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

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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Enzyme replacement therapy rescues weakness and improves muscle pathology in mice with X-linked myotubular myopathy

By Lawlor Michael W.   Armstrong Dustin   Viola Marissa G.   Widrick Jeffrey J.   Meng Hui   Grange Robert W.   Childers Martin K.   Hsu Cynthia P.   O'Callaghan Michael   Pierson Christopher R.   Buj-Bello Anna   Beggs Alan H.  

Human Molecular Genetics, Vol. 22, Iss. 8, 2013-04 ,pp. : 1525-1538

Oxford University Press

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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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Nuclear genetic control of mitochondrial translation in skeletal muscle revealed in patients with mitochondrial myopathy

By Sasarman F.   Karpati G.   Shoubridge E.A.  

Human Molecular Genetics, Vol. 11, Iss. 14, 2002-07 ,pp. : 1669-1681

Oxford University Press

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