Accelerating Medical Solutions in Israel: Building a Global Life Science Industry
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Assessing the Impacts of Changes in the Information Technology R&D Ecosystem: Retaining Leadership in an Increasingly Global Environment
This PDF is available from The National Academies Press at http://www.nap.edu/catalog.php?record_id=12174 Assessing the Impacts of Changes in the Information Technology R&D Ecosystem: Retaining Leadership in an Increasingly Global Environment ISBN Committee on Assessing the Impacts of Changes in the Information 978-0-309-11882-8 Technology R & D Ecosystem: Retaining Leadership in an Increasingly Global Environment; National Research Council 204 pages 6 x 9 PAPERBACK (2009) Visit the National Academies Press online and register for... Instant access to free PDF downloads of titles from the NATIONAL ACADEMY OF SCIENCES NATIONAL ACADEMY OF ENGINEERING INSTITUTE OF MEDICINE NATIONAL RESEARCH COUNCIL 10% off print titles Custom notification of new releases in your field of interest Special offers and discounts Distribution, posting, or copying of this PDF is strictly prohibited without written permission of the National Academies Press. Unless otherwise indicated, all materials in this PDF are copyrighted by the National Academy of Sciences. Request reprint permission for this book Copyright © National Academy of Sciences. All rights reserved. Assessing the Impacts of Changes in the Information Technology R&D Ecosystem: Retaining Leadership in an Increasingly Global Environment Committee on Assessing the Impacts of Changes in the Information Technology Research and Development Ecosystem Computer Science and Telecommunications Board Division on Engineering and Physical Sciences Copyright © National Academy of Sciences. All rights reserved. Assessing the Impacts of Changes in the Information Technology R&D Ecosystem: Retaining Leadership in an Increasingly Global Environment THE NATIONAL ACADEMIES PRESS 500 Fifth Street, N.W. Washington, DC 20001 NOTICE: The project that is the subject of this report was approved by the Gov- erning Board of the National Research Council, whose members are drawn from the councils of the National Academy of Sciences, the National Academy of Engi- neering, and the Institute of Medicine. -
United States Patent (19) 11 Patent Number: 4,871,835 Aviv Et Al
United States Patent (19) 11 Patent Number: 4,871,835 Aviv et al. (45) Date of Patent: Oct. 3, 1989 54 ANALOGS OF HGH HAVING Lewis et al., Biochem. Biophys, Res. Comm., 92(2), 1980, ANTAGONISTIC ACTIVITY, AND USES pp. 511-516. THEREOF DeGeeter, CA, vol. 99, 1983, #157232u. Russell et al., JBC, 256, 1981, pp. 296-300. (75) Inventors: Haim Aviv; Marian Gorecki, both of Lewis et al., JBC, 253(8), 1978, pp. 2679-2687. Rehovot; Avigdor Levanon, Netania; Goeddel et al., Nature, 281, 1979, pp. 544-548. Amos Oppenheim, Jerusalem; Tikva Seebury et al., Nature, 276, 1978, pp. 795-798. Vogel, Rehovot; Pinhas E. Zeelon, Ross et al., Hormone Design, 1982, pp. 313-318. Hashiva; Menachen Zeevi, Ramat Arieh Gertler et al., Endocrinology, 116(4): 1636-1644 Gan, all of Israel (1985). Alejandro C. Paladini et al., CRC Critical Reviews in 73) Assignee: Bio-Technology General Corp., New Biochemistry, 15(1): 25-56. York, N.Y. Primary Examiner-J. R. Brown 21 Appl. No.: 691,230 Assistant Examiner-Garnette D. Draper Attorney, Agent, or Firm-John P. White 22 Filed: Jan. 14, 1985 57 ABSTRACT Related U.S. Application Data Analogs of hCGH having the activity of naturally occur ring hCH and a similar amino acid sequence varying 63 Continuation-in-part of Ser. No. 514,188, Jul. 15, 1983. from the sequence of natural hCGh by the addition of one or more amino acids, e.g. methione or methionine-leu 511 Int. Cl." .............................................. CO7K 13/00 cine, to the N-terminus of natural hCGH have been pro 52 U.S. -
List of Section 13F Securities
