Duchenne muscular dystrophy (DMD) is a devastating and debilitating muscle degenerative
disease affecting 1 in every 3,500 male births worldwide. DMD is progressive and fatal; …

Abstract Duchenne Muscular Dystrophy (DMD) is an inherited genetic disorder
characterized by progressive degeneration of muscle tissue, leading to functional disability …

Somatic stem cell populations participate in the development and regeneration of their host
tissues. Skeletal muscle is capable of complete regeneration due to stem cells that reside in …

Mutations in the dystrophin gene cause an X‐linked genetic disorder: Duchenne muscular
dystrophy (DMD). Stem cell therapy is an attractive method to treat DMD because a small …

Muscular dystrophies are heritable and heterogeneous neuromuscular disorders
characterized by the primary wasting of skeletal muscle, usually caused by mutations in the …

Muscular dystrophies are heterogeneous neuromuscular disorders of inherited origin,
including Duchenne muscular dystrophy (DMD). Cell-based therapies were used to promote …

Duchenne muscular dystrophy (DMD) is a genetic disease characterised by skeletal muscle
degeneration and progressive muscle wasting, which is caused by loss-of-function …

Neuromuscular disorders encompass a heterogeneous group of conditions that impair the
function of muscles, motor neurons, peripheral nerves, and neuromuscular junctions. Being …

Duchenne muscular dystrophy (DMD) is caused by an out-of-frame mutation in the DMD
gene that results in the absence of a functional dystrophin protein, leading to a devastating …

Duchenne muscular dystrophy (DMD), the most common and most severe form of all
muscular dystrophies, leads to progressive muscle fiber necrosis, fibroblast proliferation …