Skeletal muscle repair in a mouse model of nemaline myopathy

By Sanoudou Despina   Corbett Mark A.   Han Mei   Ghoddusi Majid   Nguyen Mai-Anh T.   Vlahovich Nicole   Hardeman Edna C.  

Human Molecular Genetics, Vol. 15, Iss. 17, 2006-09 ,pp. : 2603-2612

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

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Thin filament length dysregulation contributes to muscle weakness in nemaline myopathy patients with nebulin deficiency

By Ottenheijm Coen A.C.   Witt Christian C.   Stienen Ger J.   Labeit Siegfried   Beggs Alan H.   Granzier Henk  

Human Molecular Genetics, Vol. 18, Iss. 13, 2009-07 ,pp. : 2359-2369

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Over-expression of BCL2 rescues muscle weakness in a mouse model of oculopharyngeal muscular dystrophy

By Davies Janet E.   Rubinsztein David C.  

Human Molecular Genetics, Vol. 20, Iss. 6, 2011-03 ,pp. : 1154-1163

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A mouse model offers novel insights into the myopathy and tendinopathy often associated with pseudoachondroplasia and multiple epiphyseal dysplasia

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Human Molecular Genetics, Vol. 19, Iss. 1, 2010-01 ,pp. : 52-64

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