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Wangzhen Shen

Showing results (41-50 of 52) with videos related to

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Epilepsia|December 10, 2022
Heterozygous GABA<sub>A</sub> receptor β3 subunit N110D knock-in mice have epileptic spasmsShimian Qu, Laurel G Jackson, Chengwen Zhou, et al.
Brain Communications|April 23, 2024
γ-Aminobutyric acid transporter and GABA<sub>A</sub> receptor mechanisms in <i>Slc6a1</i> and <i>Slc6a1</i> mice associated with developmental and epileptic encephalopathiesWangzhen Shen, Gerald Nwosu, Michael Honer, et al.
Brain : a Journal of Neurology|August 23, 2019
Synaptic clustering differences due to different GABRB3 mutations cause variable epilepsy syndromesYi-Wu Shi, Qi Zhang, Kefu Cai, et al.
Brain : a Journal of Neurology|May 24, 2021
Common molecular mechanisms of SLC6A1 variant-mediated neurodevelopmental disorders in astrocytes and neuronsFelicia Mermer, Sarah Poliquin, Kathryn Rigsby, et al.
Brain : a Journal of Neurology|May 7, 2019
Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathiesCiria C Hernandez, Wenshu XiangWei, Ningning Hu, et al.
Neurobiology of Disease|July 15, 2022
Astrocytic GABA transporter 1 deficit in novel SLC6A1 variants mediated epilepsy: Connected from protein destabilization to seizures in mice and humansFelicia Mermer, Sarah Poliquin, Shuizhen Zhou, et al.
Molecular Brain|May 14, 2020
Endoplasmic reticulum retention and degradation of a mutation in SLC6A1 associated with epilepsy and autismJie Wang, Sarah Poliquin, Felicia Mermer, et al.
Experimental Neurology|June 10, 2019
A missense mutation in SLC6A1 associated with Lennox-Gastaut syndrome impairs GABA transporter 1 protein trafficking and functionKefu Cai, Jie Wang, Jaclyn Eissman, et al.
Brain : a Journal of Neurology|November 20, 2016
De novo GABRG2 mutations associated with epileptic encephalopathiesDingding Shen, Ciria C Hernandez, Wangzhen Shen, et al.
Neurobiology of Disease|January 11, 2014
A novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypesAnn J Johnston, Jing-Qiong Kang, Wangzhen Shen, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Epilepsia|December 10, 2022
Heterozygous GABA<sub>A</sub> receptor β3 subunit N110D knock-in mice have epileptic spasmsShimian Qu, Laurel G Jackson, Chengwen Zhou, et al.
Brain Communications|April 23, 2024
γ-Aminobutyric acid transporter and GABA<sub>A</sub> receptor mechanisms in <i>Slc6a1</i> and <i>Slc6a1</i> mice associated with developmental and epileptic encephalopathiesWangzhen Shen, Gerald Nwosu, Michael Honer, et al.
Brain : a Journal of Neurology|August 23, 2019
Synaptic clustering differences due to different GABRB3 mutations cause variable epilepsy syndromesYi-Wu Shi, Qi Zhang, Kefu Cai, et al.
Brain : a Journal of Neurology|May 24, 2021
Common molecular mechanisms of SLC6A1 variant-mediated neurodevelopmental disorders in astrocytes and neuronsFelicia Mermer, Sarah Poliquin, Kathryn Rigsby, et al.
Brain : a Journal of Neurology|May 7, 2019
Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathiesCiria C Hernandez, Wenshu XiangWei, Ningning Hu, et al.
Neurobiology of Disease|July 15, 2022
Astrocytic GABA transporter 1 deficit in novel SLC6A1 variants mediated epilepsy: Connected from protein destabilization to seizures in mice and humansFelicia Mermer, Sarah Poliquin, Shuizhen Zhou, et al.
Molecular Brain|May 14, 2020
Endoplasmic reticulum retention and degradation of a mutation in SLC6A1 associated with epilepsy and autismJie Wang, Sarah Poliquin, Felicia Mermer, et al.
Experimental Neurology|June 10, 2019
A missense mutation in SLC6A1 associated with Lennox-Gastaut syndrome impairs GABA transporter 1 protein trafficking and functionKefu Cai, Jie Wang, Jaclyn Eissman, et al.
Brain : a Journal of Neurology|November 20, 2016
De novo GABRG2 mutations associated with epileptic encephalopathiesDingding Shen, Ciria C Hernandez, Wangzhen Shen, et al.
Neurobiology of Disease|January 11, 2014
A novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypesAnn J Johnston, Jing-Qiong Kang, Wangzhen Shen, et al.
Pageof 6