Heme oxygenase and carbon monoxide protect from muscle dystrophy.

Mun Chun ChanOlivia ZieglerLaura LiuGlenn C RoweSaumya DasLeo E OtterbeinZoltan Arany

Published in: Skeletal muscle (2016)

These data identify HO-1 and CO as novel therapeutic agents for the treatment of DMD. Safety profiles and clinical testing of inhaled CO already exist, underscoring the translational potential of these observations.

Keyphrases

duchenne muscular dystrophy
cystic fibrosis
early onset
electronic health record
big data
human health
deep learning
pi k akt