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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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.  

Human Molecular Genetics, Vol. 7, Iss. 13, 1998-12 ,pp. : 2135-2140

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans

By Dobrowolski Radoslaw   Sasse Philipp   Schrickel Jan W.   Watkins Marcus   Kim Jung-Sun   Rackauskas Mindaugas   Troatz Clemens   Ghanem Alexander   Tiemann Klaus   Degen Joachim   Bukauskas Feliksas F.   Civitelli Roberto   Lewalter Thorsten   Fleischmann Bernd K.   Willecke Klaus  

Human Molecular Genetics, Vol. 17, Iss. 4, 2008-02 ,pp. : 539-554

Oxford University Press

Access to resources Recommend Favorite