AAV-based shRNA silencing of NF-κB ameliorates muscle pathologies in mdx mice-Reference-Cited by-同舟云学术

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AAV-based shRNA silencing of NF-κB ameliorates muscle pathologies in mdx mice

Published:2012-01-26 Issue:12 Volume:19 Page:1196-1204
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Yang Q,Tang Y,Imbrogno K,Lu A,Proto J D,Chen A,Guo F,Fu F H,Huard J,Wang B

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/gt2011207.pdf

Reference35 articles.

1. Hoffman EP, Monaco AP, Feener CC, Kunkel LM . Conservation of the Duchenne muscular dystrophy gene in mice and humans. Science 1987; 238: 347–350.

2. Lapidos KA, Kakkar R, McNally EM . The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma. Circ Res 2004; 94: 1023–1031.

3. Bonilla E, Samitt CE, Miranda AF, Hays AP, Salviati G, DiMauro S et al. Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface. Cell 1988; 54: 447–452.

4. Koenig M, Kunkel LM . Detailed analysis of the repeat domain of dystrophin reveals four potential hinge segments that may confer flexibility. J Biol Chem 1990; 265: 4560–4566.

5. Koenig M, Monaco AP, Kunkel LM . The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein. Cell 1988; 53: 219–226.

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