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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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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | 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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