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Increased Expression of CC16 in Patients with Idiopathic Pulmonary Fibrosis
Idiopathic pulmonary fibrosis (IPF) is a devastating disease of unknown etiology. The pathogenic mechanisms are unclear, but evidence indicates that aberrantly activated alveolar epithelial cells secrete a variety of mediators which induce the migration, proliferation and activation of fibroblasts a...
Hauptverfasser: | , , , , , , , , , , |
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Format: | Online Artikel Text |
Sprache: | English |
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Public Library of Science
2016
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Schlagworte: | |
Online Zugang: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5158056/ https://www.ncbi.nlm.nih.gov/pubmed/27977812 http://dx.doi.org/10.1371/journal.pone.0168552 |