Jo SH - Search Results

1

The Ca(2+) channel inhibitor efonidipine decreases voltage-dependent K(+) channel activity in rabbit coronary arterial smooth muscle cells.

Park MH, Son YK, Hong DH, Choi IW, Kim DJ, Lee H, Bang H, Na SH, Li H, Jo SH, Park WS. Park MH, et al. Among authors: jo sh. Vascul Pharmacol. 2013 Sep-Oct;59(3-4):90-5. doi: 10.1016/j.vph.2013.07.005. Epub 2013 Jul 19. Vascul Pharmacol. 2013. PMID: 23876554

2

Block of HERG human K(+) channel and IKr of guinea pig cardiomyocytes by chlorpromazine.

Lee SY, Choi SY, Youm JB, Ho WK, Earm YE, Lee CO, Jo SH. Lee SY, et al. Among authors: jo sh. J Cardiovasc Pharmacol. 2004 May;43(5):706-14. doi: 10.1097/00005344-200405000-00014. J Cardiovasc Pharmacol. 2004. PMID: 15071359

3

Clomipramine block of the hERG K+ channel: accessibility to F656 and Y652.

Jo SH, Hong HK, Chong SH, Won KH, Jung SJ, Choe H. Jo SH, et al. Eur J Pharmacol. 2008 Sep 11;592(1-3):19-25. doi: 10.1016/j.ejphar.2008.06.094. Epub 2008 Jul 2. Eur J Pharmacol. 2008. PMID: 18634780

4

Papaverine, a vasodilator, blocks the pore of the HERG channel at submicromolar concentration.

Kim YJ, Hong HK, Lee HS, Moh SH, Park JC, Jo SH, Choe H. Kim YJ, et al. Among authors: jo sh. J Cardiovasc Pharmacol. 2008 Dec;52(6):485-93. doi: 10.1097/FJC.0b013e31818e65c2. J Cardiovasc Pharmacol. 2008. PMID: 19034039 Free article.

5

Block of the human ether-a-go-go-related gene (hERG) K+ channel by the antidepressant desipramine.

Hong HK, Park MH, Lee BH, Jo SH. Hong HK, et al. Among authors: jo sh. Biochem Biophys Res Commun. 2010 Apr 9;394(3):536-41. doi: 10.1016/j.bbrc.2010.03.010. Epub 2010 Mar 6. Biochem Biophys Res Commun. 2010. PMID: 20211602

6

A Carbohydrate Fraction, AIP1, from Artemisia Iwayomogi Reduces the Action Potential Duration by Activation of Rapidly Activating Delayed Rectifier K Channels in Rabbit Ventricular Myocytes.

Park WS, Son YK, Ko EA, Choi SW, Kim N, Choi TH, Youn HJ, Jo SH, Hong DH, Han J. Park WS, et al. Among authors: jo sh. Korean J Physiol Pharmacol. 2010 Jun;14(3):119-25. doi: 10.4196/kjpp.2010.14.3.119. Epub 2010 Jun 30. Korean J Physiol Pharmacol. 2010. PMID: 20631882 Free PMC article.

7

The inhibitory effect of Ca2+-activated K+ channel activator, BMS on L-type Ca2+ channels in rat ventricular myocytes.

Son YK, Choi SW, Jung WK, Jo SH, Jung ID, Park YM, Choi IW, Sin JI, Shim EB, Kim N, Han J, Park WS. Son YK, et al. Among authors: jo sh. Life Sci. 2011 Aug 29;89(9-10):331-6. doi: 10.1016/j.lfs.2011.06.017. Epub 2011 Jul 7. Life Sci. 2011. PMID: 21763323

8

Acute alteration of cardiac ECG, action potential, I(Kr) and the human ether-a-go-go-related gene (hERG) K+ channel by PCB 126 and PCB 77.

Park MH, Park WS, Jo SH. Park MH, et al. Among authors: jo sh. Toxicol Appl Pharmacol. 2012 Jul 1;262(1):60-9. doi: 10.1016/j.taap.2012.04.019. Epub 2012 Apr 28. Toxicol Appl Pharmacol. 2012. PMID: 22676973

9

Block of hERG K+ channel and prolongation of action potential duration by fluphenazine at submicromolar concentration.

Hong HK, Lee BH, Park MH, Lee SH, Chu D, Kim WJ, Choe H, Hee Choi B, Jo SH. Hong HK, et al. Among authors: jo sh. Eur J Pharmacol. 2013 Feb 28;702(1-3):165-73. doi: 10.1016/j.ejphar.2013.01.039. Epub 2013 Feb 6. Eur J Pharmacol. 2013. PMID: 23395964

10

Effect of azelastine on cardiac repolarization of guinea-pig cardiomyocytes, hERG K⁺ channel, and human L-type and T-type Ca²⁺ channel.

Park MH, Lee SH, Chu DH, Won KH, Choi BH, Choe H, Jo SH. Park MH, et al. Among authors: jo sh. J Pharmacol Sci. 2013 Sep 20;123(1):67-77. doi: 10.1254/jphs.12239fp. Epub 2013 Sep 3. J Pharmacol Sci. 2013. PMID: 24005046 Free article.

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