Host and Vector-dependent Effects on the Risk of Germline Transmission of AAV Vectors-Reference-Cited by-同舟云学术

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Host and Vector-dependent Effects on the Risk of Germline Transmission of AAV Vectors

Published:2009-06 Issue:6 Volume:17 Page:1022-1030
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Favaro Patricia,Downey Harre D,Zhou J Shangzhen,Wright J Fraser,Hauck Bernd,Mingozzi Federico,High Katherine A,Arruda Valder R

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

Reference36 articles.

1. Evidence of multiyear factor IX expression by AAV-mediated gene transfer to skeletal muscle in an individual with severe hemophilia B;Jiang;Mol Ther,2006

2. Safety and efficacy of gene transfer for Leber's congenital amaurosis;Maguire;N Engl J Med,2008

3. Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response;Manno;Nat Med,2006

4. Self-complementary adeno-associated virus vectors containing a novel liver-specific human factor IX expression cassette enable highly efficient transduction of murine and nonhuman primate liver;Nathwani;Blood,2006

5. Factor IX variants improve gene therapy efficacy for hemophilia B;Schuettrumpf;Blood,2005

Cited by 34 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. A Comprehensive Atlas of AAV Tropism in the Mouse;2024-09-10

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

3. Hemophilia B and gene therapy: a new chapter with etranacogene dezaparvovec;Blood Advances;2024-04-09

4. Selection of appropriate non-clinical animal models to ensure translatability of novel AAV-gene therapies to the clinic;Gene Therapy;2023-08-23

5. Use of Mesenchymal Stem Cells to Enhance the Efficacy of Gene Therapy;Methods in Molecular Biology;2022-11-19

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