Duchenne muscular dystrophy (DMD), myotonic dystrophy type 1 (DM1), and spinal
muscular atrophy (SMA) are the most prevalent neuromuscular disorders (NMDs) in children …

Repeat expansion diseases are a group of neuromuscular and neurodegenerative
disorders characterized by expansions of several successive repeated DNA sequences …

Parkinson's disease (PD) is the second most common rapidly progressive
neurodegenerative disease and has serious health and socio-economic consequences …

Background: Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy in
adults. In DM1 patients, skeletal muscle is severely impaired, even atrophied and patients …

Mitochondria are energy factories that sustain life activities in the body, and their dysfunction
can cause various metabolic diseases that threaten human health. Mitophagy, an essential …

Mitochondria form a dynamic network within skeletal muscle. This network is not only
responsible for producing adenine triphosphate through oxidative phosphorylation, but also …

Over the past years, researchers increased awareness of the connection of muscle tissue to
the rest of the human body and of the possibilities to tweak the muscles' metabolism in order …

Динамика митохондриальных преобразований в клетке вызывает в последние годы
все больший интерес как представителей фундаментальной науки, так и …

La dystrophie myotonique de type I (DM1) est une maladie génétique responsable d'une
altération multi-systémique de l'épissage alternatif. En conséquence, de nombreuses voies …

Abstract Myotonic dystrophy type 1 (DM1) is the most prevalent form of adult-onset muscular
dystrophy and arises from a CTG trinucleotide repeat expansion mutation in the dystrophia …