Zhuo Huang

Affiliations: 
School of Pharmacy, University of London, London, England, United Kingdom 
Area:
cellular phsiology
Google:
"Zhuo Huang"
Mean distance: 15.6 (cluster 11)
 
SNBCP
Cross-listing: Chemistry Tree

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Publications

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Wang Z, Zheng H, Yang H, et al. (2024) Cannabichromene from full-spectrum hemp extract exerts acute anti-seizure effects through allosteric activation of GABA receptors. Fundamental Research. 4: 1357-1364
Zheng R, Li Z, Wang Q, et al. (2024) Discovery of Potent and Selective Blockers Targeting the Epilepsy-Associated K1.1 Channel. Journal of Medicinal Chemistry
Di C, Wu T, Gao K, et al. (2024) Carvedilol inhibits neuronal hyperexcitability caused by epilepsy-associated KCNT1 mutations. British Journal of Pharmacology
Wang Y, Yang H, Li N, et al. (2024) A Novel Ubiquitin Ligase Adaptor PTPRN Suppresses Seizure Susceptibility through Endocytosis of Na1.2 Sodium Channels. Advanced Science (Weinheim, Baden-Wurttemberg, Germany). e2400560
Chen H, Xia Z, Dong J, et al. (2024) Structural mechanism of voltage-gated sodium channel slow inactivation. Nature Communications. 15: 3691
Wei Y, Yu Z, Wang L, et al. (2024) Structural bases of inhibitory mechanism of Ca1.2 channel inhibitors. Nature Communications. 15: 2772
Yuan T, Wang Y, Jin Y, et al. (2024) Coupling of Slack and Na1.6 sensitizes Slack to quinidine blockade and guides anti-seizure strategy development. Elife. 12
Zhang J, Liu S, Fan J, et al. (2023) Structural basis of human Slo2.2 channel gating and modulation. Cell Reports. 42: 112858
Gu J, Ke P, Guo H, et al. (2023) KCTD13-mediated ubiquitination and degradation of GluN1 regulates excitatory synaptic transmission and seizure susceptibility. Cell Death and Differentiation
Li Y, Yuan T, Huang B, et al. (2023) Structure of human Na1.6 channel reveals Na selectivity and pore blockade by 4,9-anhydro-tetrodotoxin. Nature Communications. 14: 1030
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