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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
632 related items for 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 [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 15; 499 ( Pt 3)(Pt 3):715-20. PubMed ID: 9130167 [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 15; 58(6):1318-25. PubMed ID: 11093769 [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 15; 435(5):595-603. PubMed ID: 9479011 [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; 15(4):258-66. PubMed ID: 12934053 [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 15; 141(7):1098-105. PubMed ID: 15023854 [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 15; 139(1):122-8. PubMed ID: 12746230 [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 15; 59(2):225-30. PubMed ID: 11160857 [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 15; 56(5):955-61. PubMed ID: 10531400 [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 31; 523(1-3):109-18. PubMed ID: 16226739 [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 31; 39(1):1-6. PubMed ID: 15978900 [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 01; 17(19):5529-35. PubMed ID: 9755153 [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 01; 292(1):131-5. PubMed ID: 10604939 [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 01; 149(5):573-80. PubMed ID: 17001304 [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 15; 511 ( Pt 3)(Pt 3):663-74. PubMed ID: 9714850 [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 15; 282(1):G137-44. PubMed ID: 11751167 [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 15; 85(1):39-53. PubMed ID: 10674713 [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 10; 87(10):873-80. PubMed ID: 11073882 [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 10; 587(1-3):204-8. PubMed ID: 18471810 [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 10; 100(2):338-46. PubMed ID: 14739809 [Abstract] [Full Text] [Related] Page: [Next] [New Search]