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Wharton's Jelly-Derived Mesenchymal Stem Cells Reduce Fibrosis in a Mouse Model of...
Preclinical characterization of antagomiR-218 as a potential treatment for myotonic...
Mouse Models of Muscle Fibrosis
A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion...
Nutritional intervention with cyanidin hinders the progression of muscular dystrophy
Functional rescue in a mouse model of congenital muscular dystrophy with megaconial...
Development of novel NEMO-binding domain mimetics for inhibiting IKK/NF-κB activation
Involvement of adiponectin in the pathogenesis of dystrophinopathy
Arginine butyrate: a therapeutic candidate for Duchenne muscular dystrophy.