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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Antunes FTT, Huang S, Chen L, et al. (2024) Effect of ABT-639 on Cav3.2 channel activity and its analgesic actions in mouse models of inflammatory and neuropathic pain. European Journal of Pharmacology. 967: 176416
Weiss N, Zamponi GW. (2023) The T-type calcium channelosome. Pflugers Archiv : European Journal of Physiology
Stringer RN, Cmarko L, Zamponi GW, et al. (2023) Electrophysiological characterization of a Ca3.2 calcium channel missense variant associated with epilepsy and hearing loss. Molecular Brain. 16: 68
Alonso-Matielo H, Zhang Z, Gambeta E, et al. (2023) Inhibitory insula-ACC projections modulate affective but not sensory aspects of neuropathic pain. Molecular Brain. 16: 64
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
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