Hydrogen Sulfide and T-Type Ca²⁺ Channels in Pain Processing, Neuronal Differentiation and Neuroendocrine Secretion

Publisher： Karger

E-ISSN： 1423-0313|99|3-4|196-203

ISSN： 0031-7012

Source： Pharmacology, Vol.99, Iss.3-4, 2016-12, pp. : 196-203

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Effects of Raloxifene on Voltage- Dependent T-Type Ca²⁺ Channels in Mouse Spermatogenic Cells

Pharmacology, Vol. 87, Iss. 1-2, 2011-01 ,pp. : 70-80

Karger

Access to resources Recommend Favorite

Inhibition of T-Type and L-Type Ca²⁺ Currents by Aranidipine, a Novel Dihydropyridine Ca²⁺ Antagonist

Pharmacology, Vol. 61, Iss. 2, 2000-08 ,pp. : 57-61

Karger

Access to resources Recommend Favorite

Voltage-Dependent and Frequency-Independent Inhibition of Recombinant Ca_v3.2 T-Type Ca²⁺ Channel by Bepridil

Pharmacology, Vol. 74, Iss. 4, 2005-07 ,pp. : 174-181

Karger

Access to resources Recommend Favorite

Lysophosphatidylcholine Augments Ca_v3.2 but Not Ca_v3.1 T-Type Ca²⁺ Channel Current Expressed in HEK-293 Cells

Pharmacology, Vol. 76, Iss. 4, 2006-04 ,pp. : 192-200

Karger

Access to resources Recommend Favorite

Actions of Mibefradil, Efonidipine and Nifedipine Block of Recombinant T- and L-Type Ca²⁺ Channels with Distinct Inhibitory Mechanisms

Pharmacology, Vol. 78, Iss. 1, 2006-09 ,pp. : 11-20

Karger

Access to resources Recommend Favorite