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Wu Shi

Showing results (131-140 of 180) with videos related to

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Epilepsy Research|January 1, 2021
Ilepcimide inhibited sodium channel activity in mouse hippocampal neuronsYang Zeng, Bing Qin, Yi-Wu Shi, et al.
Neurogenetics|November 14, 2017
ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variationJing-Yang Wang, Peng Zhou, Jie Wang, et al.
Nature Communications|March 24, 2024
Tunable anisotropic van der Waals films of 2M-WS<sub>2</sub> for plasmon canalizationQiaoxia Xing, Jiasheng Zhang, Yuqiang Fang, et al.
Physical Review Letters|March 7, 2025
Large Tunneling Magnetoresistance in Nonvolatile 2D Hybrid Spin FiltersXiaoyu Wang, Lihao Zhang, Miao He, et al.
Physical Review Letters|August 11, 2018
Correlation of Electron Tunneling and Plasmon Propagation in a Luttinger LiquidSihan Zhao, Sheng Wang, Fanqi Wu, et al.
Human Genetics|January 28, 2014
A novel variant in the 3' UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH's bindingTao Zeng, Zhao-Fei Dong, Shu-Jing Liu, et al.
Molecular Neurobiology|March 13, 2016
A Point Mutation in SCN1A 5' Genomic Region Decreases the Promoter Activity and Is Associated with Mild Epilepsy and Seizure Aggravation Induced by Antiepileptic DrugQu-Wen Gao, Li-Dong Hua, Jie Wang, et al.
ACS Nano|May 15, 2023
Robust Threshold-Switching Behavior Assisted by Cu Migration in a Ferroionic CuInP<sub>2</sub>S<sub>6</sub> HeterostructureZhipeng Zhong, Shuaiqin Wu, Xiang Li, et al.
Frontiers in Genetics|November 16, 2020
Heterozygous <i>PGM3</i> Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete PenetranceXiao-Rong Liu, Wen-Jun Bian, Jie Wang, et al.
Frontiers in Aging Neuroscience|April 25, 2022
Novel <i>PANK2</i> Mutations in Patients With Pantothenate Kinase-Associated Neurodegeneration and the Genotype-Phenotype CorrelationWen-Bin Li, Nan-Xiang Shen, Chao Zhang, et al.
Pageof 18

Showing results (131-140 of 180) with videos related to

Sort By:
Pageof 18
Epilepsy Research|January 1, 2021
Ilepcimide inhibited sodium channel activity in mouse hippocampal neuronsYang Zeng, Bing Qin, Yi-Wu Shi, et al.
Neurogenetics|November 14, 2017
ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variationJing-Yang Wang, Peng Zhou, Jie Wang, et al.
Nature Communications|March 24, 2024
Tunable anisotropic van der Waals films of 2M-WS<sub>2</sub> for plasmon canalizationQiaoxia Xing, Jiasheng Zhang, Yuqiang Fang, et al.
Physical Review Letters|March 7, 2025
Large Tunneling Magnetoresistance in Nonvolatile 2D Hybrid Spin FiltersXiaoyu Wang, Lihao Zhang, Miao He, et al.
Physical Review Letters|August 11, 2018
Correlation of Electron Tunneling and Plasmon Propagation in a Luttinger LiquidSihan Zhao, Sheng Wang, Fanqi Wu, et al.
Human Genetics|January 28, 2014
A novel variant in the 3' UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH's bindingTao Zeng, Zhao-Fei Dong, Shu-Jing Liu, et al.
Molecular Neurobiology|March 13, 2016
A Point Mutation in SCN1A 5' Genomic Region Decreases the Promoter Activity and Is Associated with Mild Epilepsy and Seizure Aggravation Induced by Antiepileptic DrugQu-Wen Gao, Li-Dong Hua, Jie Wang, et al.
ACS Nano|May 15, 2023
Robust Threshold-Switching Behavior Assisted by Cu Migration in a Ferroionic CuInP<sub>2</sub>S<sub>6</sub> HeterostructureZhipeng Zhong, Shuaiqin Wu, Xiang Li, et al.
Frontiers in Genetics|November 16, 2020
Heterozygous <i>PGM3</i> Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete PenetranceXiao-Rong Liu, Wen-Jun Bian, Jie Wang, et al.
Frontiers in Aging Neuroscience|April 25, 2022
Novel <i>PANK2</i> Mutations in Patients With Pantothenate Kinase-Associated Neurodegeneration and the Genotype-Phenotype CorrelationWen-Bin Li, Nan-Xiang Shen, Chao Zhang, et al.
Pageof 18