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Journal Abstract Search

489 related items for PubMed ID: 10087049

  • 21. 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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  • 22. Pinacidil relaxes porcine and human coronary arteries by activating ATP-dependent potassium channels in smooth muscle cells.
    Gollasch M, Bychkov R, Ried C, Behrendt F, Scholze S, Luft FC, Haller H.
    J Pharmacol Exp Ther; 1995 Nov; 275(2):681-92. PubMed ID: 7473155
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  • 24. BL-1249 [(5,6,7,8-tetrahydro-naphthalen-1-yl)-[2-(1H-tetrazol-5-yl)-phenyl]-amine]: a putative potassium channel opener with bladder-relaxant properties.
    Tertyshnikova S, Knox RJ, Plym MJ, Thalody G, Griffin C, Neelands T, Harden DG, Signor L, Weaver D, Myers RA, Lodge NJ.
    J Pharmacol Exp Ther; 2005 Apr; 313(1):250-9. PubMed ID: 15608074
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  • 25. 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(4):258-66. PubMed ID: 12934053
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  • 26. Pharmacological characterization of urinary bladder smooth muscle contractility following partial bladder outlet obstruction in pigs.
    Milicic I, Buckner SA, Daza A, Coghlan M, Fey TA, Brune ME, Gopalakrishnan M.
    Eur J Pharmacol; 2006 Feb 17; 532(1-2):107-14. PubMed ID: 16487510
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  • 29. The molecular composition of K(ATP) channels in human pulmonary artery smooth muscle cells and their modulation by growth.
    Cui Y, Tran S, Tinker A, Clapp LH.
    Am J Respir Cell Mol Biol; 2002 Jan 17; 26(1):135-43. PubMed ID: 11751213
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  • 31. Characterization of human urinary bladder KATP channels containing SUR2B splice variants expressed in L-cells.
    Scott VE, Davis-Taber RA, Silvia C, Hoogenboom L, Choi W, Kroeger P, Whiteaker KL, Gopalakrishnan M.
    Eur J Pharmacol; 2004 Jan 12; 483(2-3):195-205. PubMed ID: 14729107
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  • 33. Actions of ZD0947, a novel ATP-sensitive K+ channel opener, on membrane currents in human detrusor myocytes.
    Aishima M, Tomoda T, Yunoki T, Nakano T, Seki N, Yonemitsu Y, Sueishi K, Naito S, Ito Y, Teramoto N.
    Br J Pharmacol; 2006 Nov 12; 149(5):542-50. PubMed ID: 17016513
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  • 35. Pharmacological characterization of a 1,4-dihydropyridine analogue, 9-(3,4-dichlorophenyl)-3,3,6,6-tetramethyl-3,4,6,7,9,10-hexahydro-1,8(2H,5H)-acridinedione (A-184209) as a novelK(ATP) channel inhibitor.
    Gopalakrishnan M, Miller TR, Buckner SA, Milicic I, Molinari EJ, Whiteaker KL, Davis-Taber R, Scott VE, Cassidy C, Sullivan JP, Carroll WA.
    Br J Pharmacol; 2003 Jan 12; 138(2):393-9. PubMed ID: 12540531
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  • 38. Inhibition of Na(+)-K+ pump alleviates the shortening of action potential duration caused by metabolic inhibition via blockade of KATP channels in coronary perfused ventricular muscles of guinea-pigs.
    Abe T, Sato T, Kiyosue T, Saikawa T, Sakata T, Arita M.
    J Mol Cell Cardiol; 1999 Mar 12; 31(3):533-42. PubMed ID: 10198185
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  • 39. Fluorescence-based functional assay for sarcolemmal ATP-sensitive potassium channel activation in cultured neonatal rat ventricular myocytes.
    Whiteaker KL, Davis-Taber R, Scott VE, Gopalakrishnan M.
    J Pharmacol Toxicol Methods; 2001 Mar 12; 46(1):45-50. PubMed ID: 12164259
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