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Journal Abstract Search

247 related items for PubMed ID: 11809866

  • 1. 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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  • 3. 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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  • 4. 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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  • 7. Glibenclamide binding to sulphonylurea receptor subtypes: dependence on adenine nucleotides.
    Hambrock A, Löffler-Walz C, Quast U.
    Br J Pharmacol; 2002 Aug; 136(7):995-1004. PubMed ID: 12145099
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  • 8. 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
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  • 9. 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
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  • 10. The mutation Y1206S increases the affinity of the sulphonylurea receptor SUR2A for glibenclamide and enhances the effects of coexpression with Kir6.2.
    Stephan D, Stauss E, Lange U, Felsch H, Löffler-Walz C, Hambrock A, Russ U, Quast U.
    Br J Pharmacol; 2005 Apr 01; 144(8):1078-88. PubMed ID: 15711591
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  • 13. 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
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  • 14. Interaction of the sulfonylthiourea HMR 1833 with sulfonylurea receptors and recombinant ATP-sensitive K(+) channels: comparison with glibenclamide.
    Russ U, Lange U, Löffler-Walz C, Hambrock A, Quast U.
    J Pharmacol Exp Ther; 2001 Dec 31; 299(3):1049-55. PubMed ID: 11714894
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  • 15. Lipids modulate ligand binding to sulphonylurea receptors.
    Klein A, Lichtenberg J, Stephan D, Quast U.
    Br J Pharmacol; 2005 Aug 31; 145(7):907-15. PubMed ID: 15895108
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  • 17. 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 31; 58(6):1318-25. PubMed ID: 11093769
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  • 18. 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
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  • 19. Role of the amino-terminal transmembrane domain of sulfonylurea receptor SUR2B for coupling to K(IR)6.2, ligand binding, and oligomerization.
    Winkler M, Kühner P, Russ U, Ortiz D, Bryan J, Quast U.
    Naunyn Schmiedebergs Arch Pharmacol; 2012 Mar 15; 385(3):287-98. PubMed ID: 22089636
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  • 20. 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
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