Direct activation of cystic fibrosis transmembrane conductance regulator channels by 8-cyclopentyl-1,3-dipropylxanthine (CPX) and 1,3-diallyl-8-cyclohexylxanthine (DAX). (Q41052360)

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English	Direct activation of cystic fibrosis transmembrane conductance regulator channels by 8-cyclopentyl-1,3-dipropylxanthine (CPX) and 1,3-diallyl-8-cyclohexylxanthine (DAX).	scientific article

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scholarly article

1 reference

Europe PubMed Central

26 September 2017

Direct activation of cystic fibrosis transmembrane conductance regulator channels by 8-cyclopentyl-1,3-dipropylxanthine (CPX) and 1,3-diallyl-8-cyclohexylxanthine (DAX). (English)

1 reference

Europe PubMed Central

26 September 2017

cystic fibrosis

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transmembrane protein

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Kenneth A. Jacobson

3

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Europe PubMed Central

26 September 2017

author name string

N Arispe

1

1 reference

Europe PubMed Central

26 September 2017

J Ma

2

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Europe PubMed Central

26 September 2017

H B Pollard

4

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Europe PubMed Central

26 September 2017

language of work or name

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publication date

1 March 1998

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Europe PubMed Central

26 September 2017

number of pages

8

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based on heuristic

inferred from page(s)

Journal of Biological Chemistry

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Europe PubMed Central

26 September 2017

273

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Europe PubMed Central

26 September 2017

5727-5734

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Europe PubMed Central

26 September 2017

10

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Europe PubMed Central

26 September 2017

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Identification of the cystic fibrosis gene: genetic analysis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Generation of cAMP-Activated Chloride Currents by Expression of CFTR

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Cl- channels in CF: lack of activation by protein kinase C and cAMP-dependent protein kinase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Mutant (delta F508) cystic fibrosis transmembrane conductance regulator Cl- channel is functional when retained in endoplasmic reticulum of mammalian cells.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

A1 adenosine-receptor antagonists activate chloride efflux from cystic fibrosis cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

A1 receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine selectively activates chloride efflux from human epithelial and mouse fibroblast cell lines expressing the cystic fibrosis transmembrane regulator delta F508 mutation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Adenosine receptors: pharmacology, structure-activity relationships, and therapeutic potential

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Stimulation by alkylxanthines of chloride efflux in CFPAC-1 cells does not involve A1 adenosine receptors

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Intracellular loop between transmembrane segments IV and V of cystic fibrosis transmembrane conductance regulator is involved in regulation of chloride channel conductance state

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Human epithelial cystic fibrosis transmembrane conductance regulator without exon 5 maintains partial chloride channel function in intracellular membranes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Phosphorylation-dependent block of cystic fibrosis transmembrane conductance regulator chloride channel by exogenous R domain protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Slow conversions among subconductance states of cystic fibrosis transmembrane conductance regulator chloride channel

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Intrinsic anion channel activity of the recombinant first nucleotide binding fold domain of the cystic fibrosis transmembrane regulator protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Cystic fibrosis transmembrane conductance regulator activation stimulates endosome fusion in vivo

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Locating the anion-selectivity filter of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Cystic fibrosis transmembrane conductance regulator: the first nucleotide binding fold targets the membrane with retention of its ATP binding function.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

The nucleotide binding folds of the cystic fibrosis transmembrane conductance regulator are extracellularly accessible

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

ATP alters current fluctuations of cystic fibrosis transmembrane conductance regulator: evidence for a three-state activation mechanism

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Cyclic AMP-dependent protein kinase opens chloride channels in normal but not cystic fibrosis airway epithelium

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.10.5727

21 January 2018

Identifiers

10.1074/JBC.273.10.5727

1 reference

Europe PubMed Central

26 September 2017

1 reference

Europe PubMed Central

26 September 2017

ResearchGate publication ID

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