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TRPC3, but not TRPC1, as a good therapeutic target for standalone or complementary treatment of DMD

Archive ouverte | Creisméas, Anna | CCSD

International audience. Background Duchenne muscular dystrophy (DMD) is an X-linked inherited disease caused by mutations in the gene encoding dystrophin that leads to a severe and ultimately life limiting muscle-wa...

Evaluation of the dystrophin carboxy-terminal domain for micro-dystrophin gene therapy in cardiac and skeletal muscles in the DMDmdx rat model

Archive ouverte | Bourdon, Audrey | CCSD

International audience. Duchenne muscular dystrophy (DMD) is a muscle wasting disorder caused by mutations in the gene encoding dystrophin. Gene therapy using micro-dystrophin (MD) transgenes and recombinant adeno-a...

Extensive characterisation of a new rat model of Duchenne muscular dystrophy.

Archive ouverte | Larcher, Thibaut | CCSD

Extensive characterisation of a new rat model of Duchenne muscular dystrophy.. Congress of the ESVP, ECVP and ESTP

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