(Q42686007)

English

Genistein improves regulatory interactions between G551D-cystic fibrosis transmembrane conductance regulator and the epithelial sodium channel in Xenopus oocytes

scientific article published on 16 October 2002

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scholarly article

1 reference

Europe PubMed Central

4 November 2017

Genistein improves regulatory interactions between G551D-cystic fibrosis transmembrane conductance regulator and the epithelial sodium channel in Xenopus oocytes (English)

1 reference

Europe PubMed Central

4 November 2017

cystic fibrosis

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transmembrane protein

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Ronald C. Rubenstein

4

1 reference

Europe PubMed Central

4 November 2017

author name string

Laurence Suaud

1

1 reference

Europe PubMed Central

4 November 2017

Marcelo Carattino

2

1 reference

Europe PubMed Central

4 November 2017

Thomas R Kleyman

3

1 reference

Europe PubMed Central

4 November 2017

language of work or name

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publication date

16 October 2002

1 reference

Europe PubMed Central

4 November 2017

number of pages

7

1 reference

based on heuristic

inferred from page(s)

Journal of Biological Chemistry

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Europe PubMed Central

4 November 2017

277

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Europe PubMed Central

4 November 2017

50341-50347

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Europe PubMed Central

4 November 2017

52

1 reference

Europe PubMed Central

4 November 2017

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Cystic fibrosis transmembrane conductance regulator-dependent up-regulation of Kir1.1 (ROMK) renal K+ channels by the epithelial sodium channel

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Cl- transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Downregulation of epithelial sodium channel (ENaC) by CFTR co-expressed in Xenopus oocytes is independent of Cl- conductance.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Regulation of epithelial sodium channels by the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

The cytosolic termini of the beta- and gamma-ENaC subunits are involved in the functional interactions between cystic fibrosis transmembrane conductance regulator and epithelial sodium channel.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Epithelial sodium channels regulate cystic fibrosis transmembrane conductance regulator chloride channels in Xenopus oocytes.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Genistein restores functional interactions between Delta F508-CFTR and ENaC in Xenopus oocytes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Activation of the epithelial Na+ channel (ENaC) requires CFTR Cl- channel function

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Cystic fibrosis transmembrane conductance regulator inhibits epithelial Na+ channels carrying Liddle's syndrome mutations.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Inhibition of epithelial Na+ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Wild type but not deltaF508 CFTR inhibits Na+ conductance when coexpressed in Xenopus oocytes.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Activation of deltaF508 CFTR in a cystic fibrosis respiratory epithelial cell line by 4-phenylbutyrate, genistein and CPX.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Expression of the cystic fibrosis phenotype in a renal amphibian epithelial cell line

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Direct action of genistein on CFTR.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Conformational and temperature-sensitive stability defects of the delta F508 cystic fibrosis transmembrane conductance regulator in post-endoplasmic reticulum compartments.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Cystic fibrosis transmembrane conductance regulator inverts protein kinase A-mediated regulation of epithelial sodium channel single channel kinetics

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M209641200

21 January 2018

Identifiers

10.1074/JBC.M209641200

1 reference

Europe PubMed Central

4 November 2017

1 reference

Europe PubMed Central

4 November 2017

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