Hanmi Pharmaceutical announced on September 23 that it has scientifically elucidated the mechanism of action for a "novel ...

Patients aged 10-50 are being sought for a clinical trial testing SAR446268, a gene therapy for myotonic dystrophy type 1 ...

Humanin is a mitochondria‑derived micropeptide encoded within the mitochondrial 16S rRNA gene. This small peptide, ...

Type IIb fast-twitch myofibers, known for their rapid contraction speed, are plentiful in small mammals but have largely ...

Our understanding of the molecular pathogenesis of LAMA2 -related muscular dystrophy ( LAMA2 -MD) requires improving. Here, we report the phenotype, neuropathology, and transcriptomics data (scRNA-seq ...

Inherited metabolic diseases are rare monogenic conditions that disrupt biochemical pathways, affecting energy production and ...

A new role for extracellular matrix remodelling in Rheumatoid Arthritis (RA) pathology has been discovered. Dynamic collagen ...