Sputum biomarkers of inflammation and lung function decline in children with cystic fibrosis
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Neutrophil elastase and matrix metalloproteinase 12 in cystic fibrosis lung diseaseIdentification of OprF as a complement component C3 binding acceptor molecule on the surface of Pseudomonas aeruginosaRelease of cystic fibrosis airway inflammatory markers from Pseudomonas aeruginosa-stimulated human neutrophils involves NADPH oxidase-dependent extracellular DNA trap formation.Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infection.Update in cystic fibrosis 2012.2-O, 3-O-desulfated heparin inhibits neutrophil elastase-induced HMGB-1 secretion and airway inflammation.Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.Anti-PcrV antibody in cystic fibrosis: a novel approach targeting Pseudomonas aeruginosa airway infection.Lack of neutrophil elastase reduces inflammation, mucus hypersecretion, and emphysema, but not mucus obstruction, in mice with cystic fibrosis-like lung disease.miR-31 dysregulation in cystic fibrosis airways contributes to increased pulmonary cathepsin S production.Clinical mechanism of the cystic fibrosis transmembrane conductance regulator potentiator ivacaftor in G551D-mediated cystic fibrosisIdentification of neutrophil activation markers as novel surrogate markers of CF lung disease.IP-10 is a potential biomarker of cystic fibrosis acute pulmonary exacerbationsAirway, but not serum or urinary, levels of YKL-40 reflect inflammation in early cystic fibrosis lung disease.Assessment of airway microbiota and inflammation in cystic fibrosis using multiple sampling methodsPharmacokinetics and tolerability of oral sildenafil in adults with cystic fibrosis lung diseaseSputum club cell protein concentration is associated with pulmonary exacerbation in cystic fibrosisCholesteryl esters are elevated in the lipid fraction of bronchoalveolar lavage fluid collected from pediatric cystic fibrosis patients.Mature cystic fibrosis airway neutrophils suppress T cell function: evidence for a role of arginase 1 but not programmed death-ligand 1.Hypoxic epithelial necrosis triggers neutrophilic inflammation via IL-1 receptor signaling in cystic fibrosis lung disease.Metabolomics analysis identifies novel plasma biomarkers of cystic fibrosis pulmonary exacerbation.Correlations of salivary biomarkers with clinical assessments in patients with cystic fibrosis.Sputum induction improves detection of pathogens in children with cystic fibrosis.Complement Effectors of Inflammation in Cystic Fibrosis Lung Fluid Correlate with Clinical Measures of DiseaseCystic fibrosis-adapted Pseudomonas aeruginosa quorum sensing lasR mutants cause hyperinflammatory responses.Complement effectors, C5a and C3a, in cystic fibrosis lung fluid correlate with disease severity.Transforming growth factor β1 genotypes in relation to TGFβ1, interleukin-8, and tumor necrosis factor alpha in induced sputum and blood in cystic fibrosis.Automated CT scan scores of bronchiectasis and air trapping in cystic fibrosisRole of IRE1α/XBP-1 in Cystic Fibrosis Airway Inflammation.Phase I Studies of Acebilustat: Biomarker Response and Safety in Patients with Cystic Fibrosis.Interactions between Neutrophils and Pseudomonas aeruginosa in Cystic Fibrosis.Defining severity in non-cystic fibrosis bronchiectasis.Novel outcome measures for clinical trials in cystic fibrosisA survey of state-of-the-art surface chemistries to minimize fouling from human and animal biofluids.Clinically Promising Biomarkers in Cystic Fibrosis Pulmonary Exacerbations.Biomarkers for cystic fibrosis drug development.Neutrophil Elastase Activity Is Associated with Exacerbations and Lung Function Decline in Bronchiectasis.Cystic Fibrosis: Microbiology and Host ResponseAirway mucus, inflammation and remodeling: emerging links in the pathogenesis of chronic lung diseases.Immunomodulatory indications of azithromycin in respiratory disease: a concise review for the clinician.
P2860
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P2860
Sputum biomarkers of inflammation and lung function decline in children with cystic fibrosis
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Sputum biomarkers of inflammat ...... children with cystic fibrosis
@ast
Sputum biomarkers of inflammat ...... children with cystic fibrosis
@en
type
label
Sputum biomarkers of inflammat ...... children with cystic fibrosis
@ast
Sputum biomarkers of inflammat ...... children with cystic fibrosis
@en
prefLabel
Sputum biomarkers of inflammat ...... children with cystic fibrosis
@ast
Sputum biomarkers of inflammat ...... children with cystic fibrosis
@en
P2093
P2860
P921
P1476
Sputum biomarkers of inflammat ...... children with cystic fibrosis
@en
P2093
Margaret M Anthony
Peggy Emmett
Scott D Sagel
P2860
P304
P356
10.1164/RCCM.201203-0507OC
P407
P577
2012-08-16T00:00:00Z