALTH, WELLNESS AND FITNESS ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 22.06.2001 602537 ]32[ 23.06.2000 Int. Cl.8 A61B 005/00 BODYMEDIA, INC., U.S.A. WO/2002/000111 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] An apparatus for monitoring and reporting human physiological information, comprising a sensor device housing (10) adapted to be placed in proximity with an individual's body, a processor supported by said sensor device housing, said processor being in electrical communication with at least two sensors selected from the group consisting of physiological sensors and contextual sensors, at least one of said at least two sensors being adapted to generate data July 24, 2007– ט' באב התשס"ז 153516 שביעות רצון,מערכת לניטור בריאות וכשירות ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם indicative of at least a first parameter of said individual, said first parameter being physiological, and a second parameter of said individual, and means in electrical communication with said processor for providing information to said individual, characterized in that said processor is adapted to derive physiological state information from at least a portion of said data indicative of at least a first parameter and at least a portion of said data indicative of at least a second parameter. 2054 ___________ ]11[]21[ 153538 שיטה והתקן לטיפול בניגרים ]54[ METHOD AND APPARATUS FOR TREATING FLUIDS ]22[ ]31[ ]51[ ]71[ 05.07.2001 60/216444 ]32[ 06.07.2000 ]33[ US Int. Cl.8 B01F 005/06, B02C 019/06, B05B 001/34 LANCER PARTNERSHIP, LTD., U.S.A. WO/2002/004124 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]87[ ]74[ [57] A method of rotating a fluid, comprising: inletting a fluid flow tangential and normal to a tapered passageway (31) of a vortex nozzle (29) 2055 via a plurality of ports (37, 38, 39) and rotating the fluid flow in the tapered passageway. July 24, 2007– ט' באב התשס"ז The applications for division from this application have not yet been published ,175207,175206,175205,175204 בקשות חלוקה מבקשה זו .שטרם פורסמו __________ ]11[]21[ ]54[ METHOD AND ROTARY MILKING PARLOR FOR IDENTIFYING A MILKING STALL AND AN ANIMAL, ESPECIALLY A COW, IN A ROTARY MILKING PARLOR ]22[ ]31[ ]51[ ]71[ 21.06.2001 10033706.6 ]32[ 12.07.2000 Int. Cl.8 A01K 001/12 WESTFALIASURGE GMBH, GERMANY WO/2002/003783 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] Method for the identification of a milking stall (4) and of an animnal located in the milking stall, in particular a cow, in a rotary milking parlor with a plurality of milking stalls, which are disposed on a rotatable milking platform (3), as well with July 24, 2007– ט' באב התשס"ז 153580 שיטה ומתקן חליבה מעגלי לזיהוי בעל חיים בתא חליבה במיוחד פרה ומתקן חליבה מעגלי ]33[ DE ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם an entrance path (1) and an exit path (2), characterized by guiding of an animal with a recognition device into a milking stall, identification of the animal and of the milking stall, in which the animal is located, wherein the milking platform with 2056 the animal is passed by a fixed unit (10) for animal recognition, said fixed unit being disposed downstream of the entrance path, as observed in the direction of rotation of the milking platform, and by transmission and evaluation of the recognition data for the animal and for the milking stall in a data processing system. _________ ]11[]21[ 153632 נגזרות של בנזופורן והמלחים שלהם המתאימים לשימוש תרופתי ]54[ BENZOFURAN DERIVATIVES AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS ]22[ ]31[ ]51[ 21.08.2001 00/10834 ]32[ 23.08.2000 ]33[ FR Int. Cl.8 A61K 031/357, 031/41, 031/4155, 031/4525, 031/496, A61P 009/06, 009/10, 009/12, C07D 307/00, 307/78, 307/84, 405/12, 405/14, 407/04, 409/12, 409/14 SANOFI AVENTIS, FRANCE WO/2002/016339 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]71[ ]87[ ]74[ [57] Benzofuran derivatives of the formula: and their pharmaceutically acceptable salts, in which formula: A represents a linear or branched C3-C5 alkylene group 2057 optionally subsituted by a hydroxyl group or A represents a group of the formula: July 24, 2007– ט' באב התשס"ז -R19-O-R20in which R19 and R20, which are identical or different, each represent a linear or branched C1-C4 alkylene group, R30 and R31, taken together, represent a carbonyl -O-R29-Oin which R29 represents a C1-C4 alkylene group, T represents hydrogen or a C1-C4 alkyl radical, group with the carbon to which they are attached or represent a group of general formula: R represents: the cyano, hydroxymethyl, formyl or tetrazolyl group, or an ester group of the formula: in which R4 represents a linear or branched C1-C6 alkyl group or a C3-C6 cycloalkyl group, R1 represents hydrogen, a linear or branched C1-C6 alkyl group, a C3-C6 cycloalkyl group, a benzyl group or a phenyl group optionally substituted by one or more substituents selected from halogen atoms, C1-C4 alkyl groups or C1-C4 alkoxy groups or R1 represents a group of the formula: in which R21 represents a linear or branched C1-C4 alkylene group and R22 represents a linear or branched C1-C4 alkyl group, or R1 represents a group of the formula: -R23-OH in which R23 represents a linear or branched C1-C6 alkylene group, R2 and R3, which are identical or different, represent hydrogen, a linear or branched C1-C6 alkyl group optionally substituted by one or more halogen atoms or by a pyrrolidinyl group, a C3-C6 cycloalkyl group or a group of the formula: -R24-O-R25 in which R24 represents a linear or branched C1-C4 alkylene group and R25 represents a linear or branched C1-C4 alkyl group, or R2 and R3, when they are taken together, represent a linear or branched C3-C10 July 24, 2007– ט' באב התשס"ז alkylene group, W, W'; and Z are such that: when W and W', which are identical, represent CH, Z represents –O- or –S-, when W represents CH and W' represents C-R13, Z represents 2058 R13 and R14 being identical or different and representing hydrogen, a halogen atom, a C1-C4 alkyl radical or a C3-c4 alkoxy radical, X represents –O-, these benzofuran derivatives being in the form of individual isomers or of mixtures of the latter. ____________ ]11[]21[ ]54[ FUNGICIDAL COMPOSITION COMPRISING IN PARTICULAR AN OIL OF VEGETABLE ORIGIN WITH HIGH DRYING POWER ]22[ ]31[ ]51[ ]71[ 19.07.2001 00/09898 ]32[ 28.07.2000 Int. Cl.8 A01N 025/24, 043/36, 043/76 BAYER CROPSCIENCE S.A., FRANCE WO/2002/009517 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]87[ ]74[ [57] Fungicidal composition comprising iprodione and at least one oil chosen from linseed, sunflower, soya bean, maize, cottonseed, safflower and rapeseed oil, this oil being of plant origin and possessing a 153786 תכשיר קוטל פטריות המכיל במיוחד שמן ממקור צמחי בעל יכולת ייבוש גבוה ]33[ FR ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה high siccative power characterized by an iodine value which is greater than 90, the oil/iprodione weight ratio being between 0.15 and 1.6. ___________ 2059 July 24, 2007– ט' באב התשס"ז ]11[]21[ 153934 אלפא על16 אסטרגונים מותמרים בעמדה ידי מתיל או אתיל ]54[ 16 ALPHA-METHYL OR ETHYL SUBSTITUTED ESTROGENS ]22[ ]31[ ]51[ ]71[ 23.07.2001 00202697.9 ]32[ 28.07.2000 ]33[ EP Int. Cl.8 A61K 031/565, A61P 005/30, C07J 001/00 N.V. ORGANON, THE NETHERLANDS WO/2002/010188 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A 16α-substituted steroidal compound of the formula wherein: the dotted ring is a fully saturated, a fully aromatic or saturated ring with a ∆5-10 double bond; R1 is (C1-C3) alkyl or (C2-C3) alkenyl, and each of these groups can be substituted with one or more halogens; R2 is (C1-C4) alkyl, (C2-C4) alkenyl or methylene, and each of these groups can be substituted with one or more halogens; R3 is methyl or ethyl. ____________ July 24, 2007– ט' באב התשס"ז 2060 ]11[]21[ ]54[ METHOD AND ARRANGEMENT IN ASEPTIC PREPARATION ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 09.08.2001 0002868-8 ]32[ 10.08.2000 Int. Cl.8 A61M 005/31 CARMEL PHARMA AB, SWEDEN WO/2002/011794 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] A method for antiseptic preparation by means of an injection syringe, said injection syringe comprising a container for an injection agent and an immovable connection nozzle attached to the container, the method involving the 153998 שיטה והתקנים להכנה נקיה ]33[ SE ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם charging of the container with air, characterized in that charging the container with air causes air to pass through the connection nozzle and an air filter arranged on the connection nozzle. _________ 2061 July 24, 2007– ט' באב התשס"ז ]11[]21[ 154144 שימוש במנה רפואית יעילה של פלווונואיד להכנת תרופה לטיפול בתסמינים של דלקת אלרגית באף ודלקות,ששפעת הקשורות במערכת הנשימה ]54[ USE OF A THERAPEUTICALY EFFECTIVE DOSAGE OF A FLAVONOID FOR PREPARING MEDICAMENT FOR TREATING SYMPTOMS OF COMMON COLD, ALLERGIC RHINITIS AND INFECTIONS RELATING TO THE RESPIRATORY TRACT ]22[ ]31[ 23.07.2001 PA200001152 ]32[ 28.07.2000 ]33[ DK PA200001316 04.09.2000 DK PA200001935 23.12.2000 DK PA200100007 03.01.2001 DK PA200100827 22.05.2001 DK Int. Cl.8 A61K 031/315, 031/7048, A61P 011/00, 027/14, C07D 311/00, C07F 003/06, 019/00, C07H 003/04 IMMUPHARM APS, DENMARK WO/2002/009699 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]51[ ]71[ ]87[ ]74[ [57] Use of a therapeutically effective dosage of a flavonoid selected from the group consisting of hydroxyethylrutosides and pharmaceutically acceptable salts thereof together with a pharmaceutically acceptable carrier for the preparation of a medicament for ameliorating and/or curative treatment of a condition selected from the group consisting of common cold, viral and/or bacterial infection of the upper and/or lower respiratory tract and/or eyes, rhinitis and hay fever. ____________ July 24, 2007– ט' באב התשס"ז 2062 ]11[]21[ ]54[ COMPOSITION AND METHOD FOR COATING FOODSTUFFS ]22[ ]31[ ]51[ ]71[ 17.02.2003 1016018 ]32[ 25.08.2000 Int. Cl.8 A23L 001/0532 W. RUITENBERG CZN. N.V., THE NETHERLANDS WO/2002/015715 BLUM, GADOR & CO.,, 53 HASHALOM RD, GIVATAYIM 53454 ]87[ ]74[ [57] Composition for coating foodstuffs which comprises a first polysaccharide that is negatively charged in the composition and gels under the influence of cations, the first polysaccharide comprising alginate, and at least a second polysaccaharide, 154489 תכשיר ושיטה לציפוי מאכלים ]33[ NL ,' גדור ושות,בלום , מגדל הורד23 קומה,53 דרך השלום גבעתיים which is neutral in the composition, the second polysaccharide comprising galactomannans, the composition comprising 2-7 w/w % alginate and having a viscosity of 80-110 Pa.s at a temperature of 20oC. ____________ ]11[]21[ ]54[ VACUUM TUBE HOUSING COMPRISING A PLURALITY OF INTERMEDIATE PLANAR PLATES HAVING NONMONOTONICALLY APERTURE ARRANGEMENT ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 15.08.2001 652516 ]32[ 31.08.2000 Int. Cl.8 H01J 001/62 INTEVAC, INC., U.S.A. WO/2002/019365 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] A housing (10) for a vacuum microelectronic imaging device, said housing comprising: (a) a laminated structure (32) comprising 2063 154517 שרוול לצינור ואקום המורכב ממספר לוחות ביניים מישוריות בעלי סידור לא מונוטוני ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם first and second planar end plates and a plurality of intermediate planar plates disposed therebetween, July 24, 2007– ט' באב התשס"ז (b) at least three of said intermediate plates each comprising an aperture of respective area and said three plates disposed serially in substantial alignment of said apertures whereby a cavity is formed in said laminated structure, said at least three aperture areas varying nonmonotonically in said series, one of said end plates comprising a transparent electrically insulating wall positioned The applications for division from this application have not yet been published across said cavity, a photocathode (29) on the surface of said transparent end plate positioned facing said cavity, a seal (31) bonding the surface of said transparent end plate facing said cavity to the surface of the adjacent intermediate plate, and a vacuum pocket within said cavity and between said photocathode surface and said other end plate. ,174680 בקשות חלוקה מבקשה זו .שטרם פורסמו __________ ]11[]21[ 154828 שיטה,–פלואורואלקיל סטרואידיםα17 ליצורם ותכשירי רוקחות המכילים אותם ]54[ 17 α FLUOROALKYL STEROIDS, METHOD FOR PRODUCING THE SAME AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAID COMPOUNDS ]22[ ]31[ ]51[ 28.09.2001 10049736.5 ]32[ 29.09.2000 ]33[ DE Int. Cl.8 A61K 031/565, 035/00, A61P 005/24, C07J 001/00, 011/00, 053/00, 071/00, 073/00 SCHERING AKTIENGESELLSCHAFT, GERMANY WO/2002/026759 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST., תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.B. 4060, TEL AVIV 61040 ]71[ ]87[ ]74[ July 24, 2007– ט' באב התשס"ז 2064 [57] 17α-Fluoroalkyl steroids of the formula in which R1 stands for a C1-4-alkyl group, R2 stands for a hydroxy group, a group OC(O)-R20 or OR21, whereby R20 and R21 mean a C1-12-alkyl group, a C3-8-cycloalkyl group, an aryl group or an aryl -C1-4-alkyl group, R3 stands for a radical of formula CnF2n+1, whereby n = 1, 2, 3, 4,. 5 or 6, R4 and R5 in each case stand for a hydrogen atom, together for a double bond or a methylene bridge, R5 and R6 each stand for a hydrogen atom, together for a double bond or a methylene bridge, STEROID stands for a steroidal ABC-ring system of the partial formulas C whereby an additional double bond can be found in A and C in 1, 2-position, and one or two additional double bonds can be found in B in 8, 9-position and 11, 12position, R7 means a hydrogen atom, a halogen atom, a hydroxyl group or a trifluoromethyl group, X means an oxygen atom or two hydrogen atoms, R8 means a hydrogen atom, a methyl or ethyl group, R9 means a hydrogen atom or a halogen 2065 atom or together with R10 stands for a double bond, R10 means a hydrogen atom, a hydroxyl group, a methyl or ethyl group or together with R9 stands for a double bond, R11 means a hydrogen atom, a C1-4-alkyl, group, a nitrile group, a hydroxymethylene group or a formyl group, R12 means a hydrogen atom, a C1-4-alkyl group or a nitrile group, R11 and R12, in addition to the abovementioned meanings, together mean a methylene bridge, July 24, 2007– ט' באב התשס"ז R13 means a hydrogen atom or together with R7 means a double bond, R14 and R15 together stand for a double bond, an oxirane ring., a thiirane ring, a [2,3c] oxadiazole ring, a [3,2c] isoxazole ring or a [3, 2c] pyrazole ring, Y stands for an oxygen or nitrogen atom, and the wavy lines at R7, R8, R11, R12, R13, R14 and R15 mean that these substituents can be in α-or β-position, and the following compounds are excluded: 17β-Hydroxy-17α-trifluoromethyl-androst4-en-3-one, 17β-Hydroxy-17α-trifluoromethyl-estr-4en-one, 17β-Hydroxy-17α-trifluoromethyl-estra4,9-dien-3-one, 17β-Hydroxy-17α-trifluoromethyl-estra4,9,11-trien-3-one, 13-Ethyl-17β-hydroxy-17αtrifluoromethyl-gon-4-en-3-one, 13-Ethyl-17β-hydroxy-17αtrifluoromethyl-gona-4,9-dien-3-one and 13-Ethyl-17β-hydroxy-17α-trifluromethylgona-4,9,11-trien-3-one. ___________ ]11[]21[ 155179 פולימרים ספחי שטח פנים והשימוש בהם לטיפול במשטחים ]54[ SURFACE ADSORBING POLYMERS AND THEIR USE IN TREATING SURFACES ]22[ ]31[ 10.10.2001 60/239316 ]32[ 10.10.2000 ]33[ US 60/326091 28.09.2001 US Int. Cl.8 B01L 011/00, B05D 001/00, G01N 033/543 SERONO GENETICS INSTITUTE S.A., FRANCE JAN SUDOR WO/2002/030571 BEN-AMI & ASSOCIATES, P.O.BOX 94, REHOVOT 76100 ]51[ ]71[ ]72[ ]87[ ]74[ [57] A method of decreasing adsorption of an organic material to a surface, comprising: (a) providing a fluid sample comprising an organic material; (b) adding an effective amount of a surface adsorbing polymer to said fluid sample; (c) contacting said fluid sample comprising said organic material and said surface adsorbing polymer to a surface; and (d) performing a fluid operation; wherein: (1) said surface adsorbing polymer binds noncovalently to said surface; (2) said surface adsorbing polymer reduces the amount of adsorption of said organic material to said July 24, 2007– ט' באב התשס"ז ,'עמי ושות-בן רחובות,94 .