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British Journal of Pharmacology|May 30, 2024
Pronociceptive role of spinal Cav2.3 (R-type) calcium channels in a mouse model of postoperative painMarcella de Amorim Ferreira, Debora Denardin Lückemeyer, Fernanda Martins, et al.
Pflugers Archiv : European Journal of Physiology|September 11, 2015
Effect of the T-type channel blocker KYS-05090S in mouse models of acute and neuropathic painSaïd M'Dahoma, Vinicius M Gadotti, Fang-Xiong Zhang, et al.
Channels (Austin, Tex.)|June 9, 2012
AKAP79 modulation of L-type channels involves disruption of intramolecular interactions in the CaV1.2 subunitChristophe Altier, Stefan J Dubel, Christian Barrere, et al.
ACS Chemical Neuroscience|February 3, 2022
A Synthetically Accessible Small-Molecule Inhibitor of USP5-Cav3.2 Calcium Channel Interactions with Analgesic PropertiesAgustin Garcia-Caballero, Vinicius M Gadotti, Md Yousof Ali, et al.
Annals of Neurology|February 19, 2009
Glutamate receptors on myelinated spinal cord axons: I. GluR6 kainate receptorsMohamed Ouardouz, Elaine Coderre, Ajoy Basak, et al.
The Journal of Cell Biology|April 30, 2008
Prion protein attenuates excitotoxicity by inhibiting NMDA receptorsHouman Khosravani, Yunfeng Zhang, Shigeki Tsutsui, et al.
Epilepsia|March 15, 2006
Functional analysis of Ca3.2 T-type calcium channel mutations linked to childhood absence epilepsyJean B Peloquin, Houman Khosravani, Wendy Barr, et al.
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