Dysferlin function in skeletal muscle: Possible pathological mechanisms and therapeutical targets in dysferlinopathies-Reference-Cited by-同舟云学术

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Dysferlin function in skeletal muscle: Possible pathological mechanisms and therapeutical targets in dysferlinopathies

Published:2016-09 Issue: Volume:283 Page:246-254
ISSN:0014-4886
Container-title:Experimental Neurology
language:en
Short-container-title:Experimental Neurology

Author:

Cárdenas Ana M.,González-Jamett Arlek M.,Cea Luis A.,Bevilacqua Jorge A.,Caviedes Pablo

Funder

CONICYT

FONDECYT

PAI/Conicyt Proyecto de Inserción en la Academia

ICM-ECONOMIA

Publisher

Elsevier BV

Subject

Developmental Neuroscience,Neurology

Reference146 articles.

1. Quantitation of the calcium and membrane binding properties of the C2 domains of dysferlin;Abdullah;Biophys. J.,2014

2. Intracellular localization of dysferlin and its association with the dihydropyridine receptor;Ampong;Acta Myol.,2005

3. Dysferlin is a plasma membrane protein and is expressed early in human development;Anderson;Hum. Mol. Genet.,1999

4. Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy;Aoki;Neurology,2001

5. Expression of connexins during differentiation and regeneration of skeletal muscle: functional relevance of connexin43;Araya;J. Cell Sci.,2005

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1. Secondary mitochondrial dysfunction across the spectrum of hereditary and acquired muscle disorders;Mitochondrion;2024-09

2. Pilot investigations into the mechanistic basis for adverse effects of glucocorticoids in dysferlinopathy;Skeletal Muscle;2024-08-09

3. Changes in the pathomorphological condition of the myocardium in dysferlinopathy mice (Bla/J type);Morphology;2024-05-27

4. On the role of dysferlin in striated muscle: membrane repair, t‐tubules and Ca²⁺ handling;The Journal of Physiology;2024-04-14

5. A novel homozygous variant (c.5876T > C: p. Leu1959Pro) in DYSF segregates with limb-girdle muscular dystrophy: a case report;BMC Musculoskeletal Disorders;2024-03-27

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