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Moran Rubinstein
Moran Rubinstein
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Cited by
Year
Dissecting the phenotypes of Dravet syndrome by gene deletion
M Rubinstein, S Han, C Tai, RE Westenbroek, A Hunker, T Scheuer, ...
Brain 138 (8), 2219-2233, 2015
1302015
Mitochondrial regulation of the hippocampal firing rate set point and seizure susceptibility
B Styr, N Gonen, D Zarhin, A Ruggiero, R Atsmon, N Gazit, G Braun, ...
Neuron 102 (5), 1009-1024. e8, 2019
1162019
Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome
M Rubinstein, RE Westenbroek, HY Frank, CJ Jones, T Scheuer, ...
Neurobiology of disease 73, 106-117, 2015
1012015
Reciprocal changes in phosphorylation and methylation of mammalian brain sodium channels in response to seizures
JH Baek, M Rubinstein, T Scheuer, JS Trimmer
Journal of Biological Chemistry 289 (22), 15363-15373, 2014
662014
Divergent regulation of GIRK1 and GIRK2 subunits of the neuronal G protein gated K+ channel by GαiGDP and Gβγ
M Rubinstein, S Peleg, S Berlin, D Brass, T Keren‐Raifman, ...
The Journal of physiology 587 (14), 3473-3491, 2009
662009
Transcriptional activation of the insulin-like growth factor I receptor gene by the Kruppel-like factor 6 (KLF6) tumor suppressor protein: potential interactions between KLF6 …
M Rubinstein, G Idelman, SR Plymate, G Narla, SL Friedman, H Werner
Endocrinology 145 (8), 3769-3777, 2004
622004
Gαi and Gβγ jointly regulate the conformations of a Gβγ effector, the neuronal G protein-activated K+ channel (GIRK)
S Berlin, T Keren-Raifman, R Castel, M Rubinstein, CW Dessauer, ...
Journal of Biological Chemistry 285 (9), 6179-6185, 2010
592010
A novel EWS-WT1 gene fusion product in desmoplastic small round cell tumor is a potent transactivator of the insulin-like growth factor-I receptor (IGF-IR) gene
H Werner, G Idelman, M Rubinstein, P Pattee, SR Nagalla, CT Roberts Jr
Cancer letters 247 (1), 84-90, 2007
592007
Gαi3 primes the G protein‐activated K+ channels for activation by coexpressed Gβγ in intact Xenopus oocytes
M Rubinstein, S Peleg, S Berlin, D Brass, N Dascal
The Journal of physiology 581 (1), 17-32, 2007
502007
Novel ADNP syndrome mice reveal dramatic sex-specific peripheral gene expression with brain synaptic and tau pathologies
G Karmon, S Sragovich, G Hacohen-Kleiman, I Ben-Horin-Hazak, ...
Biological psychiatry 92 (1), 81-95, 2022
432022
Association of rare missense variants in the second intracellular loop of NaV1. 7 sodium channels with familial autism
M Rubinstein, A Patowary, IB Stanaway, E McCord, RR Nesbitt, M Archer, ...
Molecular psychiatry 23 (2), 231-239, 2018
382018
Developmental alterations in firing properties of hippocampal CA1 inhibitory and excitatory neurons in a mouse model of Dravet syndrome
Y Almog, S Fadila, M Brusel, A Mavashov, K Anderson, M Rubinstein
Neurobiology of disease 148, 105209, 2021
372021
Transfer of SCN1A to the brain of adolescent mouse model of Dravet syndrome improves epileptic, motor, and behavioral manifestations
L Mora-Jimenez, M Valencia, R Sanchez-Carpintero, J Tønnesen, ...
Molecular Therapy-Nucleic Acids 25, 585-602, 2021
332021
Convulsive seizures and some behavioral comorbidities are uncoupled in the Scn1aA1783V Dravet syndrome mouse model
S Fadila, S Quinn, A Turchetti Maia, D Yakubovich, M Ovadia, ...
Epilepsia 61 (10), 2289-2300, 2020
292020
Recruitment of Gβγ controls the basal activity of G‐protein coupled inwardly rectifying potassium (GIRK) channels: crucial role of distal C terminus of GIRK1
U Kahanovitch, V Tsemakhovich, S Berlin, M Rubinstein, B Styr, R Castel, ...
The Journal of physiology 592 (24), 5373-5390, 2014
282014
In vivo, in vitro and in silico correlations of four de novo SCN1A missense mutations
A Nissenkorn, Y Almog, I Adler, M Safrin, M Brusel, M Marom, S Bercovich, ...
PLoS One 14 (2), e0211901, 2019
272019
A quantitative model of the GIRK1/2 channel reveals that its basal and evoked activities are controlled by unequal stoichiometry of Gα and Gβγ
D Yakubovich, S Berlin, U Kahanovitch, M Rubinstein, I Farhy-Tselnicker, ...
PLOS Computational Biology 11 (11), e1004598, 2015
272015
Viral vector–mediated expression of NaV1.1, after seizure onset, reduces epilepsy in mice with Dravet syndrome
S Fadila, B Beucher, IG Dopeso-Reyes, A Mavashov, M Brusel, ...
The Journal of clinical investigation 133 (12), 2023
132023
Functional investigation of a neuronal microcircuit in the CA1 area of the hippocampus reveals synaptic dysfunction in Dravet syndrome mice
Y Almog, A Mavashov, M Brusel, M Rubinstein
Frontiers in Molecular Neuroscience 15, 823640, 2022
132022
Transcriptional activation of the IGF-I receptor gene by the Kruppel-like factor-6 (KLF6) tumor suppressor protein: potential interactions between KLF6 and p53
M Rubinstein, G Idelman, SR Plymate, G Narla, SL Friedman, H Werner
Endocrinology 145 (8), 3769-3777, 2004
132004
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