Modifier locus of the skeletal muscle involvement in Emery–Dreifuss muscular dystrophy

By Granger B.   Gueneau L.   Drouin-Garraud V.   Pedergnana V.   Gagnon F.   Ben Yaou R.   Tezenas du Montcel S.   Bonne G.  

Human Genetics, Vol. 129, Iss. 2, 2011-02 ,pp. : 149-159

Springer Publishing Company

Access to resources Recommend Favorite

Dominant-negative inhibition of Ca 2 influx via TRPV2 ameliorates muscular dystrophy in animal models

By Iwata Yuko   Katanosaka Yuki   Arai Yuji   Shigekawa Munekazu   Wakabayashi Shigeo  

Human Molecular Genetics, Vol. 18, Iss. 5, 2009-03 ,pp. : 824-834

Oxford University Press

Access to resources Recommend Favorite

Read-through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy

By Kayali Refik   Ku Jin-Mo   Khitrov Gregory   Jung Michael E.   Prikhodko Olga   Bertoni Carmen  

Human Molecular Genetics, Vol. 21, Iss. 18, 2012-09 ,pp. : 4007-4020

Oxford University Press

Access to resources Recommend Favorite

Myogenic Akt signaling attenuates muscular degeneration, promotes myofiber regeneration and improves muscle function in dystrophin-deficient mdx mice

By Kim Michelle H.   Kay Danielle I.   Rudra Renuka T.   Chen Bo Ming   Hsu Nigel   Izumiya Yasuhiro   Martinez Leonel   Spencer Melissa J.   Walsh Kenneth   Grinnell Alan D.   Crosbie Rachelle H.  

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1324-1338

Oxford University Press

Access to resources Recommend Favorite

Temporal gene expression profiling of dystrophin-deficient ( mdx ) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy

By Porter John D.  

Human Molecular Genetics, Vol. 13, Iss. 3, 2004-02 ,pp. : 257-269

Oxford University Press

Access to resources Recommend Favorite