Pharmaco-topology of Sulfonylurea Receptors
Open Access
- 1 January 2000
- journal article
- Published by Elsevier
- Vol. 275 (2) , 717-720
- https://doi.org/10.1074/jbc.275.2.717
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- The tolbutamide site of SUR1 and a mechanism for its functional coupling to KATP channel closureFEBS Letters, 1999
- The C Terminus of SUR1 Is Required for Trafficking of KATP ChannelsJournal of Biological Chemistry, 1999
- The N-Terminus of KIR6.2 Limits Spontaneous Bursting and Modulates the ATP-Inhibition of KATPChannelsBiochemical and Biophysical Research Communications, 1999
- Mg2+ and ATP dependence of KATP channel modulator binding to the recombinant sulphonylurea receptor, SUR2BBritish Journal of Pharmacology, 1998
- Truncation of Kir6.2 produces ATP-sensitive K+ channels in the absence of the sulphonylurea receptorNature, 1997
- A Family of Sulfonylurea Receptors Determines the Pharmacological Properties of ATP-Sensitive K+ ChannelsPublished by Elsevier ,1996
- Reconstitution of I KATP : An Inward Rectifier Subunit Plus the Sulfonylurea ReceptorScience, 1995
- The Pharmacology of ATP-Sensitive Potassium ChannelsAnnual Review of Pharmacology and Toxicology, 1993
- The potassium channel opener cromakalim (BRL 34915) activates ATP-dependent K+ channels in isolated cardiac myocytesBiochemical and Biophysical Research Communications, 1988
- Intracellular ATP directly blocks K+ channels in pancreatic B-cellsNature, 1984