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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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Detalles Bibliográficos
Autores principales:	Overed-Sayer, Catherine, Rapley, Laura, Mustelin, Tomas, Clarke, Deborah L.
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/PMC3896884/ https://www.ncbi.nlm.nih.gov/pubmed/24478701 http://dx.doi.org/10.3389/fphar.2013.00174

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