Laminin 111 prevents injury and loss of muscle function in DMD mice
posted on April 24, 2009 - 11:55am
A protein called laminin 111 had a marked therapeutic effect in mice that lack the dystrophin protein and have a muscle disease resembling human Duchenne muscular dystrophy (DMD), say researchers at the University of Nevada School of Medicine.
Recently published findings from two independent groups have suggested possible treatment pathways for the merosin-deficient and integrin-deficient forms of congenital muscular dystrophy (CMD).
Doxycycline fights cell death and lessens disease severity in merosin-deficient mice