Suggestions

Du même auteur

Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human.

Archive ouverte | Roux-Buisson, Nathalie | CCSD

International audience

Functional characterization of a Central Core Disease RyR1 mutation (p.Y4864H) associated with quantitative defect in RyR1 protein

Archive ouverte | Cacheux, Marine | CCSD

International audience. BACKGROUND: Central Core Disease (CCD) is a congenital myopathy often resulting from a mutation in RYR1 gene. Mutations in RyR1 can increase or decrease channel activity, or induce a reductio...

Deletion of the microtubule-associated protein 6 (MAP6) results in skeletal muscle dysfunction

Archive ouverte | Sébastien, Muriel | CCSD

International audience. Background : The skeletal muscle fiber has a specific and precise intracellular organization which is at the basis ofan efficient muscle contraction. Microtubules are long known to play a maj...

Chargement des enrichissements...