The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel-Reference-Cited by-同舟云学术

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

Published:1999-04-27 Issue:9 Volume:96 Page:5310-5315
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Schreiber R.,Hopf A.,Mall M.,Greger R.,Kunzelmann K.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference31 articles.

1. Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.

2. Na+ and Cl? conductances in airway epithelial cells: increased Na+ conductance in cystic fibrosis

3. The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.

4. Wild type but not ΔF508 CFTR inhibits Na+ conductance when coexpressed in Xenopus oocytes

5. Colonic and esophageal transepithelial potential difference in cystic fibrosis

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