List of Section 13F Securities 1st Quarter FY 2004 Copyright (c) 2004 American Bankers Association. CUSIP Numbers and descriptions are used with permission by Standard & Poors CUSIP Service Bureau, a division of The McGraw-Hill Companies, Inc. All rights reserved. No redistribution without permission from Standard & Poors CUSIP Service Bureau. Standard & Poors CUSIP Service Bureau does not guarantee the accuracy or completeness of the CUSIP Numbers and standard descriptions included herein and neither the American Bankers Association nor Standard & Poor's CUSIP Service Bureau shall be responsible for any errors, omissions or damages arising out of the use of such information. U.S. Securities and Exchange Commission OFFICIAL LIST OF SECTION 13(f) SECURITIES USER INFORMATION SHEET General This list of “Section 13(f) securities” as defined by Rule 13f-1(c) [17 CFR 240.13f-1(c)] is made available to the public pursuant to Section13 (f) (3) of the Securities Exchange Act of 1934 [15 USC 78m(f) (3)]. It is made available for use in the preparation of reports filed with the Securities and Exhange Commission pursuant to Rule 13f-1 [17 CFR 240.13f-1] under Section 13(f) of the Securities Exchange Act of 1934. An updated list is published on a quarterly basis. This list is current as of March 15, 2004, and may be relied on by institutional investment managers filing Form 13F reports for the calendar quarter ending March 31, 2004. Institutional investment managers should report holdings--number of shares and fair market value--as of the last day of the calendar quarter as required by Section 13(f)(1) and Rule 13f-1 thereunder. -
Cyber Security Cryptography and Machine Learning
Lecture Notes in Computer Science 12716 Founding Editors Gerhard Goos Karlsruhe Institute of Technology, Karlsruhe, Germany Juris Hartmanis Cornell University, Ithaca, NY, USA Editorial Board Members Elisa Bertino Purdue University, West Lafayette, IN, USA Wen Gao Peking University, Beijing, China Bernhard Steffen TU Dortmund University, Dortmund, Germany Gerhard Woeginger RWTH Aachen, Aachen, Germany Moti Yung Columbia University, New York, NY, USA More information about this subseries at http://www.springer.com/series/7410 Shlomi Dolev · Oded Margalit · Benny Pinkas · Alexander Schwarzmann (Eds.) Cyber Security Cryptography and Machine Learning 5th International Symposium, CSCML 2021 Be’er Sheva, Israel, July 8–9, 2021 Proceedings Editors Shlomi Dolev Oded Margalit Ben-Gurion University of the Negev Ben-Gurion University of the Negev Be’er Sheva, Israel Be’er Sheva, Israel Benny Pinkas Alexander Schwarzmann Bar-Ilan University Augusta University Tel Aviv, Israel Augusta, GA, USA ISSN 0302-9743 ISSN 1611-3349 (electronic) Lecture Notes in Computer Science ISBN 978-3-030-78085-2 ISBN 978-3-030-78086-9 (eBook) https://doi.org/10.1007/978-3-030-78086-9 LNCS Sublibrary: SL4 – Security and Cryptology © Springer Nature Switzerland AG 2021 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. The use of general descriptive names, registered names, trademarks, service marks, etc. -
Alvin Toffler
A Bantam Book I published in association with William Morrow & Co., Inc. PRINTING HISTORY William Morrow edition published March 1980 5 printings September 1980 A Literary Guild Selection October 1979 A Selection of Preferred Choice Bookplan October 1979 and the Macmillan Book Club May 1980. Serialized in Industry Week, February 1980; East/West Network, February 1980; Across the Board, March 1980; Independent News Alliance, March 1980; Rotarian, April 1980; Mechanix Illustrated, May 1980; Reader's Digest, May 1980; Video Review, May 1980; Journal of Insurance, July 1980; Reader's Digest (Canada), August 1980; and Modern Office Procedures, September 1980. Bantam edition /April 1981 13 printings through May 1989 THE THIRD WAVE also appears in translation: French (Editions Deneol); German (Bertelsmann); Japanese (NHK Books); Spanish (Plaza y Janes and Editorial Diana); Danish (Chr. Erichsens Forlag); Dutch (Uilgenerij L.J. Veen); Hebrew (Am Oved); Portuguese (Distribuidora Record); Serbo-Croatian (Jugoslavia); Swedish) (Esselte Info AB); Turkish (Altin Kitaplar); Chinese (Dushu-Peking); U.K. (William Collins & Sons); India (Pan Books); Greece (Edition Cactus); Poland (Pantswowy Instytut Wydawniczy); Romania (Editura Politica); Portuguese (Livros do Brazil); Indonesia (P.T. Pantja Simpati); Korea (Korean Economic Daily). All rights reserved. Copyright © 1980 by Alvin Toffler. Cover art copyright © 1981 by Bantam Books. No part of this book may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system, without permission in writing from the publisher. For information address: Bantam Books. ISBN 0-553-24698-4 Published simultaneously in the United States and Canada Bantam Books are published by Bantam Books, a division of Bantam Doubleday Dell Publishing Group, Inc. -
