These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
631 related articles for article (PubMed ID: 9692785)
1. SUR2 subtype (A and B)-dependent differential activation of the cloned ATP-sensitive K+ channels by pinacidil and nicorandil. Shindo T; Yamada M; Isomoto S; Horio Y; Kurachi Y Br J Pharmacol; 1998 Jul; 124(5):985-91. PubMed ID: 9692785 [TBL] [Abstract][Full Text] [Related]
2. Sulphonylurea receptor 2B and Kir6.1 form a sulphonylurea-sensitive but ATP-insensitive K+ channel. Yamada M; Isomoto S; Matsumoto S; Kondo C; Shindo T; Horio Y; Kurachi Y J Physiol; 1997 Mar; 499 ( Pt 3)(Pt 3):715-20. PubMed ID: 9130167 [TBL] [Abstract][Full Text] [Related]
3. Differential response of K(ATP) channels containing SUR2A or SUR2B subunits to nucleotides and pinacidil. Reimann F; Gribble FM; Ashcroft FM Mol Pharmacol; 2000 Dec; 58(6):1318-25. PubMed ID: 11093769 [TBL] [Abstract][Full Text] [Related]
4. The effects of nucleotides and potassium channel openers on the SUR2A/Kir6.2 complex K+ channel expressed in a mammalian cell line, HEK293T cells. Okuyama Y; Yamada M; Kondo C; Satoh E; Isomoto S; Shindo T; Horio Y; Kitakaze M; Hori M; Kurachi Y Pflugers Arch; 1998 Apr; 435(5):595-603. PubMed ID: 9479011 [TBL] [Abstract][Full Text] [Related]
5. Molecular basis and characteristics of KATP channel in human corporal smooth muscle cells. Insuk SO; Chae MR; Choi JW; Yang DK; Sim JH; Lee SW Int J Impot Res; 2003 Aug; 15(4):258-66. PubMed ID: 12934053 [TBL] [Abstract][Full Text] [Related]
6. Interaction of a novel dihydropyridine K+ channel opener, A-312110, with recombinant sulphonylurea receptors and KATP channels: comparison with the cyanoguanidine P1075. Felsch H; Lange U; Hambrock A; Löffler-Walz C; Russ U; Carroll WA; Gopalakrishnan M; Quast U Br J Pharmacol; 2004 Apr; 141(7):1098-105. PubMed ID: 15023854 [TBL] [Abstract][Full Text] [Related]
7. Different molecular sites of action for the KATP channel inhibitors, PNU-99963 and PNU-37883A. Cui Y; Tinker A; Clapp LH Br J Pharmacol; 2003 May; 139(1):122-8. PubMed ID: 12746230 [TBL] [Abstract][Full Text] [Related]
8. Pharmacological comparison of native mitochondrial K(ATP) channels with molecularly defined surface K(ATP) channels. Liu Y; Ren G; O'Rourke B; Marbán E; Seharaseyon J Mol Pharmacol; 2001 Feb; 59(2):225-30. PubMed ID: 11160857 [TBL] [Abstract][Full Text] [Related]
9. Coexpression with the inward rectifier K(+) channel Kir6.1 increases the affinity of the vascular sulfonylurea receptor SUR2B for glibenclamide. Russ U; Hambrock A; Artunc F; Löffler-Walz C; Horio Y; Kurachi Y; Quast U Mol Pharmacol; 1999 Nov; 56(5):955-61. PubMed ID: 10531400 [TBL] [Abstract][Full Text] [Related]
10. Characterization of K(ATP)-channels in rat basilar and middle cerebral arteries: studies of vasomotor responses and mRNA expression. Jansen-Olesen I; Mortensen CH; El-Bariaki N; Ploug KB Eur J Pharmacol; 2005 Oct; 523(1-3):109-18. PubMed ID: 16226739 [TBL] [Abstract][Full Text] [Related]
