Duchenne muscular dystrophy (DMD) is a rare hereditary disease that is associated with progressive muscle wasting. The ...

Utrophin increase in muscle cells after transcriptional adaptation normalises cell function in Duchenne muscular ...

The researchers noted that in DMD, dystrophin mutations not only disrupt the dystrophin protein that is made, the mutant gene that is transcribed (as mRNA) breaks apart into pieces that can then take ...

SAST and syntrophin were highly associated with purified microtubules and microtubule-associated proteins, whereas utrophin and dystrophin ... Figure 2: Expression of MAST205 and SAST in adult ...