Israeli Biotechnology Strategy Project Realizing Our Potential
Israeli Biotechnology Strategy Project *** Realizing Our Potential Final Report Tel Aviv, March 2001 Submitted to The Chief Scientist, Ministry of Industry and Trade The Ministry of Finance The IBO by Amsterdam Athens Cambridge Frankfurt Hong Kong Istanbul Johannesburg London Los Angeles Madrid Manila Milan Moscow Munich New Delhi New York Paris S?o Paulo Seoul Singapore Stockholm Tel Aviv Tokyo Toronto Zurich Content A. INTRODUCTION..................................................................................................3 B. EXECUTIVE SUMMARY ....................................................................................4 C. GLOBAL TRENDS AND POTENTIAL FOR ISRAEL ..................................13 D. KEY ISSUES IDENTIFIED IN ISRAEL AND BENCHMARK OF FOREIGN CLUSTERS .......................................................................................23 E. AREAS OF RECOMMENDATIONS ................................................................40 F. CONCLUSION- LONG TERM OBJECTIVES FOR ISRAEL.......................58 G. GLOSSARY OF TERMS....................................................................................59 H. LIST OF INTERVIEWEES................................................................................60 I. BIBLIOGRAPHY..................................................................................................63 APPENDIX .................................................................................................................66 Page 2 /80– March 2001 © 2001 Monitor Company, Inc Introduction -
Galactosidase Gene Arie Rosner, Marian Gorecki *, and Haim Aviv Departments of Virology and Organic Chemistry*, Weizmann Institute of Science, Rehovot, Israel, 76100
Screening for Highly Active Plasmid Promoters via Fusion to /?-Galactosidase Gene Arie Rosner, Marian Gorecki *, and Haim Aviv Departments of Virology and Organic Chemistry*, Weizmann Institute of Science, Rehovot, Israel, 76100 Z. Naturforsch. 37 c, 441 —444 (1982); received January 13, 1982 Plasmid Promoter, /?-Galactosidase Gene, Escherichia coli A plasmid containing promoter-deleted inactive /?-galactosidase gene [1] was used to select promoters of the pEP121 plasmid [2]. Colonies of cells harboring reactivated /?-galactosidase gene were identified by their red color on McConkey plates. The quantitative amounts of /?-galactosidase produced in each clone were estimated by assaying enzyme activity and by measuring the specific /?-galactosidase protein following fractionation of total cells’ proteins on polyacrylamide gel. A wide range of enzyme activities was observed. The most active promoter isolated was shown to promote /?-galactosidase production more efficiently, compared with the original /?-galactosidase promoter, amounting to 20% of all cell proteins. Such highly active promoters may be utilized in the future, to promote expression of cloned genes in bacteria. Introduction gene and E. coli strain MC 1061, restriction minus, deleted in the lactoase operon [1] were received It was previously shown that bacterial promoters from Dr. M. J. Casadaban and given to us by Dr. M. can promote expression of foreign genes in bacteria Mevorach. [3, 4]. The amount of protein produced depends Preparation of plasmid: Extraction of plasmid mainly on the activity of the promoter itself. The DNA was performed according to Betlach et al. [5]. isolation and molecular manipulation of bacterial Transformation of cells with plasmid DNA was promoters became, therefore, of prime interest in carried out as described by Cohen et al. -
Life Sciences in Israel
