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

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.

A protein long understood to drive inflammation by producing nitric oxide has a second, previously unknown role—it physically ...

Protein droplets serve important biological functions within cells, but in neurodegenerative diseases like Alzheimer's, these ...