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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Public Library of Science 2013
Gaiak:
Research Article
Sarrera elektronikoa: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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