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Heterogeneity in fibroblast proliferation and survival in idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is the most common form of interstitial lung disease characterized by the persistence of activated myofibroblasts resulting in excessive deposition of extracellular matrix proteins and profound tissue remodeling. Myofibroblasts have been shown to arise from inters...

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Detalhes bibliográficos
Main Authors: Habiel, David M., Hogaboam, Cory
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3899580/
https://ncbi.nlm.nih.gov/pubmed/24478703
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2014.00002
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