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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 28, 2020
Interneuron Desynchronization Precedes Seizures in a Mouse Model of Dravet Syndrome
Conny H Tran, Michael Vaiana, Johan Nakuci, et al.
Elife
|
February 25, 2022
Corticohippocampal circuit dysfunction in a mouse model of Dravet syndrome
Joanna Mattis, Ala Somarowthu, Kevin M Goff, et al.
Translational Psychiatry
|
November 20, 2019
Mitochondrial deficits in human iPSC-derived neurons from patients with 22q11.2 deletion syndrome and schizophrenia
Jianping Li, Sean K Ryan, Erik Deboer, et al.
Biorxiv : the Preprint Server for Biology
|
February 12, 2026
Developmental dysregulation of chandelier cell excitability in a mouse model of Dravet Syndrome
Sophie F Hill, Emiola A Enakhimion, Elisabetta Furlanis, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 9, 2024
A structurally precise mechanism links an epilepsy-associated <i>KCNC2</i> potassium channel mutation to interneuron dysfunction
Jerome Clatot, Christopher B Currin, Qiansheng Liang, et al.
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 encephalopathy
Eric R Wengert, Melody A Cheng, Sophie R Liebergall, et al.
Brain : a Journal of Neurology
|
November 7, 2023
Targeted blockade of aberrant sodium current in a stem cell-derived neuron model of SCN3A encephalopathy
Guojie Qu, Julie P Merchant, Jérôme Clatot, et al.
Neuron
|
February 11, 2003
The CD26-related dipeptidyl aminopeptidase-like protein DPPX is a critical component of neuronal A-type K+ channels
Marcela S Nadal, Andrés Ozaita, Yimy Amarillo, et al.
Annals of Neurology
|
February 22, 2018
Mutations in SCN3A cause early infantile epileptic encephalopathy
Tariq Zaman, Ingo Helbig, Ivana Babić Božović, et al.
The Journal of Clinical Investigation
|
May 16, 2023
Viral vector-mediated expression of NaV1.1, after seizure onset, reduces epilepsy in mice with Dravet syndrome
Saja Fadila, Bertrand Beucher, Iria González Dopeso-Reyes, et al.
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Search research articles
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Showing results (41-50 of 74) with videos related to
Sort By:
Page
of 8
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 28, 2020
Interneuron Desynchronization Precedes Seizures in a Mouse Model of Dravet Syndrome
Conny H Tran, Michael Vaiana, Johan Nakuci, et al.
Elife
|
February 25, 2022
Corticohippocampal circuit dysfunction in a mouse model of Dravet syndrome
Joanna Mattis, Ala Somarowthu, Kevin M Goff, et al.
Translational Psychiatry
|
November 20, 2019
Mitochondrial deficits in human iPSC-derived neurons from patients with 22q11.2 deletion syndrome and schizophrenia
Jianping Li, Sean K Ryan, Erik Deboer, et al.
Biorxiv : the Preprint Server for Biology
|
February 12, 2026
Developmental dysregulation of chandelier cell excitability in a mouse model of Dravet Syndrome
Sophie F Hill, Emiola A Enakhimion, Elisabetta Furlanis, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 9, 2024
A structurally precise mechanism links an epilepsy-associated <i>KCNC2</i> potassium channel mutation to interneuron dysfunction
Jerome Clatot, Christopher B Currin, Qiansheng Liang, et al.
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 encephalopathy
Eric R Wengert, Melody A Cheng, Sophie R Liebergall, et al.
Brain : a Journal of Neurology
|
November 7, 2023
Targeted blockade of aberrant sodium current in a stem cell-derived neuron model of SCN3A encephalopathy
Guojie Qu, Julie P Merchant, Jérôme Clatot, et al.
Neuron
|
February 11, 2003
The CD26-related dipeptidyl aminopeptidase-like protein DPPX is a critical component of neuronal A-type K+ channels
Marcela S Nadal, Andrés Ozaita, Yimy Amarillo, et al.
Annals of Neurology
|
February 22, 2018
Mutations in SCN3A cause early infantile epileptic encephalopathy
Tariq Zaman, Ingo Helbig, Ivana Babić Božović, et al.
The Journal of Clinical Investigation
|
May 16, 2023
Viral vector-mediated expression of NaV1.1, after seizure onset, reduces epilepsy in mice with Dravet syndrome
Saja Fadila, Bertrand Beucher, Iria González Dopeso-Reyes, et al.
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of 8