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Human Molecular Genetics|November 11, 2010
Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of tuberous sclerosis complexLing-Hui Zeng, Nicholas R Rensing, Bo Zhang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 26, 2007
Kainate seizures cause acute dendritic injury and actin depolymerization in vivoLing-Hui Zeng, Lin Xu, Nicholas R Rensing, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 28, 2022
Non-sedative cortical EEG signatures of allopregnanolone and functional comparatorsPeter M Lambert, Richard Ni, Ann Benz, et al.
Journal of Neurophysiology|February 7, 2024
Periodic and aperiodic changes to cortical EEG in response to pharmacological manipulationSofia V Salvatore, Peter M Lambert, Ann Benz, et al.
Biorxiv : the Preprint Server for Biology|October 4, 2023
Periodic and aperiodic changes to cortical EEG in response to pharmacological manipulationSofia V Salvatore, Peter M Lambert, Ann Benz, et al.
Scientific Reports|July 5, 2022
Effects of chronic cannabidiol in a mouse model of naturally occurring neuroinflammation, neurodegeneration, and spontaneous seizuresJoshua T Dearborn, Hemanth R Nelvagal, Nicholas R Rensing, et al.
The Journal of Clinical Investigation|April 27, 2023
Gene therapy ameliorates spontaneous seizures associated with cortical neuron loss in a Cln2R207X mouse modelKeigo Takahashi, Elizabeth M Eultgen, Sophie H Wang, et al.
Brain Pathology (Zurich, Switzerland)|March 31, 2021
Upregulation of the pathogenic transcription factor SPI1/PU.1 in tuberous sclerosis complex and focal cortical dysplasia by oxidative stressTill S Zimmer, Anatoly Korotkov, Susan Zwakenberg, et al.
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