Are mast cells instrumental for fibrotic diseases?

Idiopathic pulmonary fibrosis (IPF) is a fatal lung disorder of unknown etiology characterized by accumulation of lung fibroblasts and extracellular matrix deposition, ultimately leading to compromised tissue architecture and lung function capacity. IPF has a heterogeneous clinical course; however t...

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Bibliografske podrobnosti
Main Authors: Overed-Sayer, Catherine, Rapley, Laura, Mustelin, Tomas, Clarke, Deborah L.
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2014
Teme:
Pharmacology
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3896884/
https://ncbi.nlm.nih.gov/pubmed/24478701
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2013.00174
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