ד. ת, surface; (3) said surface adsorbing polymer is not one of the reactants of said fluid operation or is added in excess of the amount normally added to said fluid sample; (4) said surface adsorbing polymer does not inhibit the fluid operation; (5) said fluid operation is a chemical reaction, a dilution, a titration, a detection, a mixing and drug screening assay, or a biochemical reaction; and (6) said surface is part of an apparatus and said surface is selected from the group consisting of ninety-six well microtiter plates, three hundred eightyfour well microtiter plates, one thousand 2066 five hundred thirty-six well microtiter plates, microtiter plates comprising more than one thousand five hundred thirty-six wells, microcentrifuge tubes, test tubes, pipettes, pipette tips, and multi-well plates. ____________ ]11[]21[ ]54[ PROCESS AND APPARATUS FOR TREATING WASTEWATER ]22[ ]31[ 04.10.2001 678229 ]32[ 04.10.2000 678095 04.10.2000 Int. Cl.8 C02F 001/24, 001/44, 009/00 GREAT CIRCLE TECHNOLOGIES, INC., U.S.A. WO/2002/028786 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]51[ ]71[ ]87[ ]74[ [57] A method for treating wastewater containing settleable solids to form a reusable liquid fraction, comprising: flowing a wastewater stream into a first containment zone to create forces separating the wastewater stream into a first component and a second component in the first containment zone, the first component including an amount of settleable solids greater than an amount of settleable solids in the second component, 2067 155248 תהליך ומתקן לטיפול במי שופכין ]33[ US US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם and either: passing the second component into a second containment zone including a gas flotation separation system to form a froth fraction and a reusable liquid fraction; or applying the second component to a membrane permeable to selected ingredients of the second component and concentrating the second component on a surface of the membrane to form a solids concentrate and a reusable solids fraction. July 24, 2007– ט' באב התשס"ז The applications for division from this application have not yet been published ,182907 בקשות חלוקה מבקשה זו .שטרם פורסמו __________ ]11[]21[ 155263 תמיסות רוקחיות של תרכובות מודאפיניל ]54[ PHARMACEUTICAL SOLUTIONS OF MODAFINIL COMPOUNDS ]22[ ]31[ 11.10.2001 60/239488 ]32[ 11.10.2000 ]33[ US 09/974473 10.10.2001 US Int. Cl.8 A61K 009/08, 031/16, 047/10, C07C 317/44 CEPHALON, INC., U.S.A. WO/2002/030413 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]51[ ]71[ ]87[ ]74[ [57] A pharmaceutical composition comprising a modafinil compound in solution. ____________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 155409 2068 אלקטרוליט פולימרי מסוג ג'ל ושימושים שלו ]54[ GEL-TYPE POLYMER ELECTROLYTE AND USE THEREOF ]22[ ]31[ ]51[ ]71[ 18.10.2001 2000-318169 ]32[ 18.10.2000 ]33[ JP Int. Cl.8 C08G 065/00, C08J 005/22, H01M 006/22, 010/40 E.I. DUPONT DE NEMOURS AND COMPANY, U.S.A. NOBORU OYAMA, JAPAN WO/2002/033765 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]87[ ]74[ [57] A gel-type polymer electrolyte, wherein sad polymer comprises (A) an ethylene-unsaturated carboxylic acid copolymer or a derivative thereof and (B) a polyalkylene oxide having a hydroxyl group at one terminal thereof or a derivative thereof, which are bonded together by an ester bond, wherein the polyalkylene oxide having a hydroxyl group at one terminal thereof or the derivative thereof (B) has a number average molecular weight of from 200 to 100,000 and contains the ethylene oxide in an amount of from 30 to 100 mol% and wherein said gel-type polymer is impregnated with an electrolytic solution comprising an electrolytic salt and a non- aqueous electrolytic solution, and wherein said ethylene-unsaturated carboxylic acid copolymer or the derivative thereof (A) – has a composition containing ethylene in an amount of from 50 to 98% by weight, an unsaturated carboxylic acid or an anhydride thereof in an amount of from 2 to 50% by weight, and other monomers in an amount of from 0 to 30% by weight, and wherein said ester bond is formed by the esterification of a carboxylic acid group of the ethylene-unsaturated carboxylic acid copolymer with the polyalkylene oxide having a hydroxyl group at one terminal thereof or with a derivative thereof. _____________ ]11[]21[ 2069 155480 July 24, 2007– ט' באב התשס"ז ]54[ FLAT SOFFIT, DOUBLY PRESTRESSED, COMPOSITE, ROOF-CEILING CONSTRUCTION FOR LARGE SPAN INDUSTRIAL BUILDINGS ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 02.10.2001 P20000906A ]32[ 28.12.2000 Int. Cl.8 E04B 007/08, E04C 003/293 MARA-INSTITUT D.O.O., CROATIA WO/2002/053852 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] A double prestressed, composite, roof-ceiling construction with flat-soffit construction for constructing large-span buildings, the prestressed, composite, roofceiling construction with flat-soffit comprising a wide and thin, finished, centrally prestressed concrete soffit plate (1) and two-part upper steel beam (2), the two-part upper steel beam being connected ,מבנה תקרה–הגג עם תחתית שטוחה ,בעל הרכב מרוכב כלחץ מראש פעמיים עבור מבני תעשיה בעלי ממתח גדול ]33[ HR ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם to the concrete soffit-plate by vertical elements (3), the concrete soffit plate being prestressed centrally, the two-part upper steel beam being prestressed by a wedge (7) located in a central gap in the two-part upper steel beam and the wedge separating the two steel parts at centrally located ends of the two steel parts. __________ July 24, 2007– ט' באב התשס"ז 2070 ]11[]21[ ]54[ PALLET CONTAINER ]22[ ]31[ ]51[ ]71[ 18.08.2001 20018362.1 ]32[ 26.10.2000 Int. Cl.8 B65D 077/06 MAUSER-WERKE GMBH & CO. KG, GERMANY WO/2002/034642 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] Pallet container (10) having a thinwalled inner container (12) made of thermoplastic material for the storage and transportation of liquid or free-flowing contents, having a tubular frame which is made of metal bars and tightly encloses the inner container as a supporting casing (14), and having a base pallet (16), on which the inner container rests and to which the supporting casing is fixed, characterized in that, for the case where a container is dropped, special measures in the form of a bending location, with reduction in the 2071 155579 מיכל על משטח ]33[ DE ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם tube cross section at certain predeterminable locations, are taken only in the vertical tubular bars (20) of the supporting casing, these allowing plastic deformation of the supporting casing without individual tubular bars rupturing or breaking off, in which case, in order to produce the bending locations in the vertical tubular bars of the two longer side walls, shaped recesses (22) are formed in a direction running parallel to the longer side walls July 24, 2007– ט' באב התשס"ז __________ ]11[]21[ ]54[ TENNIS BALL COLLECTING AND STORING CART ]22[ ]51[ ]71[ ]74[ 06.05.2003 Int. Cl.8 A63B 047/00 ILAN SHERR DANIEL FREIMANN & CO., 5 DROYANOV ST. ,10TH FLOOR , TEL AVIV 63143 [57] A tennis ball collecting and storage device comprising: a receptacle (12) supported on castors (16a-16d) at an elevated level; a chute-like member (20) vertically mounted to the receptacle, having a bottom opening slightly less than the diameter of a tennis ball, and an open top; the chute being vertically displaceable between a first position wherein the opening is located July 24, 2007– ט' באב התשס"ז 155796 עגלה לאיסוף ולאחסון כדורי טניס ראשון לציון,אילן שר ,'דניאל פריימן ושות תל אביב,10 בית כלל קומה5דרויאנוב above the ground by a distance slightly greater that the diameter of the ball, and a second position wherein the opening reaches down to the ground level; means for selectively operating the chute between the first and the second positions; and means for rollingly guiding the balls piledup in the chute from the open top into the receptacle. 2072 __________ ט' באב התשס"ז –July 24, 2007 2073 ]11[]21[ 155995 4 – תהליך להכנת תרכובות של דיאריל – אמינו – פיפרידיניל ]54[ PROCESS FOR THE PREPARATION OF DIARYL - 4 - AMINOPIPERIDINYL COMPOUNDS ]22[ ]31[ 13.12.2001 PCT/SE00/02560 ]32[ 15.12.2000 ]33[ WO 0101764-9 18.05.2001 SE Int. Cl.8 C07D 211/58, 401/06, 405/06, 409/06, 413/06, 417/06 ASTRAZENECA AB, SWEDEN ANDREW GRIFFIN WO/2002/048108 LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו INDUSTRIAL PARK, OMER, באר שבע,5352 .ד. ת, עומר,גן תעשייה P.O.B. 5352, BEER-SHEVA 84152 ]51[ ]71[ ]72[ ]87[ ]74[ [57] A process for the preparation of 1subsituted diaryl-4-amino-piperidinyl compounds of the formula wherein R1 and R2 are independently selected from the group consisting of hydrogen, hydroxy, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 acyl, C1-C6 acyloxy, cyano, amino, nitro, C1-C6 acylamino, C1-C6 alkylamino, (C1-C6 alkyl)2 amino, C1-C6 alkylthio, C1-C6 alkylsulfonyl, halogenated C1-C6 alkyl, halogenated C1-C6 alkoxy, CO—NR8R9 and C1-C6 alkoxycarbonyl; R3, R4, R5 and R6 are independently selected from hydrogen and C1-C6 alkyl; R7 is selected from the group consisting of imidazolyl, thienyl, furanyl, pyrrolyl, July 24, 2007– ט' באב התשס"ז thiazolyl, oxazolyl, pyridinyl, pyrazinyl, pyrimidinyl and phenyl, all optionally and independently mono-, di-, or tri-substituted with a R' group; R8 and R9 are independently selected from hydrogen, C1-C6 alkyl, halogenated C1-C6 alkyl, phenyl, benzyl, all optionally and independently mono-, di-, or tri-substituted with a R" group; Ar—is phenyl, 1naphthyl or 2-naphthyl, each optionally substituted with 0 to 3 R2 groups; R' is independently selected from the group consisting of hydroxy, halogen, C1C6 alkyl, C1-C6 alkoxy, C1-C6 acyl, C1-C6 2074 acyloxy, cyano, amino, nitro, C1-C6 acylamino, (C1-C6 alkyl)2 amino, C1-C6 alkylthio C1-C6 alkylsulfonyl, halogenated C1-C6 alkyl, halogenated C1-C6 alkoxy; R" is independently selected from the group consisting of hydroxy; halogen, C1C6 alkyl, C1-C6 alkoxy, cyano, amino, nitro, C1-C6 alkylthio, halogenated C1-C6 alkyl, halogenated C1-C6 alkoxy; and n is 1, 2, 3, 4, 5, 5 or 6; comprising the steps of; (A) a one-pot double arylation by (a) reacting 4-amino piperidine of the formula wherein R3 to R7, n, and R' are as described above, with a first bromo compound of the the formula wherein R1, R8, R9, and R" are as described above, in the presence of a strong base, a palladium catalyst and a phosphine ligand and (b) thereafter reacting the product of reaction step(a) with second bromo compound of the formula R0-32-Ar-Br wherein R , R , R , R" and Ar are as 1-substituted diaryl-4-amino-piperidinyl described above; and a strong base to give compounds of formula I. 1 8 9 __________ 2075 July 24, 2007– ט' באב התשס"ז ]11[]21[ ]54[ HYBRID POWER SYSTEM FOR CONTINUOUS RELIABLE POWER AT REMOTE LOCATIONS ]22[ ]31[ ]51[ ]71[ 21.05.2003 10/152356 ]32[ 22.05.2002 Int. Cl.8 F01K 001/00, 023/10 ORMAT TECHNOLOGIES INC., U.S.A. Y. BECK, P.O.BOX 68 YAVNE, ISRAEL ]74[ [57] A hybrid ultra reliable power generating system comprising: (a) a primary power unit producing electric power that is supplied to a load; and (b) a secondary power unit in the form of a closed cycle vapor turbine (CCVT) system that is capable of producing 100% of the electric power that is produced by the primary power unit and which is heated in 156048 מערכת לאספקה קבועה ואמינה של כח למקומות מרוחקים המבססת על שני אמצעי המרת אנרגיה חלופיים ]33[ US ,יונה בק יבנה86 .ד. ת,אורמת תעשיות בע"מ hot standby by rejected heat of the primary power unit, wherein the vaporizer of the CCVT is maintained during hot standby at a temperature above its nominal operating temperature and the vapor turbine of the CCVT is maintained at idle hot standby at a rotating speed above its nominal rotating speed. ___________ July 24, 2007– ט' באב התשס"ז 2076 ]11[]21[ ]54[ INSULATED BEVERAGE OR FOOD CONTAINER ]22[ ]31[ 07.06.2002 60/298386 ]32[ 18.06.2001 923332 08.08.2001 Int. Cl.8 B32B 027/10, B65D 081/38 APPLETON PAPERS INC., U.S.A. WO/2002/102682 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]51[ ]71[ ]87[ ]74[ [57] An insulated beverage container comprising: a container wall (1) having an upper side portion (7), a lower side portion (8), and a bottom portion (9) engaging said lower side portion to define a beverage containing space (11) inside the container wall (1); wherein said container wall comprises: a paper stock layer (2) arranged along an exterior surface of said container wall; a laminated or extruded foam layer (3) arranged inside said paper stock layer; and a thin polyethylene film layer (4) also 2077 156108 מיכל מקודד עבור מזון או משקה ]33[ US US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם arranged inside said paper stock layer, and wherein either: (A) the foam layer forms the innermost layer of the container wall and the thin polyethylene film layer is sandwiched between the foam layer and the paper stock layer; or (B) the thin polyethylene film layer is applied onto the surface of the foam layer such that the layer is sandwiched between the paper stock layer and the thin polyethylene film layer whereby the thin polyethylene film layer forms the innermost layer of the container wall. July 24, 2007– ט' באב התשס"ז ___________ ]11[]21[ ]54[ TRIBOLOGICAL DEBRIS ANALYSIS SYSTEM ]22[ ]31[ ]51[ ]71[ 27.05.2003 162380 ]32[ 04.06.2002 Int. Cl.8 G01N 015/02 LOCKHEED MARTIN CORPORATION, U.S.A. REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]74[ [57] A tribological debris analysis system comprising: a general purpose computer (16); and a tribological sensor system for placing a fluid in a field of view and generating data, said sensor system comprising: an optical flow cell (24); a fluid delivery system (20, 22) for delivering said fluid to said optical flow cell; a laser (26) for illuminating the fluid flowing through said optical flow cell; and an imaging device (14) for collecting imagery information of July 24, 2007– ט' באב התשס"ז 156143 מערכת בדיקה לנוכחות חלקיקי מתכת זעירים ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם debris in the fluid illuminated by said laser and generating a digital video signal, said imaging device having an internal field programmable gate array for receiving said video signal and for processing said imagery information and generating object segments comprising a contiguous group of pixels in a row which are collectively representative of the debris, said field programmable gate array sending said object segments to said general purpose computer for analysis. 