Cystic fibrosis transmembrane conductance regulator facilitates ATP release by stimulating a separate ATP release channel for autocrine control of cell volume regulation (Q31663553)

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English	Cystic fibrosis transmembrane conductance regulator facilitates ATP release by stimulating a separate ATP release channel for autocrine control of cell volume regulation	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

3 July 2017

Cystic fibrosis transmembrane conductance regulator facilitates ATP release by stimulating a separate ATP release channel for autocrine control of cell volume regulation (English)

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PubMed publication ID

3 July 2017

cystic fibrosis

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transmembrane protein

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author name string

Braunstein GM

1

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3 July 2017

Roman RM

2

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3 July 2017

Clancy JP

3

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3 July 2017

Kudlow BA

4

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3 July 2017

Taylor AL

5

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PubMed publication ID

3 July 2017

Shylonsky VG

6

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3 July 2017

Jovov B

7

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3 July 2017

Peter K

8

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3 July 2017

Jilling T

9

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3 July 2017

Ismailov II

10

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3 July 2017

Benos DJ

11

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3 July 2017

Schwiebert LM

12

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3 July 2017

Fitz JG

13

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3 July 2017

Schwiebert EM

14

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3 July 2017

language of work or name

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publication date

10 November 2000

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3 July 2017

number of pages

10

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based on heuristic

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Journal of Biological Chemistry

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3 July 2017

276

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3 July 2017

9

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3 July 2017

6621-6630

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3 July 2017

G protein-coupled receptors for ATP and other nucleotides: a new receptor family

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

P2X receptors: an emerging channel family

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

A new class of ligand-gated ion channel defined by P2X receptor for extracellular ATP

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Extracellular ATP: effects, sources and fate

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https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Autocrine signaling through ATP release represents a novel mechanism for cell volume regulation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Regulation of intracellular Ca(2+) by CFTR in Chinese hamster ovary cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Propagation of mechanically induced intercellular calcium waves via gap junctions and ATP receptors in rat liver epithelial cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Autocrine regulation of volume-sensitive anion channels in airway epithelial cells by adenosine

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https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

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https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Adenosine receptors on human airway epithelia and their relationship to chloride secretion

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

The multidrug resistance (mdr1) gene product functions as an ATP channel

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Cystic fibrosis transmembrane conductance regulator-associated ATP release is controlled by a chloride sensor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

CFTR Cl- channel and CFTR-associated ATP channel: distinct pores regulated by common gates.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Failure of the cystic fibrosis transmembrane conductance regulator to conduct ATP.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Cystic fibrosis transmembrane regulator-independent release of ATP. Its implications for the regulation of P2Y2 receptors in airway epithelia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Purified cystic fibrosis transmembrane conductance regulator (CFTR) does not function as an ATP channel

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

The ABC of channel regulation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Volume-regulated chloride channels associated with the human multidrug-resistance P-glycoprotein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Separation of drug transport and chloride channel functions of the human multidrug resistance P-glycoprotein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Cystic fibrosis and the salt controversy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

An Immortalized Cystic Fibrosis Tracheal Epithelial Cell Line Homozygous for the ΔF508 CFTR Mutation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

A transformed human epithelial cell line that retains tight junctions post crisis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

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.M005893200

21 January 2018

Generation of cAMP-Activated Chloride Currents by Expression of CFTR

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

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.M005893200

21 January 2018

Interaction between cystic fibrosis transmembrane conductance regulator and outwardly rectified chloride channels

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Hepatocellular ATP-binding cassette protein expression enhances ATP release and autocrine regulation of cell volume

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Impaired cell volume regulation in intestinal crypt epithelia of cystic fibrosis mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Characterization of the voltage-dependent properties of a volume-sensitive anion conductance

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Further evidence for multitopological localization of mammalian porin (VDAC) in the plasmalemma forming part of a chloride channel complex affected in cystic fibrosis and encephalomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M005893200

21 January 2018

Identifiers

10.1074/JBC.M005893200

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2017

ResearchGate publication ID

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