Latest papers

Proteomic profiling of antisense-induced exon skipping reveals reversal of pathobiochemical abnormalities in dystrophic mdx diaphragm

Skeletal myogenesis by human primordial germ cell-derived progenitors.

Can a newer MR contrast agent be used to monitor disease progression in muscular dystrophy?

Overexpression of follistatin in human myoblasts increases their proliferation and differentiation, and improves the graft success in SCID mice.

Cell-penetrating peptide-conjugated antisense oligonucleotides restore systemic muscle and cardiac dystrophin expression and function.

Dysfunction of mitochondria and sarcoplasmic reticulum in the pathogenesis of collagen VI muscular dystrophies.

Abnormal cardiac morphology, function and energy metabolism in the dystrophic mdx mouse: an MRI and MRS study.

Dysferlin-deficient muscular dystrophy: gadofluorine M suitability at MR imaging in a mouse model.

Letter to the Editor: Overexpression of Myostatin2 in zebrafish reduces the expression of dystrophin associated protein complex(DAPC) which leads to muscle dystrophy.

Early mechanical dysfunction of the diaphragm in the muscular dystrophy with myositis (Ttnmdm) model.

Dystrophin knockdown mice suggest that early, transient dystrophin expression might be enough to prevent later pathology.

Gentamicin treatment in exercised mdx mice: Identification of dystrophin-sensitive pathways and evaluation of efficacy in work-loaded dystrophic muscle.

Ringo, a Golden Retriever Muscular Dystrophy (GRMD) dog with absent dystrophin but normal strength.

Prevention of muscle fibrosis and improvement in muscle performance in the mdx mouse by halofuginone.

Investigation of Debio 025, a cyclophilin inhibitor, in the dystrophic mdx mouse, a model for Duchenne muscular dystrophy.

Adaptive and nonadaptive responses to voluntary wheel running by mdx mice.

Cell therapies for muscular dystrophy.

Long-term survival of transplanted stem cells in immunocompetent mice with muscular dystrophy.

[Rupture of the ventral serrate muscles (Flying Scapulas) as a symptom of muscular dystrophy in Holstein-Friesian heifers on a Dutch dairy farm]

RNAi-mediated knockdown of dystrophin expression in adult mice does not lead to overt muscular dystrophy pathology.