Duchenne muscular dystrophy (DMD) is a severe, progressive, muscle-wasting disease,
characterized by progressive deterioration of skeletal muscle that causes rapid loss of …

Skeletal muscle regeneration is a complex process involving the generation of new
myofibers after trauma, competitive physical activity, or disease. In this context, adult skeletal …

Skeletal muscle disorders are mostly genetic and include several rare diseases. With
disease progression, muscle fibrosis and adiposis occur, resulting in limited mobility. The …

Duchenne muscular dystrophy (DMD), caused by mutations in the dystrophin (DMD) gene,
is associated with fatal muscle degeneration and atrophy. Patients with DMD have …

Duchenne muscular dystrophy (DMD) is caused by the lack of dystrophin, a cytoskeletal
protein essential for the preservation of the structural integrity of the muscle cell membrane …

The absence of dystrophin hypersensitizes skeletal muscle of lower and higher vertebrates
to eccentric contraction (ECC)-induced strength loss. Loss of strength can be accompanied …

ABSTRACT Spinocerebellar ataxia type 1 (SCA1) is a fatal neurodegenerative disease
caused by an expanded polyglutamine tract in the widely expressed ATXN1 protein. To …

Duchenne muscular dystrophy (DMD) is a severe muscular disorder caused by mutations in
the dystrophin gene. It leads to respiratory and cardiac failure and premature death at a …

FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-
amino-3-phenylpropanoyl] amino]-3-phenylpropanoyl] amino]-4-methylpentanoyl] amino] …

First worldwide family litigation filed litigation Critical https://patents. darts-ip. com/? family=
58503696&utm_source= google_patent&utm_medium= platform_link&utm_campaign …