2078 ____________ ]11[]21[ ]54[ LIQUID FUEL COMPOSITIONS FOR ELECTROCHEMICAL FUEL CELLS ]22[ ]31[ ]51[ ]71[ ]72[ 03.01.2002 09/752551 ]32[ 03.01.2001 Int. Cl.8 C10L 001/00, H01M 008/04 MORE ENERGY LTD. GENNADI FINKELSHTAIN, YURI KATSMAN, BORIS FILANOVSKY ]87[ ]74[ WO/2002/054506 DR. MARK FRIEDMAN LTD., MOSHE AVIV TOWER, 54TH FLOOR 7 JABOTINSKY STREET 52520 RAMAT GAN [57] A fuel composition for use in an electrochemical fuel cell, comprising: (a) a primary fuel including at least one surface-active compound; (b) an auxiliary fuel including at least one hydrogen-containing compound with a reduction potential such that a 156624 הרכבי ד לק נוזלי עבור תאי אלקטרוכימיים ]33[ US לוד,מור אנרגיה בע"מ בוריס, יורי קצמן,גנדי פינקלשטיין פילנובסקי ,ד"ר מרק פרידמן בע"מ ,77 ז'בוטינסקי54 קומה,מגדל משה אביב גן-רמת thermodynamic reversible potential of an electrochemical cell including said compound at an anode and an oxygen cathode is greater than or equal to 1.56 V; (c) an electrolyte with a pH about 7; and (d) at least one additional compound. __________ 2079 July 24, 2007– ט' באב התשס"ז ]11[]21[ ]54[ PENETRATION-RESISTANT MATERIAL COMPRISING FABRIC WITH HIGH LINEAR DENSITY RATIO OF TWO SETS OF THREADS ]22[ ]31[ ]51[ ]71[ 08.03.2002 01200979.1 ]32[ 15.03.2001 Int. Cl.8 F41H 001/02 TEIJIN TWARON GMBH, GERMANY WO/2002/075238 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A penetration-resistant material comprising at least a double layer of woven fabric, wherein the double layer comprises: a first layer of fabric composed of: a first set of threads comprising 3.5 to 20 threads/cm, having a linear density of at least 210 dtex, and at least 65% of the fabric weight, and a second set of threads comprising 0.5 to 16 threads/cm and having a linear density of at least 50 dtex, with the second set of threads being transverse to the first set of threads, and the ratio of the number of threads/cm of the first set to that of the second set is greater than 1:1; and a second layer of fabric composed of: a first set of threads 156645 חומר עמיד לחדירה המכיל אריג בעל יחס צפיפות לינארי של שתי מערכות של חוטים ]33[ EP ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם comprising 0.5 to 16 threads/cm and having a linear density of at least 50 dtex; and a second set of threads comprising 3.5 to 20 threads/cm, having a linear density of at least 210 dtex, and comprising at least 65% of the fabric weight, with the second set of threads being transverse to the first set of threads, and the ratio of the number of threads/cm of the second set to that of the first set is greater than 1:1, and wherein the first and second sets of threads of the first layer have a parallel orientation towards the first and second sets, respectively, of threads of the second layer. _____________ July 24, 2007– ט' באב התשס"ז 2080 ]11[]21[ ]54[ PESTICIDAL AND ANTIPARASITIC COMPOSITIONS ]22[ ]31[ ]51[ ]71[ 17.12.2001 20010004 ]32[ 03.01.2001 Int. Cl.8 A01N 063/00 CENTRO DE INGENIERIA GENETICA Y BIOTECNOLOGIA, CUBA WO/2002/052934 EITAN, PEARL, LATZER AND COHEN ZEDEK, P.O.B. 12688, HERZLIYA 46733 ]87[ ]74[ [57] A composition for agricultural and veterinary use that comprises at least one chitinolytic agent or a chitinolytic activity- 156700 רכיבים להדברת מזיקים וטפילים ]33[ CU , לצר וכהן צדק, פרל,איתן הרצליה,12688 .ד. ת, 7 רחוב שנקר inducing agent, and sulfide or a sulfideproducing agent. _____________ ]11[]21[ ]54[ PROCESS FOR PREPARING THE L – TARTRATE SALT OF (3AR) – 2, 3A, 4, 5, 6, 7 – HEXAHYDRO – 2 – METHYL – 3A (PHENYLMETHYL) – 3H – PYRAZOLO [4,3-C] PYRIDIN – 3 – ONE ]22[ ]31[ ]51[ ]62[ ]71[ ]74[ 17.02.2000 60/122745 ]32[ 26.02.1999 Int. Cl.8 C07K 005/023 DIVISION FROM 134599 PFIZER PRODUCTS, INC., U.S.A. LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 157103 aR) 3( תהליך להכנת מלח הטרטראט של – מתיל2 – – – הקסאהידרו2, 3a, 4, 5, 6, 7 ] c–3,4[ – פיראזולוH3 – ) (פנילמתילa3 – – און3 – פירידינ ]33[ US ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה [57] A process for preparing a L-tartrate salt of formula XX, 2081 July 24, 2007– ט' באב התשס"ז comprising the following consecutive steps: (a) reacting 4-oxo-piperidine-3-carboxylic acid methyl ester, hydrocholoride with d-tbutyl-dicarbonate and triethylamine in isopropyl ether to form 4-oxo-1,3piperidinedicarboxylic acid 1-(1,1dimethylethyl) 3-methyl ester; (b) reacting said 4-oxo-1,3piperidinedicarboxylic acid 1-(1,1dimethylethyl) 3-methyl ester with benzyl bromide and potassium carbonate in tetrahydrofuran to form 4-oxo-3(phenylmethyl)-1,3-piperidinedicarboxylic acid 1-(1,1-dimethylethyl) 3-methyl ester; (c) reacting said 4-oxo-3-(phenylmethyl)1,3-piperidinedicarboxylic acid 1-(1,1dimethylethyl) 3-methyl ester with methylhydrazine in acetic acid and methylt-butyl ether to form 2,3a,4,5,6,7hexahydro-2-methyl-3-oxo-3a(phenylmethyl)-3H-pyrazolo[4,3c]pyridine-4-carboxylic acid 1,1dimethylethyl ester; and (d) reacting said 2,3a, 4,5,6,7-hexahydro2-methyl-3-oxo-3a- (phenylmethyl)-3Hpyrazolo[4,3-c] pyridine-5-carboxylic acid 1,1-dimethylethyl ester with trifluoroacetic acid to form (3aR)-2,3a, 4, 5, 6, 7hexahydro-2-methyl-3a-(phenylmethyl)3H-pyrazolo[4,3-c] pyridine-3-one; (e) reacting said (3aR)-2,3a, 4, 5, 6, 7hexahydro-2-methyl-3a- (phenylmethyl)3H-pyrazolo[4,3-c] pyridine-3-one with Ltartaric acid in acetone and water to form said L-tartrate salt of formula XX. __________ July 24, 2007– ט' באב התשס"ז 2082 ]11[]21[ ]54[ STABILIZED HYPOBROMOUS ACID SOLUTIONS ]22[ ]31[ 01.03.2002 2001/1795 ]32[ 02.03.2001 2001/6301 31.07.2001 Int. Cl.8 C01B 011/00 MILBRIDGE INVESTMENTS (PTY) LTD., SOUTH AFRICA JAN BASTIAAN CILLIERS, MARTHA SOPHIA CILLIERS WO/2002/070404 JEREMY M. BEN-DAVID & CO. LTD., HAR HOTZVIM HI-TECH PARK, P.O.B. 45087, JERUSALEM 91450 ]51[ ]71[ ]72[ ]87[ ]74[ [57] A method for preparing a stabilized stock hypobromous acid solution including the following step: preparing a hypochlorous acid solution with a pH of less than 7,5; preparing a bromide solution with a pH of less than 7.0; mixing the 157717 תמיסות חומצת היפוברומית מיוצבות ]33[ ZA ZA ,דוד ושות' בע"מ- בן.ירמיהו מ ,45087 .ד. ת, הר חוצבים,רחוב המרפא ירושלים hypochlorous acid solution with the bromide solution to form a hypobromous acid solution; and immediately adding stabilizer to the solution to provide a stabilized stock hypobromous acid solution with a pH of from 8 to 9. _____________ ]11[]21[ ]54[ RECHARGEABLE ZINC ELECTRODE ]22[ ]31[ ]51[ ]71[ 15.03.2002 510554 ]32[ 15.03.2001 Int. Cl.8 H01M 004/60 MASSEY UNIVERSITY, NEW ZEALAND WO/2002/075830 SANFORD T.COLB & CO., P.O.B. 2273, REHOVOT ]87[ ]74[ [57] A rechargeable zinc electrode including an active composition comprising at least: (a) a source of zinc capable of being repeatedly cycled between an oxidized and 2083 157862 אלקטרודת אבץ הניתנת לטעינה מחדש ]33[ NZ ,' קולב ושות.סנפורד ט רחובות,2273 .ד. ת, מרמורק,4 שער הגיא a reduced state; and (b) at least one compound selected from the group consisting of C6-C30 fatty acids, salts, esters and other derivatives thereof, July 24, 2007– ט' באב התשס"ז and C6-C30 alkyl sulfonic acids, salts, esters and other derivatives thereof. ___________ ]11[]21[ ]54[ METHOD OF TREATING ATMOSPHERIC POLLUTANTS ]22[ ]31[ ]51[ ]71[ 15.05.2002 0111801.7 ]32[ 15.05.2001 Int. Cl.8 B01D 053/60, B01J 023/80 JOHNSON MATTHEY PUBLIC LIMITED COMPANY, UNITED KINGDOM WO/2002/092197 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A method of treating atmospheric pollutants, which method comprises contacting a first reducing agent with the at least one atmospheric oxidizing pollutant and contacting the gas leaving the first reducing agent with at least one second reducing agent for reducing at least one atmospheric oxidizing pollutant, wherein the first reducing agent comprises a precious metal-free trap material including at least one trapped atmospheric reducing 158439 שיטה לטיפול במזהמים אטמוספריים ]33[ GB ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם pollutant coated on a heat exchanged device and wherein the at least one second reducing agent comprises a manganesebased reducing agent, one or more precious metals, copper, zinc, iron or a mixture of any two or more of copper, zinc and iron, whereby as the at least one atmospheric oxidizing pollutant is reduced the at least one trapped atmospheric reducing pollutant is oxidized. __________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 158490 2084 ]54[ PROCESS FOR THE STEREOSELECTIVE PREPARATION OF INSECTICIDE 6,7,8,9,10, 10 – HEXAHALO – 1,5,5A,6,9,9A – HEXAHYDRO – 6,9 – METHANO – 2,4,3 – BENZODIOXATHIEPIN – 3 – OXIDE ]22[ ]51[ ]71[ 24.04.2001 Int. Cl.8 C07D 327/00, 327/10 EXCEL INDUSTRIES LIMITED, INDIA ASHWIN CHAMPRAJ SHROFF, ABHIJIT PREMVALLABH PUROHIT, SANJAY DHIRAJLAL VADORARIA WO/2002/085884 JEREMY M. BEN-DAVID & CO. LTD., HAR HOTZVIM HI-TECH PARK, P.O.B. 45087, JERUSALEM 91450 ]72[ ]87[ ]74[ תהליך להכנה סטריוסלקטיבית של מדביר – – הקסאהלו6,7,8,9,10,10 – החרקים – מתנו6 ,9 – – הקסאהידרוA,6,9,9A1,5,5 – תחמוצת3 – – בנזודיוקסאתיאפינ2,4,3 – ,דוד ושות' בע"מ- בן.ירמיהו מ ,45087 .ד. ת, הר חוצבים,רחוב המרפא ירושלים [57] A process for the stereoselective preparation of insecticide 6,7,8,9,10,10hexahalo-1,5,5a, 6,9,9a-hexahydro-6,9- methano-2,4,3-benzodioxathiepin-3-oxide of the formula wherein X is a halogen selected from fluorine, chlorine or bromine, comprising reacting 1, 4, 5, 6, 7, 7-hexahalo-5norbornene-2,3-dimethanol of the formula 2085 July 24, 2007– ט' באב התשס"ז wherein X is a halogen selected from fluorine, chlorine or bromine, with a cyclic sulfite ring forming reagent optionally in an inert organic solvent at ambient to 139o C, wherein the reaction is carried out in the presence of a stereoisomer directing agent comprising an isomer of the compound of the formula I different from the desired isomer, the molar ratio of the stereoisomer directing agent to the dimethanol compound of the formula IV at least 0.07. __________ ]11[]21[ ]54[ BRAKE CONTROL SYSTEM DEFINED BY FIELD PROGRAMABLE GATE ARRAY ]22[ ]31[ ]51[ ]71[ 25.02.2003 60/359867 ]32[ 25.02.2002 Int. Cl.8 B60T 008/88, 017/18 AIR-CRAFT BRAKING SYSTEMS CORPORATION, U.S.A. WO/2003/072408 DR. SHLOMO COHEN & CO., 124 IBN GABIROL ST., P.O.B. 11490, TEL AVIV 62038 ]87[ ]74[ [57] A brake control system (10) for a wheeled vehicle, comprising: a field programmable gate array (12) configured to perform an algorithm of brake control subsystems taken from the group comprising anti-skid control, nosewheel steering, brake temperature monitoring, and built-in tests; a wheel speed interface (14) interposed between wheel speed transducers of said wheeled vehicle and July 24, 2007– ט' באב התשס"ז 158541 מערכת בקרת בלם המוגדרת באמצעות מערך שערים שניתן לתכנות בשדה ]33[ US ,'ד"ר שלמה כהן ושות תל אביב,11490 .ד. ת, 124 אבן גבירול said field programmable gate array for presenting signals to said field programmable array corresponding to instantaneous wheel speed; and a brake temperature interface (16) interposed between brakes of said vehicle and said field programmable gate array and providing signals corresponding to brake temperature. 2086 _____________ ]11[]21[ 159891 או/חומר המבוסס על סיבים אורגניים ו אנאורגנים ועל כיטוזן לשימוש לקיבוע של איונים מתכתיים ]54[ MATERIAL BASED ON ORGANIC AND/OR INORGANIC FIBERS AND CHITOSAN FOR USE IN FIXING METAL IONS ]22[ ]31[ ]51[ ]71[ 15.07.2002 01/09949 ]32[ 25.07.2001 ]33[ FR Int. Cl.8 B01D 015/00, B01J 045/00, C02F 001/28 AHLSTROM CORPORATION, FINLAND WO/2003/009939 SANFORD T.COLB & CO., ,' קולב ושות.סנפורד ט P.O.B. 2273, רחובות,2273 .ד. ת, מרמורק,4 שער הגיא REHOVOT ]87[ ]74[ [57] A material based on organic and/or inorganic fibres and chitosan manufactured by means of a paper-machine process, for use in fixing metal ions contained in an effluent, characterised in that the chitosan represents between 0.01 and 20% by dry weight of fibres and that its degree of deacetylation is higher than 90%. ___________ ]11[]21[ 2087 159990 July 24, 2007– ט' באב התשס"ז ]54[ DEVICE, METHOD AND SYSTEM FOR THE APPLICATION OF CONTENT ONTO THE SURFACE OF A BEVERAGE ]22[ ]51[ ]71[ 21.01.2004 Int. Cl.8 A23L 001/27, A47G 019/14 EYAL ELIAV DANNY LAVIE ]74[ NAOMI ASSIA & CO. LAW OFFICES, 32 HABARZEL ST. RAMAT HACHAYAL TEL AVIV 69710 [57] A content application system for applying content onto the surface of a beverage comprising: (a) a computing device adapted to receive a baring signal from a distributed data network; and מכשיר ומערכת להטבעת תוכן על,שיטה פני שטחו של משקה תל אביב,אייל אליאב רמת השרון,דני לביא ,נעמי אסיא ושות' משרד עורכי דין אביב- תל, רמת החייל32 רח' הברזל (b) a contenting application head adapted to apply the received content by agitating the surface of the beverage in a pattern correlated to the content. __________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 160153 2088 –שיטות להכנת חומצה כלורית וכלור דיאוקסיד ]54[ METHODS FOR MAKING CHLOROUS ACID AND CHLORINE DIOXIDE ]22[ ]31[ ]51[ ]71[ 29.07.2002 09/919918 ]32[ 02.08.2001 ]33[ Int. Cl.8 B01J 039/04, C01B 011/02, 011/08 RICHARD SAMPSON, U.S.A. ALLISON SAMPSON, U.S.A. ]87[ ]74[ WO/2003/011750 DR. MARK FRIEDMAN LTD., MOSHE AVIV TOWER, 54TH FLOOR 7 JABOTINSKY STREET 52520 RAMAT GAN [57] A process for generating chlorous acid which comprises contacting a chlorite salt solution with a cation exchange material in the hydrogen form in a moist environment for a time sufficient to effect US ,ד"ר מרק פרידמן בע"מ ,77 ז'בוטינסקי54 קומה,מגדל משה אביב גן-רמת an essentially complete substitution of cations in the chlorite salt with hydrogen ions on the cation exchange material to form chlorous acid. ___________ ]11[]21[ ]54[ PRINTING CARTRIDGE WITH BARCODE IDENTIFICATION ]22[ ]31[ ]51[ ]71[ 09.07.2002 09/922158 ]32[ 06.08.2001 Int. Cl.8 B41J 002/175 SILVERBROOK RESEARCH PTY. LTD., AUSTRALIA WO/2003/013866 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]87[ ]74[ [57] A printing cartridge (1230) that is releasably engageable with a printing device having a linear reader (1236) for reading a barcode and a central processor capable of interpreting data carried on a barcode, the printing cartridge comprising a housing (1234); a media supply 2089 160172 מחסנית הדפסה עם זיהוי ברקוד ]33[ US ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה arrangement positioned within the housing and containing a supply of media; a feed mechanism positioned in the housing for feeding the media to a printing mechanism; and a barcode (1232) depicted on the housing, the barcode being readable July 24, 2007– ט' באב התשס"ז by the linear reader and defining a code representing data relating to the media. ___________ ]11[]21[ ]54[ KEYBOARD ]22[ ]31[ ]51[ ]71[ 06.08.2002 09/966293 ]32[ 28.09.2001 Int. Cl.7 B41J 003/44 SILVERBROOK RESEARCH PTY. LTD., AUSTRALIA WO/2003/029012 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]87[ ]74[ [57] A keyboard (10) which includes a housing (12); an alphanumeric keypad (14) carried by the housing, the keypad including key switches mounted on a circuit board; a page width printer arranged in the housing; and a feed July 24, 2007– ט' באב התשס"ז 161088 מקלדת ]33[ US ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה mechanism for feeding sheets (24) from an input slot (22) to the printer, the feed mechanism being positioned between the circuit board and an underside of the housing. 