Gene transfer vectors for clinical application /
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| Imprint: | Amsterdam, Netherlands ; Boston, Mass. : Elsevier/Academic Press, 2012. |
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| Description: | 1 online resource (l, 385 pages, [14] pages of plates) : illustrations (some color). |
| Language: | English |
| Series: | Methods in enzymology ; v. 507 Methods in enzymology ; v. 507. |
| Subject: | |
| Format: | E-Resource Book |
| URL for this record: | http://pi.lib.uchicago.edu/1001/cat/bib/11148531 |
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].
- 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.