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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869779/
https://www.ncbi.nlm.nih.gov/pubmed/24376648
http://dx.doi.org/10.1371/journal.pone.0083120

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869779/
https://www.ncbi.nlm.nih.gov/pubmed/24376648
http://dx.doi.org/10.1371/journal.pone.0083120

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