Dystrophin deficiency in canine X-linked muscular dystrophy in Japan (CXMDJ) alters myosin heavy chain expression profiles in the diaphragm more markedly than in the tibialis cranialis muscle

Author:

Yuasa Katsutoshi,Nakamura Akinori,Hijikata Takao,Takeda Shinichi

Publisher

Springer Science and Business Media LLC

Subject

Orthopedics and Sports Medicine,Rheumatology

Reference36 articles.

1. Emery AEH: Duchenne Muscular Dystrophy. 1993, Oxford: Oxford University Press, 2

2. Nonaka I: Animal models of muscular dystrophies. Lab Anim Sci. 1998, 48: 8-17.

3. Valentine BA, Cooper BJ, Cummings JF, De Lahunta A: Canine X-linked muscular dystrophy: morphologic lesions. J Neurol Sci. 1990, 97: 1-23. 10.1016/0022-510X(90)90095-5.

4. Howell JM, Fletcher S, Kakulas BA, O'Hara M, Lochmuller H, Karpati G: Use of the dog model for Duchenne muscular dystrophy in gene therapy trials. Neuromuscul Disord. 1997, 7: 325-328. 10.1016/S0960-8966(97)00057-6.

5. Shimatsu Y, Yoshimura M, Yuasa K, Urasawa N, Tomohiro M, Nakura M, Tanigawa M, Nakamura A, Takeda S: Major clinical and histopathological characteristics of canine X-linked muscular dystrophy in Japan, CXMDJ. Acta Myol. 2005, 24: 145-154.

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