Are mast cells instrumental for fibrotic diseases?

Idiopathic pulmonary fibrosis (IPF) is a fatal lung disorder of unknown etiology characterised 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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Bibliographic Details
Main Authors: Catherine eOvered-Sayer (Author), Laura eRapley (Author), Tomas eMustelin (Author), Deborah Lee Clarke (Author)
Format: Book
Published: Frontiers Media S.A., 2014-01-01T00:00:00Z.
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3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available