Browse by author
Lookup NU author(s): Dr Michael Gray
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
New research reveals a reciprocal regulation between the CFTR chloride channel, implicated in cystic fibrosis, and several members of the SLC26 family of chloride-bicarbonate exchangers. These findings provide new insights into the mechanism of epithelial bicarbonate and fluid transport and may lead to better treatments for cystic fibrosis and congenital chloride diarrhoeas.
Author(s): Gray MA
Publication type: Article
Publication status: Published
Journal: Nature Cell Biology
Year: 2004
Volume: 6
Issue: 4
Pages: 292-294
Print publication date: 01/04/2004
ISSN (print): 1465-7392
ISSN (electronic): 1476-4679
Publisher: Nature Publishing Group
URL: http://dx.doi.org/10.1038/ncb0404-292
DOI: 10.1038/ncb0404-292
PubMed id: 15057243
Altmetrics provided by Altmetric