Han Choe, Ph.D.
Affiliations: | Physiology | University of Ulsan College of Medicine |
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"Han Choe"Mean distance: 23748
Parents
Sign in to add mentor| Lawrence G. Palmer | grad student | 1994-1999 | Weill Cornell Medical College |
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Publications
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| Lee SH, Sung MJ, Lee HM, et al. (2014) Blockade of HERG human K+ channels by the antidepressant drug paroxetine. Biological & Pharmaceutical Bulletin. 37: 1495-504 |
| Choi SW, Kim KS, Shin DH, et al. (2013) Class 3 inhibition of hERG K+ channel by caffeic acid phenethyl ester (CAPE) and curcumin. Pflã¼Gers Archiv : European Journal of Physiology. 465: 1121-34 |
| Hong HK, Lee BH, Park MH, et al. (2013) Block of hERG K+ channel and prolongation of action potential duration by fluphenazine at submicromolar concentration. European Journal of Pharmacology. 702: 165-73 |
| Lee SH, Sung MJ, Hahn SJ, et al. (2012) Blockade of human HERG K⺠channels by rosiglitazone, an antidiabetic drug. Archives of Pharmacal Research. 35: 1655-64 |
| Jeon J, Hong C, Park E, et al. (2012) Selective Gαi Subunits as Novel Direct Activators of TRPC4 and TRPC5 Channels Biophysical Journal. 102: 535a |
| Lee SH, Hahn SJ, Min G, et al. (2011) 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 |
| Lee BH, Lee SH, Chu D, et al. (2011) Effects of the histamine H(1) receptor antagonist hydroxyzine on hERG K(+) channels and cardiac action potential duration. Acta Pharmacologica Sinica. 32: 1128-37 |
| Choi SH, Shin TJ, Hwang SH, et al. (2011) Ginsenoside Rg(3) decelerates hERG K(+) channel deactivation through Ser631 residue interaction. European Journal of Pharmacology. 663: 59-67 |
| Choi SH, Shin TJ, Lee BH, et al. (2010) 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 |
| Jo SH, Hong HK, Chong SH, et al. (2009) H(1) antihistamine drug promethazine directly blocks hERG K(+) channel. Pharmacological Research : the Official Journal of the Italian Pharmacological Society. 60: 429-37 |