What has the mdx mouse model of duchenne muscular dystrophy contributed to our understanding of this disease?-Reference-Cited by-同舟云学术

What has the mdx mouse model of duchenne muscular dystrophy contributed to our understanding of this disease?

Published:2015-02-11 Issue:2 Volume:36 Page:155-167
ISSN:0142-4319
Container-title:Journal of Muscle Research and Cell Motility
language:en
Short-container-title:J Muscle Res Cell Motil

Author:

Manning Jennifer,O’Malley Dervla

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Biochemistry,Physiology

Link

http://link.springer.com/content/pdf/10.1007/s10974-015-9406-4.pdf

Reference161 articles.

1. Abdel-Salam E, Abdel-Meguid I, Korraa SS (2009) Markers of degeneration and regeneration in duchenne muscular dystrophy. Acta Myol 28(3):94–100

2. Abresch R, Seyden N, Wineinger M (1998) Quality of life. Issues for persons with neuromuscular diseases. Phys Med Rehabil Clin N Am 9(1):233–248

3. Andreetta F et al (2003) Immunomodulation of TGF-beta1 in mdx mouse inhibits connective tissue proliferation in diaphragm but increases inflammatory response: implications for antifibrotic therapy. J Neuroimmunol, 15(5), p. II

4. Anderson J, Weber M, Vargas C (2000) Deflazacort increases laminin expression and myogenic repair, and induces early persistant functional gain in mdx mouse muscular dystrophy. Cell Transpl 9(4):551–564

5. Aoki Y et al (2012) Bodywide skipping of exons 45–55 in dystrophic mdx52 mice by systemic antisense delivery. Proc Natl Acad Sci USA 109(34):13763–13768

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