CFTR Expression in human neutrophils and the phagolysosomal chlorination defect in cystic fibrosis. - Wikidata - awgldk - TriplyDB

CFTR Expression in human neutrophils and the phagolysosomal chlorination defect in cystic fibrosis.

CFTR Expression in human neutrophils and the phagolysosomal chlorination defect in cystic fibrosis.

http://www.wikidata.org/entity/Q38466689

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Epithelial Anion Transport as Modulator of Chemokine Signaling Key mechanisms governing resolution of lung inflammation Inhaled hypertonic saline for cystic fibrosis: Reviewing the potential evidence for modulation of neutrophil signalling and function MicroRNA Dysregulation in Cystic Fibrosis What really happens in the neutrophil phagosome?Neutrophil plasticity enables the development of pathological microenvironments: implications for cystic fibrosis airway disease Cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis: current perspectives Molecular physiology of bestrophins: multifunctional membrane proteins linked to best disease and other retinopathies Myeloperoxidase: a front-line defender against phagocytosed microorganisms Defective CFTR expression and function are detectable in blood monocytes: development of a new blood test for cystic fibrosis Voltage-gated proton channels: molecular biology, physiology, and pathophysiology of the H(V) family Influence of neutrophil defects on Burkholderia cepacia complex pathogenesis.Pseudomonas aeruginosa alginate promotes Burkholderia cenocepacia persistence in cystic fibrosis transmembrane conductance regulator knockout mice.Comparisons of resistance of CF and non-CF pathogens to hydrogen peroxide and hypochlorous acid oxidants in vitro Bacteraemia and fungaemia in cystic fibrosis patients with febrile pulmonary exacerbation: a prospective observational study.Lipoxin A4 and platelet activating factor are involved in E. coli or LPS-induced lung inflammation in CFTR-deficient mice.Proinflammatory phenotype and increased caveolin-1 in alveolar macrophages with silenced CFTR mRNA Comparative study of HOCl-inflicted damage to bacterial DNA ex vivo and within cells The cystic fibrosis transmembrane conductance regulator (CFTR) is expressed in maturation stage ameloblasts, odontoblasts and bone cells CFTR-mediated halide transport in phagosomes of human neutrophils.Harnessing Neutrophil Survival Mechanisms during Chronic Infection by Pseudomonas aeruginosa: Novel Therapeutic Targets to Dampen Inflammation in Cystic Fibrosis Dysfunctional CFTR alters the bactericidal activity of human macrophages against Pseudomonas aeruginosa.CFTR inhibition provokes an inflammatory response associated with an imbalance of the annexin A1 pathway.Neutrophil extracellular trap (NET)-mediated killing of Pseudomonas aeruginosa: evidence of acquired resistance within the CF airway, independent of CFTR.A neutrophil intrinsic impairment affecting Rab27a and degranulation in cystic fibrosis is corrected by CFTR potentiator therapy.Neutrophil-mediated phagocytic host defense defect in myeloid Cftr-inactivated mice.RNA interference against CFTR affects HL60-derived neutrophil microbicidal function.Myeloperoxidase in human neutrophil host defence.Impaired functions of macrophage from cystic fibrosis patients: CD11b, TLR-5 decrease and sCD14, inflammatory cytokines increase Abnormal trafficking and degradation of TLR4 underlie the elevated inflammatory response in cystic fibrosis.Critical modifier role of membrane-cystic fibrosis transmembrane conductance regulator-dependent ceramide signaling in lung injury and emphysema.Physiological impact of abnormal lipoxin A₄ production on cystic fibrosis airway epithelium and therapeutic potential.Cystic Fibrosis Gene Therapy in the UK and Elsewhere.Defective innate immunity and hyperinflammation in newborn cystic fibrosis transmembrane conductance regulator-knockout ferret lungs Neutrophils in cystic fibrosis display a distinct gene expression pattern Pro-resolving lipid mediator Resolvin D1 serves as a marker of lung disease in cystic fibrosis.Absence of the cystic fibrosis transmembrane regulator (Cftr) from myeloid-derived cells slows resolution of inflammation and infection.Salt, chloride, bleach, and innate host defense.Modulating Innate and Adaptive Immunity by (R)-Roscovitine: Potential Therapeutic Opportunity in Cystic Fibrosis.Reduced caveolin-1 promotes hyperinflammation due to abnormal heme oxygenase-1 localization in lipopolysaccharide-challenged macrophages with dysfunctional cystic fibrosis transmembrane conductance regulator.

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P2860

CFTR Expression in human neutrophils and the phagolysosomal chlorination defect in cystic fibrosis.

http://www.wikidata.org/entity/Q38466689

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2006 nî lūn-bûn

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CFTR Expression in human neutr ...... ion defect in cystic fibrosis.

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CFTR Expression in human neutr ...... ion defect in cystic fibrosis.

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CFTR Expression in human neutr ...... ion defect in cystic fibrosis.

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CFTR Expression in human neutr ...... ion defect in cystic fibrosis.

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Anand Viswanathan

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Connie Thompson

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Gisele Lombard

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Guangdi Wang

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Guoshun Wang

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Kevin Leidal

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Nicholas A Lanson

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Qiang Zhang

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Richard G Painter

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Vincent G Valentine

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P2860

Identification of the cystic fibrosis gene: chromosome walking and jumping

A component of innate immunity prevents bacterial biofilm development

Anion channels, including ClC-3, are required for normal neutrophil oxidative function, phagocytosis, and transendothelial migration

Biological reactivity of hypochlorous acid: implications for microbicidal mechanisms of leukocyte myeloperoxidase

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

The biochemical basis of phagocytosis. I. Metabolic changes during the ingestion of particles by polymorphonuclear leukocytes

Direct measurement of free chloride concentrations in the phagolysosomes of human neutrophils

Structure and function of the CFTR chloride channel

Myeloperoxidase: friend and foe

A comparison of 14 antibodies for the biochemical detection of the cystic fibrosis transmembrane conductance regulator protein.

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10.1021/BI060490T

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16922501

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cystic fibrosis

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2931333

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