Muscular dystrophy exerts significant and dramatic impacts on affected patients, including
progressive muscle wasting leading to lung and heart failure, and results in severely …

Duchenne muscular dystrophy (DMD) is a genetic progressive muscle-wasting disorder that
leads to rapid loss of mobility and premature death. The absence of functional dystrophin in …

Aims Type 1 diabetes mellitus (T1DM) has been linked to the occurrence of skeletal muscle
atrophy. Insulin monotherapy may lead to excessive blood glucose fluctuations. N …

Duchenne muscular dystrophy (DMD), the severest form of muscular dystrophy, is
characterized by progressive muscle weakness with fatal outcomes most often before the …

Non-communicable chronic diseases (NCDs) are most commonly characterized by age-
related loss of homeostasis and/or by cumulative exposures to environmental factors, which …

Sphingosine-1-phosphate lyase (SPL) resides at the endpoint of the sphingolipid metabolic
pathway, catalyzing the irreversible breakdown of sphingosine-1-phosphate. Depletion of …

Duchenne muscular dystrophy (DMD) is characterised by respiratory muscle injury,
inflammation, fibrosis and weakness, ultimately culminating in respiratory failure. The …

ABSTRACT Duchenne Muscular Dystrophy (DMD) is a severe issue in the field of
neuromuscular disorders, needing novel treatment strategies. Natural substances with …

The skeletal muscle is pivotal for conferring and regulating movement, posture, and body
heat. Within the muscle fibres, the sarcoplasmic reticulum-mitochondria interaction is …