2090 ____________ ]11[]21[ ]54[ DUPLEX STAINLESS STEEL ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 20.03.2002 981074 ]32[ 16.10.2001 Int. Cl.8 C21D 009/00, C22C 038/44 ATI PROPERTIES, INC., U.S.A. WO/2003/033755 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] A duplex stainless steel comprising, in weight percent: up to 0.06 percent carbon; 15 up to 22.5 percent chromium; greater than 3 up to less than 4 percent nickel; up to 3.75 percent manganese; 0.14 up to 0.35 percent nitrogen; up to 2 percent silicon; greater than 1.4 up to less than 2.5 161175 חלד דו שכבתית-פלדת אל ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם percent molybdenum; up to less than 0.5 percent copper; up to less than 0.2 percent cobalt; up to 0.05 percent phosphorus; up to 0.005 percent sulfur; 0.001 up to 0.0035 percent boron; iron and incidental impurities. __________ 2091 July 24, 2007– ט' באב התשס"ז ]11[]21[ ]54[ DUPLEX STAINLESS STEELS ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 01.03.2002 012908 ]32[ 30.10.2001 Int. Cl.8 C21D 009/00, C22C 038/40 ATI PROPERTIES, INC., U.S.A. WO/2003/038136 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] A duplex stainless steel comprising, in weight percent: up to 0.06 percent carbon; 15 to less than 19 percent chromium; 1 to less than 2 percent nickel; greater than 2 percent up to 3.75 percent manganese; greater than 0.12 up to 0.35 161289 שכבתית-חלד דו-פלדת אל ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם percent nitrogen; up to 2 percent silicon; up to 1.5 percent molybdenum; up to 0.5 percent copper; up to 0.2 percent cobalt; up to 0.05 percent phosphorus; up to 0.005 percent sulfur; up to 0.03 percent boron; iron and incidental impurities. __________ ]11[]21[ 161841 –אמינו–תיאזולין והשימוש בהן2נגזרות סינטאז בר–השראהNO – כמעכבות ]54[ 2-AMINO-THIAZOLINE DERIVATIVES AND THEIR USE AS INHIBITORS OF INDUCIBLE NO-SYNTHASE ]22[ ]31[ 07.11.2002 01/14510 ]32[ 09.11.2001 ]33[ FR 60/352797 30.01.2002 US Int. Cl.8 A61K 031/4439, 031/497, 031/506, A61P 025/00, 025/16, C07D 265/00, 265/06, 417/06, 417/12, 417/14 AVENTIS PHARMA S.A., FRANCE WO/2003/040115 EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688, HERZLIYA 46733 ]51[ ]71[ ]87[ ]74[ [57] Compounds of the formula July 24, 2007– ט' באב התשס"ז 2092 in which either Y is a methylene (CH2) and X is selected from the following groups: O, H, N-(C1-C4) alkyl, N-Bn, N-Ph, N-(2-Py), N(3-Py), N-(4-Py), N-2-pyrimidyl, N-5pyrimidiyl, S, SO, SO2, CH2 or CHPh; or Y is a carbonyl (C=O) and X is selected from the following groups: NH, N-Ph, N(2-Py), N-(3-Py), N-(4-Py), N-2pyrimidiyl or N-5-pyrimidiyl with the proviso that the (C1-C4) alkyl radicals contain 1 to 4 carbons in a straight or branched chain wherein the abbreviations Bn, Py and Ph signify benzyl, pyridyl and phenyl respectively, their racemic mixtures, enantiomers, diastereoisomers and mixtures thereof, their tautomers and their pharmaceutically acceptable salts. _____________ ]11[]21[ 162871 מוצר,שיטה להכנת מוצר תחליף לבשר תחליף לבשר אשר הוכן לפי השיטה ומוצר תחליף לבשר מוכן לאכילה ]54[ METHOD FOR THE PREPARATION OF A MEAT SUBSTITUTE PRODUCT, MEAT SUBSTITUTE PRODUCT OBTAINED WITH THE METHOD AND READY TO CONSUME MEAT SUBSTITUTE PRODUCT ]22[ ]31[ ]51[ ]71[ 17.09.2002 1019816 ]32[ 22.01.2002 ]33[ NL Int. Cl.8 A23J 003/08, 003/22, A23L 001/0532, 001/059 NUG NAHRUNG-UND GENUSSMITTEL VERTRIEBSGESELLSCHAFT MBH, GERMANY WO/2003/061400 DVORA GADOR, גדור,בלום דבורה גדור עו"ד DERECH HASHLOM 53, ,'ושות GIVATAYIM 53454 קומה,53 גדור ושות' דרך השלום,בלום גבעתיים,23 ]87[ ]74[ [57] Method for the preparation of a meat substitute product which comprises protein, wherein: (1) a protein material, a hydrocolloid which precipitates with metal cations and water are added to one another, (2) the composition from step (1) is formed 2093 into a homogeneous mixture, (3) the mixture from (2) is mixed with a solution of metal cation with a valency of at least 2, in order to form a fibrous product, (4) the fibrous product is isolated, characterized in that July 24, 2007– ט' באב התשס"ז (5) the protein material comprises a milk protein material, and (6) the mixture of milk protein material, hydrocolloid which precipitates with metal cations and water is formed in the presence of an amount of a calcium complexforming agent. ,182324 The applications for division from this application have not yet been published בקשות חלוקה מבקשה זו .שטרם פורסמו __________ ]11[]21[ 163061 מערכת בריאות מקוונת ושיטה לניהולה ]54[ SYSTEM AND METHOD FOR ADMINISTRATION OF ON-LINE HEALTHCARE ]22[ ]51[ ]71[ ]72[ ]74[ 15.07.2004 Int. Cl.8 A61B 001/00, 005/00, A61N 005/00 MED DYNAMICS LTD. AVNER MAN, AVNER AMIR DR. EYAL BRESSLER, 11 TOVAL ST. RAMAT GAN 52522 [57] A healthcare administration system useful for the management of anamnesis and medical records, data analysis, guided diagnosis, medical treatment, and clinical investigation; said system comprising: (a) a plurality of self-sufficient subsystems (12, 13, 14, 15, 16) adated to record, store, share, clinically investigate and analyze information by means of a common medical information protocol (CMIP) (17); (b) at least one end-unit device (11) adapted to diagnose and/or treat patients, July 24, 2007– ט' באב התשס"ז מגדל העמק,מדדינמיקס בע"מ אבנר עמיר,אבנר מן ,דר' אייל ברסלר עו"פ רמת – גן,11 תובל in communication with a subsystem for controlling, monitoring and recording the treatment process and its outcome by means of a medical protocol; (c) a least one module adapted for a CMIP; wherein said end-unit device is guided by said CMIP so that anamnesis, diagnosis and targeted treatment is dictated, provided, monitored, recorded and/or clinically investigated. 2094 ___________ ]11[]21[ 163486 התקן הניתן להפעלה בריבוי ברמות ביצוע ושיטה למדידת שימושו ]54[ DEVICE OPERABLE AT A PLURALITY OF PERFORMANCE LEVELS AND A METHOD OF METERING ITS USAGE ]22[ ]31[ ]51[ ]71[ 12.02.2003 PS0481 ]32[ 13.02.2002 ]33[ AU Int. Cl.7 B41F 031/02, 033/02, B41J 029/38, B41L 039/02, G07C 003/00 SILVERBROOK RESEARCH PTY. LTD., AUSTRALIA WO/2003/068517 LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו INDUSTRIAL PARK, OMER, באר שבע,5352 .ד. ת, עומר,גן תעשייה P.O.B. 5352, BEER-SHEVA 84152 ]87[ ]74[ [57] A device (100) operable at a plurality of different performance levels, the device including a metering system (118) configured to measure usage of the device in units of use, configured such that 2095 the number of units metered for performing a particular task of the device is varied in reliance on a level of performance of the device for that task. July 24, 2007– ט' באב התשס"ז _________ ]11[]21[ ]54[ PHARMACEUTICAL FORMULATION OF IRESSA COMPRISING A WATERSOLUBLE CELLULOSE DERIVATIVE ]22[ ]31[ 24.02.2003 0204392.5 ]32[ 26.02.2002 0212462.6 30.05.2002 0213267.8 11.06.2002 Int. Cl.8 A61K 047/38 ASTRAZENECA AB, SWEDEN PAUL RICHARD GELLERT, MICHAEL DAVIS PARKER, MARCEL DE MATAS WO/2003/072139 S. HOROWITZ & CO., ZION HOUSE, 41-45 ROTHSCHILD BLVD., TEL AVIV 65784 ]51[ ]71[ ]72[ ]87[ ]74[ [57] A pharmaceutical composition comprising 4-(3'-chloro-4'-fluoroanilino)7-methoxy-6-(3-morpholinopropoxy) quinazoline or a pharmaceuticallyacceptable salt thereof and a water-soluble cellulose ether or an ester of a water- 163642 תכשיר רוקחות של אירסה המכיל נגזרת תאית מסיסה במים ]33[ GB GB GB ,' הורוביץ ושות.ש תל,41-45 שדרות רוטשילד,בית ציון אביב soluble cellulose ether. The water-soluble cellulose ether is preferably selected from hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropyl methyl cellulose and a water-soluble salt of carboxymethylcellulose. ___________ July 24, 2007– ט' באב התשס"ז 2096 ]11[]21[ ]54[ METHOD FOR REDUCING SULFUR CONTENT OF CARBONACEOUS MATERIALS ]22[ ]31[ ]51[ ]71[ 05.03.2003 PS0911 ]32[ 05.03.2002 Int. Cl.8 C01B 031/02, C10L 009/02 KARALEE RESEARCH PTY LTD., AUSTRALIA WO/2003/074639 SANFORD T.COLB & CO., P.O.B. 2273, REHOVOT ]87[ ]74[ [57] A process for reducing the amount of sulfur-containing impurities in carbonanceous materials, comprising (a) contacting said materials with an aqueous solution of hydroflurosilicic acid in the absence of hydrogen fluoride under 163835 שיטה להפחתת כמות גפרית בחומרים פחמניים ]33[ AU ,' קולב ושות.סנפורד ט רחובות,2273 .ד. ת, מרמורק,4 שער הגיא conditions wherein at least some of said sulfur-containing impurities react with said hydrofluorosilicic acid to form reaction products, and (b) separating said reaction products from said carbonanceous materials. _____________ ]11[]21[ ]54[ MOTION TRANSMITTING STRUCTURE FOR A NOZZLE ARRANGEMENT OF A PRINTHEAD ]22[ ]31[ ]51[ ]71[ 13.06.2002 10/120347 ]32[ 12.04.2002 Int. Cl.8 B41J 002/14 SILVERBROOK RESEARCH PTY.LTD., AUSTRALIA WO/2003/086769 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]87[ ]74[ [57] A printhead chip for an inkjet printhead, the printhead chip comprising: a substrate; and a plurality of nozzle arrangements (100) positioned on the 2097 164503 מבנה שידור תנועה לסידור נחיר של שבב ראש הדפסה למדפסת הזרקת דיו ]33[ US ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה substrate (32), each nozzle arrangement comprising: a nozzle chamber structure that defines a nozzle chamber (106) in which ink is received; an ink-ejecting July 24, 2007– ט' באב התשס"ז member (140) that is positioned in the nozzle chamber and is displaceable in the nozzle chamber to eject ink from the nozzle chamber; at least one actuator (148) that is positioned on the substrate, the, or each, actuator having a working position that is displaceable with respect to the substrate when the actuator receives a drive signal; a sealing structure (130) that is positioned on the substrate and is interposed between the, or each, actuator and the ink-ejecting member to inhibit a passage of ink between the ink-ejecting member and actuator; and a motion transmitting structure (122) that bridges the sealing structure, the motion transmitting structure comprising an effort formation (124) that is connected to the working portion (156) of the actuator, a load formation that is connected to the inkejecting member and a lever arm formation that interconnects the effort formation and the load formation, the lever arm formation being pivotal with respect to the nozzle chamber structure so that reciprocal movement of the working portion of the actuator is accommodated by pivotal movement of the lever arm formation with the result that the ink-ejecting member is reciprocally displaced towards and away form an ink ejection port. _____________ ]11[]21[ ]54[ INFLATABLE PLUSH TOY ]22[ ]31[ ]51[ ]71[ ]74[ 02.11.2004 03380286.9 ]32[ 10.12.2003 Int. Cl.8 A63H 003/06 VICTORY PRODUCTS, S.L., SPAIN EITAN, PEARL, LATZER AND COHEN ZEDEK, P.O.B. 12688, HERZLIYA 46733 [57] Inflatable plush toy, comprising an exterior covering (1) having a central body portion and appendages, and an interior July 24, 2007– ט' באב התשס"ז 164992 צעצוע מקטיפה שניתן לניפוח ]33[ EP , לצר וכהן צדק, פרל,איתן הרצליה,12688 .ד. ת, 7 רחוב שנקר bag (2) located in only said central body portion and being made of an airtight, flexible material, the configuration 2098 of the interior bag, in an expanded form, is shaped close to a shape of the central body portion in final form, said interior bag including an air valve (3) extending through the exterior covering and being accessible from outside the exterior covering and being located in a place that is at least partially hidden by at least one of the appendages, said air valve including a closure cap (4) to facilitate filling of the toy with air and expelling of the air from the toy. _____________ ]11[]21[ 2099 165464 July 24, 2007– ט' באב התשס"ז ]54[ MAGNETICALLY ACTIVE SHEET PRODUCT AND A METHOD OF USING SUCH A PRODUCT FOR STORING AND READING DIGITAL DATA ]22[ ]31[ ]51[ ]71[ 19.05.2003 0212358.6 ]32[ 29.05.2002 Int. Cl.8 B41M 005/30, G11B 005/70 ARJO WIGGINS LIMITED, UNITED KINGDOM DAVID JOHN TAYLOR, RICHARD DAVID SAUNDERS, MICHAEL ERIC HOBSON WO/2003/102926 JEREMY M. BEN-DAVID & CO. LTD., HAR HOTZVIM HI-TECH PARK, P.O.B. 45087, JERUSALEM 91450 ]72[ ]87[ ]74[ [57] A magnetically-activatable sheet product (1) comprising a pair of laminated outer sheets (2) at least one of which is provided with a pigment/binder primer coat on its inward facing surface, between מוצר פעיל– מגנטי מורכב מיריעות ושיטה לשימוש במוצר כזה לאחסון וקריאה של נתונים דיגיטאליים ]33[ GB ,דוד ושות' בע"מ- בן.ירמיהו מ ,45087 .ד. ת, הר חוצבים,רחוב המרפא ירושלים which is a magnetic layer (3) comprising magnetically-activatable particles in a binder matrix, the outer sheets having sufficient opacity to mask the appearance of the magnetic layer. __________ ]11[]21[ July 24, 2007– ט' באב התשס"ז 165759 2100 ]54[ SPLIT VANE FLOW BLOCKER ]22[ ]31[ ]51[ ]71[ 14.12.2004 10/737599 ]32[ 16.12.2003 Int. Cl.8 F01D 017/00, F02C 001/00 UNITED TECHNOLOGIES CORPORATION, U.S.A. WOLFF, BREGMAN AND GOLLER, 19B KEREN HAYESOD ST., P.O.B. 1352, JERUSALEM 91013 ]74[ [57] A gas path flow blocker assembly (10) for use in a gas turbine engine having a gas flowpath between an outer duct and an inner support structure comprising: a plurality of vanes (21) located in said gas flowpath beween said outer duct and said inner support structure of said gas turbine engine, each of said vanes having an airfoil shape and comprising a forward portion (25) and an aft portion (23) defining a plurality of gas paths; שבשבת חצויה חוסמת זרימה ]33[ US , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד said flowpath being a secondary flowpath; a forward ring (15) comprising a central axis about which is circumferentially disposed said plurality of forward portions; and an aft ring (17) disposed about said central axis about which is circumferentially disposed said plurality of aft portions (23), wherein said forward ring and said aft ring are moveable with respect to each other to at least partially block the flow of a gas through said gas paths. ___________ ]11[]21[ 2101 165917 July 24, 2007– ט' באב התשס"ז ]54[ TRANSDERMAL DELIVERY SYSTEM ]22[ ]31[ ]51[ ]71[ 28.07.2003 02016864.7 ]32[ 30.07.2002 Int. Cl.8 A61K 009/00 SCHWARZ PHARMA AG, GERMANY WO/2004/012719 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 ]87[ ]74[ [57] A transdermal delivery system (TDS) comprising a backing layer inert to the components of the matrix, a selfadhesive matrix containing an aminefunctional drug and a protective foil or sheet to be removed prior to use, characterized in that the self-adhesive matrix consists of a solid or semi-solid semi-permeable polymer (1) wherein an amine functional drug in its free base form has been incorporated, מערכת למתן תרופות דרך העור ]33[ EP ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם (2) which is saturated with the amine functional drug and contains said drug as a multitude of microreservoirs within the matrix, (3) which is highly permeable for the free base of the amine functional drug, (4) which is impermeable for the protonated form of the amine functional drug, (5) wherein the maximum diameter of the microreservoirs is less than the thickness of the matrix. ___________ ]11[]21[ ]54[ SEPARATING DEVICE FOR A PRINT ENGINE ]22[ ]51[ ]62[ ]71[ 30.06.2000 Int. Cl.8 B41J 011/70 DIVISION FROM 153727 SILVERBROOK RESEARCH PTY. LTD., AUSTRALIA WO/2002/002344 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]87[ ]74[ [57] A motor arrangement for a printer having a printhead with a nozzle guard, July 24, 2007– ט' באב התשס"ז 166725 התקן מוטורי עבור מנוע הדפסה ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה print media cartridge (504) and an air pump (522) for reducing build up on the nozzle guard, the motor comprising first 2102 (532) and second (538) gear trains, wherein the first gear train is configured for driving the air pump and the second gear train is configured for driving a roller assembly of the print media cartridge, such that the air pump is only operational during printing on the print media. _____________ ]11[]21[ 166726 שיטה לחלוקת דיו ואוויר בראש המדפסת ]54[ PAPER THICKNESS SENSOR IN A PRINTER ]22[ ]51[ ]62[ ]71[ 24.05.2000 Int. Cl.8 B41J 002/01, 002/21, 011/04, 011/20 DIVISION FROM 153032 SILVERBROOK RESEARCH PTY. LTD., AUSTRALIA WO/2001/089837 LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו INDUSTRIAL PARK, OMER, באר שבע,5352 .