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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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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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  

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Mouse model of muscleblind-like 1 overexpression: skeletal muscle effects and therapeutic promise

By Chamberlain Christopher M.   Ranum Laura P.W.  

Human Molecular Genetics, Vol. 21, Iss. 21, 2012-11 ,pp. : 4645-4654

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Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy

By Bonaldo P.   Braghetta P.   Zanetti M.   Piccolo S.   Volpin D.   Bressan G.M.  

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