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Dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient muscular dystrophy

BACKGROUND: MDC1A is a congenital neuromuscular disorder with developmentally complex and progressive pathologies that results from a deficiency in the protein laminin α(2). MDC1A is associated with a multitude of pathologies, including increased apoptosis, inflammation and fibrosis. In order to ass...

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Bibliografski detalji
Glavni autori: Mehuron, Thomas, Kumar, Ajay, Duarte, Lina, Yamauchi, Jenny, Accorsi, Anthony, Girgenrath, Mahasweta
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2014
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4114446/
https://ncbi.nlm.nih.gov/pubmed/25075272
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2044-5040-4-14
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