Adult skeletal muscle is a tissue with a high capacity for regeneration due to the existence of stem cell population, termed ...
A potential way to treat muscular dystrophy directly targets muscle repair instead of the underlying genetic defect that usually leads to the disease, researchers say. Muscular dystrophies are a group ...
A single-dose gene replacement therapy is found to improve movement ability in children over 2 years of age and teenagers ...
For more than two decades, researchers at the University of Basel, Switzerland, have been investigating a severe form of ...
First patient with facioscapulohumeral muscular dystrophy (FSHD) dosed with Restem-L umbilical lining modified progenitor cells (UMPCs)− The ...
Registrational Expansion Cohort (REC) met primary endpoint, demonstrating statistically significant increase in dystrophin to 5.46% at 6 months ...
Capricor jumps after Phase 3 data show Deramiocel improves heart function and slows muscle decline in Duchenne muscular ...
Results that may be inaccessible to you are currently showing.
Hide inaccessible results
Feedback