Plasma Surfactant Protein-D, Matrix Metalloproteinase-7, and Osteopontin Index Distinguishes Idiopathic Pulmonary Fibrosis from Other Idiopathic Interstitial Pneumonias

Rationale: Idiopathic pulmonary fibrosis (IPF) is a progressive, fatal interstitial lung disease (ILD) characterized by abnormal extracellular matrix (ECM) remodeling. We hypothesized that ECM remodeling might result in a plasma profile of proteins specific for IPF that could distinguish patients wi...

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Xehetasun bibliografikoak
Argitaratua izan da:Am J Respir Crit Care Med
Egile Nagusiak: White, Eric S., Xia, Meng, Murray, Susan, Dyal, Rachel, Flaherty, Candace M., Flaherty, Kevin R., Moore, Bethany B., Cheng, Ling, Doyle, Tracy J., Villalba, Julian, Dellaripa, Paul F., Rosas, Ivan O., Kurtis, Jonathan D., Martinez, Fernando J.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Thoracic Society 2016
Gaiak:
Original Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5114439/
https://ncbi.nlm.nih.gov/pubmed/27149370
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201505-0862OC
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