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Wangzhen Shen

Showing results (11-20 of 52) with videos related to

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Epilepsia|September 18, 2020
Endoplasmic reticulum stress increases inflammatory cytokines in an epilepsy mouse model Gabrg2<sup>+/Q390X</sup> knockin: A link between genetic and acquired epilepsy?Wangzhen Shen, Sarah Poliquin, Robert L Macdonald, et al.
Biochemical and Biophysical Research Communications|July 14, 2023
Ginsenoside Rg1 improved learning and memory ability and reduces neuronal apoptosis in epileptic rats through ERK/CREB/BDNF signal pathwayJiawei Zhang, Chaochao Zhu, Yun Jin, et al.
Organic & Biomolecular Chemistry|September 13, 2022
A review on the assembly of multi-substituted pyridines <i>via</i> Co-catalyzed [2 + 2 + 2] cycloaddition with nitrilesKaili Cen, Muhammad Usman, Wangzhen Shen, et al.
Nature Neuroscience|May 26, 2015
The human epilepsy mutation GABRG2(Q390X) causes chronic subunit accumulation and neurodegenerationJing-Qiong Kang, Wangzhen Shen, Chengwen Zhou, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 20, 2002
Modulation of the human Kv1.5 channel by protein kinase C activation: role of the Kvbeta1.2 subunitChristine P Williams, NingNing Hu, Wangzhen Shen, et al.
Journal of Molecular and Cellular Cardiology|February 9, 2005
Rapid stimulation causes electrical remodeling in cultured atrial myocytesZhenjiang Yang, Wangzhen Shen, Jeffrey N Rottman, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 15, 2010
Slow degradation and aggregation in vitro of mutant GABAA receptor gamma2(Q351X) subunits associated with epilepsyJing-Qiong Kang, Wangzhen Shen, Melissa Lee, et al.
International Journal of Molecular Sciences|May 11, 2024
Modulating Endoplasmic Reticulum Chaperones and Mutant Protein Degradation in GABRG2(Q390X) Associated with Genetic Epilepsy with Febrile Seizures Plus and Dravet SyndromeSarah Poliquin, Gerald Nwosu, Karishma Randhave, et al.
Epilepsy Research|February 9, 2025
4-Phenylbutyrate restored GABA uptake, mitigated seizures in SLC6A1 and SLC6A11 microdeletions/3p- syndrome: From cellular models to human patientsMelissa B DeLeeuw, Wangzhen Shen, Xiaojuan Tian, et al.
Human Molecular Genetics|June 25, 2016
Differential molecular and behavioural alterations in mouse models of GABRG2 haploinsufficiency versus dominant negative mutations associated with human epilepsyTimothy A Warner, Wangzhen Shen, Xuan Huang, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Epilepsia|September 18, 2020
Endoplasmic reticulum stress increases inflammatory cytokines in an epilepsy mouse model Gabrg2<sup>+/Q390X</sup> knockin: A link between genetic and acquired epilepsy?Wangzhen Shen, Sarah Poliquin, Robert L Macdonald, et al.
Biochemical and Biophysical Research Communications|July 14, 2023
Ginsenoside Rg1 improved learning and memory ability and reduces neuronal apoptosis in epileptic rats through ERK/CREB/BDNF signal pathwayJiawei Zhang, Chaochao Zhu, Yun Jin, et al.
Organic & Biomolecular Chemistry|September 13, 2022
A review on the assembly of multi-substituted pyridines <i>via</i> Co-catalyzed [2 + 2 + 2] cycloaddition with nitrilesKaili Cen, Muhammad Usman, Wangzhen Shen, et al.
Nature Neuroscience|May 26, 2015
The human epilepsy mutation GABRG2(Q390X) causes chronic subunit accumulation and neurodegenerationJing-Qiong Kang, Wangzhen Shen, Chengwen Zhou, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 20, 2002
Modulation of the human Kv1.5 channel by protein kinase C activation: role of the Kvbeta1.2 subunitChristine P Williams, NingNing Hu, Wangzhen Shen, et al.
Journal of Molecular and Cellular Cardiology|February 9, 2005
Rapid stimulation causes electrical remodeling in cultured atrial myocytesZhenjiang Yang, Wangzhen Shen, Jeffrey N Rottman, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 15, 2010
Slow degradation and aggregation in vitro of mutant GABAA receptor gamma2(Q351X) subunits associated with epilepsyJing-Qiong Kang, Wangzhen Shen, Melissa Lee, et al.
International Journal of Molecular Sciences|May 11, 2024
Modulating Endoplasmic Reticulum Chaperones and Mutant Protein Degradation in GABRG2(Q390X) Associated with Genetic Epilepsy with Febrile Seizures Plus and Dravet SyndromeSarah Poliquin, Gerald Nwosu, Karishma Randhave, et al.
Epilepsy Research|February 9, 2025
4-Phenylbutyrate restored GABA uptake, mitigated seizures in SLC6A1 and SLC6A11 microdeletions/3p- syndrome: From cellular models to human patientsMelissa B DeLeeuw, Wangzhen Shen, Xiaojuan Tian, et al.
Human Molecular Genetics|June 25, 2016
Differential molecular and behavioural alterations in mouse models of GABRG2 haploinsufficiency versus dominant negative mutations associated with human epilepsyTimothy A Warner, Wangzhen Shen, Xuan Huang, et al.
Pageof 6