ד. ת, עומר,גן תעשייה P.O.B. 5352, BEER-SHEVA 84152 ]87[ ]74[ [57] A method of distributing ink and air to print chips (27) in a printhead assembly (11) of a printer, the method utilizing a laminated ink distributing structure formed as a number of micro-molded layers adhered to one another with each layer including a plurality of ink holes formed therethrough, at least some of the ink holes in each layer communicating with a channel formed in one side of the said layer allowing passage of at least one of 2103 ink and air to a transversely located position within the structure, which transversely located position aligns with an aperture formed through an adjacent layer of the structure via which at least one of ink and air pass to the print chips, the method including selectively supplying different inks to pre-determined ones of the holes to thereby transfer the different inks to the printhead chips as required and selectively supplying air to predetermined July 24, 2007– ט' באב התשס"ז ones of the holes to thereby transfer air to the printhead chips as required. ____________ ]11[]21[ ]54[ PRINTHEAD ASSEMBLY WITH CAPPING ARRANGEMENT ]22[ ]51[ ]62[ ]71[ 24.05.2000 Int. Cl.8 B41J 002/165, 002/21 DIVISION FROM 153034 SILVERBROOK RESEARCH PTY. LTD., AUSTRALIA WO/2001/089848 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]87[ ]74[ [57] An inkjet printhead assembly comprising: July 24, 2007– ט' באב התשס"ז 166874 מכלול ראש הדפסה עם הסדר כיסוי ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה a printhead having plurality of print nozzles (30) for selectively ejecting drops 2104 of ink towards a print medium (31) passing the nozzles; a plurality of apertures (44) spaced from the nozzles in the direction of the ink ejection, each aperture being aligned with a corresponding nozzle so that ink drops ejected from the nozzles pass through the apertures; and means for sealing the space between the nozzles and the apertures when the printhead assembly is in a non-printing mode so as to reduce drying of the ink. __________ ]11[]21[ ]54[ INK SUPPLY ASSEMBLY FOR A PRINT ENGINE ]22[ ]51[ ]62[ ]71[ 30.06.2000 Int. Cl.8 B41J 002/175 DIVISION FROM 153664 SILVERBROOK RESEARCH PTY. LTD., AUSTRALIA WO/2002/002335 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]87[ ]74[ [57] An ink supply arrangement for a printhead (516) of a print engine, the printhead comprising a nozzle guard (757) adjacent to a first surface (730) of a wafer (724), an array of microelectromechanical system (MEMS) ink ejection devices mounted on the first surface of the wafer and a plurality of ink supply passages (734) extending through the wafer from an opposed surface of the wafer to respective ink ejection devices, the ink ejection devices being arranged in a plurality of groups, the ink supply arrangement comprising: a block (726) of material 2105 166875 התקן לאספקת דיו למנוע הדפסה ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה mountable on the opposed surface of the wafer, the block having a number of channels (728) defined therein, each channel corresponding to one of the groups, and opening out into a first surface of the block in abutment with the opposed surface of the wafer; and a plurality of ink supply inlet openings into a second surface (746) of the block, the opening being configured such that each of the channels is in communication with at least one opening, wherein ink from each ink ejection device is ejected through the nozzle guard. July 24, 2007– ט' באב התשס"ז ____________ ]11[]21[ ]54[ INKJET PRINTER HAVING COMPENSATION FOR OVERLAPPING PRINTHEAD ELEMENTS ]22[ ]51[ ]62[ ]71[ 24.05.2000 Int. Cl.8 B41J 002/145 DIVISION FROM 153025 SILVERBROOK RESEARCH PTY. LTD., AUSTRALIA WO/2001/089845 LUZZATTO & LUZZATTO, INDUSTRIAL PARK, OMER, P.O.B. 5352, BEER-SHEVA 84152 ]87[ ]74[ [57] A printer comprising an inkjet printhead comprising a plurality of spaced apart spatially overlapping print head segments (2, 3) the printer further comprising at least one means for measurement of the degree of overlap between adjacent print head segments; July 24, 2007– ט' באב התשס"ז 166876 מדפסת דיו בעלת פיצוי לרכיבי ראש מדפסת חופפים ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשייה means for providing a half toning of a continuous tone image and means for adjusting said half toning means in a region (10, 11, 12, 13) of overlap between adjacent print head segments to reduce artifacts between said adjacent segments. 2106 __________ ]11[]21[ 173678 גישה מרוחקת למחשב ]54[ REMOTE COMPUTER ACCESS ]22[ ]51[ ]62[ ]71[ ]87[ ]74[ 27.07.1998 Int. Cl.8 G06F 019/00, H04L 012/00, H04N 007/10 DIVISION FROM 141104 MICROSOFT CORPORATION WO/2000/007091 REINHOLD COHN AND ,ריינהולד כהן ושותפיו PARTNERS, תל אביב,4060 .ד. ת, 21 רחוב אחד העם 21 AHAD HA'AM ST., P.O.B. 4060, TEL AVIV 61040 [57] A method of bandwidth allocation for transmitting video on a cable network, the method comprising: providing a plurality of data sources; differentially converting said data sources into compressed video streams, responsive to an instantaneous resource restriction; and multiplexing said compressed video streams on a single transmission line; wherein differentially converting said data sources comprises identifying compression . 2107 parameters to be used to compress the data that is received from the plurality of data sources to a desired depth of compression, the compression parameters being based on a function of types of data to be displayed and a function of client capabilities, wherein the types of data are determined from content of data received from the respective plurality of data sources July 24, 2007– ט' באב התשס"ז _____________ ]11[]21[ 174850 תרכובות המשמשות בהכנת תולדות של פיפרידין אנטיהיסטמיניות ]54[ COMPOUNDS USEFUL IN THE PREPARATION OF ANTIHISTAMINIC PIPERIDINE DERIVATIVES ]22[ ]31[ ]51[ ]62[ ]71[ ]74[ 22.06.1994 08/082693 ]32[ 25.06.1993 ]33[ US 08/144084 27.10.1993 US 08/237466 11.05.1994 US Int. Cl.8 C07C 049/82, 049/86, 069/76, 255/16, C07D 211/22 DIVISION FROM 143611 AVENTIS INC., U.S.A. DR. SHLOMO COHEN & CO., ,'ד"ר שלמה כהן ושות 124 IBN GABIROL ST., תל אביב,11490 .ד. ת, 124 אבן גבירול P.O.B. 11490, TEL AVIV 62038 [57] A compound of the formula July 24, 2007– ט' באב התשס"ז 2108 wherein Hal is Cl, Br or I; n is an integer of from 1 to 5; A is hydrogen or hydroxy; and R5 is CH2OD wherein D is hydrogen, acetate or benzoate, CHO, Br, Cl, I or CN; or a compound of the formula wherein n is an integer of from 1 to 5; A is a hydrogen or hydroxy; and R5 is Br, Cl or I; or a compound of the formula wherein R5 is Br, Cl or I; or a compound of the formula and individual optical isomers thereof; or a compound of the formula 2109 July 24, 2007– ט' באב התשס"ז wherein W represents –C(==O)-or –CH(OH)-; R1 represents hydrogen or hydroxy; R2 represents hydrogen; or R1 and R2 taken together form a second bond between the carbon atoms bearing R1 and R2; m is an integer 0 or 1; R5 is H, Br, Cl, I or CN; A is hydrogen or hydroxy; and pharmaceutically acceptable salts and individual optical isomers thereof, with the proviso that where R1 and R2 are taken together to form a second bond between the carbon atoms bearing R1 and R2 or where R1 represented hydroxy, m is an integer 0. __________ ]11[]21[ 179054 יחידת לקוח ורשת תיקשורות,יחידת שרת עבור יישומי מכפל–משתמשים ]54[ SERVER UNIT, CLIENT UNIT AND COMMUNICATIONS NETWORK FOR MULTI-USER APPLICATIONS ]22[ ]31[ 10.05.2000 9901694-1 ]32[ 10.05.1999 ]33[ SE 09/307712 10.05.1999 US Int. Cl.8 A63F 009/24, G06F 017/30, 019/00, 161/00 DIVISION FROM 146348 TERRAPLAY SYSTEMS AB, SWEDEN WO/2000/068864 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף 19B KEREN HAYESOD ST., ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352, JERUSALEM 91013 ]51[ ]62[ ]71[ ]87[ ]74[ [57] A server unit connectable to at least a July 24, 2007– ט' באב התשס"ז 2110 first and a second client unit and adapted to enable communication between the first and the second client unit through the server unit for running a distributed interactive application having a state that can be simultaneously affected and contributed to by both the first and the second client unit, the server unit being characterized in that it includes; first receiving means for receiving application state information about the state of the application from at least the first client unit; state information storing means for storing application state information; second receiving means for receiving priority information from at least the first client unit about application state information to be sent to the first client unit; priority information storing means for storing the received priority information; first transmission means cooperating with the state information storing means for transmitting application state information to the first client unit in the dependence of the priority information; at least one application router including the first and second transmission means and the first and second receiving means, an application server including the information storing means. ___________ 2111 July 24, 2007– ט' באב התשס"ז פטנטים PATENTS פטנטים שניתנו PATENTS GRANTED 125894 141922 142549 142813 143279 143816 144117 144379 144642 144911 145080 145320 145639 169779 129332 131436 132437 146102 146374 146685 146840 147211 147542 147840 148078 148377 148691 148964 149212 149649 150037 150982 117420 138113 138987 139780 140241 141505 157986 2112 125143 141912 142470 142799 143184 143809 144049 144377 144626 144884 145057 145286 145619 168036 129085 131396 132166 146068 146277 146669 146835 147210 147540 147807 148058 148366 148548 148955 149165 149643 149998 150969 116216 137768 138746 139775 140234 141503 157899 124941 141902 142439 142732 143115 143731 143937 144325 144602 144813 145050 145244 145590 145807 129035 130995 132095 146037 146262 146609 146833 147178 147395 147746 148049 148357 148520 148888 149150 149622 149975 150938 151298 137639 138737 139607 140206 141399 141705 124579 141822 142400 142728 143028 143697 143928 144246 144559 144809 145036 145240 145523 145777 128741 130967 132062 145957 146224 146549 146831 147116 147380 147694 148020 148330 148438 148804 149143 149503 149886 150654 151276 137571 138733 139368 140199 141294 141665 124473 141794 142130 142669 142996 143575 143923 144136 144549 144794 145018 145206 145516 145748 114775 130333 131794 145877 146216 146532 146804 147058 147346 147682 147974 148242 148435 148794 149104 149482 149852 150378 151237 137517 138705 139283 140151 141194 141661 124112 141742 142106 142605 142969 143502 143831 144127 144545 144785 145012 145155 145488 145699 101769 130129 131770 132676 146200 146519 146750 147014 147304 147625 147945 148241 148434 148765 149094 149310 149732 150355 151181 137490 138442 139255 140144 141124 141651 108788 127813 141926 142571 142854 143347 143829 144124 144539 144758 144977 145105 145475 145647 101288 129851 131767 132632 146167 146504 146746 146995 147263 147609 147903 148219 148428 148764 149023 149272 149693 150282 151069 137410 138224 139216 139917 140981 141592 108586 127365 141923 142567 142833 143303 143818 144123 144382 144718 144935 145104 145326 145640 170293 129527 131508 132557 146159 146394 146700 146985 147241 147607 147877 148082 148379 148705 149007 149239 149663 150183 151038 137347 138223 139186 139890 140260 141549 ט' באב התשס"ז –July 24, 2007 159359 160854 162998 164980 132886 133973 134880 136655 137146 151984 152677 153378 153843 154432 155021 155902 156706 159137 160566 162626 164957 122942 133678 134763 136483 137099 151929 152664 153302 153544 154300 155017 155630 156535 159121 159958 161567 164690 167541 133586 134656 136250 136888 151698 152526 153256 153515 154174 154951 155578 156503 157790 ט' באב התשס"ז –July 24, 2007 158994 159761 161556 164648 166283 133449 134599 136030 136886 151682 152513 153216 153502 154154 154766 155336 156456 157646 158649 159608 161321 164446 166281 133386 134430 135836 136839 151587 152425 153126 153467 154105 154763 155308 156318 157403 158578 159574 161221 164251 165698 133319 134188 135508 136831 151582 152365 152954 153466 154104 154749 155264 156170 157346 158375 159505 161087 163942 164982 133101 134073 135503 136782 151366 152311 152755 153381 154019 154706 155114 156141 157035 158077 159425 161011 163370 164981 133060 134042 135384 136737 137216 152010 152728 153379 153969 154597 155028 156102 157034 2113 פטנטים שחודשו PATENTS RENEWED 89686 89779 89841 89931 90484 90542 90622 90795 103939 104954 105146 105207 105268 105337 105372 105413 105516 105818 105946 106013 106076 106218 114775 119874 120399 120483 120547 120654 120725 120910 120985 121044 121076 121115 121174 122117 122526 123441 123840 125849 126083 126190 2114 89670 89763 89831 89896 90462 90533 90599 90775 103813 104926 105141 105205 105264 105325 105371 105410 105513 105817 105945 105988 106074 106155 113988 119728 120388 120481 120542 120651 120722 120907 120976 121032 121075 121112 121173 122101 122525 123336 123835 125812 126075 126187 89669 89749 89807 89880 90453 90527 90594 90752 103152 104923 105135 105204 105252 105323 105369 105403 105468 105746 105944 105987 106071 106142 113232 119727 120365 120465 120522 120623 120701 120890 120959 121018 121068 121109 121161 121316 122521 123259 123676 125795 126073 126186 89593 89748 89794 89879 90062 90510 90592 90731 101520 104915 105119 105203 105251 105306 105366 105400 105464 105744 105941 105970 106040 106135 109049 118578 120358 120436 120517 120587 120700 120889 120953 121013 121060 121102 121158 121230 122520 123130 123656 125628 126044 126185 89557 89735 89791 89875 90059 90502 90583 90730 101288 104912 105077 105187 105246 105303 105345 105396 105457 105706 105933 105969 106036 106116 108316 118418 120328 120435 120512 120586 120696 120857 120951 121009 121057 121092 121151 121195 122447 123025 123655 125006 125987 126177 89470 89692 89790 89867 90019 90501 90551 90674 97688 104911 105051 105161 105244 105302 105344 105383 105449 105702 105905 105959 106033 106111 107868 118279 120187 120429 120498 120584 120695 120820 120946 121008 121053 121089 121139 121194 122438 122998 123629 124941 125895 126146 89460 89691 89789 89847 89982 90500 90550 90665 97687 104910 105027 105153 105243 105279 105340 105382 105432 105662 105895 105958 106027 106109 107709 116609 120076 120420 120492 120574 120670 120814 120943 121007 121046 121079 121138 121186 122423 122765 123531 124617 125894 126123 89403 89688 89781 89845 89963 90488 90545 90662 90802 104839 104957 105152 105221 105276 105338 105377 105430 105658 105876 105956 106020 106099 107563 116398 119928 120416 120490 120554 120669 120800 120930 121005 121045 121078 121128 121179 122318 122699 123514 124072 125850 126120 ט' באב התשס"ז –July 24, 2007 126251 126318 126367 126394 126484 126551 126612 126717 126901 127013 127126 127231 127325 127378 127476 127542 127715 127770 128632 131396 132095 133544 135406 136655 137579 138984 139775 139983 140661 141741 141836 142112 142227 142400 142553 142783 143190 143457 143649 143787 143928 144105 144358 144626 144907 145244 126248 126314 126363 126393 126479 126545 126596 126716 126842 126989 127113 127218 127312 127365 127475 127540 127657 127769 128163 130955 132071 133264 135295 136388 137493 138837 139704 139982 140636 141707 141790 142098 142226 142373 142524 142781 143112 143443 143631 143731 143915 144100 144352 144599 144905 145131 126245 126311 126354 126392 126470 126541 126594 126690 126831 126985 127111 127212 127296 127364 127473 127539 127651 127766 128108 130287 132062 133162 134980 136287 137490 138737 139283 139981 140495 141702 141780 142020 142208 142345 142484 142728 143111 143425 143606 143727 143913 144084 144260 144545 144867 145080 ט' באב התשס"ז –July 24, 2007 126237 126307 126351 126384 126459 126535 126591 126677 126823 126976 127062 127208 127295 127360 127468 127534 127629 127741 127861 130129 132000 133078 134699 136250 137475 138711 139255 139980 140491 141676 141777 142004 142177 142335 142470 142716 142966 143423 143576 143721 143836 144058 144227 144544 144771 145036 126231 126304 126343 126381 126458 126534 126590 126655 126793 126975 127049 127207 127279 127357 127446 127526 127619 127740 127860 129814 131841 132845 134126 135811 137410 138425 139252 139979 140434 141642 141771 141963 142156 142325 142457 142649 142958 143315 143575 143697 143818 144036 144198 144488 144770 145018 126207 126299 126338 126380 126449 126532 126584 126646 126779 126934 127033 127180 127250 127349 127415 127519 127604 127735 127859 129789 131794 132437 134087 135618 137347 138317 139244 139978 140260 141501 141766 141961 142140 142293 142455 142606 142954 143285 143572 143694 143790 144035 144160 144486 144762 145012 126204 126283 126337 126371 126431 126497 126583 126643 126770 126924 127016 127144 127249 127343 127409 127510 127603 127730 127783 129561 131770 132166 134073 135610 137277 138099 139199 139977 140199 140804 141765 141926 142125 142245 142416 142601 142832 143248 143503 143658 143789 144010 144119 144382 144699 144968 126199 126282 126324 