Gene Transfer Vectors for Clinical Application: Methods in Enzymology, cartea 507
Theodore C. Friedmanen Limba Engleză Hardback – 17 apr 2012
- Chapters provide an invaluable resource for academics, researchers and students alike
- 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
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Specificații
ISBN-13: 9780123865090
ISBN-10: 0123865093
Pagini: 440
Dimensiuni: 152 x 229 x 28 mm
Greutate: 0.8 kg
Editura: ELSEVIER SCIENCE
Seria Methods in Enzymology
ISBN-10: 0123865093
Pagini: 440
Dimensiuni: 152 x 229 x 28 mm
Greutate: 0.8 kg
Editura: ELSEVIER SCIENCE
Seria Methods in Enzymology
Public țintă
Biochemists, biophysicists, molecular biologists, analytical chemists, and physiologistsCuprins
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