The Carboxyl Terminus of the Cystic Fibrosis Transmembrane Conductance Regulator Binds to AP-2 Clathrin Adaptors
Open Access
- 1 February 2000
- journal article
- Published by Elsevier
- Vol. 275 (5) , 3655-3660
- https://doi.org/10.1074/jbc.275.5.3655
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- A3adenosine receptors regulate Cl−channels of nonpigmented ciliary epithelial cellsAmerican Journal of Physiology-Cell Physiology, 1999
- Subcellular localization of CFTR to endosomes in a ductal epitheliumAmerican Journal of Physiology-Cell Physiology, 1994
- Functional CFTR in endosomal compartment of CFTR-expressing fibroblasts and T84 cellsAmerican Journal of Physiology-Cell Physiology, 1994
- Cell surface labeling of CFTR in T84 cellsAmerican Journal of Physiology-Cell Physiology, 1993
- Immunocytochemical localization of the cystic fibrosis gene product CFTR.Proceedings of the National Academy of Sciences, 1991
- Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductanceCell, 1991
- Generation of cAMP-Activated Chloride Currents by Expression of CFTRScience, 1991
- Cystic fibrosis: a disease in electrolyte transportThe FASEB Journal, 1990
- Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNAScience, 1989
- Cyclic AMP-dependent protein kinase opens chloride channels in normal but not cystic fibrosis airway epitheliumNature, 1988