Regulatory Interaction between the Cystic Fibrosis Transmembrane Conductance Regulator and HCO Salvage Mechanisms in Model Systems and the Mouse Pancreatic Duct
Open Access
- 1 May 2001
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 276 (20) , 17236-17243
- https://doi.org/10.1074/jbc.m011763200
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Aberrant CFTR-dependent HCO-3 transport in mutations associated with cystic fibrosisNature, 2001
- E3KARP Mediates the Association of Ezrin and Protein Kinase A with the Cystic Fibrosis Transmembrane Conductance Regulator in Airway CellsJournal of Biological Chemistry, 2000
- Na+-dependent transporters mediate HCO3– salvage across the luminal membrane of the main pancreatic ductJournal of Clinical Investigation, 2000
- Novel amiloride-sensitive sodium-dependent proton secretion in the mouse proximal convoluted tubuleJournal of Clinical Investigation, 2000
- Cystic Fibrosis Transmembrane Conductance Regulator Regulates Luminal Cl−/HCO3−Exchange in Mouse Submandibular and Pancreatic DuctsPublished by Elsevier ,1999
- Regulation of Cl−/ HCO3−Exchange by Cystic Fibrosis Transmembrane Conductance Regulator Expressed in NIH 3T3 and HEK 293 CellsPublished by Elsevier ,1999
- Structure-function of recombinant Na/H exchanger regulatory factor (NHE-RF).Journal of Clinical Investigation, 1998
- cAMP-mediated inhibition of the epithelial brush border Na + /H + exchanger, NHE3, requires an associated regulatory proteinProceedings of the National Academy of Sciences, 1997
- CFTR as a cAMP-Dependent Regulator of Sodium ChannelsScience, 1995
- CYSTIC FIBROSIS OF THE PANCREASThe Lancet, 1968