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Journal Abstract Search

250 related items for PubMed ID: 7568338

  • 21. The individual enantiomers of cis-cromakalim possess K+ channel opening activity.
    Quast U, Villhauer EB.
    Eur J Pharmacol; 1993 Apr 15; 245(2):165-71. PubMed ID: 8491256
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  • 29. Comparison of the in vitro effects of K+ channel modulators on detrusor and portal vein strips from guinea pigs.
    Zografos P, Li JH, Kau ST.
    Pharmacology; 1992 Apr 15; 45(4):216-30. PubMed ID: 1438528
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  • 33. 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 15; 52(3):473-81. PubMed ID: 9281610
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  • 34. ATP-Sensitive K+ channel modulator binding to sulfonylurea receptors SUR2A and SUR2B: opposite effects of MgADP.
    Hambrock A, Löffler-Walz C, Kloor D, Delabar U, Horio Y, Kurachi Y, Quast U.
    Mol Pharmacol; 1999 May 15; 55(5):832-40. PubMed ID: 10220561
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  • 35. Effects of K+ channel blockers and cromakalim (BRL 34915) on the mechanical activity of guinea pig detrusor smooth muscle.
    Grant TL, Zuzack JS.
    J Pharmacol Exp Ther; 1991 Dec 15; 259(3):1158-64. PubMed ID: 1722252
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  • 36. 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 15; 356(2):210-5. PubMed ID: 9272727
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  • 38. 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 15; 125(3):577-83. PubMed ID: 9806343
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  • 39. Effects of rubidium on responses to potassium channel openers in rat isolated aorta.
    Greenwood IA, Weston AH.
    Br J Pharmacol; 1993 Aug 15; 109(4):925-32. PubMed ID: 8401946
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