1α,25(OH)(2)-Vitamin D3 Increases Dysferlin Expression in vitro and in a Human Clinical Trial

Dysferlinopathies are a heterogenous group of autosomal recessive inherited muscular dystrophies caused by mutations in DYSF gene. Dysferlin is expressed mainly in skeletal muscle and in monocytes and patients display a severe reduction or absence of protein in both tissues. Vitamin D3 promotes diff...

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Dettagli Bibliografici
Autori principali: Luna, Noemi De, Díaz-Manera, Jordi, Paradas, Carmen, Iturriaga, Cristina, Rojas-García, Ricardo, Araque, Josefa, Genebriera, Mireia, Gich, Ignasi, Illa, Isabel, Gallardo, Eduard
Natura: Artigo
Lingua:Inglês
Pubblicazione: Nature Publishing Group 2012
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Original Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3464637/
https://ncbi.nlm.nih.gov/pubmed/22910291
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mt.2012.156
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