Moran Rubinstein

Tel Aviv, TA, Israel

Last Updated: 09/26/2026

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Found 24 publications

Behavioral and epileptic phenotypes in a CHD2-related developmental delay model.

Behavioral and epileptic phenotypes in a CHD2-related developmental delay model.

Journal: Epilepsia

Published: April 06, 2025

Disrupted temperature-sleep coupling mechanism in a Dravet syndrome mouse model.

Disrupted temperature-sleep coupling mechanism in a Dravet syndrome mouse model.

Journal: Nature communications

Published: March 10, 2025

A mouse model of GRIN2D developmental and epileptic encephalopathy recapitulates the human disease.

A mouse model of GRIN2D developmental and epileptic encephalopathy recapitulates the human disease.

Journal: Brain : a journal of neurology

Published: October 16, 2024

Synaptic dysregulation in a mouse model of GRIN2D developmental and epileptic encephalopathy.

Synaptic dysregulation in a mouse model of GRIN2D developmental and epileptic encephalopathy.

Journal: Brain : a journal of neurology

Published: October 15, 2024

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

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

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: December 17, 2023

Preferential expression of SCN1A in GABAergic neurons improves survival and epileptic phenotype in a mouse model of Dravet syndrome.

Preferential expression of SCN1A in GABAergic neurons improves survival and epileptic phenotype in a mouse model of Dravet syndrome.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: May 05, 2023

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

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

Journal: Frontiers in cellular neuroscience

Published: January 21, 2023

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

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

Journal: Frontiers in pharmacology

Published: December 07, 2022

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

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

Journal: The Journal of clinical investigation

Published: February 14, 2022

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

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

Journal: Frontiers in molecular neuroscience

Published: November 27, 2021

Transfer of SCN1A to the brain of adolescent mouse model of Dravet syndrome improves epileptic, motor, and behavioral manifestations.

Transfer of SCN1A to the brain of adolescent mouse model of Dravet syndrome improves epileptic, motor, and behavioral manifestations.

Journal: Molecular therapy. Nucleic acids

Published: May 04, 2021

Novel ADNP Syndrome Mice Reveal Dramatic Sex-Specific Peripheral Gene Expression With Brain Synaptic and Tau Pathologies.

Novel ADNP Syndrome Mice Reveal Dramatic Sex-Specific Peripheral Gene Expression With Brain Synaptic and Tau Pathologies.

Journal: Biological psychiatry

Published: April 19, 2021

Showing 1-12 of 24

Last Updated: 09/26/2026