126368 126403 126496 126556 126628 126727 126911 127015 127133 127235 127342 127385 127509 127595 127726 127782 129193 131436 132101 133976 135503 137096 137605 138987 139917 140179 140710 141742 141918 142124 142228 142413 142571 142804 143201 143487 143657 143788 143937 144106 144379 144698 144911 2115 145400 145774 146224 146602 146807 146965 147425 148082 148548 148794 149039 149503 149989 150433 151095 151404 151643 151792 151997 152267 152459 152914 153106 153338 154104 154662 154979 155264 156169 156918 158456 159798 161031 162418 164448 173676 2116 145365 145651 146205 146588 146804 146953 147369 148058 148520 148765 149005 149499 149920 150373 151072 151366 151587 151773 151984 152175 152400 152851 153057 153294 154066 154511 154924 155211 156141 156639 158406 159763 160854 161963 164445 170201 145363 145619 146103 146460 146759 146927 147247 147849 148470 148764 148998 149476 149853 150282 151038 151336 151582 151770 151983 152171 152392 152833 153047 153260 153448 154440 154766 155187 155902 156631 158177 159762 160735 161962 163942 165734 145336 145616 146068 146394 146746 146926 147178 147694 148391 148725 148955 149441 149852 150183 150887 151298 151565 151756 151975 152056 152376 152789 153007 153256 153416 154355 154765 155114 155722 156535 158052 159760 160258 161961 163503 165710 145327 145561 146014 146374 146721 146925 147119 147614 148379 148691 148932 149440 149819 150138 150654 151276 151560 151750 151966 152050 152308 152752 152992 153146 153380 154330 154749 155076 155624 156503 157833 159245 160234 161820 163292 164782 145318 145523 145986 146261 146702 146917 146995 147607 148302 148684 148910 149338 149731 150098 150616 151273 151536 151701 151963 152010 152286 152619 152977 153145 153379 154253 154746 155028 155541 156456 157790 159213 160186 161612 162974 164576 145316 145517 145807 146260 146669 146876 146992 147557 148291 148629 148897 149214 149675 150038 150532 151241 151516 151678 151850 152000 152282 152558 152974 153126 153378 154174 154714 155003 155358 156279 157524 159121 159958 161556 162626 164505 145286 145486 145777 146259 146609 146835 146985 147542 148242 148553 148840 149087 149589 150017 150469 151204 151449 151677 151813 151999 152281 152534 152915 153112 153344 154171 154681 154983 155308 156170 157194 158994 159799 161065 162575 164504 ט' באב התשס"ז –July 24, 2007 פטנטים שתוקפם פקעו בגלל אי תשלום אגרת חידוש PATENTS NOT IN FORCE DUE TO NON-PAYMENT OF RENEWAL FEES 87275 87369 87436 87564 87664 87740 87836 88348 88443 102686 102794 102873 102947 103060 103630 103732 103825 103897 110804 119009 119112 119190 119255 119313 119381 119491 119542 119615 119704 120968 122826 123155 123372 123455 123489 123605 123724 123901 123977 124040 124095 124198 2117 87292 87377 87448 87568 87676 87755 87868 88350 88453 102703 102797 102881 102951 103062 103642 103753 103827 103900 116942 119019 119121 119192 119256 119317 119392 119492 119550 119616 119705 121050 122865 123164 123375 123471 123539 123614 123745 123902 123987 124046 124096 124200 87303 87390 87458 87623 87686 87756 87882 88354 88493 102711 102809 102884 102985 103065 103644 103776 103832 103906 117592 119020 119132 119201 119257 119327 119403 119493 119552 119659 119709 121051 122987 123165 123424 123480 123560 123615 123771 123915 123991 124048 124107 124205 87312 87392 87468 87632 87694 87760 88289 88365 88498 102745 102816 102898 103010 103078 103665 103778 103847 103936 118674 119021 119144 119207 119259 119330 119424 119501 119571 119668 119740 121196 123042 123213 123427 123482 123581 123650 123797 123916 123999 124049 124121 124212 87323 87413 87487 87636 87697 87802 88330 88377 88531 102760 102821 102904 103018 103096 103694 103782 103879 103953 118984 119055 119149 119212 119264 119331 119433 119512 119586 119672 119746 121341 123056 123250 123430 123484 123589 123662 123808 123918 124003 124056 124136 124217 87329 87415 87513 87642 87704 87816 88345 88397 88544 102784 102854 102906 103054 103123 103703 103798 103884 103962 118992 119064 119174 119230 119274 119369 119434 119521 119587 119678 119970 121432 123080 123319 123434 123485 123597 123692 123816 123941 124021 124067 124156 124227 87332 87427 87542 87658 87713 87828 88346 88410 101332 102791 102856 102924 103055 103128 103713 103802 103887 103963 118997 119083 119182 119246 119285 119374 119466 119525 119602 119692 120742 121459 123136 123345 123438 123486 123599 123696 123851 123950 124022 124087 124158 124241 87341 87430 87554 87661 87731 87829 88347 88429 102681 102792 102858 102936 103056 103150 103729 103821 103895 104695 119000 119094 119188 119251 119311 119377 119482 119533 119609 119703 120780 121916 123147 123371 123443 123488 123603 123705 123885 123966 124037 124094 124185 124290 July 24, 2007– ט' באב התשס"ז 124411 124662 124776 129813 137770 138919 139650 141259 145340 148608 152236 2118 124396 124658 124775 128643 137437 138537 139633 141228 144682 148197 151728 165945 124385 124649 124774 128627 135768 138364 139622 140162 143877 148009 150884 154667 124375 124611 124765 127347 135032 138282 139581 140123 143476 146736 150264 154664 124365 124499 124730 125460 134592 138023 139550 140007 143134 146592 149629 153108 124340 124464 124729 124884 130805 137909 139490 139892 142898 145817 149284 152579 124339 124420 124677 124833 130440 137864 139211 139712 142849 145809 149198 152374 124338 124415 124668 124792 129872 137861 139174 139657 142646 145341 148660 152255 ט' באב התשס"ז –July 24, 2007 פטנטים שחודשו לעשרים שנה PATENTS RENEWED FOR 20 YEARS 163265 ט' באב התשס"ז –July 24, 2007 163074 146159 145350 138891 2119 פטנטים שפג תוקפם PATENTS EXPIRED 81572 81649 81713 81775 81841 81920 81967 82032 82073 82120 82213 82250 82323 82397 82474 82512 82604 82709 101990 2120 81542 81639 81712 81769 81838 81919 81960 82017 82072 82118 82192 82245 82311 82395 82472 82511 82601 82700 99897 81520 81633 81709 81750 81835 81913 81959 82016 82061 82116 82176 82244 82298 82387 82464 82510 82592 82693 98886 81481 81618 81695 81749 81803 81892 81952 82005 82054 82113 82165 82242 82271 82377 82456 82508 82564 82692 91062 81456 81611 81686 81748 81802 81888 81948 81988 82053 82103 82152 82231 82266 82373 82454 82504 82550 82687 82758 81450 81607 81669 81744 81795 81886 81946 81984 82050 82101 82149 82230 82265 82353 82430 82491 82541 82641 82746 81448 81597 81663 81740 81791 81855 81937 81973 82045 82091 82148 82225 82260 82343 82411 82481 82535 82624 82743 119895 81438 81573 81652 81737 81788 81851 81927 81970 82044 82085 82127 82220 82251 82331 82398 82478 82513 82615 82719 119484 ט' באב התשס"ז –July 24, 2007 צווי הארכה שחודשו EXTENSION ORDERS RENEWED 70311 2121 73534 77111 77243 84054 84601 July 24, 2007– ט' באב התשס"ז הודעה NOTICE לחוק60 לפי סעיף 1967- תשכ"ז,הפטנטים הוגשה בקשה להחזר תוקפו של הפטנט המפורט שתוקפו פקע מחמת,מטה אי תשלום אגרות החידוש :הקבועות Under section 60 of the Patent Law, 5727-1967 Application has been filed for the restoration of the patent recorded below, which has lapsed through non-payment of the prescribed renewal fees: No. of Patent Acceptance published in journal no: Proprietors: 114731 2/2005 מס' הפטנט :'קיבול פורסם ביומן מס :שם בעל הפטנט מדינול בע"מ MEDINOL LTD. :שם האמצאה Title of invention: סטנט מפרקי ARTICULATED STENT Any person may oppose the said application within three months from the date of this Patents Journal, as prescribed by section 61 of the law and by regulation 92 of the Patent Regulations, 5728-1968 July 24, 2007– ט' באב התשס"ז כל אדם רשאי להתנגד לבקשה האמורה תוך שלושה חודשים מתאריך כפי שנקבע,יומן פטנטים זה 92 לחוק ובתקנה61 בסעיף - תשכ"ח,לתקנות הפטנטים 1968 2122 הודעה NOTICE לחוק60 לפי סעיף 1967- תשכ"ז,הפטנטים הוגשה בקשה להחזר תוקפו של הפטנט המפורט שתוקפו פקע מחמת,מטה אי תשלום אגרות החידוש :הקבועות Under section 60 of the Patent Law, 5727-1967 Application has been filed for the restoration of the patent recorded below, which has lapsed through non-payment of the prescribed renewal fees: No. of Patent Acceptance published in journal no: Proprietors: 116685 2/2000 מס' הפטנט :'קיבול פורסם ביומן מס :שם בעל הפטנט וסקולאר טכנולגיות בע"מ VASCULAR TECHNOLOGIES LIMITED :שם האמצאה ציין חדירה לכלי דם BLOOD VESSEL ENTRY INDICATOR Any person may oppose the כל אדם רשאי להתנגד said application within three לבקשה האמורה תוך months from the date of this שלושה חודשים מתאריך Patents Journal, as כפי שנקבע,יומן פטנטים זה prescribed by section 61 of 92 לחוק ובתקנה61 בסעיף the law and by regulation 92 - תשכ"ח,לתקנות הפטנטים of the Patent Regulations, 5728-1968 1968 Title of invention: 2123 July 24, 2007– ט' באב התשס"ז הודעה NOTICE לחוק60 לפי סעיף 1967- תשכ"ז,הפטנטים הוגשה בקשה להחזר תוקפו של הפטנט המפורט שתוקפו פקע מחמת,מטה אי תשלום אגרות החידוש :הקבועות Under section 60 of the Patent Law, 5727-1967 Application has been filed for the restoration of the patent recorded below, which has lapsed through non-payment of the prescribed renewal fees: No. of Patent Acceptance published in journal no: Proprietors: 116722 9/2000 מס' הפטנט :'קיבול פורסם ביומן מס :שם בעל הפטנט פסקל אביזרי קשירה בע"מ PASKAL BINDING ACCESSORIES LTD. :שם האמצאה מתלה משחרר חוט סלילי להדליית ירקות ROPE RELEASING HOOK WITH SPOOL FOR TRELLISING VEGETABLES Any person may oppose the כל אדם רשאי להתנגד said application within three לבקשה האמורה תוך months from the date of this שלושה חודשים מתאריך Patents Journal, as כפי שנקבע,יומן פטנטים זה prescribed by section 61 of 92 לחוק ובתקנה61 בסעיף the law and by regulation 92 - תשכ"ח,לתקנות הפטנטים of the Patent Regulations, 5728-1968 1968 Title of invention: July 24, 2007– ט' באב התשס"ז 2124 הודעה NOTICE לחוק60 לפי סעיף 1967- תשכ"ז,הפטנטים הוגשה בקשה להחזר תוקפו של הפטנט המפורט שתוקפו פקע מחמת,מטה אי תשלום אגרות החידוש :הקבועות Under section 60 of the Patent Law, 5727-1967 Application has been filed for the restoration of the patent recorded below, which has lapsed through non-payment of the prescribed renewal fees: No. of Patent Acceptance published in journal no: Proprietors: 123446 7/2000 מס' הפטנט :'קיבול פורסם ביומן מס :שם בעל הפטנט T-SYSTEMS INTERNATIONAL, INC. Title of invention: :שם האמצאה שיטה לחיבור טמפטות תוך שימוש באמצעיי פנימיים לטפטפות METHOD FOR SPLICING DRIP IRRIGATION HOSES USING SPLICING MEANS INTERNAL TO THE HOSES Any person may oppose the כל אדם רשאי להתנגד said application within three לבקשה האמורה תוך months from the date of this שלושה חודשים מתאריך Patents Journal, as כפי שנקבע,יומן פטנטים זה prescribed by section 61 of 92 לחוק ובתקנה61 בסעיף the law and by regulation 92 - תשכ"ח,לתקנות הפטנטים of the Patent Regulations, 5728-1968 1968 2125 July 24, 2007– ט' באב התשס"ז הודעה NOTICE לחוק60 לפי סעיף 1967- תשכ"ז,הפטנטים הוגשה בקשה להחזר תוקפו של הפטנט המפורט שתוקפו פקע מחמת,מטה אי תשלום אגרות החידוש :הקבועות Under section 60 of the Patent Law, 5727-1967 Application has been filed for the restoration of the patent recorded below, which has lapsed through non-payment of the prescribed renewal fees: No. of Patent Acceptance published in journal no: Proprietors: 126729 5/2001 מס' הפטנט :'קיבול פורסם ביומן מס :שם בעל הפטנט CABOT CORPORATION Title of invention: :שם האמצאה שיטה לייצור אבקת מתכת טנטל עם פיזור גודל מבוקר ומוצרים המיוצרים ממנה METHOD OF MAKING TANTALUM METAL POWDER WITH CONTROLLED SIZE DISTRIBUTION AND PRODUCTS MADE THEREFROM Any person may oppose the כל אדם רשאי להתנגד said application within three לבקשה האמורה תוך months from the date of this שלושה חודשים מתאריך Patents Journal, as כפי שנקבע,יומן פטנטים זה prescribed by section 61 of 92 לחוק ובתקנה61 בסעיף the law and by regulation 92 - תשכ"ח,לתקנות הפטנטים of the Patent Regulations, 5728-1968 1968 July 24, 2007– ט' באב התשס"ז 2126 הודעה NOTICE לחוק60 לפי סעיף 1967- תשכ"ז,הפטנטים הוגשה בקשה להחזר תוקפו של הפטנט המפורט שתוקפו פקע מחמת,מטה אי תשלום אגרות החידוש :הקבועות Under section 60 of the Patent Law, 5727-1967 Application has been filed for the restoration of the patent recorded below, which has lapsed through non-payment of the prescribed renewal fees: No. of Patent Acceptance published in journal no: Proprietors: מס' הפטנט :'קיבול פורסם ביומן מס 137470 9/2004 :שם בעל הפטנט ) בע"מ1993( טבעול TIVALL (1993) LIMITED :שם האמצאה מוצר מזון תזונתי ותהליך להכנתו NUTRITIONAL FOOD PRODUCT AND PROCESS FOR ITS PREPARATION Any person may oppose the כל אדם רשאי להתנגד said application within three לבקשה האמורה תוך months from the date of this שלושה חודשים מתאריך Patents Journal, as כפי שנקבע,יומן פטנטים זה prescribed by section 61 of 92 לחוק ובתקנה61 בסעיף the law and by regulation 92 - תשכ"ח,לתקנות הפטנטים of the Patent Regulations, 5728-1968 1968 Title of invention: 2127 July 24, 2007– ט' באב התשס"ז הודעה NOTICE לחוק60 לפי סעיף 1967- תשכ"ז,הפטנטים הוגשה בקשה להחזר תוקפו של הפטנט המפורט שתוקפו פקע מחמת,מטה אי תשלום אגרות החידוש :הקבועות Under section 60 of the Patent Law, 5727-1967 Application has been filed for the restoration of the patent recorded below, which has lapsed through non-payment of the prescribed renewal fees: No. of Patent Acceptance published in journal no: Proprietors: 151651 6/2005 מס' הפטנט :'קיבול פורסם ביומן מס :שם בעל הפטנט PLASTICOS MONDRAGON S.A. Title of invention: :שם האמצאה שסטום הידרולי דיאפרגמתי לוויסות זרם נוזלים HYDRAULIC DIAPHRAGM VALVE FOR FLUID FLOW REGULATION Any person may oppose the כל אדם רשאי להתנגד said application within three לבקשה האמורה תוך months from the date of this שלושה חודשים מתאריך Patents Journal, as כפי שנקבע,יומן פטנטים זה prescribed by section 61 of 92 לחוק ובתקנה61 בסעיף the law and by regulation 92 תשכ"ח,לתקנות הפטנטים of the Patent Regulations, 5728-1968 1968 July 24, 2007– ט' באב התשס"ז 2128 הודעה NOTICE לחוק60 לפי סעיף 1967- תשכ"ז,הפטנטים הוגשה בקשה להחזר תוקפו של הפטנט המפורט שתוקפו פקע מחמת,מטה אי תשלום אגרות החידוש :הקבועות Under section 60 of the Patent Law, 5727-1967 Application has been filed for the restoration of the patent recorded below, which has lapsed through non-payment of the prescribed renewal fees: No. of Patent Acceptance published in journal no: Proprietors: 151728 10/2005 מס' הפטנט :'קיבול פורסם ביומן מס :שם בעל הפטנט איתמר בורשטיין ITAMAR BURSTEIN :שם האמצאה שיטה והתקן לשמירת פריטי לבוש יחדיו METHOD AND DEVICE FOR SECURING APPAREL ARTICLES TOGETHER Any person may oppose the כל אדם רשאי להתנגד said application within three לבקשה האמורה תוך months from the date of this שלושה חודשים מתאריך Patents Journal, as כפי שנקבע,יומן פטנטים זה prescribed by section 61 of 92 לחוק ובתקנה61 בסעיף the law and by regulation 92 - תשכ"ח,לתקנות הפטנטים of the Patent Regulations, 5728-1968 1968 Title of invention: 2129 July 24, 2007– ט' באב התשס"ז NOTICE under section 64E of the Patents Law, 5727-1967 ה לחוק64 הודעה לפי סעיף 1967-הפטנטים התשכ"ז בכוונת רשם הפטנטים ליתן צו להארכת תקופת הגנה ע"פ פרק , לחוק הפטנטים1 סימן ב,'ד לגבי הפטנט1967-התשכ"ז :המפורט מטה It is the intention of the Commissioner of Patents to grant an order for the extension of the period of protection of the following patent in accordance with Chapter Four, Article Two bis, of the Patents Law, 5727-1967 No. of basic patent: 84863 :מס' פטנט בסיסי Title of invention: :שם האמצאה תהליך להכנתם ותכשירים תרופתיים,3 –אריאלאוקסי פרפאנאמינים מותמרים בעמדה3 המכילים אותם -3ARYLOXY-3-SUBSTITUTED PROPANAMINES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM Proprietors: :בעלי הפטנט ELI LILLY AND COMPANY Any person desiring to oppose the כל המעוניין להתנגד למתן צו said grant of an order may, within הארכה רשאי תוך שלושה three months from the date of this להגיש,חודשים מתאריך יומן זה journal, serve to the Commissioner התנגדות לרשם הפטנטים הודעה of Patents a notice of opposition בדרך ,ו לחוק64 לפי סעיף under Section 64F of the Law, as לתקנות3 הקבועה בתקנה prescribed by Rule 3 of the Patent Regulations (extension of period of הפטנטים (הארכת תקופה הגנה protection – procedure of ,– סדרי דין בבקשה לצו application for order, opposition to ,) ובבקשה לביטול,בהתנגדות לצו order, application to annul) 57581998-התשנ"ח 1998. July 24, 2007– ט' באב התשס"ז 