Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid.
about
The sense of smell, its signalling pathways, and the dichotomy of cilia and microvilli in olfactory sensory cellsA C-terminal motif found in the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatory factor family of PDZ proteinsInnate lung defenses and compromised Pseudomonas aeruginosa clearance in the malnourished mouse model of respiratory infections in cystic fibrosisMolecular cloning and characterization of rat genes encoding homologues of human beta-defensinsRhesus monkey (Macaca mulatta) mucosal antimicrobial peptides are close homologues of human moleculesDrosophila as a model host for Pseudomonas aeruginosa infectionRoles of Pseudomonas aeruginosa las and rhl quorum-sensing systems in control of twitching motilityEffects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patientsAntimicrobial polypeptides in host defense of the respiratory tractHuman beta-defensin 2 is a salt-sensitive peptide antibiotic expressed in human lungA polymicrobial perspective of pulmonary infections exposes an enigmatic pathogen in cystic fibrosis patientsA novel host defense system of airways is defective in cystic fibrosisEngineering disulfide bridges to dissect antimicrobial and chemotactic activities of human beta-defensin 3The peptide antibiotic LL-37/hCAP-18 is expressed in epithelia of the human lung where it has broad antimicrobial activity at the airway surfaceThe lactoperoxidase system links anion transport to host defense in cystic fibrosisEpithelial antimicrobial peptides in host defense against infectionSafety assessment of inhaled xylitol in mice and healthy volunteersReduced interleukin-8 production by cystic fibrosis airway epithelial cellsMidkine in host defenceIntegrin α6β4 identifies human distal lung epithelial progenitor cells with potential as a cell-based therapy for cystic fibrosis lung diseaseGlucose depletion in the airway surface liquid is essential for sterility of the airwaysStructural Basis for Substrate Specificity in ArnB. A Key Enzyme in the Polymyxin Resistance Pathway of Gram-Negative BacteriaBeta-defensin expression in human mammary gland epitheliaRegulation of channel gating by AMP-activated protein kinase modulates cystic fibrosis transmembrane conductance regulator activity in lung submucosal cellsEpithelial antimicrobial peptides: review and significance for oral applicationsFunctional characterization of the peptide transporter PEPT2 in primary cultures of human upper airway epitheliumExpression of beta-defensin genes in bovine alveolar macrophages.Role of flagella in pathogenesis of Pseudomonas aeruginosa pulmonary infectionThe Pseudomonas aeruginosa flagellar cap protein, FliD, is responsible for mucin adhesionRoles of Pseudomonas aeruginosa las and rhl quorum-sensing systems in control of elastase and rhamnolipid biosynthesis genesDeletion of the ubiquitin ligase Nedd4L in lung epithelia causes cystic fibrosis-like diseasebeta-Defensin 1 contributes to pulmonary innate immunity in miceMicrobial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepaciaLung infections associated with cystic fibrosis.Influence of neutrophil defects on Burkholderia cepacia complex pathogenesis.Genes of non-typeable Haemophilus influenzae expressed during interaction with human epithelial cell lines.Osmotic water permeabilities of cultured, well-differentiated normal and cystic fibrosis airway epitheliaIdentification of virulence genes in a pathogenic strain of Pseudomonas aeruginosa by representational difference analysis.Mucin glycosylation and sulphation in airway epithelial cells is not influenced by cystic fibrosis transmembrane conductance regulator expression.Cystic fibrosis transmembrane conductance regulator facilitates ATP release by stimulating a separate ATP release channel for autocrine control of cell volume regulation.
P2860
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P2860
Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid.
description
1996 nî lūn-bûn
@nan
1996 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Cystic fibrosis airway epithel ...... abnormal airway surface fluid.
@ast
Cystic fibrosis airway epithel ...... abnormal airway surface fluid.
@en
Cystic fibrosis airway epithel ...... abnormal airway surface fluid.
@nl
type
label
Cystic fibrosis airway epithel ...... abnormal airway surface fluid.
@ast
Cystic fibrosis airway epithel ...... abnormal airway surface fluid.
@en
Cystic fibrosis airway epithel ...... abnormal airway surface fluid.
@nl
prefLabel
Cystic fibrosis airway epithel ...... abnormal airway surface fluid.
@ast
Cystic fibrosis airway epithel ...... abnormal airway surface fluid.
@en
Cystic fibrosis airway epithel ...... abnormal airway surface fluid.
@nl
P2093
P1433
P1476
Cystic fibrosis airway epithel ...... abnormal airway surface fluid
@en
P2093
P304
P356
10.1016/S0092-8674(00)81099-5
P407
P577
1996-04-01T00:00:00Z