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...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en: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: American Thoracic Society 2016
Assuntos:
Original Article
Acceso en liña: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
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares