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Eric R Wengert

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Biorxiv : the Preprint Server for Biology|October 10, 2024
Impaired excitability of fast-spiking neurons in a novel mouse model of <i>KCNC1</i> epileptic encephalopathyEric R Wengert, Melody A Cheng, Sophie R Liebergall, et al.
Epilepsia|May 22, 2018
The novel sodium channel modulator GS-458967 (GS967) is an effective treatment in a mouse model of SCN8A encephalopathyErin M Baker, Christopher H Thompson, Nicole A Hawkins, et al.
Human Mutation|May 5, 2018
Partial loss-of-function of sodium channel SCN8A in familial isolated myoclonusJacy L Wagnon, Niccolò E Mencacci, Bryan S Barker, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 21, 2021
Somatostatin-Positive Interneurons Contribute to Seizures in <i>SCN8A</i> Epileptic EncephalopathyEric R Wengert, Raquel M Miralles, Kyle C A Wedgwood, et al.
JCI Insight|October 22, 2024
Parvalbumin interneuron impairment causes synaptic transmission deficits and seizures in SCN8A developmental and epileptic encephalopathyRaquel M Miralles, Alexis R Boscia, Shrinidhi Kittur, et al.
Elife|February 18, 2026
Impaired excitability of fast-spiking neurons in a novel mouse model of <i>KCNC1</i> epileptic encephalopathyEric R Wengert, Sophie R Liebergall, Teresa Jimenez, et al.
Annals of Neurology|February 19, 2021
Postictal Death Is Associated with Tonic Phase Apnea in a Mouse Model of Sudden Unexpected Death in EpilepsyIan C Wenker, Frida A Teran, Eric R Wengert, et al.
Brain : a Journal of Neurology|January 3, 2019
Prominent role of forebrain excitatory neurons in SCN8A encephalopathyRosie K A Bunton-Stasyshyn, Jacy L Wagnon, Eric R Wengert, et al.
Cell Reports. Medicine|January 24, 2024
Targeted therapy improves cellular dysfunction, ataxia, and seizure susceptibility in a model of a progressive myoclonus epilepsyHuijie Feng, Jerome Clatot, Keisuke Kaneko, et al.
Epilepsia|October 19, 2019
Biallelic inherited SCN8A variants, a rare cause of SCN8A-related developmental and epileptic encephalopathyEric R Wengert, Cathrine E Tronhjem, Jacy L Wagnon, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Biorxiv : the Preprint Server for Biology|October 10, 2024
Impaired excitability of fast-spiking neurons in a novel mouse model of <i>KCNC1</i> epileptic encephalopathyEric R Wengert, Melody A Cheng, Sophie R Liebergall, et al.
Epilepsia|May 22, 2018
The novel sodium channel modulator GS-458967 (GS967) is an effective treatment in a mouse model of SCN8A encephalopathyErin M Baker, Christopher H Thompson, Nicole A Hawkins, et al.
Human Mutation|May 5, 2018
Partial loss-of-function of sodium channel SCN8A in familial isolated myoclonusJacy L Wagnon, Niccolò E Mencacci, Bryan S Barker, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 21, 2021
Somatostatin-Positive Interneurons Contribute to Seizures in <i>SCN8A</i> Epileptic EncephalopathyEric R Wengert, Raquel M Miralles, Kyle C A Wedgwood, et al.
JCI Insight|October 22, 2024
Parvalbumin interneuron impairment causes synaptic transmission deficits and seizures in SCN8A developmental and epileptic encephalopathyRaquel M Miralles, Alexis R Boscia, Shrinidhi Kittur, et al.
Elife|February 18, 2026
Impaired excitability of fast-spiking neurons in a novel mouse model of <i>KCNC1</i> epileptic encephalopathyEric R Wengert, Sophie R Liebergall, Teresa Jimenez, et al.
Annals of Neurology|February 19, 2021
Postictal Death Is Associated with Tonic Phase Apnea in a Mouse Model of Sudden Unexpected Death in EpilepsyIan C Wenker, Frida A Teran, Eric R Wengert, et al.
Brain : a Journal of Neurology|January 3, 2019
Prominent role of forebrain excitatory neurons in SCN8A encephalopathyRosie K A Bunton-Stasyshyn, Jacy L Wagnon, Eric R Wengert, et al.
Cell Reports. Medicine|January 24, 2024
Targeted therapy improves cellular dysfunction, ataxia, and seizure susceptibility in a model of a progressive myoclonus epilepsyHuijie Feng, Jerome Clatot, Keisuke Kaneko, et al.
Epilepsia|October 19, 2019
Biallelic inherited SCN8A variants, a rare cause of SCN8A-related developmental and epileptic encephalopathyEric R Wengert, Cathrine E Tronhjem, Jacy L Wagnon, et al.
Pageof 2