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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Detalhes bibliográficos
Publicado no:Am J Respir Crit Care Med
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2016
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Original Article
Acesso em linha: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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