Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy

By Kariya Shingo   Park Gyu-Hwan   Maeno-Hikichi Yuka   Leykekhman Olga   Lutz Cathleen   Arkovitz Marc S.   Landmesser Lynn T.   Monani Umrao R.  

Human Molecular Genetics, Vol. 17, Iss. 16, 2008-08 ,pp. : 2552-2569

Oxford University Press

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A mutation in α-tropomyosin slow affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy

By Hardeman E.C.  

Human Molecular Genetics, Vol. 10, Iss. 4, 2001-02 ,pp. : 317-328

Oxford University Press

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Defects in neuromuscular junction structure in dystrophic muscle are corrected by expression of a NOS transgene in dystrophin-deficient muscles, but not in muscles lacking α- and 1-syntrophins

By Shiao Terry  

Human Molecular Genetics, Vol. 13, Iss. 17, 2004-09 ,pp. : 1873-1884

Oxford University Press

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Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies

By Chan Yiumo Michael   Keramaris-Vrantsis Elizabeth   Lidov Hart G.   Norton James H.   Zinchenko Natalia   Gruber Helen E.   Thresher Randy   Blake Derek J.   Ashar Jignya   Rosenfeld Jeffrey   Lu Qi L.  

Human Molecular Genetics, Vol. 19, Iss. 20, 2010-10 ,pp. : 3995-4006

Oxford University Press

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Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice

By Ito Kaori   Kimura Shigemi   Ozasa Shiro   Matsukura Makoto   Ikezawa Makoto   Yoshioka Kowashi   Ueno Hiroe   Suzuki Misao   Araki Kimi   Yamamura Ken-ichi   Miwa Takeshi   Dickson George   Thomas Gail D.   Miike Teruhisa  

Human Molecular Genetics, Vol. 15, Iss. 14, 2006-07 ,pp. : 2266-2275

Oxford University Press

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