Plasma Surfactant Protein-D, Matrix Metalloproteinase-7, and Osteopontin Index Distinguishes Idiopathic Pulmonary Fibrosis from Other Idiopathic Interstitial Pneumonias.
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MMP-7 is a predictive biomarker of disease progression in patients with idiopathic pulmonary fibrosisBaseline serum syndecan-4 predicts prognosis after the onset of acute exacerbation of idiopathic interstitial pneumoniaImpact of serum SP-A and SP-D levels on comparison and prognosis of idiopathic pulmonary fibrosis: A systematic review and meta-analysis.The diagnosis of idiopathic pulmonary fibrosis: current and future approaches.Increased Expression of CC16 in Patients with Idiopathic Pulmonary FibrosisiTRAQ-Based Proteomics Reveals Novel Biomarkers for Idiopathic Pulmonary Fibrosis.Serum Matrix Metalloproteinase-7, Respiratory Symptoms, and Mortality in Community-dwelling Adults: The Multi-Ethnic Study of Atherosclerosis.An Official American Thoracic Society Workshop Report: Use of Animal Models for the Preclinical Assessment of Potential Therapies for Pulmonary Fibrosis.Influences of innate immunity, autophagy, and fibroblast activation in the pathogenesis of lung fibrosis.Blood Biomarkers in Idiopathic Pulmonary Fibrosis.The MUC5B promoter polymorphism and telomere length in patients with chronic hypersensitivity pneumonitis: an observational cohort-control study.Pulmonary fibrosis, part I: epidemiology, pathogenesis, and diagnosis.Diagnosis of Idiopathic Pulmonary Fibrosis "Pragmatic Challenges in Clinical Practice"Usual Interstitial Pneumonia Can Be Detected in Transbronchial Biopsies Using Machine Learning.The role of periostin in lung fibrosis and airway remodeling.A Recombinant Fragment of Human Surfactant Protein D Suppresses Basophil Activation and T-Helper Type 2 and B-Cell Responses in Grass Pollen-induced Allergic Inflammation.Validation of the prognostic value of MMP-7 in idiopathic pulmonary fibrosis.An Official American Thoracic Society Workshop Report: Translational Research in Rare Respiratory Diseases.Delving Deep into the Proteome of Lung Fibrosis Brings Plasma Cells to the Surface.An ex vivo model to induce early fibrosis-like changes in human precision-cut lung slices.Update in Interstitial Lung Disease 2016.Surfactant Protein D in Respiratory and Non-Respiratory Diseases.Phosphodiesterase 4 inhibition reduces lung fibrosis following targeted type II alveolar epithelial cell injury.Idiopathic Pulmonary Fibrosis (IPF): An OverviewIdentification of MMP28 as a biomarker for the differential diagnosis of idiopathic pulmonary fibrosisPirfenidone in patients with unclassifiable progressive fibrosing interstitial lung disease: design of a double-blind, randomised, placebo-controlled phase II trial
P2860
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P2860
Plasma Surfactant Protein-D, Matrix Metalloproteinase-7, and Osteopontin Index Distinguishes Idiopathic Pulmonary Fibrosis from Other Idiopathic Interstitial Pneumonias.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Plasma Surfactant Protein-D, M ...... athic Interstitial Pneumonias.
@en
Plasma Surfactant Protein-D, M ...... athic Interstitial Pneumonias.
@nl
type
label
Plasma Surfactant Protein-D, M ...... athic Interstitial Pneumonias.
@en
Plasma Surfactant Protein-D, M ...... athic Interstitial Pneumonias.
@nl
prefLabel
Plasma Surfactant Protein-D, M ...... athic Interstitial Pneumonias.
@en
Plasma Surfactant Protein-D, M ...... athic Interstitial Pneumonias.
@nl
P2093
P2860
P50
P1476
Plasma Surfactant Protein-D, M ...... pathic Interstitial Pneumonias
@en
P2093
Candace M Flaherty
Fernando J Martinez
Ivan O Rosas
Jonathan D Kurtis
Julian Villalba
Kevin R Flaherty
Ling Cheng
Paul F Dellaripa
Rachel Dyal
P2860
P304
P356
10.1164/RCCM.201505-0862OC
P407
P577
2016-11-01T00:00:00Z