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Molecular Pharmacology|August 15, 2001
Ca(v)3.2 channel is a molecular substrate for inhibition of T-type calcium currents in rat sensory neurons by nitrous oxideS M Todorovic, V Jevtovic-Todorovic, S Mennerick, et al.
American Journal of Physiology. Cell Physiology|February 24, 2001
alpha1H T-type Ca2+ channel is the predominant subtype expressed in bovine and rat zona glomerulosaA D Schrier, H Wang, E M Talley, et al.
FEBS Letters|January 29, 2000
Molecular cloning and functional expression of Ca(v)3.1c, a T-type calcium channel from human brainL L Cribbs, J C Gomora, A N Daud, et al.
FEBS Letters|August 3, 2000
Overexpression of T-type calcium channels in HEK-293 cells increases intracellular calcium without affecting cellular proliferationJ Chemin, A Monteil, C Briquaire, et al.
The Journal of Biological Chemistry|April 15, 1992
Molecular cloning of a human serotonin receptor (S12) with a pharmacological profile resembling that of the 5-HT1D subtypeF O Levy, T Gudermann, E Perez-Reyes, et al.
The American Journal of Physiology|March 1, 1995
Molecular characterization of renal calcium channel beta-subunit transcriptsA S Yu, M Boim, S C Hebert, et al.
The Journal of Biological Chemistry|November 10, 1995
Molecular determinants of cardiac Ca2+ channel pharmacology. Subunit requirement for the high affinity and allosteric regulation of dihydropyridine bindingX Wei, S Pan, W Lang, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 19, 2000
Mibefradil block of cloned T-type calcium channelsR L Martin, J H Lee, L L Cribbs, et al.
The Journal of Biological Chemistry|November 15, 1991
Heterologous regulation of the cardiac Ca2+ channel alpha 1 subunit by skeletal muscle beta and gamma subunits. Implications for the structure of cardiac L-type Ca2+ channelsX Y Wei, E Perez-Reyes, A E Lacerda, et al.
The Journal of Biological Chemistry|January 21, 1994
Modification of Ca2+ channel activity by deletions at the carboxyl terminus of the cardiac alpha 1 subunitX Wei, A Neely, A E Lacerda, et al.
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