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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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Bibliografiske detaljer
Main Authors: Habiel, David M., Hogaboam, Cory
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2014
Fag:
Online adgang: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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