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Journal Abstract Search


104 related items for PubMed ID: 9604853

  • 1. The natriuretic activity of the K+ channel blocker U-37883A displays an ADH-dependence.
    Clark MA, Lawson JA, Ludens JH.
    Methods Find Exp Clin Pharmacol; 1998 Mar; 20(2):115-23. PubMed ID: 9604853
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  • 2. Effects of a K+ channel blocker on glomerular filtration rate and electrolyte excretion in conscious rats.
    Ludens JH, Clark MA, Lawson JA.
    J Pharmacol Exp Ther; 1995 Jun; 273(3):1375-81. PubMed ID: 7791110
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  • 3. Interaction of the diuretics torasemide and U-37883A with the K(ATP) channel in rat isolated aorta.
    Löffler-Walz C, Quast U.
    Naunyn Schmiedebergs Arch Pharmacol; 1998 Aug; 358(2):230-7. PubMed ID: 9750009
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  • 4. Renal and vascular effects of chemically distinct ATP-sensitive K+ channel blockers in rats.
    Ludens JH, Clark MA, Smith MP, Humphrey SJ.
    J Cardiovasc Pharmacol; 1995 Mar; 25(3):404-9. PubMed ID: 7769805
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  • 6. Cardiovascular effects of the K-ATP channel blocker U-37883A and structurally related morpholinoguanidines.
    Humphrey SJ, Smith MP, Cimini MG, Buchanan LV, Gibson JK, Khan SA, Meisheri KD.
    Methods Find Exp Clin Pharmacol; 1996 May; 18(4):247-60. PubMed ID: 8803957
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  • 7. Eukaliuric diuresis and natriuresis in response to the KATP channel blocker U37883A: micropuncture studies on the tubular site of action.
    Huang DY, Osswald H, Vallon V.
    Br J Pharmacol; 1999 Aug; 127(8):1811-8. PubMed ID: 10482911
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  • 11. Diuretic activity of N'-disubstituted morpholinoguanidine analogs of U-37883A in rats and dogs.
    Humphrey SJ, Ludens JH, Perricone SC, Skaletzky LL, Graham BE, Zins GR.
    Methods Find Exp Clin Pharmacol; 1995 May; 17(4):255-66. PubMed ID: 7475512
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  • 12. Potassium diet as a determinant for the renal response to systemic potassium channel modulation in anesthetized rats.
    Vallon V, Kirschenmann D, Brenner I, Albinus M, Osswald H.
    Naunyn Schmiedebergs Arch Pharmacol; 1998 Aug; 358(2):245-52. PubMed ID: 9750011
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  • 13. Sodium reabsorption in thick ascending limb of Henle's loop: effect of potassium channel blockade in vivo.
    Huang DY, Osswald H, Vallon V.
    Br J Pharmacol; 2000 Jul; 130(6):1255-62. PubMed ID: 10903963
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  • 14. 4-morpholinecarboximidine-N-1-adamantyl-N'-cyclohexylhydrochloride (U-37883A): pharmacological characterization of a novel antagonist of vascular ATP-sensitive K+ channel openers.
    Meisheri KD, Humphrey SJ, Khan SA, Cipkus-Dubray LA, Smith MP, Jones AW.
    J Pharmacol Exp Ther; 1993 Aug; 266(2):655-65. PubMed ID: 8355199
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  • 16. Guanidine derivative U-37883A, inhibits mitochondrial K+ uniport.
    Szewczyk A, Wójcik G, Jabłonowska A, Nałecz.
    Pol J Pharmacol; 1995 Aug; 47(4):339-44. PubMed ID: 8616514
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  • 17. Multiple actions of U-37883A, an ATP-sensitive K+ channel blocker, on membrane currents in pig urethra.
    Tomoda T, Yunoki T, Naito S, Ito Y, Teramoto N.
    Eur J Pharmacol; 2005 Nov 07; 524(1-3):1-10. PubMed ID: 16242124
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  • 18. Inhibition of ROMK blocks macula densa tubuloglomerular feedback yet causes renal vasoconstriction in anesthetized rats.
    Araujo M, Welch WJ, Zhou X, Sullivan K, Walsh S, Pasternak A, Wilcox CS.
    Am J Physiol Renal Physiol; 2017 Jun 01; 312(6):F1120-F1127. PubMed ID: 28228405
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  • 19. Receptor binding characterization in kidney membrane of [3H]U-37883, a novel ATP-sensitive K+ channel blocker with diuretic/natriuretic properties.
    Meisheri K, Fosset M, Humphrey S, Lazdunski M.
    Mol Pharmacol; 1995 Jan 01; 47(1):155-63. PubMed ID: 7838124
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