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Laminin α2 Chain-Deficiency is Associated with microRNA Deregulation in Skeletal Muscle and Plasma

microRNAs (miRNAs) are widespread regulators of gene expression, but little is known of their potential roles in congenital muscular dystrophy type 1A (MDC1A). MDC1A is a severe form of muscular dystrophy caused by mutations in the gene encoding laminin α2 chain. To gain insight into the pathophysio...

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Detalhes bibliográficos
Main Authors: Holmberg, Johan, Alajbegovic, Azra, Gawlik, Kinga Izabela, Elowsson, Linda, Durbeej, Madeleine
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4080261/
https://ncbi.nlm.nih.gov/pubmed/25071564
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnagi.2014.00155
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