STATE OF ISRAEL Ministry of Industry Trade and Labor Investment Promotion Center Inspiration Invention Innovation Life Sciences in Israel www.investinisrael.gov.il Table of Contents .......................................... 3 Israel: A Powerhouse of Opportunities ............................................................ 3 Israel’s Life Science Sectors Medical Devices ........................................................................ 4 Healthcare IT ............................................................................ 4 BioPharmaceutical .................................................................... 7 Israel’s Biomedical Engineering - ................................................... 11 Spotlight on Stem Cell Research ....................................... 15 Israel’s Life Sciences Competitive Edge ..................................................................... 19 Government Support 2 Life Sciences in Israel Israel: A Powerhouse of Opportunities Why Israel’s Life Sciences Over the last decade, Israel has introduced a wealth of groundbreaking More than 1,000 Life and valuable innovations in Life Sciences. Israel’s Life Sciences sector Sciences Companies - is supported by a strong foundation of academic excellence, including Biopharma and Medical some of the world’s leading research institutes, renowned R&D Devices facilities and cutting-edge medical centers. Bolstered by a highly skilled Over 1/3 of LS Start-Ups workforce, a flourishing high-tech environment, and an entrepreneurial already generate revenue -
Galactosidase Gene Arie Rosner, Marian Gorecki *, and Haim Aviv Departments of Virology and Organic Chemistry*, Weizmann Institute of Science, Rehovot, Israel, 76100
Screening for Highly Active Plasmid Promoters via Fusion to /?-Galactosidase Gene Arie Rosner, Marian Gorecki *, and Haim Aviv Departments of Virology and Organic Chemistry*, Weizmann Institute of Science, Rehovot, Israel, 76100 Z. Naturforsch. 37 c, 441 —444 (1982); received January 13, 1982 Plasmid Promoter, /?-Galactosidase Gene, Escherichia coli A plasmid containing promoter-deleted inactive /?-galactosidase gene [1] was used to select promoters of the pEP121 plasmid [2]. Colonies of cells harboring reactivated /?-galactosidase gene were identified by their red color on McConkey plates. The quantitative amounts of /?-galactosidase produced in each clone were estimated by assaying enzyme activity and by measuring the specific /?-galactosidase protein following fractionation of total cells’ proteins on polyacrylamide gel. A wide range of enzyme activities was observed. The most active promoter isolated was shown to promote /?-galactosidase production more efficiently, compared with the original /?-galactosidase promoter, amounting to 20% of all cell proteins. Such highly active promoters may be utilized in the future, to promote expression of cloned genes in bacteria. Introduction gene and E. coli strain MC 1061, restriction minus, deleted in the lactoase operon [1] were received It was previously shown that bacterial promoters from Dr. M. J. Casadaban and given to us by Dr. M. can promote expression of foreign genes in bacteria Mevorach. [3, 4]. The amount of protein produced depends Preparation of plasmid: Extraction of plasmid mainly on the activity of the promoter itself. The DNA was performed according to Betlach et al. [5]. isolation and molecular manipulation of bacterial Transformation of cells with plasmid DNA was promoters became, therefore, of prime interest in carried out as described by Cohen et al. -
Laws Encouraging Technological Innovation in Israel : Ⲳstrings Attachedⲵ Heather A
Laws Encouraging Technological Innovation in Israel : ⲳStrings AttachedⲴ Heather A. Stone* Ɇ. Introduction ɇ. The Laws Encouraging Technological Innovation in Israel A. Venture Capital B. Tax Incentives C. Capital Markets Ɉ. The R&D Law A. OCS Administration; Technology Administered by Technolo- gists B. Grants and Royalties C. Periodic Reporting D. Transfer of Manufacturing Activities E. Transfer of Technology F. Licensing Arrangements ɉ. Summary and Conclusion * The author is a partner in the Mergers & Acquisitions department, and head of the Intellectual Property practice, of the Tel Aviv, Israel law firm Gross, Kleinhendler, Hodak, Halevy, Greenberg & Co. The information in this article should not be construed as legal advice. Opinions in this article are those of the author and not of the firm. The author wishes to thank Messrs. Aviram Zolti, Uri Gabai and Shlomi Nezry from the OCS, and Shmil Levy from