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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Detalles Bibliográficos
Autores principales: Habiel, David M., Hogaboam, Cory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899580/
https://www.ncbi.nlm.nih.gov/pubmed/24478703
http://dx.doi.org/10.3389/fphar.2014.00002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899580/
https://www.ncbi.nlm.nih.gov/pubmed/24478703
http://dx.doi.org/10.3389/fphar.2014.00002

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