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Han Choe, Ph.D. - Publications

Affiliations: 
Physiology University of Ulsan College of Medicine 
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28 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2014 Lee SH, Sung MJ, Lee HM, Chu D, Hahn SJ, Jo SH, Choe H, Choi BH. Blockade of HERG human K+ channels by the antidepressant drug paroxetine. Biological & Pharmaceutical Bulletin. 37: 1495-504. PMID 25177033 DOI: DN/JST.JSTAGE/bpb/b14-00244  0.409
2013 Choi SW, Kim KS, Shin DH, Yoo HY, Choe H, Ko TH, Youm JB, Kim WK, Zhang YH, Kim SJ. Class 3 inhibition of hERG K+ channel by caffeic acid phenethyl ester (CAPE) and curcumin. Pflã¼Gers Archiv : European Journal of Physiology. 465: 1121-34. PMID 23440458 DOI: 10.1007/s00424-013-1239-7  0.335
2013 Hong HK, Lee BH, Park MH, Lee SH, Chu D, Kim WJ, Choe H, Hee Choi B, Jo SH. Block of hERG K+ channel and prolongation of action potential duration by fluphenazine at submicromolar concentration. European Journal of Pharmacology. 702: 165-73. PMID 23395964 DOI: 10.1016/j.ejphar.2013.01.039  0.363
2012 Lee SH, Sung MJ, Hahn SJ, Kim J, Min G, Jo SH, Choe H, Choi BH. Blockade of human HERG K⁺ channels by rosiglitazone, an antidiabetic drug. Archives of Pharmacal Research. 35: 1655-64. PMID 23054723 DOI: 10.1007/S12272-012-0917-X  0.383
2012 Jeon J, Hong C, Park E, Jeon J, Choe H, Suh C, Kim H, So I. Selective Gαi Subunits as Novel Direct Activators of TRPC4 and TRPC5 Channels Biophysical Journal. 102: 535a. DOI: 10.1016/J.Bpj.2011.11.2922  0.341
2011 Lee SH, Hahn SJ, Min G, Kim J, Jo SH, Choe H, Choi BH. Inhibitory actions of HERG currents by the immunosuppressant drug cyclosporin a. The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology. 15: 291-7. PMID 22128262 DOI: 10.4196/Kjpp.2011.15.5.291  0.385
2011 Lee BH, Lee SH, Chu D, Hyun JW, Choe H, Choi BH, Jo SH. Effects of the histamine H(1) receptor antagonist hydroxyzine on hERG K(+) channels and cardiac action potential duration. Acta Pharmacologica Sinica. 32: 1128-37. PMID 21892192 DOI: 10.1038/aps.2011.66  0.349
2011 Choi SH, Shin TJ, Hwang SH, Lee BH, Kang J, Kim HJ, Jo SH, Choe H, Nah SY. Ginsenoside Rg(3) decelerates hERG K(+) channel deactivation through Ser631 residue interaction. European Journal of Pharmacology. 663: 59-67. PMID 21586280 DOI: 10.1016/j.ejphar.2011.05.006  0.461
2010 Choi SH, Shin TJ, Lee BH, Chu DH, Choe H, Pyo MK, Hwang SH, Kim BR, Lee SM, Lee JH, Kim DH, Kim HC, Rhim HW, Nah SY. Ginsenoside Rg3 activates human KCNQ1 K+ channel currents through interacting with the K318 and V319 residues: a role of KCNE1 subunit. European Journal of Pharmacology. 637: 138-47. PMID 20399767 DOI: 10.1016/j.ejphar.2010.04.001  0.4
2009 Jo SH, Hong HK, Chong SH, Lee HS, Choe H. H(1) antihistamine drug promethazine directly blocks hERG K(+) channel. Pharmacological Research : the Official Journal of the Italian Pharmacological Society. 60: 429-37. PMID 19497368 DOI: 10.1016/j.phrs.2009.05.008  0.373
2008 Kim YJ, Hong HK, Lee HS, Moh SH, Park JC, Jo SH, Choe H. Papaverine, a vasodilator, blocks the pore of the HERG channel at submicromolar concentration. Journal of Cardiovascular Pharmacology. 52: 485-93. PMID 19034039 DOI: 10.1097/FJC.0b013e31818e65c2  0.395
2008 Jo SH, Hong HK, Chong SH, Won KH, Jung SJ, Choe H. Clomipramine block of the hERG K+ channel: accessibility to F656 and Y652. European Journal of Pharmacology. 592: 19-25. PMID 18634780 DOI: 10.1016/j.ejphar.2008.06.094  0.392
2008 Jo SH, Hong HK, Chong SH, Choe H. Protriptyline block of the human ether-à-go-go-related gene (HERG) K+ channel. Life Sciences. 82: 331-40. PMID 18191158 DOI: 10.1016/j.lfs.2007.12.004  0.333
