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

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

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  

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

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

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Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb

By Kurapati Ramakrishna   McKenna Caoimhe   Lindqvist Johan   Williams Debbie   Simon Michelle   LeProust Emily   Baker Jane   Cheeseman Michael   Carroll Natalie   Denny Paul   Laval Steve   Lochmüller Hanns   Ochala Julien   Blanco Gonzalo  

Human Molecular Genetics, Vol. 21, Iss. 8, 2012-04 ,pp. : 1706-1724

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