UID:
almahu_9949251584902882
Umfang:
1 online resource (XIII, 462 p. 43 illus., 20 illus. in color.)
Ausgabe:
1st ed. 2011.
ISBN:
1-61779-370-1
Serie:
Methods in Molecular Biology, 807
Inhalt:
Today, progress in rAAV-mediated gene transfer is so robust that long-term, efficient, and regulatable transgene expression is reproducibly achieved in large animal models. The complexity of gene transfer agents in the context of their clinical use requires investigators from a wide variety of backgrounds to have an understanding — or at least an appreciation of — the regulatory environment and constraints that affect vector design, manufacturing, pre-clinical testing, and clinical use, with an emphasis on patient protection. In Adeno-Associated Virus: Methods and Protocols, experts from the United States and Europe have contributed current knowledge of this multi-dimensional field relating to the biology of AAV, rAAV vector design, vector manufacturing and product testing, performance of rAAV vectors in major organs, rAAV-related immunological issues, design of animal and clinical studies, and clinical experience. Written in the successful Methods in Molecular Biology™ series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and notes on troubleshooting and avoiding known pitfalls. Authoritative and accessible, Adeno-Associated Virus: Methods and Protocols provides a complete and comprehensive understanding of this multi-disciplinary and rapidly progressing field.
Anmerkung:
Bibliographic Level Mode of Issuance: Monograph
,
Adeno-Associated Virus Biology -- Design and Construction of Functional AAV Vectors -- AAV Capsid Structure and Cell Interactions -- Exploiting Natural Diversity of AAV for the Design of Vectors With Novel Properties -- Gene Therapy in Skeletal Muscle Mediated by Adeno-Associated Virus (AAV) Vectors -- AAV-Mediated Liver-Directed Gene Therapy -- Recombinant AAV Delivery to the Central Nervous System -- AAV Mediated Gene Therapy for Retinal Degenerative Diseases -- Adeno-Associated Virus Vector Delivery to the Heart -- Evaluation of the Fate of rAAV Genomes Following in vivo Administration -- Measuring Immune Responses to Recombinant AAV Gene Transfer -- Modification and Labeling of AAV Vector Particles -- AAV-mediated Gene Targeting -- Preclinical Study Design for rAAV -- Biodistribution and Shedding of AAV Vectors -- Production and Purification of Recombinant Adeno-Associated Vectors -- rAAV Vector Product Characterization and Stability Studies -- rAAV Human Trial Experience.
,
English
Weitere Ausg.:
ISBN 1-61779-369-8
Sprache:
Englisch
DOI:
10.1007/978-1-61779-370-7
