(Q41695434)

7 October 2017

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

1 reference

7 October 2017

0 references

Illek B

1

1 reference

7 October 2017

Zhang L

2

1 reference

7 October 2017

Lewis NC

3

1 reference

7 October 2017

Moss RB

4

1 reference

7 October 2017

Dong JY

5

1 reference

7 October 2017

Fischer H

6

1 reference

7 October 2017

language of work or name

English

0 references

publication date

1 October 1999

1 reference

American Journal of Physiology

7 October 2017

1 reference

7 October 2017

277

1 reference

7 October 2017

4 Pt 1

1 reference

7 October 2017

C833-9

1 reference

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

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

1 reference

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

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

21 January 2018

1 reference

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

1 reference

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

1 reference

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

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

1 reference

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

0 references

1 reference