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Moran Rubinstein

Tel Aviv University

31

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548

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Reprogramming of two induced pluripotent stem cell lines from a heterozygous GRIN2D developmental and epileptic encephalopathy (DEE) patient (BGUi011-A) and from a healthy family relative (BGUi012-A).

2021 Stem Cell Research
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Developmental alterations in firing properties of hippocampal CA1 inhibitory and excitatory neurons in a mouse model of Dravet syndrome.

2021 Neurobiology of Disease
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Transfer of SCN1A to the brain of adolescent mouse model of Dravet syndrome improves epileptic, motor, and behavioral manifestations

2021 Molecular therapy. Nucleic acids
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Novel ADNP syndrome mice reveal dramatic sex-specific peripheral gene expression with brain synaptic and Tau pathologies

2021 Biological Psychiatry
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Striatin is required for hearing and affects inner hair cells and ribbon synapses

2020 Frontiers in Cell and Developmental Biology
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Early EEG and behavioral alterations in Dravet mice

2020 bioRxiv
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Convulsive seizures and some behavioral comorbidities are uncoupled in the Scn1a A1783V Dravet syndrome mouse model

2020 Epilepsia
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Striatin is required for hearing and affects inner hair cells and ribbon synapses

2020 bioRxiv
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Mitochondrial Regulation of the Hippocampal Firing Rate Set Point and Seizure Susceptibility

2019 Neuron
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In vivo, in vitro and in silico correlations of four de novo SCN1A missense mutations

2019 PLOS ONE
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