Gerald W. Zamponi

Affiliations: 
Physiology and Pharmacology University of Calgary, Calgary, Alberta, Canada 
Area:
calcium channels
Website:
http://www.ucalgary.ca/physiology/faculty/primary-members/gerald-w-zamponi
Google:
"Gerald Zamponi"
Mean distance: 15.82 (cluster 11)
 
SNBCP
Cross-listing: Chemistry Tree

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Publications

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Martins DF, Sorrentino V, Mazzardo-Martins L, et al. (2023) Antihyperalgesic effect of joint mobilization requires Cav3.2 calcium channels. Molecular Brain. 16: 60
Ferron L, Gandini MA, Zamponi GW. (2023) Fighting pain: the structure of gabapentin and its binding site in the Caαδ subunit. Nature Structural & Molecular Biology. 30: 717-719
de Maria Gadotti V, Antunes FTT, Zamponi GW. (2023) Analgesia by intrathecal delta-9-tetrahydrocannabinol is dependent on Cav3.2 calcium channels. Molecular Brain. 16: 47
Ali MY, Gadotti VM, Huang S, et al. (2023) Icariside II, a Prenyl-Flavonol, Alleviates Inflammatory and Neuropathic Pain by Inhibiting T-Type Calcium Channels and USP5-Cav3.2 Interactions. Acs Chemical Neuroscience
Alaklabi AM, Gambeta E, Zamponi GW. (2023) Electrophysiological characterization of a Ca3.1 calcium channel mutation linked to trigeminal neuralgia. Pflugers Archiv : European Journal of Physiology
Harding EK, Souza IA, Gandini MA, et al. (2023) Differential regulation of Cav3.2 and Cav2.2 calcium channels by CB1 receptors and cannabidiol. British Journal of Pharmacology
Caminski ES, Antunes FTT, Souza IA, et al. (2022) Regulation of N-type calcium channels by nociceptin receptors and its possible role in neurological disorders. Molecular Brain. 15: 95
Mustafá ER, Gambeta E, Stringer RN, et al. (2022) Electrophysiological and computational analysis of Ca3.2 channel variants associated with familial trigeminal neuralgia. Molecular Brain. 15: 91
Ferron L, Zamponi GW. (2022) The road to the brain in Timothy syndrome is paved with enhanced CaV1.2 activation gating. The Journal of General Physiology. 154
Duran P, Loya-López S, Ran D, et al. (2022) The natural product Argentatin C attenuates postoperative pain via inhibition of voltage-gated sodium and T-type voltage-gated calcium channels. British Journal of Pharmacology
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