Association between pulmonary function and sputum biomarkers in cystic fibrosis. - Wikidata - wikimedia - TriplyDB

Association between pulmonary function and sputum biomarkers in cystic fibrosis.

Association between pulmonary function and sputum biomarkers in cystic fibrosis.

http://www.wikidata.org/entity/Q37287157

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Antioxidant supplementation for lung disease in cystic fibrosis Antioxidant micronutrients for lung disease in cystic fibrosis Neutrophil elastase and matrix metalloproteinase 12 in cystic fibrosis lung disease Advancing clinical development pathways for new CFTR modulators in cystic fibrosis Cleavage of CXCR1 on neutrophils disables bacterial killing in cystic fibrosis lung disease Lung transplantation for cystic fibrosis Polymorphonuclear leukocytes restrict growth of Pseudomonas aeruginosa in the lungs of cystic fibrosis patients.Smartphone-Based pH Sensor for Home Monitoring of Pulmonary Exacerbations in Cystic Fibrosis.Release of cystic fibrosis airway inflammatory markers from Pseudomonas aeruginosa-stimulated human neutrophils involves NADPH oxidase-dependent extracellular DNA trap formation.Update in cystic fibrosis 2012.2-O, 3-O-desulfated heparin inhibits neutrophil elastase-induced HMGB-1 secretion and airway inflammation.Anti-PcrV antibody in cystic fibrosis: a novel approach targeting Pseudomonas aeruginosa airway infection.Year-to-year changes in lung function in individuals with cystic fibrosis.Acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with cystic fibrosis.Isolation and characterization of microparticles in sputum from cystic fibrosis patients Sputum biomarkers and the prediction of clinical outcomes in patients with cystic fibrosis.Lack of neutrophil elastase reduces inflammation, mucus hypersecretion, and emphysema, but not mucus obstruction, in mice with cystic fibrosis-like lung disease.Identification of neutrophil activation markers as novel surrogate markers of CF lung disease.IP-10 is a potential biomarker of cystic fibrosis acute pulmonary exacerbations The blood neutrophil to lymphocyte ratio correlates with clinical status in children with cystic fibrosis: a retrospective study FRET-based and other fluorescent proteinase probes.Using bacterial biomarkers to identify early indicators of cystic fibrosis pulmonary exacerbation onset Pharmacokinetics and tolerability of oral sildenafil in adults with cystic fibrosis lung disease The ferrous iron-responsive BqsRS two-component system activates genes that promote cationic stress tolerance.Potential of anti-inflammatory treatment for cystic fibrosis lung disease.Correlations of salivary biomarkers with clinical assessments in patients with cystic fibrosis.SerpinB1 in cystic fibrosis airway fluids: quantity, molecular form and mechanism of elastase inhibition.Metabolomic Evaluation of Neutrophilic Airway Inflammation in Cystic Fibrosis.Omics approaches in cystic fibrosis research: a focus on oxylipin profiling in airway secretions.Cystic fibrosis-adapted Pseudomonas aeruginosa quorum sensing lasR mutants cause hyperinflammatory responses.Transcription of Interleukin-8: How Altered Regulation Can Affect Cystic Fibrosis Lung Disease.Sputum biomarkers of inflammation and lung function decline in children with cystic fibrosis Exhaled breath condensate adenosine tracks lung function changes in cystic fibrosis.Advancing outcome measures for the new era of drug development in cystic fibrosis.Sputum biomarkers of inflammation in cystic fibrosis lung disease Proteases and cystic fibrosis.Update in cystic fibrosis 2007.Interleukin-17 Pathophysiology and Therapeutic Intervention in Cystic Fibrosis Lung Infection and Inflammation.Progress in cystic fibrosis and the CF Therapeutics Development Network Highlights of a workshop to discuss targeting inflammation in cystic fibrosis

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Association between pulmonary function and sputum biomarkers in cystic fibrosis.

http://www.wikidata.org/entity/Q37287157

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 18 January 2007

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Association between pulmonary function and sputum biomarkers in cystic fibrosis.

@en

Association between pulmonary function and sputum biomarkers in cystic fibrosis.

@nl

type

label

Association between pulmonary function and sputum biomarkers in cystic fibrosis.

@en

Association between pulmonary function and sputum biomarkers in cystic fibrosis.

@nl

prefLabel

Association between pulmonary function and sputum biomarkers in cystic fibrosis.

@en

Association between pulmonary function and sputum biomarkers in cystic fibrosis.

@nl

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RCCM.200609-1354OC

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American Journal of Respiratory and Critical Care Medicine

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Association between pulmonary function and sputum biomarkers in cystic fibrosis.

@en

P2093

Bonnie W Ramsey

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Frank J Accurso

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Jane L Burns

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Michael W Konstan

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Moira L Aitken

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Nicole Mayer-Hamblett

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Richard A Kronmal

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Scott D Sagel

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P2860

Risk Factors for Death of Patients with Cystic Fibrosis Awaiting Lung Transplantation

Sputum induction as a research tool for sampling the airways of subjects with cystic fibrosis

Predictive 5-year survivorship model of cystic fibrosis.

Gender differences in cystic fibrosis: Pseudomonas aeruginosa infection.

Changes in the normal maximal expiratory flow-volume curve with growth and aging.

The role of inflammation in the pathophysiology of CF lung disease.

Noninvasive biomarkers of airway inflammation in cystic fibrosis.

Pathophysiology and management of pulmonary infections in cystic fibrosis.

Outcome measures for clinical trials in cystic fibrosis. Summary of a Cystic Fibrosis Foundation consensus conference.

Effect of clarithromycin on airway obstruction and inflammatory markers in induced sputum in cystic fibrosis: a pilot study.

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10.1164/RCCM.200609-1354OC

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2007-01-18T00:00:00Z

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cystic fibrosis

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2720115

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