Robert W. Grange

Dietary epicatechin promotes survival of obese diabetic mice and Drosophila melanogaster.

Fast-twitch skeletal muscles of dystrophic mouse pups are resistant to injury from acute mechanical stress.

Alterations in slow-twitch muscle phenotype in transgenic mice overexpressing the Ca2+ buffering protein parvalbumin.

Genistein activates the 3',5'-cyclic adenosine monophosphate signaling pathway in vascular endothelial cells and protects endothelial barrier function.

Adeno-associated virus-mediated microdystrophin expression protects young mdx muscle from contraction-induced injury.

Lumbar extensor fatigue and circumferential ankle pressure impair ankle joint motion sense.

Molecular and cellular contractile dysfunction of dystrophic muscle from young mice.

Increased extraocular muscle strength with direct injection of insulin-like growth factor-I.

Passive mechanical properties of maturing extensor digitorum longus are not affected by lack of dystrophin.

Recommendations to define exercise prescription for Duchenne muscular dystrophy.

Telomere shortening in diaphragm and tibialis anterior muscles of aged mdx mice.

A novel SNaPshot assay to detect the mdx mutation.

Endurance capacity in maturing mdx mice is markedly enhanced by combined voluntary wheel running and green tea extract.

Dysregulated intracellular signaling and inflammatory gene expression during initial disease onset in Duchenne muscular dystrophy.

The F-BAR protein CIP4 promotes GLUT4 endocytosis through bidirectional interactions with N-WASp and Dynamin-2.

Immune-mediated mechanisms potentially regulate the disease time-course of duchenne muscular dystrophy and provide targets for therapeutic intervention.

Green tea extract decreases muscle pathology and NF-kappaB immunostaining in regenerating muscle fibers of mdx mice.

Foxj3 transcriptionally activates Mef2c and regulates adult skeletal muscle fiber type identity.

Eccentric contractions induce rapid isometric torque drop in dystrophin-deficient dogs.

Golden retriever muscular dystrophy (GRMD): Developing and maintaining a colony and physiological functional measurements.

Exercise and Duchenne muscular dystrophy: toward evidence-based exercise prescription.

The passive mechanical properties of the extensor digitorum longus muscle are compromised in 2- to 20-mo-old mdx mice.

Myosin light-chain phosphorylation and potentiation of dynamic function in mouse fast muscle.

Concerted regulation of myofiber-specific gene expression and muscle performance by the transcriptional repressor Sox6.

Mice lacking microRNA 133a develop dynamin 2–dependent centronuclear myopathy.

Aging and physical mobility in group-housed Old World monkeys.

Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies.

The paradox of muscle hypertrophy in muscular dystrophy.

Nutrition strategies to improve physical capabilities in Duchenne muscular dystrophy.

Reply to head.

Chronic administration of a leupeptin-derived calpain inhibitor fails to ameliorate severe muscle pathology in a canine model of duchenne muscular dystrophy.

Exercise and Duchenne muscular dystrophy: where we have been and where we need to go.

Foxk1 promotes cell proliferation and represses myogenic differentiation by regulating Foxo4 and Mef2.

Muscle function in a canine model of X-linked myotubular myopathy.

Enzyme replacement therapy rescues weakness and improves muscle pathology in mice with X-linked myotubular myopathy.

Selenoprotein N deficiency in mice is associated with abnormal lung development.

Myosin phosphorylation and force potentiation in skeletal muscle: evidence from animal models.

Gene therapy prolongs survival and restores function in murine and canine models of myotubular myopathy.

Compared with that of MUFA, a high dietary intake of n-3 PUFA does not reduce the degree of pathology in mdx mice.

KLHL40 deficiency destabilizes thin filament proteins and promotes nemaline myopathy.