Researchers at the University of Basel have developed a gene therapy that could potentially treat a rare and currently fatal ...
Researchers at the University of Basel have developed a gene therapy that could potentially treat a rare and currently fatal muscle disease in ...
Dual AAV gene therapy using laminin-linking proteins ameliorates muscle and nerve defects in LAMA2-related muscular dystrophy Molecular Therapy (2026), doi: 10.1016/j.ymthe.2026.01.041 ...
A UCLA study in mice reveals that aging muscle stem cells accumulate a protein that slows repair but boosts survival. This ...
Muscle loss (atrophy) due to inactivity is common after illness, injury, hospitalization or falls, and becomes increasingly ...