The receptor for antidiabetic sulfonylureas controls the activity of the ATP-modulated K+ channel in insulin-secreting cells.
Open Access
- 1 November 1987
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 262 (33) , 15840-15844
- https://doi.org/10.1016/s0021-9258(18)47664-8
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- Two potent central convulsant peptides, a bee venom toxin, the MCD peptide, and a snake venom toxin, dendrotoxin I, known to block K+ channels, have interacting receptor sitesBiochemical and Biophysical Research Communications, 1987
- Voltage‐activated Ca2+ currents in insulin‐secreting cellsFEBS Letters, 1985
- THE SULPHONYLUREA RECEPTOR MAY BE AN ATP-SENSITIVE POTASSIUM CHANNELThe Lancet, 1985
- Quinine inhibits Ca2+‐independent K+ channels whereas tetraethylammonium inhibits Ca2+‐activated K+ channels in insulin‐secreting cellsFEBS Letters, 1985
- ATP-sensitive inward rectifier and voltage- and calcium-activated K+ channels in cultured pancreatic islet cellsThe Journal of Membrane Biology, 1985
- Glucose induces closure of single potassium channels in isolated rat pancreatic β-cellsNature, 1984
- Interaction of sulfonylurea with the pancreatic B-cellCellular and Molecular Life Sciences, 1984
- Intracellular ATP directly blocks K+ channels in pancreatic B-cellsNature, 1984
- Are dihydropyridine binding sites voltage sensitive calcium channels?Life Sciences, 1984
- Conduction and selectivity in potassium channelsThe Journal of Membrane Biology, 1983