Dystrophy Archives

Membrane Stabilization by Modified Steroid Offers a Potential Therapy for Muscular Dystrophy Due to Dysferlin Deficit

Xin-deficient mice display myopathy, impaired contractility, attenuated muscle repair and altered satellite cell functionality.

Osteoprotegerin Protects against Muscular Dystrophy.

Single muscle contractile measurements in vivo and in situ.

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

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

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

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

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

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

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.

In vivo canine muscle function assay.

In vivo canine muscle function assay.

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.

Membrane Stabilization by Modified Steroid Offers a Potential Therapy for Muscular Dystrophy Due to Dysferlin Deficit

Cellular rescue in a zebrafish model of congenital muscular dystrophy type 1A

Xin-deficient mice display myopathy, impaired contractility, attenuated muscle repair and altered satellite cell functionality.

Osteoprotegerin Protects against Muscular Dystrophy.

Single muscle contractile measurements in vivo and in situ.

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

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

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

Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions.

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

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

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.

In vivo canine muscle function assay.

In vivo canine muscle function assay.

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.

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