Cartilage Oligomeric Matrix Protein in Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is a progressive and life threatening disease with median survival of 2.5–3 years. The IPF lung is characterized by abnormal lung remodeling, epithelial cell hyperplasia, myofibroblast foci formation, and extracellular matrix deposition. Analysis of gene expressio...

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Detalhes bibliográficos
Main Authors: Vuga, Louis J., Milosevic, Jadranka, Pandit, Kusum, Ben-Yehudah, Ahmi, Chu, Yanxia, Richards, Thomas, Sciurba, Joshua, Myerburg, Michael, Zhang, Yingze, Parwani, Anil V., Gibson, Kevin F., Kaminski, Naftali
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3869779/
https://ncbi.nlm.nih.gov/pubmed/24376648
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0083120
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