Role of the cystic fibrosis transmembrane conductance regulator in innate immunity to Pseudomonas aeruginosa infections.
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Binding of protegrin-1 to Pseudomonas aeruginosa and Burkholderia cepacia.Evidence that WbpD is an N-acetyltransferase belonging to the hexapeptide acyltransferase superfamily and an important protein for O-antigen biosynthesis in Pseudomonas aeruginosa PAO1Second-hand cigarette smoke impairs bacterial phagocytosis in macrophages by modulating CFTR dependent lipid-raftsDysfunctional CFTR alters the bactericidal activity of human macrophages against Pseudomonas aeruginosa.Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung.Can a place of origin of the main cystic fibrosis mutations be identified?Pseudomonas aeruginosa acquires biofilm-like properties within airway epithelial cellsTowards a physiology of epithelial pathogens.Impaired functions of macrophage from cystic fibrosis patients: CD11b, TLR-5 decrease and sCD14, inflammatory cytokines increaseMyeloperoxidase promoter polymorphism -463G is associated with more severe clinical expression of cystic fibrosis pulmonary disease.Pseudomonas aeruginosa in cystic fibrosis patients with G551D-CFTR treated with ivacaftor.Cholesteryl esters are elevated in the lipid fraction of bronchoalveolar lavage fluid collected from pediatric cystic fibrosis patients.A genome-wide approach to identify genetic loci with a signature of natural selection in the Irish population.A haplotype framework for cystic fibrosis mutations in IranDefective innate immunity and hyperinflammation in newborn cystic fibrosis transmembrane conductance regulator-knockout ferret lungsPseudomonas aeruginosa pili and flagella mediate distinct binding and signaling events at the apical and basolateral surface of airway epithelium.First encounter: how pathogens compromise epithelial transport.Non-typeable Haemophilus influenzae invasion and persistence in the human respiratory tract.Partial Restoration of CFTR Function in cftr-Null Mice following Targeted Cell Replacement Therapy.Resistance of Porphyromonas gingivalis ATCC 33277 to direct killing by antimicrobial peptides is protease independentCystic fibrosis and other respiratory diseases of impaired mucus clearance.Cystic fibrosis transmembrane conductance regulator and caveolin-1 regulate epithelial cell internalization of Pseudomonas aeruginosa.Role of IRE1α/XBP-1 in Cystic Fibrosis Airway Inflammation.CFTR is required for cellular entry and internalization of Chlamydia trachomatis.Host mucin glycosylation plays a role in bacterial adhesion in lungs of individuals with cystic fibrosis.Binding of the non-typeable Haemophilus influenzae lipooligosaccharide to the PAF receptor initiates host cell signalling.Clinical approach to the diagnosis and treatment of cystic fibrosis and CFTR-related disorders.Elevated Mirc1/Mir17-92 cluster expression negatively regulates autophagy and CFTR (cystic fibrosis transmembrane conductance regulator) function in CF macrophages.P-113D, an antimicrobial peptide active against Pseudomonas aeruginosa, retains activity in the presence of sputum from cystic fibrosis patients.N-glycosylation augmentation of the cystic fibrosis epithelium improves Pseudomonas aeruginosa clearance.Staphylococcus aureus escapes more efficiently from the phagosome of a cystic fibrosis bronchial epithelial cell line than from its normal counterpart.Defective activation of c-Src in cystic fibrosis airway epithelial cells results in loss of tumor necrosis factor-alpha-induced gap junction regulation.Multidrug efflux systems play an important role in the invasiveness of Pseudomonas aeruginosa.Diagnostic and prognostic value of serum antibodies against Pseudomonas aeruginosa in cystic fibrosis.Abnormalities in the pulmonary innate immune system in cystic fibrosisCystic fibrosis transmembrane conductance regulator and pseudomonas.Innate defense evicts bacterial squatters.Cytokine secretion by cystic fibrosis airway epithelial cells.G551D CF mice display an abnormal host response and have impaired clearance of Pseudomonas lung disease.Pseudomonas aeruginosa pyocyanin inactivates lung epithelial vacuolar ATPase-dependent cystic fibrosis transmembrane conductance regulator expression and localization.
P2860
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P2860
Role of the cystic fibrosis transmembrane conductance regulator in innate immunity to Pseudomonas aeruginosa infections.
description
2000 nî lūn-bûn
@nan
2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Role of the cystic fibrosis tr ...... domonas aeruginosa infections.
@ast
Role of the cystic fibrosis tr ...... domonas aeruginosa infections.
@en
type
label
Role of the cystic fibrosis tr ...... domonas aeruginosa infections.
@ast
Role of the cystic fibrosis tr ...... domonas aeruginosa infections.
@en
prefLabel
Role of the cystic fibrosis tr ...... domonas aeruginosa infections.
@ast
Role of the cystic fibrosis tr ...... domonas aeruginosa infections.
@en
P2860
P921
P356
P1476
Role of the cystic fibrosis tr ...... domonas aeruginosa infections.
@en
P2093
P2860
P304
P356
10.1073/PNAS.97.16.8822
P407
P577
2000-08-01T00:00:00Z