Maria A. Gandini
Affiliations: | University of Calgary, Calgary, Alberta, Canada |
Area:
Calcium ChannelsGoogle:
"Maria Gandini"Mean distance: 17.82 (cluster 11) | S | N | B | C | P |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Kricek F, Ruf C, Meghani P, et al. (2024) A next generation peripherally restricted Cavα2δ-1 ligand with inhibitory action on Cav2.2 channels and utility in neuropathic pain. Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie. 174: 116472 |
Gandini MA, Zamponi GW. (2024) Opening the K3.1 gates: A therapeutic strategy for progressive myoclonus epilepsy type 7? Cell Reports. Medicine. 5: 101425 |
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 |
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 |
Gambeta E, Gandini MA, Souza IA, et al. (2022) CaV3.2 calcium channels contribute to trigeminal neuralgia. Pain |
Gandini MA, Souza IA, Khullar A, et al. (2021) Correction to: Regulation of Ca3.2 channels by the receptor for activated C kinase 1 (Rack-1). Pflugers Archiv : European Journal of Physiology |
Gandini MA, Souza IA, Khullar A, et al. (2021) Regulation of Ca3.2 channels by the receptor for activated C kinase 1 (Rack-1). Pflugers Archiv : European Journal of Physiology |
Souza IA, Gandini MA, Zamponi GW. (2021) Splice-variant specific effects of a CACNA1H mutation associated with writer's cramp. Molecular Brain. 14: 145 |
Gandini MA, Zamponi GW. (2021) Voltage-gated calcium channel nanodomains: molecular composition and function. The Febs Journal |
Gandini MA, Souza IA, Ferron L, et al. (2021) The de novo CACNA1A pathogenic variant Y1384C associated with hemiplegic migraine, early onset cerebellar atrophy and developmental delay leads to a loss of Cav2.1 channel function. Molecular Brain. 14: 27 |