Improvement of the mdx mouse dystrophic phenotype by systemic in utero AAV8 delivery of a minidystrophin gene-Reference-Cited by-同舟云学术

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Improvement of the mdx mouse dystrophic phenotype by systemic in utero AAV8 delivery of a minidystrophin gene

Published:2010-06-10 Issue:11 Volume:17 Page:1355-1362
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Koppanati B M,Li J,Reay D P,Wang B,Daood M,Zheng H,Xiao X,Watchko J F,Clemens P R

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/gt201084.pdf

Reference46 articles.

1. Emery AE . Population frequencies of inherited neuromuscular diseases--a world survey. Neuromuscul Disord 1991; 1: 19–29.

2. Emery AEH, Muntoni F . Duchenne Muscular Dystrophy. Oxford Univ Press: Oxford, New York, 2003.

3. Gregorevic P, Allen JM, Minami E, Blankinship MJ, Haraguchi M, Meuse L et al. rAAV6-microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice. Nat Med 2006; 12: 787–789.

4. Gregorevic P, Blankinship MJ, Allen JM, Crawford RW, Meuse L, Miller DG et al. Systemic delivery of genes to striated muscles using adeno-associated viral vectors. Nat Med 2004; 10: 828–834.

5. Liu M, Yue Y, Harper SQ, Grange RW, Chamberlain JS, Duan D . Adeno-associated virus-mediated microdystrophin expression protects young mdx muscle from contraction-induced injury. Mol Ther 2005; 11: 245–256.

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