Genistein potentiates wild-type and delta F508-CFTR channel activity (Q42835338)

8 November 2017

title

Genistein potentiates wild-type and delta F508-CFTR channel activity (English)

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8 November 2017

Hwang TC

1

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8 November 2017

Wang F

series ordinal

2

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8 November 2017

Yang IC

series ordinal

3

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8 November 2017

Reenstra WW

series ordinal

4

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8 November 2017

language of work or name

English

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publication date

1 September 1997

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American Journal of Physiology

8 November 2017

published in

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8 November 2017

volume

273

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8 November 2017

issue

3 Pt 1

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8 November 2017

page(s)

C988-98

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Defective acidification of intracellular organelles in cystic fibrosis

8 November 2017

cites work

1 reference

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Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel

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Regulation of plasma membrane recycling by CFTR.

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https://api.crossref.org/works/10.1152%2FAJPCELL.1997.273.3.C988

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

21 January 2018

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

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPCELL.1997.273.3.C988

The CFTR chloride channel of mammalian heart

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPCELL.1997.273.3.C988

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

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Activation of endogenous deltaF508 cystic fibrosis transmembrane conductance regulator by phosphodiesterase inhibition

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The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR.

21 January 2018

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Soy intake and cancer risk: a review of the in vitro and in vivo data

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

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

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The variance of sodium current fluctuations at the node of Ranvier

21 January 2018

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

21 January 2018

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CFTR as a cAMP-dependent regulator of sodium channels

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

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Mode-switching of a voltage-gated cation channel is mediated by a protein kinase A-regulated tyrosine phosphatase

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21 January 2018

Identifiers

DOI

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