2008 Lee JH, Lee BH, Choi SH, Yoon IS, Pyo MK, Shin TJ, Choi WS, Lim Y, Rhim H, Won KH, Lim YW, Choe H, Kim DH, Kim YI, Nah SY. Ginsenoside Rg3 inhibits human Kv1.4 channel currents by interacting with the Lys531 residue. Molecular Pharmacology. 73: 619-26. PMID 17959711 DOI: 10.1124/mol.107.040360  0.434
2007 Jo SH, Hong HK, Jung SJ, Chong SH, Yun JH, Koh YS, Choe H. Maprotiline block of the human ether-a-go-go-related gene (HERG) K+ channel. Archives of Pharmacal Research. 30: 453-60. PMID 17489361  0.341
2006 Lee SY, Kim YJ, Kim KT, Choe H, Jo SH. Blockade of HERG human K+ channels and IKr of guinea-pig cardiomyocytes by the antipsychotic drug clozapine. British Journal of Pharmacology. 148: 499-509. PMID 16633353 DOI: 10.1038/sj.bjp.0706744  0.303
2006 Choe H, Nah KH, Lee SN, Lee HS, Lee HS, Jo SH, Leem CH, Jang YJ. A novel hypothesis for the binding mode of HERG channel blockers. Biochemical and Biophysical Research Communications. 344: 72-8. PMID 16616004 DOI: 10.1016/j.bbrc.2006.03.146  0.326
2003 Choe H, Lee YK, Lee YT, Choe H, Ko SH, Joo CU, Kim MH, Kim GS, Eun JS, Kim JH, Chae SW, Kwak YG. Papaverine blocks hKv1.5 channel current and human atrial ultrarapid delayed rectifier K+ currents. The Journal of Pharmacology and Experimental Therapeutics. 304: 706-12. PMID 12538825 DOI: 10.1124/jpet.102.042770  0.416
2002 Park JB, Choe H, Lee YK, Ha KC, Rhee KS, Ko JK, Joo CU, Chae SW, Kwak YG. Open channel block by KCB-328 [1-(2-amino-4-methanesulfonamidophenoxy)-2-[N-(3,4-dimethoxyphenethyl)-N-methylamino]ethane hydrochloride] of the heterologously expressed human ether-a-go-go-related gene K+ channels. The Journal of Pharmacology and Experimental Therapeutics. 302: 314-9. PMID 12065732 DOI: 10.1124/JPET.302.1.314  0.42
2001 Choe H, Sackin H, Palmer LG. Gating properties of inward-rectifier potassium channels: effects of permeant ions. The Journal of Membrane Biology. 184: 81-9. PMID 11687881 DOI: 10.1007/S00232-001-0076-3  0.59
2001 Sackin H, Syn S, Palmer LG, Choe H, Walters DE. Regulation of ROMK by extracellular cations. Biophysical Journal. 80: 683-97. PMID 11159436 DOI: 10.1016/S0006-3495(01)76048-1  0.606
2000 Choe H, Sackin H, Palmer LG. Permeation properties of inward-rectifier potassium channels and their molecular determinants. The Journal of General Physiology. 115: 391-404. PMID 10736307 DOI: 10.1085/Jgp.115.4.391  0.625
1999 Choe H, Palmer LG, Sackin H. Structural determinants of gating in inward-rectifier K+ channels. Biophysical Journal. 76: 1988-2003. PMID 10096896 DOI: 10.1016/S0006-3495(99)77357-1  0.6
1998 Choe H, Sackin H, Palmer LG. Permeation and gating of an inwardly rectifying potassium channel. Evidence for a variable energy well. The Journal of General Physiology. 112: 433-46. PMID 9758862 DOI: 10.1085/Jgp.112.4.433  0.635
1997 Choe H, Zhou H, Palmer LG, Sackin H. A conserved cytoplasmic region of ROMK modulates pH sensitivity, conductance, and gating. American Journal of Physiology. Renal Physiology. 273: F516-F529. PMID 29587098 DOI: 10.1152/ajprenal.1997.273.4.F516  0.6
1997 Choe H, Zhou H, Palmer LG, Sackin H. A conserved cytoplasmic region of ROMK modulates pH sensitivity, conductance, and gating. The American Journal of Physiology. 273: F516-29. PMID 9362329 DOI: 10.1152/Ajprenal.1997.273.4.F516  0.616
1997 Palmer LG, Choe H, Frindt G. Is the secretory K channel in the rat CCT ROMK? The American Journal of Physiology. 273: F404-10. PMID 9321913 DOI: 10.1152/Ajprenal.1997.273.3.F404  0.639
1996 Zhou H, Chepilko S, Schütt W, Choe H, Palmer LG, Sackin H. Mutations in the pore region of ROMK enhance Ba2+ block. The American Journal of Physiology. 271: C1949-56. PMID 8997197 DOI: 10.1152/Ajpcell.1996.271.6.C1949  0.626
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