Similar articles for PMID: 19401195

Year	Number of Results
1984	2
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1990	2
1991	1
1992	2
1993	5
1994	4
1995	6
1996	4
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1998	3
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2001	17
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2012	14
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2014	7
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2019	10
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2024	0

1

Five different profiles of dihydropyridines in blocking T-type Ca(2+) channel subtypes (Ca(v)3.1 (alpha(1G)), Ca(v)3.2 (alpha(1H)), and Ca(v)3.3 (alpha(1I))) expressed in Xenopus oocytes.

Furukawa T, Nukada T, Namiki Y, Miyashita Y, Hatsuno K, Ueno Y, Yamakawa T, Isshiki T. Furukawa T, et al. Eur J Pharmacol. 2009 Jun 24;613(1-3):100-7. doi: 10.1016/j.ejphar.2009.04.036. Epub 2009 May 3. Eur J Pharmacol. 2009. PMID: 19401195

2

Selectivities of dihydropyridine derivatives in blocking Ca(2+) channel subtypes expressed in Xenopus oocytes.

Furukawa T, Yamakawa T, Midera T, Sagawa T, Mori Y, Nukada T. Furukawa T, et al. J Pharmacol Exp Ther. 1999 Nov;291(2):464-73. J Pharmacol Exp Ther. 1999. PMID: 10525060

3

Contrasting the effects of nifedipine on subtypes of endogenous and recombinant T-type Ca2+ channels.

Shcheglovitov A, Zhelay T, Vitko Y, Osipenko V, Perez-Reyes E, Kostyuk P, Shuba Y. Shcheglovitov A, et al. Biochem Pharmacol. 2005 Mar 1;69(5):841-54. doi: 10.1016/j.bcp.2004.11.024. Epub 2005 Jan 12. Biochem Pharmacol. 2005. PMID: 15710361

4

Differential blocking action of dihydropyridine Ca2+ antagonists on a T-type Ca2+ channel (alpha1G) expressed in Xenopus oocytes.

Furukawa T, Nukada T, Miura R, Ooga K, Honda M, Watanabe S, Koganesawa S, Isshiki T. Furukawa T, et al. J Cardiovasc Pharmacol. 2005 Mar;45(3):241-6. doi: 10.1097/01.fjc.0000154374.88283.15. J Cardiovasc Pharmacol. 2005. PMID: 15725949

5

Blockade of T-type voltage-dependent Ca2+ channels by benidipine, a dihydropyridine calcium channel blocker, inhibits aldosterone production in human adrenocortical cell line NCI-H295R.

Akizuki O, Inayoshi A, Kitayama T, Yao K, Shirakura S, Sasaki K, Kusaka H, Matsubara M. Akizuki O, et al. Eur J Pharmacol. 2008 Apr 28;584(2-3):424-34. doi: 10.1016/j.ejphar.2008.02.001. Epub 2008 Feb 12. Eur J Pharmacol. 2008. PMID: 18331727

6

Identification of R(-)-isomer of efonidipine as a selective blocker of T-type Ca2+ channels.

Furukawa T, Miura R, Honda M, Kamiya N, Mori Y, Takeshita S, Isshiki T, Nukada T. Furukawa T, et al. Br J Pharmacol. 2004 Dec;143(8):1050-7. doi: 10.1038/sj.bjp.0705944. Epub 2004 Nov 15. Br J Pharmacol. 2004. PMID: 15545287 Free PMC article.

7

A region of N-type Ca(2+) channel critical for blockade by the dihydropyridine amlodipine.

Miyashita Y, Furukawa T, Kamegaya E, Yoshii M, Nukada T. Miyashita Y, et al. Eur J Pharmacol. 2010 Apr 25;632(1-3):14-22. doi: 10.1016/j.ejphar.2010.01.006. Epub 2010 Jan 22. Eur J Pharmacol. 2010. PMID: 20097194

8

Block of cloned human T-type calcium channels by succinimide antiepileptic drugs.

Gomora JC, Daud AN, Weiergräber M, Perez-Reyes E. Gomora JC, et al. Mol Pharmacol. 2001 Nov;60(5):1121-32. Mol Pharmacol. 2001. PMID: 11641441

9

T-type Ca2+ channel blockade prevents sudden death in mice with heart failure.

Kinoshita H, Kuwahara K, Takano M, Arai Y, Kuwabara Y, Yasuno S, Nakagawa Y, Nakanishi M, Harada M, Fujiwara M, Murakami M, Ueshima K, Nakao K. Kinoshita H, et al. Circulation. 2009 Sep 1;120(9):743-52. doi: 10.1161/CIRCULATIONAHA.109.857011. Epub 2009 Aug 17. Circulation. 2009. PMID: 19687356

10

The biochemical activation of T-type Ca2+ channels in HEK293 cells stably expressing alpha1G and Kir2.1 subunits.

Kim T, Choi J, Kim S, Kwon O, Nah SY, Han YS, Rhim H. Kim T, et al. Biochem Biophys Res Commun. 2004 Nov 5;324(1):401-8. doi: 10.1016/j.bbrc.2004.09.069. Biochem Biophys Res Commun. 2004. PMID: 15465033

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