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Journal Abstract Search


99 related items for PubMed ID: 9281610

  • 1. Nucleotide regulation and characteristics of potassium channel opener binding to skeletal muscle membranes.
    Dickinson KE, Bryson CC, Cohen RB, Rogers L, Green DW, Atwal KS.
    Mol Pharmacol; 1997 Sep; 52(3):473-81. PubMed ID: 9281610
    [Abstract] [Full Text] [Related]

  • 2. Binding of K(ATP) channel modulators in rat cardiac membranes.
    Löffler-Walz C, Quast U.
    Br J Pharmacol; 1998 Apr; 123(7):1395-402. PubMed ID: 9579735
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  • 4. Binding and effects of KATP channel openers in the vascular smooth muscle cell line, A10.
    Russ U, Metzger F, Kickenweiz E, Hambrock A, Krippeit-Drews P, Quast U.
    Br J Pharmacol; 1997 Nov; 122(6):1119-26. PubMed ID: 9401776
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  • 5. Binding of the K+ channel opener [3H]P1075 in rat isolated aorta: relationship to functional effects of openers and blockers.
    Quast U, Bray KM, Andres H, Manley PW, Baumlin Y, Dosogne J.
    Mol Pharmacol; 1993 Mar; 43(3):474-81. PubMed ID: 8450836
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  • 7. Mg2+ and ATP dependence of K(ATP) channel modulator binding to the recombinant sulphonylurea receptor, SUR2B.
    Hambrock A, Löffler-Walz C, Kurachi Y, Quast U.
    Br J Pharmacol; 1998 Oct; 125(3):577-83. PubMed ID: 9806343
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  • 8. Binding of [3H]-P1075, an opener of ATP-sensitive K+ channels, to rat glomerular preparations.
    Metzger F, Quast U.
    Naunyn Schmiedebergs Arch Pharmacol; 1996 Oct; 354(4):452-9. PubMed ID: 8897448
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  • 10. Alteration of binding sites for [3H]P1075 and [3H]glibenclamide in renovascular hypertensive rat aorta.
    He HM, Long CL, Zhang LZ, Fu AL, Wang H.
    Acta Pharmacol Sin; 2005 Jan; 26(1):69-76. PubMed ID: 15659117
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  • 11. Interaction between thiol-modifying agents and P1075, a K(ATP) channel opener, in rat isolated aorta.
    Linde C, Löffler C, Kessler C, Quast U.
    Naunyn Schmiedebergs Arch Pharmacol; 1997 Oct; 356(4):467-74. PubMed ID: 9349633
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  • 12. Interaction of K(ATP) channel modulators with sulfonylurea receptor SUR2B: implication for tetramer formation and allosteric coupling of subunits.
    Löffler-Walz C, Hambrock A, Quast U.
    Mol Pharmacol; 2002 Feb; 61(2):407-14. PubMed ID: 11809866
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  • 13. Potentiation of P1075-induced K+ channel opening by stimulation of adenylate cyclase in rat isolated aorta.
    Linde C, Quast U.
    Br J Pharmacol; 1995 Jun; 115(3):515-21. PubMed ID: 7582466
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  • 14. 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
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  • 16. Characterization of the ATP-sensitive potassium channels (KATP) expressed in guinea pig bladder smooth muscle cells.
    Gopalakrishnan M, Whiteaker KL, Molinari EJ, Davis-Taber R, Scott VE, Shieh CC, Buckner SA, Milicic I, Cain JC, Postl S, Sullivan JP, Brioni JD.
    J Pharmacol Exp Ther; 1999 Apr; 289(1):551-8. PubMed ID: 10087049
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  • 18. Nucleotide modulation of pinacidil stimulation of the cloned K(ATP) channel Kir6.2/SUR2A.
    Gribble FM, Reimann F, Ashfield R, Ashcroft FM.
    Mol Pharmacol; 2000 Jun; 57(6):1256-61. PubMed ID: 10825398
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  • 19. K-channel opening activity of dihydropyridine ZM244085: effect on 86Rb efflux and 3H-P1075 binding in urinary bladder smooth muscle.
    Trivedi S, Potter-Lee L, McConville MW, Li JH, Ohnmacht CJ, Trainor DA, Kau ST.
    Res Commun Mol Pathol Pharmacol; 1995 May; 88(2):137-51. PubMed ID: 7670846
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  • 20. Characterization of binding of the ATP-sensitive potassium channel ligand, [3H]glyburide, to neuronal and muscle preparations.
    Gopalakrishnan M, Johnson DE, Janis RA, Triggle DJ.
    J Pharmacol Exp Ther; 1991 Jun; 257(3):1162-71. PubMed ID: 1904493
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