Zhuo Huang
Affiliations: | School of Pharmacy, University of London, London, England, United Kingdom |
Area:
cellular phsiologyGoogle:
"Zhuo Huang"Mean distance: 15.6 (cluster 11) | S | N | B | C | P |
Cross-listing: Chemistry Tree
Parents
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Sign in to add traineeshuai Xu | grad student | Peking University | |
Jingyun Yi | grad student | Univerisity College London | |
Na Li | grad student | 2020- | Peking University |
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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 |