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Heterogeneity of Fibroblasts and Myofibroblasts in Pulmonary Fibrosis

PURPOSE OF REVIEW: Idiopathic Pulmonary Fibrosis (IPF) is the most common form of interstitial lung diseases of unknown eathiopathogenesis, mean survival of 3-5 years and limited therapeutics. Characterized by a loss of alveolar type II epithelial cells and aberrant activation of stromal cells, cons...

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Detaylı Bibliyografya
Yayımlandı:Curr Pathobiol Rep
Asıl Yazarlar: Habiel, David M., Hogaboam, Cory M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2017
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5654579/
https://ncbi.nlm.nih.gov/pubmed/29082111
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40139-017-0134-x
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