Duchenne muscular dystrophy (DMD) leads to disability and death in young men. This
disease is caused by mutations in the DMD gene encoding diverse isoforms of dystrophin …

The systematic bioanalytical characterization of the protein product of the DMD gene, which
is defective in the pediatric disorder Duchenne muscular dystrophy, led to the discovery of …

Acute exercise and chronic exercise training elicit beneficial whole‐body changes in
physiology that ultimately depend on profound alterations to the dynamics of tissue‐specific …

Voluntary striated muscles are characterized by a highly complex and dynamic proteome
that efficiently adapts to changed physiological demands or alters considerably during …

Duchenne muscular dystrophy is an inherited disorder of early childhood that affects
multiple systems in the body. Besides late-onset cardio-respiratory syndrome and various …

The highly progressive neuromuscular disorder dystrophinopathy is triggered by primary
abnormalities in the Dmd gene, which causes cytoskeletal instability and loss of …

Introduction: Progressive skeletal muscle wasting is the manifesting symptom of Duchenne
muscular dystrophy, an X-linked inherited disorder triggered by primary abnormalities in the …

The X‐linked inherited neuromuscular disorder Duchenne muscular dystrophy is
characterised by primary abnormalities in the membrane cytoskeletal component dystrophin …

Duchenne muscular dystrophy is a highly progressive muscle wasting disease with a
complex pathophysiology that is based on primary abnormalities in the dystrophin gene. In …

Dystrophinopathies are multi-system disorders that affect the skeletal musculature, the
cardio-respiratory system and the central nervous system. The systematic screening of …