Muscle weakness in a mouse model of nemaline myopathy can be reversed with exercise and reveals a novel myofiber repair mechanism

By Joya Josephine E.  

Human Molecular Genetics, Vol. 13, Iss. 21, 2004-11 ,pp. : 2633-2645

Oxford University Press

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Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin gene

By Anderson Sylvia   Ekstein Josef   Donnelly Mary   Keefe Erin   Toto Nicole   LeVoci Lauretta   Rubin Berish  

Human Genetics, Vol. 115, Iss. 3, 2004-08 ,pp. : 185-190

Springer Publishing Company

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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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Changes in cross-bridge cycling underlie muscle weakness in patients with tropomyosin 3-based myopathy

By Ottenheijm Coen A.C.   Lawlor Michael W.   Stienen Ger J.M.   Granzier Henk   Beggs Alan H.  

Human Molecular Genetics, Vol. 20, Iss. 10, 2011-05 ,pp. : 2015-2025

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

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

Oxford University Press

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