(Q34040994)

30 July 2017

title

Rectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations (English)

1 reference

30 July 2017

0 references

transmembrane protein

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author name string

J Zhao

1

1 reference

30 July 2017

B Zerhusen

2

1 reference

30 July 2017

J Xie

3

1 reference

30 July 2017

M L Drumm

4

1 reference

30 July 2017

P B Davis

5

1 reference

30 July 2017

J Ma

6

1 reference

30 July 2017

language of work or name

English

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publication date

1 November 1996

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30 July 2017

number of pages

9

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based on heuristic

inferred from page(s)

published in

Biophysical Journal

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30 July 2017

volume

71

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30 July 2017

issue

5

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30 July 2017

page(s)

2458-2466

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

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Structural and functional similarities between the nucleotide-binding domains of CFTR and GTP-binding proteins

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Surface charge potentiates conduction through the cardiac ryanodine receptor channel

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Potassium channel block by cytoplasmic polyamines as the mechanism of intrinsic rectification

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

The CFTR chloride channel of mammalian heart

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Functions of the cystic fibrosis transmembrane conductance regulator protein

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

The cystic fibrosis transmembrane conductance regulator gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Novel pore-lining residues in CFTR that govern permeation and open-channel block

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Primary structure and expression from complementary DNA of skeletal muscle ryanodine receptor.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Cystic fibrosis: a disease in electrolyte transport.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Inhibition of an outwardly rectifying anion channel by HEPES and related buffers

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Dihydropyridine-sensitive skeletal muscle Ca channels in polarized planar bilayers. 1. Kinetics and voltage dependence of gating

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Cyclic AMP-dependent protein kinase activation of cystic fibrosis transmembrane conductance regulator chloride channels in planar lipid bilayers

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Spermine and spermidine as gating molecules for inward rectifier K+ channels.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Effects of pyrophosphate and nucleotide analogs suggest a role for ATP hydrolysis in cystic fibrosis transmembrane regulator channel gating.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Amino acid residues lining the chloride channel of the cystic fibrosis transmembrane conductance regulator.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1233734

Multi-ion pore behaviour in the CFTR chloride channel

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8913585

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8913585

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0006-3495(96)79439-0

1 reference

30 July 2017

1 reference

30 July 2017

1 reference