Genistein restores functional interactions between Delta F508-CFTR and ENaC in Xenopus oocytes (Q42666747)

4 November 2017

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

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4 November 2017

4

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4 November 2017

Laurence Suaud

1

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4 November 2017

Jinqing Li

series ordinal

2

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4 November 2017

Qinshi Jiang

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3

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4 November 2017

Thomas R Kleyman

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5

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4 November 2017

language of work or name

English

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publication date

28 December 2001

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Journal of Biological Chemistry

4 November 2017

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4 November 2017

277

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4 November 2017

8928-8933

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4 November 2017

11

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

4 November 2017

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https://api.crossref.org/works/10.1074%2FJBC.M111482200

CFTR as a cAMP-dependent regulator of sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

CFTR and outward rectifying chloride channels are distinct proteins with a regulatory relationship

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

Identification of the cystic fibrosis gene: genetic analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

Degradation of CFTR by the ubiquitin-proteasome pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

Multiple proteolytic systems, including the proteasome, contribute to CFTR processing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

Effects of 8-cpt-cAMP on the epithelial sodium channel expressed in Xenopus oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

Liddle's syndrome mutations disrupt cAMP-mediated translocation of the epithelial Na(+) channel to the cell surface

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

The CF salt controversy: in vivo observations and therapeutic approaches.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

In vivo nasal potential difference: techniques and protocols for assessing efficacy of gene transfer in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl- concentration

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

Non-specific activation of the epithelial sodium channel by the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

Strategies for correcting the delta F508 CFTR protein-folding defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

Use of protein repair therapy in the treatment of cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111482200

21 January 2018

Identifiers

DOI

10.1074/JBC.M111482200

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4 November 2017

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