rdf-syntax-grammar
mods:
  schema location: http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
  title info:
    title: Gene transfer vectors for clinical application
  name:
    name part: Friedmann, Theodore
    name part: 1935-
  type of resource: text
  genre: bibliography
  genre: Electronic books.
  origin info:
    place:
      place term: ne
    place:
      place term: Amsterdam, Netherlands
    place:
      place term: Boston, Mass
    publisher: Elsevier/Academic Press
    date issued: 2012
    issuance: monographic
  language:
    language term: eng
  physical description:
    form: remote
    extent: 1 online resource (l, 385 pages, [14] pages of plates) : illustrations (some color).
  abstract: This volume of Methods in Enzymology looks at Gene Transfer Vectors for Clinical Application. The chapters provide an invaluable resource for academics, researchers and students alike. With an international board of authors, this volume covers such topics as General principles of retrovirus vector design, Chronic granulomatous disease (CGD), Gene therapy for blindness, and Retrovirus genetic strategy and vector design. Chapters provide an invaluable resource for academics, researchers and students alike. Iinternational board of authors. This volume covers such topics as General principles of retrovirus vector design, Chronic granulomatous disease (CGD), Gene therapy for blindness, and Retrovirus genetic strategy and vector design.
  table of contents: General principles of retrovirus vector design / Tammy Chang and Jiing-Kuan Yee -- Strategies for retrovirus-based correction of severe, combined immunodeficiency (SCID) / Alain Fischer, Salima Hacein-Bey-Abina, and Marina Cavazzana-Calvo -- Retrovirus and lentivirus vector design and methods of cell conditioning / Samantha Cooray, Steven J. Howe, and Adrian J. Thrasher -- Analysis of the clonal repertoire of gene-corrected cells in gene therapy / Anna Paruzynski [and others] -- Developing novel lentiviral vectors into clinical products / Anna Leath and Kenneth Cornetta -- Lentivirus vectors in [beta]-thalassemia / Emmanuel Payen [and others] -- Gene therapy for chronic granulomatous disease / Elizabeth M. Kang and Harry L. Malech -- Alternative splicing caused by lentiviral integration in the human genome / Arianna Moiani and Fulvio Mavilio -- Genotoxicity assay for gene therapy vectors in tumor prone Cdkn2amice / Eugenio Montini and Daniela Cesana -- Lentiviral hematopoietic cell gene therapy for X-linked adrenoleukodystrophy / Nathalie Cartier [and others] -- Retroviral replicating vectors in cancer / Christopher R. Logg [and others] -- Adeno-associated virus vectorology, manufacturing, and clinical applications / Joshua C. Grieger and R. Jude Samulski -- Gene delivery to the retina : from mouse to man / Jean Bennett, Daniel C. Chung, and Albert Maguire -- Generation of hairpin-based RNAi vectors for biological and therapeutic application / Ryan L. Boudreau and Beverly L. Davidson -- Recombinant adeno-associated viral vector reference standards / Philippe Moullier and Richard O. Snyder -- NIH oversight of human gene transfer research involving retroviral, lentiviral, and adeno-associated virus vectors and the role of the NIH Recombinant DNA Advisory Committee / Marina O'Reilly [and others] -- Regulatory structures for gene therapy medicinal products in the European Union / Bettina Klug [and others].
  table of contents: Preface: The successful clinical use of viral vectors for human gene therapy. General principles of retrovirus vector design Strategies for retrovirus-based correction of severe, combined immunodeficiency (SCID) Retrovirus and lentivirus vector design and methods of cell conditioning Analysis of the clonal repertoire of gene corrected cells in gene therapy Developing novel lentiviral vectors into clinical products Lentivirus vectors in beta-thalassemia Gene Therapy for Chronic Granulomatous Disease Alternative splicing caused by lentiviral integration in the human genome Genotoxicity assay for gene therapy vectors in tumor prone Cdkn2a-/- mice Lentiviral Hematopoietic Cell Gene Therapy for X-linked Adrenoleukodystrophy Retroviral replicating vectors in cancer Adeno-associated virus vectorology, manufacturing and clinical applications Gene Delivery To The Retina: From Mouse To Man Generation of hairpin-based RNAi vectors for biological and therapeutic application Recombinant adeno-associated viral vector reference standards NIH oversight of human gene transfer research involving retroviral, lentiviral and adeno-associated virus vectors and the role of the NIH recombinant DNA advisory committee draft Regulatory structures for gene therapy medicinal products in the European Union.
  note: edited by Theodore Friedman.
  note: Includes bibliographical references and indexes.
  subject:
    topic: Gene therapy
  subject:
    topic: Genetic vectors
  subject:
    topic: Genetic transformation
  subject:
    topic: PSYCHOLOGY
    topic: Psychotherapy
    topic: General
  subject:
    topic: Gene therapy
  subject:
    topic: Genetic transformation
  subject:
    topic: Genetic vectors
  subject:
    topic: Genetic Therapy
  subject:
    topic: Genetic Vectors
  subject:
    topic: Gene Transfer Techniques
  classification: RB155.8 .G46 2012
  classification: 615.8/95
  classification: W1 ME9615K no.507 2012
  classification: QZ 52
  related item:
    title info:
      title: Gene transfer vectors for clinical application
    origin info:
      publisher: Amsterdam, Netherlands ; Boston, Mass. : Elsevier/Academic Press, 2012
      edition: 1st ed.
    identifier: (OCoLC)780075440
  related item:
    title info:
      title: Methods in enzymology ; v. 507
  identifier: 9780123865106
  identifier: 0123865107
  identifier: 9780123865090
  identifier: 0123865093
  identifier: https://www.sciencedirect.com/science/bookseries/00766879/507
  record info:
    record content source: OPELS
    record creation date: 120411
    record change date: 20180501121956.0
    record identifier: ocn785407732
    language of cataloging:
      language term: eng