CFTR activation in human bronchial epithelial cells by novel benzoflavone and benzimidazolone compounds. - Wikidata - awgldk - TriplyDB

CFTR activation in human bronchial epithelial cells by novel benzoflavone and benzimidazolone compounds.

CFTR activation in human bronchial epithelial cells by novel benzoflavone and benzimidazolone compounds.

http://www.wikidata.org/entity/Q42438647

about

Curcumin and genistein: the combined effects on disease-associated CFTR mutants and their clinical implications Rescue of the mutant CFTR chloride channel by pharmacological correctors and low temperature analyzed by gene expression profiling.Novel amino-carbonitrile-pyrazole identified in a small molecule screen activates wild-type and ΔF508 cystic fibrosis transmembrane conductance regulator in the absence of a cAMP agonist Regulatory domain phosphorylation to distinguish the mechanistic basis underlying acute CFTR modulators.Resveratrol ameliorates abnormalities of fluid and electrolyte secretion in a hypoxia-Induced model of acquired CFTR deficiency Pharmacological approaches to correcting the ion transport defect in cystic fibrosis.Endogenous protease activation of ENaC: effect of serine protease inhibition on ENaC single channel properties.Targeted therapy for cystic fibrosis: cystic fibrosis transmembrane conductance regulator mutation-specific pharmacologic strategies.Combating cystic fibrosis: in search for CF transmembrane conductance regulator (CFTR) modulators.CFTR potentiators partially restore channel function to A561E-CFTR, a cystic fibrosis mutant with a similar mechanism of dysfunction as F508del-CFTR Benzimidazolones enhance the function of epithelial Na⁺ transport.Influence of cell background on pharmacological rescue of mutant CFTR.4-Chloro-benzo[F]isoquinoline (CBIQ) activates CFTR chloride channels and KCNN4 potassium channels in Calu-3 human airway epithelial cells Mechanisms of anion secretion in Calu-3 human airway epithelial cells by 7,8-benzoquinoline Modulation of cystic fibrosis transmembrane conductance regulator (CFTR) activity and genistein binding by cytosolic pH.Stimulation of Wild-Type, F508del- and G551D-CFTR Chloride Channels by Non-Toxic Modified pyrrolo[2,3-b]pyrazine Derivatives.Curcumin and genistein additively potentiate G551D-CFTR.Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis.Bicarbonate-dependent chloride secretion in Calu-3 epithelia in response to 7,8-benzoquinoline.Molecular basis of cystic fibrosis: from bench to bedside

P2860

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P2860

CFTR activation in human bronchial epithelial cells by novel benzoflavone and benzimidazolone compounds.

http://www.wikidata.org/entity/Q42438647

description

2003 nî lūn-bûn

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2003年の論文

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2003年論文

@yue

2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

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2003年論文

@zh-tw

2003年论文

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2003年论文

@zh

2003年论文

@zh-cn

name

CFTR activation in human bronc ...... and benzimidazolone compounds.

@en

CFTR activation in human bronc ...... and benzimidazolone compounds.

@nl

type

label

CFTR activation in human bronc ...... and benzimidazolone compounds.

@en

CFTR activation in human bronc ...... and benzimidazolone compounds.

@nl

prefLabel

CFTR activation in human bronc ...... and benzimidazolone compounds.

@en

CFTR activation in human bronc ...... and benzimidazolone compounds.

@nl

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AJPLUNG.00351.2002

P1433

American Journal of Physiology - Lung Cellular and Molecular Physiology

P1476

CFTR activation in human bronc ...... and benzimidazolone compounds.

@en

P2093

A S Verkman

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

Chiara Folli

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

Emanuela Caci

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

Luis J V Galietta

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

Mark F Springsteel

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Mark J Kurth

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Michael H Nantz

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Olga Zegarra-Moran

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

Robert E Sammelson

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

Tonghui Ma

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P2860

Structure and function of the CFTR chloride channel

Novel CFTR chloride channel activators identified by screening of combinatorial libraries based on flavone and benzoquinolizinium lead compounds.

Molecular pharmacology of the CFTR Cl- channel.

Genetic risk factors for chronic obstructive pulmonary disease.

Pharmacotherapy of the ion transport defect in cystic fibrosis.

Correction of G551D-CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB-07.

Effects of low-chloride solutions on action potentials of sheep cardiac Purkinje fibers.

Functional roles of the nucleotide-binding folds in the activation of the cystic fibrosis transmembrane conductance regulator.

Development of substituted Benzo[c]quinolizinium compounds as novel activators of the cystic fibrosis chloride channel.

Modulation of CFTR chloride channels by calyculin A and genistein.

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