Muscle Pathology & Wasting Archives

Evaluation of muscle function of the extensor digitorum longus muscle ex vivo and tibialis anterior muscle in situ in mice.

Effects of prednisolone on the dystrophin-associated proteins in the blood-brain barrier and skeletal muscle of dystrophic mdx mice.

Diaphragm and ventilatory dysfunction during cancer cachexia.

Diaphragm weakness in pulmonary arterial hypertension: role of sarcomeric dysfunction.

Skeletal muscle weakness caused by carrageenan-induced inflammation.

Diaphragm weakness in pulmonary arterial hypertension: role of sarcomeric dysfunction.

Isometric and eccentric force generation assessment of skeletal muscles isolated from murine models of muscular dystrophies.

Neuromuscular Electrical Stimulation as a Method to Maximize the Beneficial Effects of Muscle Stem Cells Transplanted into Dystrophic Skeletal Muscle.

Diaphragm muscle fiber weakness in pulmonary hypertension.

Sustained release of bone morphogenetic protein-4 in adult rabbit extraocular muscle results in decreased force and muscle size: potential for strabismus treatment.

Long-term supplementation with resveratrol alleviates oxidative stress but does not attenuate sarcopenia in aged mice.

Factors underlying the early limb muscle weakness in acute quadriplegic myopathy using an experimental ICU porcine model.

In vivo canine muscle function assay.

In vivo canine muscle function assay.

Physiological characterization of muscle strength with variable levels of dystrophin restoration in mdx mice following local antisense therapy.

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

Physiological characterization of muscle strength with variable levels of dystrophin restoration in mdx mice following local antisense therapy.

Skeletal muscle weakness caused by carrageenan-induced inflammation.

Single muscle fiber contractile properties in adults with muscular dystrophy treated with MYO‐029.

Modulation of Muscle Atrophy, Fatigue and MLC Phosphorylation by MuRF1 as Indicated by Hindlimb Suspension Studies on MuRF1-KO Mice.

Combination of myostatin pathway interference and dystrophin rescue enhances tetanic and specific force in dystrophic mdx mice.

Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping.

Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping.

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

Muscle fiber size and function in elderly humans: a longitudinal study.

Evaluation of muscle function of the extensor digitorum longus muscle ex vivo and tibialis anterior muscle in situ in mice.

Effects of prednisolone on the dystrophin-associated proteins in the blood-brain barrier and skeletal muscle of dystrophic mdx mice.

Diaphragm and ventilatory dysfunction during cancer cachexia.

Diaphragm weakness in pulmonary arterial hypertension: role of sarcomeric dysfunction.

Skeletal muscle weakness caused by carrageenan-induced inflammation.

Diaphragm weakness in pulmonary arterial hypertension: role of sarcomeric dysfunction.

Isometric and eccentric force generation assessment of skeletal muscles isolated from murine models of muscular dystrophies.

Neuromuscular Electrical Stimulation as a Method to Maximize the Beneficial Effects of Muscle Stem Cells Transplanted into Dystrophic Skeletal Muscle.

Diaphragm muscle fiber weakness in pulmonary hypertension.

Sustained release of bone morphogenetic protein-4 in adult rabbit extraocular muscle results in decreased force and muscle size: potential for strabismus treatment.

Long-term supplementation with resveratrol alleviates oxidative stress but does not attenuate sarcopenia in aged mice.

Factors underlying the early limb muscle weakness in acute quadriplegic myopathy using an experimental ICU porcine model.

In vivo canine muscle function assay.

In vivo canine muscle function assay.

Physiological characterization of muscle strength with variable levels of dystrophin restoration in mdx mice following local antisense therapy.

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

Physiological characterization of muscle strength with variable levels of dystrophin restoration in mdx mice following local antisense therapy.

Skeletal muscle weakness caused by carrageenan-induced inflammation.

Single muscle fiber contractile properties in adults with muscular dystrophy treated with MYO‐029.

Modulation of Muscle Atrophy, Fatigue and MLC Phosphorylation by MuRF1 as Indicated by Hindlimb Suspension Studies on MuRF1-KO Mice.

Combination of myostatin pathway interference and dystrophin rescue enhances tetanic and specific force in dystrophic mdx mice.

Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping.

Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping.

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

Muscle fiber size and function in elderly humans: a longitudinal study.

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