Animal Models for Genetic Neuromuscular Diseases-Reference-Cited by-同舟云学术

Animal Models for Genetic Neuromuscular Diseases

Published:2008-01-18 Issue:3 Volume:34 Page:241-248
ISSN:0895-8696
Container-title:Journal of Molecular Neuroscience
language:en
Short-container-title:J Mol Neurosci

Author:

Vainzof Mariz,Ayub-Guerrieri Danielle,Onofre Paula C. G.,Martins Poliana C. M.,Lopes Vanessa F.,Zilberztajn Dinorah,Maia Lucas S.,Sell Karen,Yamamoto Lydia U.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s12031-007-9023-9.pdf

Reference37 articles.

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3. Barresi, R., Michele, D. E., Kanagawa, M., Harper, H. A., Dovico, S. A., Satz, J. S., et al. (2004). LARGE can functionally bypass alpha- dystroglycan glycosylation defects in distinct congenital muscular dystrophies. Natural Medicines, 10, 696–703.

4. Bittner, R. E., Anderson, L. V., Burkhardt, E., Bashir, R., Vafiadaki, E., Ivanova, S., et al. (1999). Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B. Nature Genetics, 23, 141–142.

5. Bogdanovich, S., Krag, T. O., Barton, E. R., Morris, L. D., Whittemore, L. A., Ahima, R. S., et al. (2002). Functional improvement of dystrophic muscle by myostatin blockade. Nature, 420, 418–421.

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