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Agricola

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Dysferlin links excitation-contraction coupling to structure and maintenance of the cardiac transverse-axial tubule system.

• Authors : Hofhuis, Julia; Bersch, Kristina; Wagner, Stefan

Subjects: RESEARCH; MUSCLE contraction; ANIMAL experimentation

• Source: EP: Europace; Jul2020, Vol. 22 Issue 7, p1119-1131, 13p

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Dysferlin-deficiency has greater impact on function of slow muscles, compared with fast, in aged BLAJ mice

• Authors : Lloyd, Erin M.; Xu, Hongyang; Murphy, Robyn M.

• Source: PLoS ONE. April 10, 2019, Vol. 14 Issue 4, e0214908

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Distinct amino acid motifs carrying multiple positive charges regulate membrane targeting of dysferlin and MG53

• Authors : Zhou, Lu; Middel, Volker; Reischl, Markus

• Source: PLoS ONE. August 9, 2018, Vol. 13 Issue 8, e0202052

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The effects of concentric and eccentric training in murine models of dysferlin-associated muscular dystrophy.

• Authors : Begam, Morium; Roche, Renuka; Hass, Joshua J.

Subjects: MUSCULAR dystrophy; BIOLOGICAL models; RESEARCH

• Source: Muscle & Nerve; Sep2020, Vol. 62 Issue 3, p393-403, 11p

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Genetic ablation of complement C3 attenuates muscle pathology in dysferlin-deficient mice.

• Authors : Renzhi Han; Frett, Ellie M.; Levy, Jennifer R.

Subjects: GENETIC mutation; MUSCLE diseases; ERYTHROCYTE membranes

• Source: Journal of Clinical Investigation. Dec2010, Vol. 120 Issue 12, p4366-4374. 9p. 2 Color Photographs, 5 Graphs.

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Dysferlin-mediated membrane repair protects the heart from stress-induced left ventricular injury.

• Authors : Han, Renzhi; Bansal, Dimple; Miyake, Katsuya

Subjects: HEART cells; CARDIOMYOPATHIES; HEART ventricle diseases

• Source: Journal of Clinical Investigation. Jul2007, Vol. 117 Issue 7, p1805-1813. 9p. 4 Color Photographs, 1 Black and White Photograph, 2 Graphs.

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Catabasis Pharmaceuticals and the Jain Foundation Announce a Preclinical Research Collaboration to Study Edasalonexent in Dysferlinopathy

• Authors : Catabasis Pharmaceuticals, Inc.

• Source: Business Wire (English). 09/26/2019.

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Secreted acid sphingomyelinase as a potential gene therapy for limb girdle muscular dystrophy 2B.

• Authors : Bittel, Daniel C.; Sreetama, Sen Chandra; Chandra, Goutam

Subjects: GENE therapy; MUSCULAR dystrophy; SPHINGOMYELINASE

• Source: Journal of Clinical Investigation. Jan2022, Vol. 132 Issue 1, preceding p1-1. 15p.

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Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21.

• Authors : Martinez‐Thompson, Jennifer M.; Niu, Zhiyv; Tracy, Jennifer A.

Subjects: MUSCLE protein metabolism; COMPARATIVE studies; CREATINE kinase

• Source: Muscle & Nerve; Apr2018, Vol. 57 Issue 4, p679-683, 5p

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