CFTR: Interacting with everything?

Kunzelmann, K. H. P. (2001) CFTR: Interacting with everything?. News in Physiological Science, 16 4: 167-170.

Author Kunzelmann, K. H. P.
Title CFTR: Interacting with everything?
Journal name News in Physiological Science   Check publisher's open access policy
ISSN 0886-1714
Publication date 2001
Sub-type Article (original research)
Volume 16
Issue 4
Start page 167
End page 170
Total pages 4
Editor S. G. Schultz
Margaret Reich
Place of publication United States
Publisher American Physiological Society
Collection year 2001
Language eng
Subject C1
270104 Membrane Biology
730110 Respiratory system and diseases (incl. asthma)
Abstract More than 1,300 different mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) are the cause for cystic fibrosis. CFTR is in charge of proper secretion and absorption of electrolytes, and thus the disease is characterized by defective epithelial Cl– secretion and enhanced Na+ absorption. Recent studies show that CFTR interacts with other proteins via PDZ domains.
Q-Index Code C1

Document type: Journal Article
Sub-type: Article (original research)
Collection: School of Pharmacy Publications
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Created: Tue, 14 Aug 2007, 15:12:13 EST