Latest papers

Inhibition of Prostaglandin D Synthase Suppresses Muscular Necrosis

[Mesenchymal stem cells transplanted in mdx mice differentiate into myocytes and express dystrophin/utrophin].

Real-time monitoring of cell transplantation in mouse dystrophic muscles by a secreted alkaline phosphatase reporter gene

Octa-guanidine Morpholino Restores Dystrophin Expression in Cardiac and Skeletal Muscles and Ameliorates Pathology in Dystrophic mdx Mice

Dystrophins carrying spectrin-like repeats 16 and 17 anchor nNOS to the sarcolemma and enhance exercise performance in a mouse model of muscular dystrophy.

NO more muscle fatigue.

Cationic PMMA Nanoparticles Bind and Deliver Antisense Oligoribonucleotides Allowing Restoration of Dystrophin Expression in the mdx Mouse

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

Identification of three distinguishable phenotypes in golden retriever muscular dystrophy.

Can a Newer MR Contrast Agent Be Used to Monitor Disease Progression in Muscular Dystrophy?

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

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

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

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

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

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

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

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

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