CFTR: Interacting With Everything?-Reference-Cited by-同舟云学术

CFTR: Interacting With Everything?

Published:2001-08 Issue:4 Volume:16 Page:167-170
ISSN:1548-9213
Container-title:Physiology
language:en
Short-container-title:Physiology

Author:

Kunzelmann Karl¹

Affiliation:

1. Department of Physiology and Pharmacology, University of Queensland, St. Lucia, Queensland 4072, Australia

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.

Publisher

American Physiological Society

Subject

Physiology

Link

https://www.physiology.org/doi/pdf/10.1152/physiologyonline.2001.16.4.167

Reference19 articles.

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2. Cytosolic Na+ controls and epithelial Na+ channel via the Go guanine nucleotide-binding regulatory protein.

3. Kunzelmann K. The cystic fibrosis transmembrane conductance regulator and its function in epithelial transport. Rev Physiol Biochem Pharmacol 137: 1–70, 1999.

4. CFTR, A Regulator of Channels

5. Osmotic water permeabilities of cultured, well-differentiated normal and cystic fibrosis airway epithelia

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