Sequoia Capital and Eyal Kishon from Genesis Partners, for their patience and kind answers to the author's questions. The author also wishes to the thank Mr. Elad Ziv for his assistance in researching this article. Email: [email protected] Abstract There are numerous laws in Israel that aim to encourage technological inno- vation in industrial research and development. One common feature of nearly all these laws is that they aim to make capital available to entrepreneurs or make the economic return on investment (ROI) for investors more attrac- tive. This is largely due to the fact that capital is the one main ingredient to a successful technology sector that Israel has historically lacked. This article will focus primarily on the Israeli Law for the Encouragement of Industrial Research and Development, 1984 (the “R&D Law”), as amended, and the regulations promulgated thereunder. -
(12) United States Patent (10) Patent No.: US 6,229,003 B1 Aviv Et Al
USOO6229003B1 (12) United States Patent (10) Patent No.: US 6,229,003 B1 Aviv et al. (45) Date of Patent: May 8, 2001 (54) PRODUCTION OF BOVINE GROWTH OTHER PUBLICATIONS HORMONE BY MICROORGANISMS Seeburg et al., Nature 276:795–798 (1978). (75) Inventors: Haim Aviv, Rehovot; Eliyahu Keshet, Lingappa et al., Cell Biol. 74:2432-2436 (1977). Ramat; Marian Gorecki, Rehovot, Cohen et al., P.N.A.S. 70 (11):3240–3244 (1973); and. Chang et al., P.N.A.S. 71 (4): 1030-1034 (1974). Arie Rosner, Nes Ziona, all of (IL) Nilson et al. (1979), “Purificatio of Pre-prolactin mRNA (73) Assignee: Yeda Research and Development from Bovine Anterior Pituitary Glands”, J. Biol. Chem. Company Ltd., Rehovot (IL) 254:1516-1520. Keiichi Itakura and Arthur D. Riggs (1980), “Chemical (*) Notice: Subject to any disclaimer, the term of this DNA Synthesis and Recombinant DNA Studies”, Science patent is extended or adjusted under 35 209:1401-1405. U.S.C. 154(b) by 0 days. Hunt and Dayhoff (1976), Atlas of Protein Sequence and Structure, (National Biomed. Res. Fund.) Washington, D.C., Vol. 5, Supp. 2, p. 11. (21) Appl. No.: 08/457,405 Edge et al. (1981), “Total Synthesis Of A Human Leukocyte (22) Filed: Jun. 1, 1995 Interferon Gene”, Nature 292:756–762. Coutelle et al. (1978), “Use of Matrix-Immobilised Recom Related U.S. Application Data binant Plasmids To Purify Chain-Specific Rabbit Globin Complementary DNAs, Gene 3:113-122. (63) Continuation of application No. 08/317.248, filed on Oct. 3, 1994, now abandoned, which is a continuation of application Sassavage et al., Federation Proceedings, Abstracts, (1979), No. -
Purification of Biologically Active Globin Messenger RNA By
Proc. Nat. Acad. Sci. USA Vol. 69, No. 6, pp. 1408-1412, June 1972 Purification of Biologically Active Globin Messenger RNA by Chromatography on Oligothymidylic acid-Cellulose (p.ly (A)-richi inRNA/rabbit globin niRN A/ascites tumiior cell-free systelml) HAIM AVIV ANI) PHILIP LEI)ER Laboratory of Molecular Genetics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20014 Coinnmunicatel by E. IR. Stadtrnan, March 22, 1972 ABSTRACT A convenient technique for the partial MATERIALS AND METHODS purification of large quantities of functional, poly(adenylic acid)-rich mRNA is described. The method depends upon The sources of many of the reagents used in this study have annealing poly(adenylic acid)-rich mRNA to oligothymi- been indicated (10). For the synthesis of oligo(dT)-cellulose, dylic acid-cellulose columns and its elution with buffers Whatman cellulose powder CC 41 was obtained from Reeve of low ionic strength. Biologically active rabbit globin Angel; thymidine-5'-monophosphate, from Schwarz-Mann; mRNA has been purified by this procedure and assayed for its ability to direct the synthesis of rabbit globin in a and NN'-dicyclohexylearbodiimide, from Aldrich. [3H]- cell-free extract of ascites tumnor. Inasmuch as various Leucine (specific activity, 26 Ci/mmol); ['4C]leucine (specific mammalian mRNAs appear to be rich in poly(adenylic activity, 263 Ci/mol) and [14C]valine (specific activity, 219 acid) and can likely be translated in the ascites cell-free Ci/mol), from New England Nuclear; [14C]lysine (specific extract, this approach should prove generally useful as an i -itial step in the isolation of specific mRNAs.