Cytokine secretion by cystic fibrosis airway epithelial cells. - Wikidata - wikimedia - TriplyDB

Cytokine secretion by cystic fibrosis airway epithelial cells.

Cytokine secretion by cystic fibrosis airway epithelial cells.

http://www.wikidata.org/entity/Q44689957

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Mechanisms of the noxious inflammatory cycle in cystic fibrosis Airway epithelial cell tolerance to Pseudomonas aeruginosa.Relation of exaggerated cytokine responses of CF airway epithelial cells to PAO1 adherence Inhaled hypertonic saline for cystic fibrosis: Reviewing the potential evidence for modulation of neutrophil signalling and function Assessment of biological responses of EpiAirway 3-D cell constructs versus A549 cells for determining toxicity of ambient air pollution High-Dose Ibuprofen in Cystic Fibrosis.Disruption of interleukin-1β autocrine signaling rescues complex I activity and improves ROS levels in immortalized epithelial cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.Bergamot (Citrus bergamia Risso) fruit extracts and identified components alter expression of interleukin 8 gene in cystic fibrosis bronchial epithelial cell lines.Alveolar inflammation in cystic fibrosis.Loss of cystic fibrosis transmembrane conductance regulator function enhances activation of p38 and ERK MAPKs, increasing interleukin-6 synthesis in airway epithelial cells exposed to Pseudomonas aeruginosa Interaction with CREB binding protein modulates the activities of Nrf2 and NF-κB in cystic fibrosis airway epithelial cells.SERCA2 regulates non-CF and CF airway epithelial cell response to ozone Comparison of nasal and bronchial epithelial cells obtained from patients with COPD Normal CFTR inhibits epidermal growth factor receptor-dependent pro-inflammatory chemokine production in human airway epithelial cells.Elevated paracellular glucose flux across cystic fibrosis airway epithelial monolayers is an important factor for Pseudomonas aeruginosa growth Neutrophil cell death, activation and bacterial infection in cystic fibrosis.Inhibition of p38 mitogen activated protein kinase controls airway inflammation in cystic fibrosis Staphylococcus aureus Inhibits IL-8 Responses Induced by Pseudomonas aeruginosa in Airway Epithelial Cells.Cystic fibrosis-adapted Pseudomonas aeruginosa quorum sensing lasR mutants cause hyperinflammatory responses.Liquid hyper-absorption as a cause of increased DTPA clearance in the cystic fibrosis airway Low sphingosine-1-phosphate impairs lung dendritic cells in cystic fibrosis cAMP-mediated regulation of cholesterol accumulation in cystic fibrosis and Niemann-Pick type C cells Novel human bronchial epithelial cell lines for cystic fibrosis research.Implication of NADPH oxidases in the early inflammation process generated by cystic fibrosis cells.Immune responses in cystic fibrosis: are they intrinsically defective?Cystic Fibrosis from Laboratory to Bedside: The Role of A20 in NF-κB-Mediated Inflammation.Oxidative stress modulates the expression of genes involved in cell survival in ΔF508 cystic fibrosis airway epithelial cells.Inflammation and its genesis in cystic fibrosis.Ibuprofen regulation of microtubule dynamics in cystic fibrosis epithelial cells.Antibacterial and anti-inflammatory activity of a temporin B peptide analogue on an in vitro model of cystic fibrosis.Viruses in cystic fibrosis patients' airways.Does the F508-CFTR mutation induce a proinflammatory response in human airway epithelial cells?Effects of decoy molecules targeting NF-kappaB transcription factors in Cystic fibrosis IB3-1 cells: recruitment of NF-kappaB to the IL-8 gene promoter and transcription of the IL-8 gene.Reduced surface toll-like receptor-4 expression and absent interferon-γ-inducible protein-10 induction in cystic fibrosis airway cells.Down-regulation of cytokine-induced interleukin-8 requires inhibition of p38 mitogen-activated protein kinase (MAPK) via MAPK phosphatase 1-dependent and -independent mechanisms.Trimethylangelicin reduces IL-8 transcription and potentiates CFTR function.A disease-relevant high-content screening assay to identify anti-inflammatory compounds for use in cystic fibrosis.Impaired interleukin-8 chemokine secretion by staphylococcus aureus-activated epithelium and T-cell chemotaxis in cystic fibrosis.Corr4A and VRT325 do not reduce the inflammatory response to P. aeruginosa in human cystic fibrosis airway epithelial cells.Effects of cystic fibrosis transmembrane conductance regulator and DeltaF508CFTR on inflammatory response, ER stress, and Ca2+ of airway epithelia.

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P2860

Cytokine secretion by cystic fibrosis airway epithelial cells.

http://www.wikidata.org/entity/Q44689957

description

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2003年學術文章

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name

Cytokine secretion by cystic fibrosis airway epithelial cells.

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Cytokine secretion by cystic fibrosis airway epithelial cells.

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type

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Cytokine secretion by cystic fibrosis airway epithelial cells.

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Cytokine secretion by cystic fibrosis airway epithelial cells.

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prefLabel

Cytokine secretion by cystic fibrosis airway epithelial cells.

@en

Cytokine secretion by cystic fibrosis airway epithelial cells.

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RCCM.200207-765OC

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American Journal of Respiratory and Critical Care Medicine

P1476

Cytokine secretion by cystic fibrosis airway epithelial cells.

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P2093

Andrew J Hirsh

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Margrith W Verghese

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Mariam S Sauer

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Marianne S Muhlebach

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Marie N Becker

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Qi Wu

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Scott H Randell

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P2860

Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

Reduced interleukin-8 production by cystic fibrosis airway epithelial cells

Tlr4: central component of the sole mammalian LPS sensor.

Role of the cystic fibrosis transmembrane conductance regulator in innate immunity to Pseudomonas aeruginosa infections.

Selective up-regulation of chemokine IL-8 expression in cystic fibrosis bronchial gland cells in vivo and in vitro

Genistein inhibits constitutive and inducible NFkappaB activation and decreases IL-8 production by human cystic fibrosis bronchial gland cells.

Cystic fibrosis transmembrane conductance regulator does not affect neutrophil migration across cystic fibrosis airway epithelial monolayers

Complement receptor expression on neutrophils at an inflammatory site, the Pseudomonas-infected lung in cystic fibrosis.

Lower respiratory infection and inflammation in infants with newly diagnosed cystic fibrosis

Inflammation in cystic fibrosis airways: relationship to increased bacterial adherence.

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P921

cystic fibrosis