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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Bibliografische gegevens
Gepubliceerd in:Am J Respir Crit Care Med
Hoofdauteurs: 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.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Thoracic Society 2016
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Original Article
Online toegang: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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