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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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Библиографические подробности
Главные авторы: Habiel, David M., Hogaboam, Cory
Формат: Artigo
Язык:Inglês
Опубликовано: Frontiers Media S.A. 2014
Предметы:
Online-ссылка: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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