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Matrix metalloproteinase (MMP)-19-deficient fibroblasts display a profibrotic phenotype

Idiopathic pulmonary fibrosis (IPF) is a progressive and usually lethal interstitial lung disease of unknown etiology characterized by aberrant activation of epithelial cells that induce the migration, proliferation and activation of fibroblasts. The resulting distinctive fibroblastic/myofibroblasti...

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Detalhes bibliográficos
Publicado no:Am J Physiol Lung Cell Mol Physiol
Main Authors: Jara, Paul, Calyeca, Jazmin, Romero, Yair, Plácido, Luis, Yu, Guoying, Kaminski, Naftali, Maldonado, Vilma, Cisneros, José, Selman, Moisés, Pardo, Annie
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2015
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5243210/
https://ncbi.nlm.nih.gov/pubmed/25575513
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00043.2014
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