Dr Aaron Holley argues that skeletal muscle — not just heart and lungs — is a key, often missed driver of activity ...

Myofibrillar myopathy type 6 (MFM6) is a rare genetic muscle disorder that leads to severe muscle weakness and a drastically ...

A. Fluorescent immunostaining of PDGFRα, showing mesenchymal progenitors, laminin surrounding skeletal muscle, and AR. Arrows indicate mesenchymal progenitors expressing AR, arrowheads indicate ...

A new research paper was published in Volume 18 of Aging-US on March 27, 2026, titled “ATF5 is required for the maintenance of mitochondrial homeostasis and skeletal muscle health during aging.” ...

The investigational cell therapy deramiocel slowed upper limb functional decline in boys and young men with Duchenne muscular ...

Myofibrillar myopathy type 6 (MFM6) is a rare genetic muscle disorder that leads to severe muscle weakness and a drastically shortened life expectancy due to a disruption in muscle protein regulation.

Here are the signs of muscle loss and what you can do to maintain your strength.

Satellos Bioscience Inc. has released promising preliminary data showing SAT-3247 can improve skeletal muscle function in a mouse model of facioscapulohumeral muscular dystrophy (FSHD).