Defective function of the cystic fibrosis-causing missense mutation G551D is recovered by genistein (Q41695434)

7 October 2017

title

Defective function of the cystic fibrosis-causing missense mutation G551D is recovered by genistein (English)

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7 October 2017

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Illek B

1

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7 October 2017

Zhang L

2

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7 October 2017

Lewis NC

3

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7 October 2017

Moss RB

4

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7 October 2017

Dong JY

5

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7 October 2017

Fischer H

6

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7 October 2017

language of work or name

English

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publication date

1 October 1999

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American Journal of Physiology

7 October 2017

published in

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7 October 2017

volume

277

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7 October 2017

issue

4 Pt 1

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7 October 2017

page(s)

C833-9

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Direct activation of cystic fibrosis transmembrane conductance regulator channels by 8-cyclopentyl-1,3-dipropylxanthine (CPX) and 1,3-diallyl-8-cyclohexylxanthine (DAX).

7 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

The Irish cystic fibrosis database

21 January 2018

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Structural basis for specificity and potency of xanthine derivatives as activators of the CFTR chloride channel.

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

CFTR displays voltage dependence and two gating modes during stimulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

The tyrosine kinase p60c-src regulates the fast gate of the cystic fibrosis transmembrane conductance regulator chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

Efficiency of gene transfer for restoration of normal airway epithelial function in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

In vivo activation of the cystic fibrosis transmembrane conductance regulator mutant deltaF508 in murine nasal epithelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

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

21 January 2018

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Cystic fibrosis transmembrane conductance regulator mutations that disrupt nucleotide binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

Heterogeneity of phenotype in two cystic fibrosis patients homozygous for the CFTR exon 11 mutation G551D

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

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/10.1152%2FAJPCELL.1999.277.4.C833

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

Shunt resistance and ion permeabilities in normal and cystic fibrosis airway epithelia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.1999.277.4.C833

10.1152/AJPCELL.1999.277.4.C833

21 January 2018

Identifiers

DOI

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