Five different profiles of dihydropyridines in blocking T-type Ca2+ channel subtypes (Cav3.1 (α1G), Cav3.2 (α1H), and Cav3.3 (α1I)) expressed in Xenopus oocytes-Reference-Cited by-同舟云学术

Five different profiles of dihydropyridines in blocking T-type Ca2+ channel subtypes (Cav3.1 (α1G), Cav3.2 (α1H), and Cav3.3 (α1I)) expressed in Xenopus oocytes

Published:2009-06 Issue:1-3 Volume:613 Page:100-107
ISSN:0014-2999
Container-title:European Journal of Pharmacology
language:en
Short-container-title:European Journal of Pharmacology

Author:

Furukawa Taiji,Nukada Toshihide,Namiki Yoshiko,Miyashita Yoriko,Hatsuno Kento,Ueno Yasunari,Yamakawa Takeshi,Isshiki Takaaki

Publisher

Elsevier BV

Subject

Pharmacology

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3. Dihydropyridine-sensitive low-threshold calcium channels in isolated rat hypothalamic neurones;Akaike;J. Physiol.,1989

4. Low-voltage activated calcium channels are differently affected by nimodipine;Formenti;Neuroreport,1993

5. Selectivities of dihydropyridine derivatives in blocking Ca(2+) channel subtypes expressed in Xenopus oocytes;Furukawa;J. Pharmacol. Exp. Ther.,1999

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