Marina Brusel

发表

Acute effect of antiseizure drugs on background oscillations in Scn1a A1783V Dravet syndrome mouse model

M. Brusel, Shir Quinn, Mor Ovadia, 2022, bioRxiv.

Functional Investigation of a Neuronal Microcircuit in the CA1 Area of the Hippocampus Reveals Synaptic Dysfunction in Dravet Syndrome Mice

M. Rubinstein, M. Brusel, Y. Almog, 2022, Frontiers in Molecular Neuroscience.

Developmental alterations in firing properties of hippocampal CA1 inhibitory and excitatory neurons in a mouse model of Dravet syndrome

M. Rubinstein, M. Brusel, Y. Almog, 2020, Neurobiology of Disease.

Early hippocampal hyperexcitability followed by disinhibition in a mouse model of Dravet syndrome

M. Brusel, Y. Almog, K. Anderson, 2019, bioRxiv.

Heat-induced seizures, premature mortality, and hyperactivity in a novel Scn1a nonsense model for Dravet syndrome

V. Dani, M. Rubinstein, M. Brusel, 2023, bioRxiv.

Viral vector–mediated expression of NaV1.1, after seizure onset, reduces epilepsy in mice with Dravet syndrome

Ethan M. Goldberg, E. Kremer, Bertrand Beucher, 2023, The Journal of clinical investigation.

Complex biophysical changes and reduced neuronal firing in an SCN8A variant associated with developmental delay and epilepsy

H. Bassan, Y. Haitin, Roy Ben-Shalom, 2023, bioRxiv.

The SCN8A p.(Gly1625Arg) variant associated with developmental and epileptic encephalopathy causes complex biophysical changes and reduced neuronal firing

H. Bassan, Y. Haitin, Roy Ben-Shalom, 2022 .

Exogenous NaV1.1 activity in excitatory and inhibitory neurons reverts Dravet syndrome comorbidities when delivered post-symptom onset in mice with Dravet

Ethan M. Goldberg, M. Rubinstein, E. Kremer, 2022, bioRxiv.

In vivo, in vitro and in silico correlations of four de novo SCN1A missense mutations

M. Rubinstein, B. Ben-Zeev, M. Brusel, 2019, PloS one.