11. A functional role of the C-terminal 42 amino acids of SUR2A and SUR2B in the physiology and pharmacology of cardiovascular ATP-sensitive K(+) channels. Yamada M; Kurachi Y J Mol Cell Cardiol; 2005 Jul; 39(1):1-6. PubMed ID: 15978900 [TBL] [Abstract][Full Text] [Related]
12. Potassium channel openers require ATP to bind to and act through sulfonylurea receptors. Schwanstecher M; Sieverding C; Dörschner H; Gross I; Aguilar-Bryan L; Schwanstecher C; Bryan J EMBO J; 1998 Oct; 17(19):5529-35. PubMed ID: 9755153 [TBL] [Abstract][Full Text] [Related]
13. MCC-134, a novel vascular relaxing agent, is an inverse agonist for the pancreatic-type ATP-sensitive K(+) channel. Shindo T; Katayama Y; Horio Y; Kurachi Y J Pharmacol Exp Ther; 2000 Jan; 292(1):131-5. PubMed ID: 10604939 [TBL] [Abstract][Full Text] [Related]
14. A key role for the subunit SUR2B in the preferential activation of vascular KATP channels by isoflurane. Fujita H; Ogura T; Tamagawa M; Uemura H; Sato T; Ishida A; Imamaki M; Kimura F; Miyazaki M; Nakaya H Br J Pharmacol; 2006 Nov; 149(5):573-80. PubMed ID: 17001304 [TBL] [Abstract][Full Text] [Related]
15. Intracellular nucleotide-mediated gating of SUR/Kir6.0 complex potassium channels expressed in a mammalian cell line and its modification by pinacidil. Satoh E; Yamada M; Kondo C; Repunte VP; Horio Y; Iijima T; Kurachi Y J Physiol; 1998 Sep; 511 ( Pt 3)(Pt 3):663-74. PubMed ID: 9714850 [TBL] [Abstract][Full Text] [Related]
16. ATP-sensitive K(+) channels composed of Kir6.1 and SUR2B subunits in guinea pig gastric myocytes. Sim JH; Yang DK; Kim YC; Park SJ; Kang TM; So I; Kim KW Am J Physiol Gastrointest Liver Physiol; 2002 Jan; 282(1):G137-44. PubMed ID: 11751167 [TBL] [Abstract][Full Text] [Related]
17. Molecular aspects of ATP-sensitive K+ channels in the cardiovascular system and K+ channel openers. Fujita A; Kurachi Y Pharmacol Ther; 2000 Jan; 85(1):39-53. PubMed ID: 10674713 [TBL] [Abstract][Full Text] [Related]
18. C-terminal tails of sulfonylurea receptors control ADP-induced activation and diazoxide modulation of ATP-sensitive K(+) channels. Matsuoka T; Matsushita K; Katayama Y; Fujita A; Inageda K; Tanemoto M; Inanobe A; Yamashita S; Matsuzawa Y; Kurachi Y Circ Res; 2000 Nov; 87(10):873-80. PubMed ID: 11073882 [TBL] [Abstract][Full Text] [Related]
19. Decreased expression of aortic KIR6.1 and SUR2B in hypertension does not correlate with changes in the functional role of K(ATP) channels. Blanco-Rivero J; Gamallo C; Aras-López R; Cobeño L; Cogolludo A; Pérez-Vizcaino F; Ferrer M; Balfagon G Eur J Pharmacol; 2008 Jun; 587(1-3):204-8. PubMed ID: 18471810 [TBL] [Abstract][Full Text] [Related]
20. Molecular mechanisms of the inhibitory effects of propofol and thiamylal on sarcolemmal adenosine triphosphate-sensitive potassium channels. Kawano T; Oshita S; Takahashi A; Tsutsumi Y; Tomiyama Y; Kitahata H; Kuroda Y; Nakaya Y Anesthesiology; 2004 Feb; 100(2):338-46. PubMed ID: 14739809 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]