Background Duchenne muscular dystrophy (DMD) is a severe X-linked neuromuscular
childhood disorder that causes progressive muscle weakness and degeneration and results …

Duchenne muscular dystrophy (DMD) is a progressive disease caused by the loss of
function of the protein dystrophin. This protein contributes to the stabilisation of striated cells …

Asynchronous skeletal muscle degeneration/regeneration is a hallmark feature of Duchenne
muscular dystrophy (DMD); however, traditional-omics technologies that lack spatial context …

Dystrophin is a large protein serving as local scaffolding repetitively bridging cytoskeleton
and the outside of striated muscle cell. As such dystrophin is a critical brick primarily in …

Skeletal muscle regeneration relies on the reciprocal interaction between many types of
cells. Regenerative capacity may be altered in different disorders. In our study, we …

Duchenne muscular dystrophy (DMD) is an incurable disease caused by mutations in the X-
linked DMD gene that encodes a structural muscle protein, dystrophin. This, in turn, leads to …

Dysregulation of autophagy may contribute to the progression of various muscle diseases,
including Duchenne muscular dystrophy (DMD). Heme oxygenase-1 (HO-1, encoded by …

Although Duchenne muscular dystrophy (DMD) primarily affects muscle tissues, the
alterations to systemic metabolism manifested in DMD patients contribute to the severe …

Duchenne muscular dystrophy (DMD) is a devastating chromosome X-linked disease that
manifests predominantly in progressive skeletal muscle wasting and dysfunctions in the …

Abstract microRNA-378a (miR-378a) is one of the most highly expressed microRNAs in the
heart. However, its role in the human cardiac tissue has not been fully understood. It was …