Login / Signup

Inhibition of myostatin improves muscle atrophy in oculopharyngeal muscular dystrophy (OPMD).

Pradeep HarishAlberto MalerbaNgoc Lu-NguyenLeysa ForrestOrnella CappellariFanny RothCapucine TrolletLinda PopplewellGeorge Dickson
Published in: Journal of cachexia, sarcopenia and muscle (2019)
Our study supports the clinical translation of such antibody-mediated inhibition of myostatin as a treatment of OPMD. This strategy has implications to be used as adjuvant therapies with gene therapy based approaches, or to stabilize the muscle prior to myoblast transplantation.
Keyphrases
  • muscular dystrophy
  • gene therapy
  • skeletal muscle
  • duchenne muscular dystrophy
  • early stage
  • cell therapy