Cytoplasmic loop three of cystic fibrosis transmembrane conductance regulator contributes to regulation of chloride channel activity. (Q41155403)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8910333 AND SRC:MED&resulttype=core&format=json

21 October 2019

title

Cytoplasmic loop three of cystic fibrosis transmembrane conductance regulator contributes to regulation of chloride channel activity (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8910333 AND SRC:MED&resulttype=core&format=json

21 October 2019

main subject

cystic fibrosis

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transmembrane protein

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author

Tip W. Loo

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8910333 AND SRC:MED&resulttype=core&format=json

21 October 2019

author name string

F S Seibert

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8910333 AND SRC:MED&resulttype=core&format=json

21 October 2019

P Linsdell

2

1 reference

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21 October 2019

J W Hanrahan

4

1 reference

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21 October 2019

J R Riordan

5

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21 October 2019

D M Clarke

6

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21 October 2019

language of work or name

English

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publication date

1 November 1996

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8910333 AND SRC:MED&resulttype=core&format=json

Journal of Biological Chemistry

21 October 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8910333 AND SRC:MED&resulttype=core&format=json

21 October 2019

volume

271

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21 October 2019

issue

44

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21 October 2019

page(s)

27493-27499

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Nucleoside triphosphates are required to open the CFTR chloride channel.

21 October 2019

cites work

1 reference

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Biocytin hydrazide--a selective label for sialic acids, galactose, and other sugars in glycoconjugates using avidin-biotin technology

21 January 2018

1 reference

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Phosphatase inhibitors activate normal and defective CFTR chloride channels

21 January 2018

1 reference

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Chemical chaperones correct the mutant phenotype of the ΔF508 cystic fibrosis transmembrane conductance regulator protein

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.271.44.27493

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

21 January 2018

1 reference

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High-efficiency transformation of mammalian cells by plasmid DNA

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Identification of the cystic fibrosis gene: genetic analysis

21 January 2018

1 reference

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Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene

21 January 2018

1 reference

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Steady-state distribution and biogenesis of endogenous Madin-Darby canine kidney glycoproteins: evidence for intracellular sorting and polarized cell surface delivery

21 January 2018

1 reference

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Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel

21 January 2018

1 reference

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

21 January 2018

1 reference

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Increasing expression of the normal human CFTR cDNA in cystic fibrosis epithelial cells results in a progressive increase in the level of CFTR protein expression, but a limit on the level of cAMP-stimulated chloride secretion

21 January 2018

1 reference

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

21 January 2018

1 reference

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Disease-associated mutations in the fourth cytoplasmic loop of cystic fibrosis transmembrane conductance regulator compromise biosynthetic processing and chloride channel activity.

21 January 2018

1 reference

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

21 January 2018

1 reference

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The cystic fibrosis transmembrane conductance regulator chloride channel. Iodide block and permeation

21 January 2018

1 reference

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

21 January 2018

1 reference

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Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.271.44.27493

CFTR: the nucleotide binding folds regulate the accessibility and stability of the activated state

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.271.44.27493

Effect of ATP concentration on CFTR Cl- channels: a kinetic analysis of channel regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.271.44.27493

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/JBC.271.44.27493

Multi-ion pore behaviour in the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.271.44.27493

21 January 2018

Identifiers

DOI

10.1074/JBC.271.44.27493

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8910333 AND SRC:MED&resulttype=core&format=json

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21 October 2019

Fatcat ID

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24 November 2022

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