The Chloride Channel ClC-4 Co-localizes with Cystic Fibrosis Transmembrane Conductance Regulator and May Mediate Chloride Flux across the Apical Membrane of Intestinal Epithelia
Open Access
- 1 January 2002
- journal article
- Published by Elsevier
- Vol. 277 (1), 566-574
- https://doi.org/10.1074/jbc.m106968200
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Tissue distribution and subcellular localization of the ClC-5 chloride channel in rat intestinal cellsAmerican Journal of Physiology-Cell Physiology, 2001
- Amelioration of Intestinal Disease Severity in Cystic Fibrosis Mice Is Associated with Improved Chloride Secretory CapacityPediatric Research, 2000
- In vivo role of CLC chloride channels in the kidneyAmerican Journal of Physiology-Renal Physiology, 2000
- From Tonus to TonicityJournal of the American Society of Nephrology, 2000
- The CLC chloride channel familyPflügers Archiv - European Journal of Physiology, 1999
- Structure and Function of the CFTR Chloride ChannelPhysiological Reviews, 1999
- Two highly homologous members of the ClC chloride channel family in both rat and human kidney.Proceedings of the National Academy of Sciences, 1994
- Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice.Proceedings of the National Academy of Sciences, 1994
- Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosisCell, 1993
- Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosisCell, 1990