(Q41083500)

26 September 2017

Function of the R domain in the cystic fibrosis transmembrane conductance regulator chloride channel (English)

1 reference

26 September 2017

transmembrane protein

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1 reference

Ma J

1

1 reference

26 September 2017

Zhao J

2

1 reference

26 September 2017

Drumm ML

3

1 reference

26 September 2017

Xie J

4

1 reference

26 September 2017

Davis PB

5

1 reference

26 September 2017

language of work or name

English

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publication date

1 October 1997

1 reference

Journal of Biological Chemistry

26 September 2017

1 reference

26 September 2017

272

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26 September 2017

28133-28141

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26 September 2017

44

1 reference

The ABC of channel regulation

26 September 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Functions of the cystic fibrosis transmembrane conductance regulator protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Nucleoside triphosphates are required to open the CFTR chloride channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

The two nucleotide-binding domains of cystic fibrosis transmembrane conductance regulator (CFTR) have distinct functions in controlling channel activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Regulation of the gating of cystic fibrosis transmembrane conductance regulator C1 channels by phosphorylation and ATP hydrolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Coupling of CFTR Cl- channel gating to an ATP hydrolysis cycle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Conformational states of CFTR associated with channel gating: the role ATP binding and hydrolysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Pyrophosphate stimulates wild-type and mutant cystic fibrosis transmembrane conductance regulator Cl- channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

AM-loading of fluorescent Ca2+ indicators into intact single fibers of frog muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Destruction of sodium conductance inactivation in squid axons perfused with pronase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Biophysical and molecular mechanisms of Shaker potassium channel inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

The amino-terminal portion of CFTR forms a regulated Cl- channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

A two-domain model for the R domain of the cystic fibrosis transmembrane conductance regulator based on sequence similarities

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

Regulation of CFTR channel gating

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.44.28133

21 January 2018

Identifiers

DOI

10.1074/JBC.272.44.28133

1 reference

26 September 2017

1 reference