CFTR directly mediates nucleotide-regulated glutathione flux. - Wikidata - awgldk - TriplyDB

CFTR directly mediates nucleotide-regulated glutathione flux.

CFTR directly mediates nucleotide-regulated glutathione flux.

http://www.wikidata.org/entity/Q39756358

about

Mechanisms of the noxious inflammatory cycle in cystic fibrosis The ABC protein turned chloride channel whose failure causes cystic fibrosis ATP-binding cassette (ABC) transporters in normal and pathological lung MicroRNA Dysregulation in Cystic Fibrosis Oxidative stress and glutathione in TGF-beta-mediated fibrogenesis Cadmium-Induced Pathologies: Where Is the Oxidative Balance Lost (or Not)?Select cyclopentenone prostaglandins trigger glutathione efflux and the role of ABCG2 transport Peroxiredoxin 6 fails to limit phospholipid peroxidation in lung from Cftr-knockout mice subjected to oxidative challenge.Expression of cystic fibrosis transmembrane conductance regulator in paracervical ganglia.Glutathione transport is a unique function of the ATP-binding cassette protein ABCG2.Dysfunctional CFTR alters the bactericidal activity of human macrophages against Pseudomonas aeruginosa.Hypertonic saline increases lung epithelial lining fluid glutathione and thiocyanate: two protective CFTR-dependent thiols against oxidative injury.Listeria monocytogenes exploits cystic fibrosis transmembrane conductance regulator (CFTR) to escape the phagosome.Volume-sensitive anion channels mediate osmosensitive glutathione release from rat thymocytes.Protection against oxidative stress in beta thalassemia/hemoglobin E erythrocytes by inhibitors of glutathione efflux transporters.Variants in the glutamate-cysteine-ligase gene are associated with cystic fibrosis lung disease.Modeling the conformational changes underlying channel opening in CFTR Emerging drug treatments for cystic fibrosis.Lung inflammation as a therapeutic target in cystic fibrosis.A phase II study on safety and efficacy of high-dose N-acetylcysteine in patients with cystic fibrosis.Functional role of anion channels in cardiac diseases.Reversible silencing of CFTR chloride channels by glutathionylation.Voltage-dependent gating of the cystic fibrosis transmembrane conductance regulator Cl- channel.The role of glutathione in disulphide bond formation and endoplasmic-reticulum-generated oxidative stress.Cystic fibrosis: a mucosal immunodeficiency syndrome.Antioxidants in cystic fibrosis. Conclusions from the CF antioxidant workshop, Bethesda, Maryland, November 11-12, 2003.Mycoplasma pneumoniae infection and environmental tobacco smoke inhibit lung glutathione adaptive responses and increase oxidative stress Mitochondrial oxidative stress in the lungs of cystic fibrosis transmembrane conductance regulator protein mutant mice Role for cystic fibrosis transmembrane conductance regulator protein in a glutathione response to bronchopulmonary pseudomonas infection CLC-0 and CFTR: chloride channels evolved from transporters.CFTR activity and mitochondrial function.Expression of Cystic Fibrosis Transmembrane Conductance Regulator in Ganglia of Human Gastrointestinal Tract Reduced NHE3-mediated Na+ absorption increases survival and decreases the incidence of intestinal obstructions in cystic fibrosis mice Plasma membrane glutathione transporters and their roles in cell physiology and pathophysiology Characterization of the ATP-dependent sphingosine 1-phosphate transporter in rat erythrocytes Glutathione dysregulation and the etiology and progression of human diseases.Phenomics of cardiac chloride channels: the systematic study of chloride channel function in the heart.Expression and distribution of cystic fibrosis transmembrane conductance regulator in neurons of the human brain.Ion channels versus ion pumps: the principal difference, in principle.Cystic fibrosis-related diabetes: from CFTR dysfunction to oxidative stress.

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P2860

CFTR directly mediates nucleotide-regulated glutathione flux.

http://www.wikidata.org/entity/Q39756358

description

2003 nî lūn-bûn

@nan

2003年の論文

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2003年学术文章

@wuu

2003年学术文章

@zh-cn

2003年学术文章

@zh-hans

2003年学术文章

@zh-my

2003年学术文章

@zh-sg

2003年學術文章

@yue

2003年學術文章

@zh

2003年學術文章

@zh-hant

name

CFTR directly mediates nucleotide-regulated glutathione flux.

@en

CFTR directly mediates nucleotide-regulated glutathione flux.

@nl

type

label

CFTR directly mediates nucleotide-regulated glutathione flux.

@en

CFTR directly mediates nucleotide-regulated glutathione flux.

@nl

prefLabel

CFTR directly mediates nucleotide-regulated glutathione flux.

@en

CFTR directly mediates nucleotide-regulated glutathione flux.

@nl

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The EMBO Journal

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CFTR directly mediates nucleotide-regulated glutathione flux

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Canhui Li

http://www.w3.org/2001/XMLSchema#string

Christine E Bear

http://www.w3.org/2001/XMLSchema#string

Elaine M Leslie

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Ilana Kogan

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Jackie F Kidd

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Mohabir Ramjeesingh

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Yanchun Wang

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P2860

Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line

Repacking of the transmembrane domains of P-glycoprotein during the transport ATPase cycle

The E. coli BtuCD structure: a framework for ABC transporter architecture and mechanism

Walker mutations reveal loose relationship between catalytic and channel-gating activities of purified CFTR (cystic fibrosis transmembrane conductance regulator)

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

Organ distribution of multidrug resistance proteins 1, 2, and 3 (Mrp1, 2, and 3) mRNA and hepatic induction of Mrp3 by constitutive androstane receptor activators in rats

ClC-3B, a novel ClC-3 splicing variant that interacts with EBP50 and facilitates expression of CFTR-regulated ORCC

The ABC of channel regulation

Perturbation of the pore of the cystic fibrosis transmembrane conductance regulator (CFTR) inhibits its atpase activity.

A common mechanism for cystic fibrosis transmembrane conductance regulator protein activation by genistein and benzimidazolone analogs.

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12727866

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