Rapid and highly efficient transduction by double-stranded adeno-associated virus vectors in vitro and in vivo-Reference-Cited by-同舟云学术

Rapid and highly efficient transduction by double-stranded adeno-associated virus vectors in vitro and in vivo

Published:2003-11-17 Issue:26 Volume:10 Page:2105-2111
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Wang Z,Ma H-I,Li J,Sun L,Zhang J,Xiao X

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/3302133.pdf

Reference31 articles.

1. Samulski RJ, Sally M, Muzyczka N . Adeno-associated viral vectors. In: Friedmann T (ed). Development of Human Gene Therapy. Cold Spring Harbor Laboratory Press: Cold Spring Harbor, 1999, pp 131–172.

2. Ferrari FK, Samulski T, Shenk T, Samulski RJ . Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors. J Virol 1996; 70: 3227–3234.

3. Fisher KJ et al. Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis. J Virol 1996; 70: 520–532.

4. Nakai H, Storm TA, Kay MA . Recruitment of single-stranded recombinant adeno-associated virus vector genomes and intermolecular recombination are responsible for stable transduction of liver in vivo. J Virol 2000; 74: 9451–9463.

5. Lewin AS et al. Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa [published erratum appears in Nat Med 1998 Sep;4(9):1081]. Nat Med 1998; 4: 967–971.

Cited by 360 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Localizedin vivogene editing of murine cancer-associated fibroblasts;2024-07-16

2. Recombinant Adeno-Associated Virus Vectors for Gene Therapy of the Central Nervous System: Delivery Routes and Clinical Aspects;Biomedicines;2024-07-09

3. Developing AAV-delivered nonsense suppressor tRNAs for neurological disorders;Neurotherapeutics;2024-07

4. Enhanced transgene expression from single-stranded AAV vectors in human cells in vitro and in murine hepatocytes in vivo;Molecular Therapy - Nucleic Acids;2024-06

5. Development of AAV-Mediated Gene Therapy Approaches to Treat Skeletal Diseases;Human Gene Therapy;2024-05-01