2130 שינויים בפרטים רשומים בפנקס CHANGES IN PARTICULARS ENTERED IN REGISTER שינוי שם הבעלים CHANGE OF NAME OF PROPRIETORS No. of Patent: ,160923 ,160922 ,156758 ,156148 ,128551 ,51634 163428 ,162232 ,162169 ,161564 :מס' פטנט :השם הקודם Previous name: SYNTHES AG CHUR :השם החדש New name: AO TECHNOLOGY AG שינוי בעלות CHANGES IN PROPRIETORSHIP No. of Patent: 113024 Previous Proprietors: RECORDATI S.A., CHEMICAL AND PHARMACEUTICAL COMPANY New Proprietors: RECORDATI IRELAND LIMITED :מס' פטנט :הבעלים הקודמים No. of Patent: 135814 Previous Proprietors: KOSLOW TECHNOLOGIES CORPORATION New Proprietors: KX INDUSTRIES, L.P. :מס' פטנט :הבעלים הקודמים No. of Patent: 138057 Previous Proprietors: RESPIRATORY SUPPORT PRODUCTS INC. New Proprietors: SMITHS MEDICAL ASD :מס' פטנט :הבעלים הקודמים 2131 :הבעלים החדשים :הבעלים החדשים :הבעלים החדשים July 24, 2007– ט' באב התשס"ז No. of Patent: 139313 Previous Proprietors: HUBERT ERIC WALTER New Proprietors: MGS MODULAR GALLERY SYSTEMS AG :מס' פטנט :הבעלים הקודמים No. of Patent: 141991 Previous Proprietors: LABORATORIOS VITA S.A. New Proprietors: VITA CIENTIFICA, S.L. :מס' פטנט :הבעלים הקודמים No. of Patent: 147701 Previous Proprietors: KOSLOW TECHNOLOGIES CORPORATION New Proprietors: KX INDUSTRIES, L.P. :מס' פטנט :הבעלים הקודמים No. of Patent: 156186 Previous Proprietors: KOSLOW TECHNOLOGIES CORPORATION New Proprietors: KX INDUSTRIES, L.P. :מס' פטנט :הבעלים הקודמים July 24, 2007– ט' באב התשס"ז :הבעלים החדשים :הבעלים החדשים :הבעלים החדשים :הבעלים החדשים 2132 No. of Patent: 158362 Previous Proprietors: KOSLOW TECHNOLOGIES CORPORATION New Proprietors: KX INDUSTRIES, L.P. :מס' פטנט :הבעלים הקודמים No. of Patent: 163057 Previous Proprietors: KOSLOW TECHNOLOGIES CORPORATION New Proprietors: KX INDUSTRIES, L.P. :מס' פטנט :הבעלים הקודמים No. of Patent: 163159 Previous Proprietors: KOSLOW TECHNOLOGIES CORPORATION New Proprietors: KX INDUSTRIES, L.P. :מס' פטנט :הבעלים הקודמים No. of Patent: 165739 Previous Proprietors: KOSLOW TECHNOLOGIES CORPORATION New Proprietors: KX INDUSTRIES, L.P. :מס' פטנט :הבעלים הקודמים 2133 :הבעלים החדשים :הבעלים החדשים :הבעלים החדשים :הבעלים החדשים July 24, 2007– ט' באב התשס"ז No. of Patent: 165740 Previous Proprietors: KOSLOW TECHNOLOGIES CORPORATION New Proprietors: KX INDUSTRIES, L.P. :מס' פטנט :הבעלים הקודמים No. of Patent: 165741 Previous Proprietors: KOSLOW TECHNOLOGIES CORPORATION New Proprietors: KX INDUSTRIES, L.P. :מס' פטנט :הבעלים הקודמים No. of Patent: 165742 Previous Proprietors: KOSLOW TECHNOLOGIES CORPORATION New Proprietors: KX INDUSTRIES, L.P. :מס' פטנט :הבעלים הקודמים July 24, 2007– ט' באב התשס"ז :הבעלים החדשים :הבעלים החדשים :הבעלים החדשים 2134 תיקוני טעויות CORRIGENDA Journal 11/2005 P. 4667 Patent application No. 118235 Correct address for service toINTERPHARM LABORATORIES LTD. KIRYAT WEIZMANN NES ZIONA 76110 יומן 118235 ' בקשת פטנט מס4667 'ע :תקן המען למסירת אינטרפארם מעבדות בע"מ פארק לתעשיות עתירות ידע,קרית ויצמן 76100 נס ציונה Journal 11/2006 P. 4359 Notice under section 35 of the law Concerning patent application No. 101769 Delete the notice under section 35. The notice was published by mistake יומן לחוק35 הודעה לפי סעיף4359 'ע 101769 'בעניין בקשת פטנט מס ההודעה פורסמה בטעות Journal 9/2006 יומן P. 3455 Patent application No. 122942 122942 ' בקשת פטנט מס3455 'ע GB 25.7.1995 9515279.9 WO 1997/05154 Correct priority claim תקן דין קדימה Correct international publication no. to תקן את מספר הפרסום הבינלאומי ל 2135 July 24, 2007– ט' באב התשס"ז קודים למדינת המופיעים ביומן COUNTRY CODES APPEARING IN THIS JOURNAL Code AR AT AU BA BE BR CA CH CN CU CZ DE DK EC EP ES FI FR GB GE GR GT HR HU IE IL IN IT JP KR LK LU LV MX Country or Organization Argentina Austria Australia Herzegovina Belgium Brazil Canada Switzerland China Cuba Czech Republic Germany Denmark Ecuador European Patent Office Spain Finland France United Kingdom Georgia Greece Guatemala Croatia Hungary Ireland Israel India Italy Japan Republic of Korea Sri Lanka Luxembourg Latvia Mexico July 24, 2007– ט' באב התשס"ז 2136 MY NL NO NZ PL PT RU SE SG SI SK TH TR TW UA US UY UZ WO ZA 2137 Malaysia The Netherlands Norway New Zealand Poland Portugal Russian Federation Sweden Singapore Slovenia Slovakia Thailand Turkey Taiwan Ukraine United States of America Uruguay Uzbekistan World Intellectual Property Organization (W.I.P.O.) South Africa July 24, 2007– ט' באב התשס"ז מדגמים DESIGNS מדגמים שנרשמו DESIGNS REGISTERED Class 38950, 38951, 38952 2(04) 23. 2.2004 סוג אשר ליאני )תאריך אמנה (ארצות הברית סוליה ASHER LIEANY Sole 39711 6(06) 21. 9.2004 Class WIEDER THE EXPERTS ON BEDS AND MATTRESSES LTD. סוג וידר המומחים למיטות ומזרונים בע"מ רגליים של ספה Feet of a couch 39798 25(01) 20.10.2004 Class סוג בודי משומשים בע"מ BODY MESHUMASHIM LTD. פרופיל Profile Class 39861, 39862 14(03) 9. 11.2004 סוג RESEARCH IN MOTION LTD. התקן תקשורת Communication device Class 39926, 42710, 42711 14(03) 16.11.2004 סוג RESEARCH IN MOTION LTD. Communication device July 24, 2007– ט' באב התשס"ז מכשיר תקשורת 2138 Class 40092, 40093 8(06) 21.12.2004 סוג אבנרס קולקשיין בע"מ AVNER'S COLLECTION LTD. ידית Handle Class 40103 21(01) 22.12.2004 סוג למדע תעשיות קלות בע"מ LEMADA LIGHT INDUSTRIES LTD. משחק Game Class 40129 19(02) 29.12.2004 סוג משה מנור MOSHE MANOR פורט כסף Money changer Class 40331 8(08) 13. 2.2005 סוג אורלי בע"מ.ב.ל L.B. ORLY LTD. תפסן Gripper Class 40424 25(01) 9. 3.2005 סוג פרס פלסט בע"מ PRESS PLAST LTD. פרופיל Profile Class MIGAL ENGINEERING AND CONSTRUCTION LTD. Building unit for acoustic wall 2139 40590 25(01) 11. 4.2005 סוג מיגל חברה להנדסה ובניין בע"מ יחידת בניה לקיר אקוסטי July 24, 2007– ט' באב התשס"ז 40998 10(02) 12. 7.2005 Class סוג אופטו ליין בע"מ-אחים סגל SEGAL BROS-OPTO LINE LTD. שעון Watch 41107 11(01) 25.7.2005 Class סוג H. STERN COMERCIO E INDUSTRIA S.A. תכשיט Jewel 41119 8(06) 27.7.2005 Class סוג UNION KNOPF GMBH ידית Handle 41204 25(01) 11. 8.2005 Class סוג יגאל בלכר IGAL BLECHER פרופיל Profile 41217 28(02) 15.8.2005 Class סוג UNILEVER PLC Soap bar 3.3.2005 Convention date (United Kingdom) Class 41240 25(02) 17. 8.2005 ALIAZER GANNY (GARTNER) Barrier July 24, 2007– ט' באב התשס"ז סבון תאריך האמנה (הממלכה )המאוחדת סוג )אליעזר גנני (גרטנר מחסום 2140 )צות הברית 41447 6(03) 2. 10.2005 Class סוג עמינח תעשית רהיטים ומזרונים בע"מ AMINACH BEDDING AND FURNITURE LTD. שולחנון צד המיטה Bedside table Class 41450 13(03) 2.10.2005 סוג LUTRON ELECTRONICS CO., INC. מתג עמעם )הברית )הברית (ארצות (ארצות האמנה תאריךאמנה תאריך Dimmer switch Convention date (U.S.A.) Class 4.4.2005 41468, 41469, 41471, 41472, 41473, 41474, 41475, 41476, 41477, 41478, 41479 6(06) 9. 10.2005 WIEDER THE EXPERTS ON BEDS AND MATTRESSES LTD. סוג וידר המומחים למיטות ומזרונים בע"מ רגליים של ספה Feet for couch Class 41489, 41491 6(06) 9. 10.2005 WIEDER THE EXPERTS ON BEDS AND MATTRESSES LTD. סוג וידר המומחים למיטות ומזרונים בע"מ מסעד לספה Support for couch Class 41495, 41496, 41497, 41498 6(06) 9. 10.2005 WIEDER THE EXPERTS ON BEDS AND MATTRESSES LTD. Frame for couch 2141 סוג וידר המומחים למיטות ומזרונים בע"מ מסגרת לספה July 24, 2007– ט' באב התשס"ז Class 41502 6(06) 9. 10.2005 WIEDER THE EXPERTS ON BEDS AND MATTRESSES LTD. סוג וידר המומחים למיטות ומזרונים בע"מ ידית לספה Handle for couch Class 41599 9(01) 15. 11.2005 סוג יפאורה תבורי בע"מ JAFORA TABORI LTD. בקבוק Bottle Class 41684 23(02) 4. 12.2005 סוג יציקות בע"מ.מ.א.ר R.A.M. CASTING LTD. מושב למקלחון Seat for shower room Class 41802 9(07) 27.12.2005 סוג PORTOLA PACKAGING LIMITED Closure for containers 8.7.2005 Convention date (OHIM) Class סגר עבור מיכלים )הברית )(אוהיים (ארצות האמנה תאריךאמנה תאריך 41855, 41856 7(07) 29.12.2004 סוג DART INDUSTRIES INC. Container Convention date (U.S.A.) Class 22.7.2004 41908 11(01) 25.1.2006 מיכל )הברית )הברית (ארצות (ארצות האמנה תאריךאמנה תאריך סוג H. STERN COMERCIO E INDUSTRIA S.A. Jewel July 24, 2007– ט' באב התשס"ז תכשיט 2142 41919 25(01) 26. 1.2006 Class GUMIX LIMITED PARTNERSHIP גומיקס שותפות מוגבלת מעבר חציה למוגבלים Crosswalk for handicapped Class סוג 42133, 42135, 42136 10(07) 26.7.2005 סוג H. STERN COMERCIO E INDUSTRIA S.A. Watch dial Convention date (EUROPE) Class 28.1.2005 42216 9(03) 22. 3.2006 לוח שעון )הברית )(אירופה (ארצות האמנה תאריךאמנה תאריך סוג ) בע"מ1990( ווק-פלסטו PLASTO-VACK (1990) LTD. מיכל Container Class 42237, 42238 8(06) 26. 3.2006 סוג אבנרס קולקשיין בע"מ AVNER'S COLLECTION LTD. ידית Handle Class SHARON BELGAZAL Profile 2143 42253 25(01) 30. 3.2006 סוג שרון בלגזל פרופיל July 24, 2007– ט' באב התשס"ז 42309 13(03) 2.10.2005 Class סוג LUTRON ELECTRONICS CO., INC. Dimmer switch Convention date (U.S.A.) 4.4.2005 42319 7(01) 11. 4.2006 Class מתג עמעם )הברית )הברית (ארצות (ארצות האמנה תאריךאמנה תאריך סוג דורון מרדינגר בע"מ DORON MERDINGER LTD. תחתית לספל Saucer for cup Class 42329, 43362 25(01) 20. 4.2006 סוג תמנון הופ בע"מ TAMNUN HOP LTD. פרופיל Profile Class 42330 20(03) 20. 4.2006 סוג תמנון הופ בע"מ TAMNUN HOP LTD. התקן תמיכה לרשימת קניות Support for shopping list Class 42361, 42362 2(04) 25.4.2006 סוג CROCS, INC. Upper Convention date (U.S.A.) Class 26.10.2005 42426 19(06) 2.5.2006 גפה )הברית )הברית (ארצות (ארצות האמנה תאריךאמנה תאריך סוג ZEBRA CO. LTD. Ballpoint pen Convention date (Japan) July 24, 2007– ט' באב התשס"ז 21.2.2006 עט כדורי )(ארצות) הברית האמנה (יפן תאריךאמנה תאריך 2144 Class 42725 10(02) 11.7.2006 סוג CARTIER CREATION STUDIO SA Wristwatch Convention date (OHIM( שעון יד )הברית )(אוהיים (ארצות האמנה תאריךאמנה תאריך 12.1.2006 Class 42763 6(01) 18.7.2006 סוג NICOLETTI S.P.A. ספה )הברית )(איטליה (ארצות האמנה תאריךאמנה תאריך Sofa 19.1.2006 Convention date (Italy) Class 42849, 42850 7(01) 6.8.2006 סוג VILLEROY & BOCH AG צלחת )הברית )(אוהיים (ארצות האמנה תאריךאמנה תאריך Plate 8.2.2006 Convention date (OHIM) Class 42851 7(01) 6.8.2006 סוג VILLEROY & BOCH AG Set of cup and saucer Convention date (OHIM) Class 8.2.2006 42911 13(03) 16. 8.2006 NISKO ELECTRICITY & ELECTRONICS PRODUCTS )1982) LTD. Socket 2145 מערכת חפצים ספל ותחתית )הברית )(אוהיים (ארצות האמנה תאריךאמנה תאריך סוג ניסקו מוצרי חשמל ) בע"מ1982( ואלקטרוניקה שקע July 24, 2007– ט' באב התשס"ז Class 42930 9(03) 21. 8.2006 סוג מנשה רוגוטנר MENASHE ROGOTNER אריזה Packaging Class 42951 9(01) 28.8.2006 סוג BULGARI S.P.A. Cream jar Convention date (OHIM) Class 3.3.2006 43126 6(06) 26. 9.2006 WIEDER THE EXPERTS ON BEDS AND MATTRESSES LTD. צנצנת למשחה )הברית )(אוהיים (ארצות האמנה תאריךאמנה תאריך סוג וידר המומחים למיטות ומזרונים בע"מ רגליים של ספה Feet for couch Class 43130 6(06) 26. 9.2006 WIEDER THE EXPERTS ON BEDS AND MATTRESSES LTD. סוג וידר המומחים למיטות ומזרונים בע"מ מסגרת לספה Frame for a couch Class 43137, 43139 6(01) 26. 9.2006 WIEDER THE EXPERTS ON BEDS AND MATTRESSES LTD. סוג וידר המומחים למיטות ומזרונים בע"מ משענת גב לספה Back rest for couch Class PAPAYA FASHION LTD. Sole July 24, 2007– ט' באב התשס"ז 43192 2(04) 15. 10.2006 סוג פאפאיה אופנה בע"מ סוליה 2146 Class 43212 24(04) 18.10.2006 סוג VECTURA GROUP PLC Inhaler Convention date (OHIM) Class 28.4.2006 43224, 43921 11(01) 22.10.2006 משאף )הברית )(אוהיים (ארצות האמנה תאריךאמנה תאריך סוג H. STERN COMERCIO E INDUSTRIA S.A. תכשיט Jewel Class 43229 25(01) 22. 10.2006 סוג שרון בלגזל SHARON BELGAZAL פרופיל Profile Class 43288 4(02) 6.11.2006 סוג GLAXOSMITHKLINE CONSUMER HEALTHCARE GMBH & CO KG Toothbrush handle Convention date (United Kingdom) Class R.A.M. CASTING LTD. Chair 2147 8.5.2006 43298 6(01) 7. 11.2006 ידית למברשת שיניים תאריך האמנה (הממלכה )המאוחדת סוג יציקות בע"מ.מ.א.ר כסא July 24, 2007– ט' באב התשס"ז )ות הברית 43321 3(03) 14. 11.2006 Class סוג אורית יצחק ORIT YIZHAK מטריה Umbrella 43357 12(15) 22.11.2006 Class סוג BRIDGESTONE CORPORATION Tire 25.5.2006 Convention date (Japan) 43382 15(07) 30.5.2006 Class צמיג )(יפן) הברית (ארצות האמנה תאריךאמנה תאריך סוג DAF TRUCKS N.V. מקרר Refrigerator Class 43406 24(04) 29.11.2006 סוג NORTON HEALTHCARE LTD. Inhaler device Convention date (OHIM) Class AVISHY COSMETIC AND HYGIENE LTD. 16.6.2006 43416 28(03) 30. 11.2005 משאף )הברית )(אוהיים (ארצות האמנה תאריךאמנה תאריך סוג אבישי תמרוקים והיגיינה בע"מ בקבוק Bottle Class 43421 10(07) 3. 12.2006 סוג EREZ BARUCH ארז ברוך Hands for watch dial מחוגים של לוח השעון July 24, 2007– ט' באב התשס"ז 2148 Class 43426 13(03) 4. 12.2006 UNITRONICS (1989) (R.G.) LTD. סוג ) (ר"ג) בע"מ1989( יוניטרוניקס בקר Controller Class 43449 24(02) 10. 12.2006 סוג יוסף פלדמן JOSEPH FELDMAN מכשיר טיפולי להקרנות Therapeutic radiation instrument Class 43463, 43464, 43465 8(06) 12. 12.2006 סוג SMILDO S.L. ידית Handle Class 43466 23(02) 12. 12.2006 DOMICILE IMPORT EXPORT LTD. סוג דומיסיל יבוא ויצוא בע"מ וו Hook Class 43468 23(02) 12. 12.2006 DOMICILE IMPORT EXPORT LTD. סוג דומיסיל יבוא ויצוא בע"מ סבוניה לקיר Wall soap-dish Class 43469 23(02) 12. 12.2006 DOMICILE IMPORT EXPORT LTD. Toilet paper holder 2149 סוג דומיסיל יבוא ויצוא בע"מ מחזיק נייר טואלט July 24, 2007– ט' באב התשס"ז Class 43471 23(02) 12. 12.2006 DOMICILE IMPORT EXPORT LTD. סוג דומיסיל יבוא ויצוא בע"מ מתלה למגבות Towel hanger Class 43472 23(02) 12. 12.2006 DOMICILE IMPORT EXPORT LTD. סוג דומיסיל יבוא ויצוא בע"מ מתלה כפול למגבות Double towel hanger Class 43478 10(04) 13.12.2006 סוג THE DIAMOND TRADING COMPANY LTD. Diamond verification instrument 1.8.2006 Convention date (EUROPE) Class 43492 28(03) 14.12.2006 מכשיר לבדיקת יהלומים )הברית )(אירופה (ארצות האמנה תאריךאמנה תאריך סוג CALOR Depilator 7.7.2006 Convention date (France) Class 43503 23(04) 14.12.2006 מסיר שערות )הברית )(צרפת (ארצות האמנה תאריךאמנה תאריך סוג SARA LEE HOUSEHOLD AND BODY CARE NEDERLAND B.V. Refill bottle for air deodorizing apparatus Convention date (OHIM) Class בקבוקון מילוי למכשיר לבישום אוויר 26.9.2006 )הברית )(אוהיים (ארצות האמנה תאריךאמנה תאריך 43504 23(04) 14.12.2006 סוג SARA LEE HOUSEHOLD AND BODY CARE NEDERLAND B.V. Air deodorizing apparatus Convention date (OHIM) July 24, 2007– ט' באב התשס"ז 26.9.2006 מכשיר לבישום אוויר )הברית )(אוהיים (ארצות האמנה תאריךאמנה תאריך 2150 Class 43546 6(09) 26. 12.2006 סוג אלמוג צחר ALMOG TSACHAR מזרון החתלה לתינוק Baby diaper changing mattress Class 43661 11(01) 4. 11.2004 סוג H. STERN COMERCIO E INDUSTRIA S.A. עגיל Earring Class 43692 26(03) 29. 1.2007 סוג ILAN NAHSON אילן נחשון Lighting fixture התקן תאורה Class 43839 23(01) 2.3.2005 סוג STRIX LIMITED Water filter Convention date (OHIM) Class 9.9.2004 43923 11(01) 10. 9.2006 מסנן למים )הברית )(אוהיים (ארצות האמנה תאריךאמנה תאריך סוג H. STERN COMERCIO E INDUSTRIA S.A. Jewel 2151 תכשיט July 24, 2007– ט' באב התשס"ז מדגמים שחודשו DESIGNS RENEWED 27961 36370 36534 37152 2152 27960 36369 36505 36983 27959 36304 36496 36803 27957 36258 36492 36689 27932 28462 36491 36688 27913 28241 36487 36681 27846 28239 36373 36610 27584 27962 36372 36609 37153 ט' באב התשס"ז –July 24, 2007 מדגמים שבוטלו DESIGNS VOID 19399 26944 27029 35749 35810 35819 35845 35882 19487 26954 27030 35795 35811 35820 35847 35883 19488 26956 27031 35796 35812 35823 35848 35884 Dr. Meir Noam Commissioner of Patents, Designs and Trade Marks 2153 19489 26958 27036 35800 35813 35824 35849 35987 19490 26959 27037 35801 35814 35841 35856 19506 26992 27038 35802 35815 35842 35866 19513 26995 27039 35804 35817 35843 35867 26934 27016 33070 35809 35818 35844 35881 ד"ר מאיר נועם המדגמים,רשם הפטנטים וסימני מסחר July 24, 2007– ט' באב התשס"ז מפתחות לבקשות שקובלו INDICES OF APPLICATIONS ACCEPTED מפתח שמי א.י .מעבדות בע"מ 159911 אבי דסקלו 132625 אבישי מלמד 165639 אברהם ניסנקורן 146534 אדוארד ג.