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99 related items for PubMed ID: 9281610
21. Inhibition by protein kinase C of the 86Rb+ efflux and vasorelaxation induced by P1075, a K(ATP) channel opener, in rat isolated aorta. Linde C, Löffler C, Quast U. Naunyn Schmiedebergs Arch Pharmacol; 1997 Sep; 356(3):425-32. PubMed ID: 9303583 [Abstract] [Full Text] [Related]
22. The identification of a potent imidazoline-based vascular K(ATP) channel antagonist. Bell K, Favaloro J, Khalil V, Iskander MM, McPherson GA. Naunyn Schmiedebergs Arch Pharmacol; 2000 Aug; 362(2):145-51. PubMed ID: 10961377 [Abstract] [Full Text] [Related]
23. Synthesis and characterization of a novel tritiated KATP channel opener with a benzopyran structure. Manley PW, Löffler-Walz C, Russ U, Hambrock A, Moenius T, Quast U. Br J Pharmacol; 2001 May; 133(2):275-85. PubMed ID: 11350864 [Abstract] [Full Text] [Related]
24. 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]
25. Binding and effects of P1075, an opener of ATP-sensitive K+ channels, in the aorta from streptozotocin-treated diabetic rats. Glocker S, Quast U. Naunyn Schmiedebergs Arch Pharmacol; 1997 Aug 31; 356(2):210-5. PubMed ID: 9272727 [Abstract] [Full Text] [Related]
26. 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]
27. Different potassium channels are involved in relaxation of rat renal artery induced by P1075. Novakovic A, Pavlovic M, Milojevic P, Stojanovic I, Nenezic D, Jovic M, Ugresic N, Kanjuh V, Yang Q, He GW. Basic Clin Pharmacol Toxicol; 2012 Jul 01; 111(1):24-30. PubMed ID: 22225832 [Abstract] [Full Text] [Related]
28. Synthesis of and radioligand binding studies with a tritiated pinacidil analogue: receptor interactions of structurally different classes of potassium channel openers and blockers. Manley PW, Quast U, Andres H, Bray K. J Med Chem; 1993 Jul 09; 36(14):2004-10. PubMed ID: 8336339 [Abstract] [Full Text] [Related]
29. Functional and electrophysiological effects of a novel imidazoline-based K(ATP) channel blocker, IMID-4F. McPherson GA, Bell KL, Favaloro JL, Kubo M, Standen NB. Br J Pharmacol; 1999 Dec 09; 128(8):1636-42. PubMed ID: 10588917 [Abstract] [Full Text] [Related]
30. Identification and properties of an ATP-sensitive K+ current in rabbit sino-atrial node pacemaker cells. Han X, Light PE, Giles WR, French RJ. J Physiol; 1996 Jan 15; 490 ( Pt 2)(Pt 2):337-50. PubMed ID: 8821133 [Abstract] [Full Text] [Related]
31. Effect of cromakalim and pinacidil on 86Rb efflux from guinea pig urinary bladder smooth muscle. Trivedi S, Stetz S, Levin R, Li J, Kau S. Pharmacology; 1994 Sep 15; 49(3):159-66. PubMed ID: 7972330 [Abstract] [Full Text] [Related]
32. Effect of MgATP on pinacidil-induced displacement of glibenclamide from the sulphonylurea receptor in a pancreatic beta-cell line and rat cerebral cortex. Schwanstecher M, Brandt C, Behrends S, Schaupp U, Panten U. Br J Pharmacol; 1992 Jun 15; 106(2):295-301. PubMed ID: 1393263 [Abstract] [Full Text] [Related]
33. A specific binding site for K+ channel openers in rat aorta. Bray KM, Quast U. J Biol Chem; 1992 Jun 15; 267(17):11689-92. PubMed ID: 1601843 [Abstract] [Full Text] [Related]
34. Characterization of sulfonylurea receptors and the action of potassium channel openers on cholinergic neurotransmission in guinea pig isolated small intestine. Zini S, Ben-Ari Y, Ashford ML. J Pharmacol Exp Ther; 1991 Nov 15; 259(2):566-73. PubMed ID: 1658303 [Abstract] [Full Text] [Related]
35. Diverse effects of pinacidil on KATP channels in mouse skeletal muscle in the presence of different nucleotides. Hehl S, Neumcke B. Cardiovasc Res; 1994 Jun 15; 28(6):841-6. PubMed ID: 7923289 [Abstract] [Full Text] [Related]
36. Regulation of ATP-sensitive K+ channels by chronic glyburide and pinacidil administration. Gopalakrishnan M, Triggle DJ. Biochem Pharmacol; 1992 Nov 03; 44(9):1843-7. PubMed ID: 1333209 [Abstract] [Full Text] [Related]
37. [125I]A-312110, a novel high-affinity 1,4-dihydropyridine ATP-sensitive K+ channel opener: characterization and pharmacology of binding. Davis-Taber R, Molinari EJ, Altenbach RJ, Whiteaker KL, Shieh CC, Rotert G, Buckner SA, Malysz J, Milicic I, McDermott JS, Gintant GA, Coghlan MJ, Carroll WA, Scott VE, Gopalakrishnan M. Mol Pharmacol; 2003 Jul 03; 64(1):143-53. PubMed ID: 12815170 [Abstract] [Full Text] [Related]
38. Stoichiometry of potassium channel opener action. Gross I, Toman A, Uhde I, Schwanstecher C, Schwanstecher M. Mol Pharmacol; 1999 Dec 03; 56(6):1370-3. PubMed ID: 10570067 [Abstract] [Full Text] [Related]