שיפרין 147954 אדוארד שיפרין 147954 אדי קרניאלי 137759 אוה -טק מדיקל 21בע"מ 147954 אורבוטק בע"מ 149588 אורמת תעשיות בע"מ 156048 איי אופטימה בע"מ 152343 אייל אליאב 159990 אילן שר 155796 אינולייז 2002בע"מ 150094 איתמר מדיקל בע"מ 154833 אלי לויס 148378 אנקו-טון בע"מ 122023 אפרון רוזן 124301 אקספנד נטוורקס בע"מ 137199 NAME INDEX טבע תעשיות פרמצבטיות בע"מ ,144679 149681 ,149308 ידע חברה למחקר ופיתוח בע"מ ,112699 145299 ,132455 ,126835 יובל זינגר 146981 יונתן לביא 172637 יישום חברה לפיתוח המחקר של האוניברסיטה העברית בירושלים 118570 יישום חברה לפיתוח המחקר של האוניברסיטה העברית בירושלים ,141370 142172 יצחק לבטון 122023 יראל יאירוב 132700 ישקר בע"מ 150015 ,150013 ,150012 ישקר בע"מ 150015 ,150013 ,150012 כרמלי אדהאן 160096 לאון ליפסיקס 144581 גדעון רוזנברג 157525 ג'ינוטק בע"מ 146534 דורון חכימי 158726 דיינמיק שלס בע"מ 148400 דני לביא 159990 הדסית שרותי מחקר רפואי ופתוח בע"מ 142172 הנדסה דנטלית מתקדמת בע''מ 149563 זולי החזקות בע"מ 142176 טאגרה ביוטכנולוגיות בע"מ 149637 i מאיר אבגנים 151060 מדדינמיקס בע"מ 163061 מדידרמיס בע"מ 132625 מדינול בע"מ 142176 מוסד הטכניון למחקר ופיתוח בע"מ 122115 מוסד הטכניון למחקר ופיתוח בע"מ 128727 מוסרות בע"מ 147685 מור אנרגיה בע"מ 156624 מטאו-טק בע"מ 147725 מיג"ל מרכז ידע גליל עליון 132666 מרדכי אלדר 152089 ט' באב התשס"ז –July 24, 2007 149180 קומברס בע"מ 151611 משה שאלתיאל אביב בע"מ-רמות ליד אוניברסיטת תל 116416 רפא"ל רשות לפיתוח אמצעי לחימה 138831 בע"מ רפא"ל רשות לפיתוח אמצעי לחימה 147370 בע"מ רשות לפיתוח אמצעי לחימה-רפא"ל 136566 בע"מ ) בע"מ1975( תעשיות מגופים-רפאל 156797 148566 נובה מכשירי מדידה בע"מ 151826 נורה מרקובייקי 144581 שמעון פרידמן 148926 סלקום ישראל בע"מ עמינח תעשית רהיטים ומזרונים בע"מ 167402 144040 פאורדסיין בע"מ מערכות חליבה- אפיקים.מ.ח.צ 162821 ממוחשבות 156362 קבוצת גל בע"מ 147260 קדנט בע"מ 149433 ,147276 קומברס בע"מ A.Y. LABORATORIES LTD. 159911 ABBOTT LABORATORIES 145135 ABRAHAM NISSENKORN 146534 ADVANCED DENTAL ENGINEERING LTD. 149563 AHLSTROM CORPORATION 159891 AHLSTROM CORPORATION 159891 AHLSTROM RESEARCH AND SERVICES 159891 AIR-CRAFT BRAKING SYSTEMS CORPORATION 158541 AKZO NOBEL N.V. 149412 AKZO NOBEL N.V. 153934 ALBANY INTERNATIONAL TECHNIWEAVE, INC. 143154 ALLELIX BIOPHARMACEUTICALS, INC. 139320 ALLISON SAMPSON 160153 ALZA CORPORATION 142808 AMINACH BEDDING & FURNITURE MANUFACTURING LTD. 167402 ANDREY SHUSTOV 151612 ANORMED, INC. 145401 ANTHONY KHOURI 148560 iv APPLETON PAPERS INC. 156108, 156109 APPLIED RESEARCH SYSTEMS ARS HOLDING N.V. 130123, 136855 APPLIED RESEARCH SYSTEMS ARS HOLDING N.V. 133686 ARES TRADING S.A. 152320, 152321 ARJO WIGGINS LIMITED 165464 ASAHI KASEI KABUSHIKI KAISHA 153377 ASK S.A. 155882 ASTRAZENECA AB 145192, 145357, 146187, 151392, 155995 ASTRAZENECA AB 163642 ASTRAZENECA UK LIMITED 151930 ATI PROPERTIES, INC. 161175, 161289 AVENTIS INC. 174850 Aventis Pharma S.A 122991, 134192 AVENTIS PHARMA S.A. 132671 AVENTIS PHARMA S.A. 161841 AVENTIS PHARMACEUTICALS INC. 146729 AVENTIS PHARMACEUTICALS INC. 147495 July 24, 2007– ט' באב התשס"ז AVI DASCXALU 132625 AVISHAI MELAMED 165639 BASF AKTIENGESELLSCHAFT 148464 BASF AKTIENGESELLSCHAFT 150528 BATTELLE MEMORIAL INSTITUTE 149080 BAYER CORPORATION 136738, 136767 BAYER CROPSCIENCE S.A. 153786 BAYER PHARMACEUTICALS CORPORATION 136738, 136767 BERNARD TECHNOLOGIES, INC. 146440 BIOGEN IDEC INC. 146005 Biogen Idec MA Inc. 127162, 128407 BIOGEN IDEC MA INC. 134593, 145898 BIONICHE LIFE SCIENCES INC. 134371 BIOSENSE, INC. 137322, 144271, 146217 BIOVITRUM AB 155875 BODYMEDIA, INC. 153516 BOEHRINGER INGELHEIM INTERNATIONAL GMBH 151465 BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG 144619, 150377, 150621 BPSI HOLDINGS, INC. 150850 BRISTOL-MYERS SQUIBB COMPANY 144910 BRISTOL-MYERS SQUIBB COMPANY 149601 BYK GULDEN LOMBERG CHEMISCHE FABRIK GMBH 141157 CADENT LTD. 147260 CARGILL, INCORPORATED 156017 CARMEL PHARMA AB 153998 CARMELI ADAHAN 160096 CATAVAULT 150728 CELLCOM ISRAEL LIMITED 148926 CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) July 24, 2007– ט' באב התשס"ז 146396 CENTRO DE INGENIERIA GENETICA Y BIOTECNOLOGIA 156700 CEPHALON, INC. 155263 CHIRON CORPORATION 123248 CIBA SPECIALTY CHEMICALS HOLDING INC. 158505 CILAG GMBH INTERNATIONAL 137808 CODENA INC. 151786 COLLATERAL THERAPEUTICS INC. 128727 COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION 152087 COMPUTER ASSOCIATES THINK, INC. 147879 COMVERSE LTD. 147276, 149433 COMVERSE LTD. 149180 COMVERSE, INC. 147137, 149697 CONCEPTO DIAGNOSTICS, INC. 137601 CONNECTIVE TISSUE IMAGINEERING LLC 138453 DADE BEHRING INC. 160418 DAINIPPON SUMITOMO PHARMA CO., LTD. 153439 DAINIPPON SUMITOMO PHARMA CO., LTD. 133512 DANNY LAVIE 159990 DAVID M. ALLEN 156757 DELAVAL HOLDING AB 151990 DENTSPLY INTERNATIONAL INC. 147320 DEPOMED, INC. 149421 DETLEF SCHUPPAN 128042 DISCOVISION ASSOCIATES 139083 DIVERSA CORPORATION 130245 DOMPE PHA.R.MA S.P.A. 137564 DOMPE S.P.A. 137564 DORON HAKIMI 158726 DR. REDDY'S LABORATORIES LIMITED 123201 DRK-BLUTSPENDEDIENDST BADEN-WUERTTEMBERG-HESSEN GEMEINNUTZIGE GMBH 137522 iii DYNAMIC SHELLS LTD. 148400 E.I. DU PONT DE NEMOURS AND COMPANY 152087 E.I. DUPONT DE NEMOURS AND COMPANY 151083, 155409 EADS DEUTSCHLAND GMBH 151466 EDDIE KARNIELI 137759 EDWARD G. SHIFRIN 147954 EDWARD G.SHIFRIN 147954 EFRON ROZAN 124301 ELI LEVIS 148378 EMORY UNIVERSITY 138281 ENCO-TONE LTD. 122023 ESSILOR INTERNATIONAL (COMPAGNIE GENERALE D'OPTIQUE) 150234 EURO - CELTIQUE S.A. 139230 EVA - TECH MEDICAL 21 LTD 147954 EVEREADY BATTERY COMPANY, INC. 157252 EXCEL INDUSTRIES LIMITED 158490 EXPAND NETWORKS LTD. 137199 EYAL ELIAV 159990 F. HOFFMANN-LA ROCHE AG 144055 F. HOFFMANN-LA ROCHE AG 144636 FEDERICO SINGER 146981 FLEXPLAY TECHNOLOGIES, INC. 147543 FORESCOUT TECHNOLOGIES INC. 149594 FRANCO BRUTTI 154335 GE HEALTHCARE AS 155475 GEA ENERGIETECHNIK GMBH 150875 GEM PHARMACEUTICALS, INC. 134494 GENENTECH, INC. 114668, 115792, 128128 GENENTECH, INC. 146005 GENERAL DYNAMICS ADVANCED INFORMATION SYSTEMS, INC. 157521 GENTIUM SPA 130405 GIDEON ROSENBERG 157525 GLAXO GROUP LIMITED 137403 iv GLAXOSMITHKLINE S.P.A. 139301 GORE ENTERPRISE HOLDINGS, INC. 157410 GRANDIS BIOTECH GMBH 147253 GREAT CIRCLE TECHNOLOGIES, INC. 155248 GRUNENTHAL GMBH 149010 GYNOTECH LTD. 146534 H. LUNDBECK A/S 145959, 149994 HADASIT MEDICAL RESEARCH SERVICES AND DEVELOPMENT LTD. 142172 HEE-SUNG CHUNG 149205 HEIDELBERGER DRUCKMASCHINEN AG 166910 HUNTER DOUGLAS INDUSTRIES B.V. 151766 I OPTIMA LTD 152343 IBM CORPORATION 140141, 153925 IBM UNITED KINGDOM LIMITED 147015 IGOR K. KOTLIAR 152017 IHARA CHEMICAL INDUSTRY CO., LTD. 147958 ILAN SHERR 155796 IMAGINATION MEDICAL, INC. 140972 IMMUNEX CORPORATION 137178 IMMUPHARM APS 154144 INDENA S.P.A. 163225 INDIVIDUAL NETWORK, LLC 150474 INEX PHARMACEUTICALS CORPORATION 153676 INNOVATA BIOMED LIMITED 149623 INOLASE 2002 LTD. 150094 INSTITUT GUSTAVE ROUSSY 130123 INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) 130123 INTEGRAGEN, S.A.S. 145141 INTEL CORPORATION 144017, 152798 INTELLIGENT ENGINEERING (BAHAMAS) LIMITED 154672 INTERDIGITAL TECHNOLOGY CORPORATION 148412 July 24, 2007– ט' באב התשס"ז INTERNATIONAL BUSINESS MACHINES CORPORATION 147015, 147630 INTERSENSE, INC. 152359 INTERTEX DATA AB 148700 INTEVAC, INC. 154517 INTRALUMINAL THERAPEUTICS, INC. 151864 ISAAC J. LABATON 122023 ISCAR LTD. 150012, 150013, 150015 ISCAR LTD. 150012, 150013, 150015 ITAMAR MEDICAL LTD. 154833 JANSSEN PHARMACEUTICA N.V. 138745, 143830 JOHNSON & JOHNSON VISION CARE, INC. 150234 JOHNSON MATTHEY PUBLIC LIMITED COMPANY 158439, 158798 KARALEE RESEARCH PTY LTD. 163835 KENNAMETAL INC. 148284 KUMIAI CHEMICAL INDUSTRY CO., LTD. 147958 KUNIFUMI KOMIYA 156426 L. MOLTENI & C. DEI FRATELLI ALITTI SOCIETA' DI ESERCIZIO S.P.A. 147876 LABORATOIRE MEDIDOM S.A. 150390 LABORATOIRE THERAMEX 149370 LACER, S.A. 142391 LAM RESEARCH CORPORATION 134926 LANCER PARTNERSHIP, LTD. 153538 LATTICE INTELLECTUAL PROPERTY LIMITED 152499 LEON LIPSICAS 144581 LEONID MIHALJOV 143453 LOCKHEED MARTIN CORPORATION 156143 LOTUS PHARMACEUTICAL CO. LTD. 153205 MACROVISION CORPORATION July 24, 2007– ט' באב התשס"ז 148002 MARA-INSTITUT D.O.O. 155480 MARGA DUMMEN 154938 MASSEY UNIVERSITY 157862 MAUSER-WERKE GMBH & CO. KG 155579 MCCOMAS TECHNOLOGIES AG 156656 MEDDYNAMICS LTD. 163061 Medidermis Ltd. 132625 MEDINOL LTD. 142176 MEDIVIR AB 141161 MEIR AVGANIM 151060 MERIDIAN MEDICAL TECHNOLOGIES, INC. 151579 METABASIS THERAPEUTICS, INC. 145052, 151248 METEO-TECH LTD. 147725 MFH HYPERTHERMIESYSTEME GMBH 142409 MICROSOFT CORPORATION 173678 MIGAL GALILEE TECHNOLOGICAL CENTER 132666 MILBRIDGE INVESTMENTS (PTY) LTD. 157717 MILOW LTD. 157525 MOBIL OIL CORPORATION 144846 MOLECULAR EXPRESS, INC. 141675 MONA INDUSTRIES, INC. 149196 MORDECHAI ELDAR 152089 MORE ENERGY LTD. 156624 MOSEROTH LTD. 147685 MOSHE SHEALTIEL 151611 N.V. ORGANON 149412, 153934 NABRIVA THERAPEUTICS FORSCHUNGS GMBH 138477 NAGRAVISION S.A. 149303, 152092 NANOSCALE MATERIALS, INC. 141747 NEKTAR THERAPEUTICS 141562, 142215 NEOTHERMIA CORPORATION 148989 NEST INTERNATIONAL N.V. 151612 NEW YORK UNIVERSITY 146228 NEWMAT, S.A. 148911 v NOBORU OYAMA 155409 NORA MARKOWIECKI 151826 NOVA MEASURING INSTRUMENTS LTD. 148566 NOVARTIS AG 143233 NOVARTIS AG 153229 NOVEN PHARMACEUTICALS, INC. 158551 NOVO NORDISK A/S 126463, 149049 NOVOGEN RESEARCH PTY LTD. 128765 NOZOMU SAHASHI 159329 NUG NAHRUNG-UND GENUSSMITTEL VERTRIEBSGESELLSCHAFT MBH 162871 NYMPHEA WATER 146846 OBSCHESTVO S OGRANICHENNOI OTVETSTVENNOSTIJU "KLINIKA INSTITUTA BIOREGUL YATSII I GERONTOLOGII" 140412 OCTAPHARMA AG 152173 OMD DEVICES, L.L.C. 132796 ORBOTECH LTD. 149588 ORION CORPORATION 141680 ORMAT INDUSTRIES LTD. 156048 ORMAT TECHNOLOGIES INC. 156048 ORTHOFIX INTERNATIONAL B.V 152563 ORTHOFIX S.R.L. 152563 ORTHOFIX S.R.L. 152563 PANACEA BIOTEC LIMITED 149030 PECHINEY EMBALLAGE FLEXIBLE EUROPE 154669 PFIZER INC. 134851, 138911 PFIZER ITALIA S.R.L 152537 PFIZER PRODUCTS, INC. 139012, 145946, 157103 PHARMACIA & UPJOHN COMPANY 152537 PHARMACIA CORPORATION 144757, 144761 POWDERJECT RESEARCH LIMITED 144380 POWER MEDICAL INTERVENTIONS, INC. 147511 vi POWERDSINE LTD. 144040 PRAECIS PHARMACEUTICALS INCORPORATED 130309 QPOD SYSTEMS LIMITED 146979 QUADLOGIC CONTROLS CORPORATION 151406 QUALCOMM INCORPORATED 145652, 147719, 147792, 148069, 148367, 148370 QUALCOMM INCORPORATED 155562 RAFAEL ARMAMENT DEVELOPMENT AUTHORITY LTD. 147370 RAFAEL-ARMAMENT DEVELOPMENT AUTHORITY LTD. 136566 RAFAEL-ARMAMENT DEVELOPMENT AUTHORITY LTD. 138831 RAMOT AT TEL-AVIV UNIVERSITY LTD. 116416 RAPHAEL VALVES INDUSTRIES (1975) LTD. 156797 RAVCO INNOVATIONS INC. 151668 REDDY-CHEMINOR, INC. 123201 REIFENHAUSER GMBH & CO. MASCHINENFABRIK 154630 RHEON AUTOMATIC MACHINERY CO., LTD. 152240 RHONE-POULENC AGRO 131750 RICHARD SAMPSON 160153 ROHM GMBH & CO. KG 150850 RTP PHARMA INC. 139779, 140276 RUBY HILL LTD. 147954 RVC LLC 139995 S.A.E. AFIKIM- COMPUTERIZED DAIRY MANAGEMENT SYSTEMS 162821 SAMSUNG ELECTRONICS CO., LTD. 149656 SAMSUNG ELECTRONICS CO., LTD. 152648, 157864 SANDOZ AG 138477, 147253 SANDOZ GMBH 138477 July 24, 2007– ט' באב התשס"ז SANKYO COMPANY LIMITED 132962, 149444 SANOFI AVENTIS 135520, 144181, 153632 SANOFI AVENTIS 147320 SANOFI-AVENTIS DEUTSCHLAND GMBH 145923 SANOFI-AVENTIS DEUTSCHLAND GMBH 146731 SAP AG 147105 SCHERING AKTIENGESELLSCHAFT 128691, 133195 SCHERING AKTIENGESELLSCHAFT 154828, 156353 SCHUCO INTERNATIONAL KG 151447 SCHWARZ PHARMA AG 165917 SEB S.A. 155352 SEQUOIA SOFTWARE CORPORATION 150106 SERONO GENETICS INSTITUTE S.A. 155179 SHIMON FREEDMAN 144581 SILVERBROOK RESEARCH PTY. LTD. 146606, 146652, 146680, 163486, 163494, 163496, 164953, 165540, 166422, 166723, 166725, 166726, 166874, 166876 SILVERBROOK RESEARCH PTY. LTD. 160172, 161088, 164691, 166875 SILVERBROOK RESEARCH PTY.LTD. 164447, 164503 SINON CORPORATION 146027 SIRAP-GEMA S.P.A. 140677 SK TELETECH CO., LTD. 147799 SKELETON TECHNOLOGIES AG 161555 SMITHKLINE BEECHAM BIOLOGICALS S.A. 139612, 145043 SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.) 149177 SOLUTIA INC. 139816 SOLYSTIC 150792 SOUTHWEST RESEARCH INSTITUTE 146440 SPECIAL CARTRIDGE COMPANY July 24, 2007– ט' באב התשס"ז LIMITED 138823 SPEEDFAM-IPEC CORPORATION 148274 SPINEVISION S.A. 149981 SUN MICROSYSTEMS INC. 150583 SWISSCOM MOBILE AG 147399, 148431 SYNGENTA LIMITED 141066 SYNGENTA LIMITED 141109, 145962 SYNGENTA PARTICIPATIONS AG 132768, 158360 T.J. BROOKS COMPANY-DIVISION OF HANNA CYLINDERS 157804 TAGRA BIOTECHNOLOGIES LTD. 149637 TECHNION RESEARCH AND DEVELOPMENT FOUNDATION LTD. 122115 TECHNION RESEARCH AND DEVELOPMENT FOUNDATION LTD. 128727 TEENESS ASA 164561 TEIJIN TWARON GMBH 156645 TELEDIFFUSION DE FRANCE 149877 TELEFONAKTIEBOLAGET LM ERICSSON (PUBL) 179054 TERRAPLAY SYSTEMS AB 179054 TEVA PHARMACEUTICAL INDUSTRIES LTD. 144679, 149308, 149681 THE BABCOCK & WILCOX COMPANY 146157 THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS 138856 THE CHIEF CONTROLLER, RESEARCH AND DEVELOPMENT 152139 THE CUPRON CORPORATION 149206 THE FACULTY OF MEDICINE OF THE UNIVERSITY OF GENEVA 128407 THE GENERAL HOSPITAL CORPORATION 127162 THE GILLETTE COMPANY 150871 THE REGENTS OF THE UNIVERSITY OF MICHIGAN 153374 vii THE SCRIPPS RESEARCH INSTITUTE 126843, 136544, 137661 THE TEXAS A&M UNIVERSITY SYSTEM 151083 THE TEXAS ENGINEERING EXPERIMENT STATION 151083 THE UNIVERSITY OF BRISTOL 151949 THOMSON LICENSING S.A. 148775 TRANSNEURONIX, INC. 150552 TRISOPLAST INTERNATIONAL B.V. 151803 TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA 150617 UNILEVER PLC 146357 UNITED TECHNOLOGIES CORPORATION 165759 UNIVERSAL PRESERVATION TECHNOLOGIES, INC. 149778 UNIVERSITE PARIS 7-DENIS DIDEROT 150839 UNIVERSITY OF PITTSBURGH OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION 141990 UNIVERSITY OF SOUTHERN CALIFORNIA 139360 UNIVERSITY OF UTAH RESEARCH FOUNDATION 133799 WISCONSIN ALUMNI RESEARCH FOUNDATION 135458 YAREL YAIROV 132700 YEDA RESEARCH AND DEVELOPMENT CO. LTD. 112699, 126835, 132455, 145299 YEHONATAN LAVEE 172637 YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM 118570 YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM 141370, 142172 YUVAL SINGER 146981 ZENTARIS GmbH 135103 ZULI HOLDINGS LTD. 142176 VELA PHARMACEUTICALS, INC. 149134 VIASAT, INC. 135786 VICTORY PRODUCTS, S.L. 164992 VLADIMIR DROBKOV 151612 VLADIMIR MELNIKOV 151612 W. RUITENBERG CZN. N.V. 154489 WALBURGA DIETERICH 128042 WALTER REED ARMY INSTITUTE OF RESEARCH 137449 WARNER-LAMBERT COMPANY LLC 145684 WAVE GROUP LTD. 156362 WESTFALIASURGE GMBH 153580 WILLIAMS INTERNATIONAL CO., L.L.C. 145349 viii July 24, 2007– ט' באב התשס"ז מפתח ענייני SUBJECT MATTER INDEX A01J – 151990 A01K – 141370 A01 N – 141109 A23G – 146357 A23J – 162871 A23L – 159990 A61B – 124301, 144271, 147511, 147954, 148989, 149981, 152343, 152359, 152563, 163061 A61C – 149563 A61F – 142176 A61K – 128765, 130405, 132666, 134371, 136767, 137808, 138453, 139230, 140276, 141562, 141990, 143233, 144757, 145898, 146005, 147253, 149308, 149421, 149994, 150390, 163642, 165917 A61M – 142215, 144380, 149623, 152320 B25B – 152089 B41F – 163486 B41J – 155512, 160172, 161088, 164503, 166725, 166726, 166874, 166875, 166876 B60T – 1585411 B65D – 140677, 146979, 155579, 156108 B01B– 157717, 160153 C02F – 155248 C07C – 128691, 155263, 174850 C07D – 123201, 133195, 135520, 138856, 142391, 143830, 144055, 144761, 144910, 145357, 145401, 145959, 145962, 146027, 147495, 149049, 149177, 153439, 153632, 155995, 158490, 161841 C07F – 142172, 145052, 145299, 153299, 154144 A63H – 164992 C07J – 149412, 153934 B01J – 141066, 158439, 159891 C07K– 138911, 146731, 152173, 157103 B02C – 146157, 153538 B07C – 150792 B23B – 148284 July 24, 2007– ט' באב התשס"ז C08G – 139816, 149196 C08J – 155409 C10L –163835 ix G01S – 151466 C12N – 114668, 122991, 123248, 126835, 127162, 128407, 130123, 133686, 133799, 136855, 139360, 139612, 149206 G01V – 146846 G02B – 151949 G03B – 139995 C12P – 134494, 136544, 137403, 141161 G06F– 147105, 147630, 149588, 149594, 179054 G06Q– 144846 C12Q – 145141, 146228 G09G –149205 C21D– 161289 G11B – 148002, 165464 C22C – 161175 H01J – 134926, 154517 C23C – 150839 H01M –150617, 156624, 157862 E04B – 155480 H01R – 132700 E04F – 151668 H01S – 132455 F01K – 156048 H03M– 140141 F02C – 165759 H04B – 145652, 149656 F16B – 151060 H04J –147719 F16L –152499 F41G – 136566, 147370 F41H– 156645 H04L – 144040, 148775, 150728, 152648 H04M – 147276, 149180, 149697, 151611 G01C – 138831, 146981 H04N – 150474, 152092, 152798 G01D – 151406 G01N – 155179, 156143 x H04Q – 147137, 147799, 148926, 149433 July 24, 2007– ט' באב התשס"ז ירושלים, משרד המשפטים,נערך ע"י רשות הפטנטים ירושלים,הופק והודפס במדפיס הממשלתי EDITED BY THE PATENT OFFICE, MINISTRY OF JUSTICE, JERUSALEM PRINTED AND PUBLISHED BY THE GOVERNMENT PRINTER