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Frontiers in Genetics
|
May 1, 2014
Chromatin regulators, phenotypic robustness, and autism risk
Reut Suliman, Eyal Ben-David, Sagiv Shifman
Plos Computational Biology
|
December 11, 2020
Value-complexity tradeoff explains mouse navigational learning
Nadav Amir, Reut Suliman-Lavie, Maayan Tal, et al.
Acta Neuropathologica Communications
|
February 26, 2026
Kcnq2 R213 knock-in mice reveal variant- and region-specific mechanisms underlying self-limited familial neonatal-infantile epilepsy and early infantile developmental and epileptic encephalopathy
Takuma Nishijo, Nanako Hamada, Reut Suliman-Lavie, et al.
Nature Communications
|
November 18, 2020
Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
Reut Suliman-Lavie, Ben Title, Yahel Cohen, et al.
Nature Communications
|
June 18, 2021
Author Correction: Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
Reut Suliman-Lavie, Ben Title, Yahel Cohen, et al.
EMBO Molecular Medicine
|
May 5, 2026
Distinct pathophysiological mechanisms of CEP152 variants in microcephaly and brain abnormalities
Nanako Hamada, Lama AlAbdi, Tomoko Uehara, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Frontiers in Genetics
|
May 1, 2014
Chromatin regulators, phenotypic robustness, and autism risk
Reut Suliman, Eyal Ben-David, Sagiv Shifman
Plos Computational Biology
|
December 11, 2020
Value-complexity tradeoff explains mouse navigational learning
Nadav Amir, Reut Suliman-Lavie, Maayan Tal, et al.
Acta Neuropathologica Communications
|
February 26, 2026
Kcnq2 R213 knock-in mice reveal variant- and region-specific mechanisms underlying self-limited familial neonatal-infantile epilepsy and early infantile developmental and epileptic encephalopathy
Takuma Nishijo, Nanako Hamada, Reut Suliman-Lavie, et al.
Nature Communications
|
November 18, 2020
Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
Reut Suliman-Lavie, Ben Title, Yahel Cohen, et al.
Nature Communications
|
June 18, 2021
Author Correction: Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
Reut Suliman-Lavie, Ben Title, Yahel Cohen, et al.
EMBO Molecular Medicine
|
May 5, 2026
Distinct pathophysiological mechanisms of CEP152 variants in microcephaly and brain abnormalities
Nanako Hamada, Lama AlAbdi, Tomoko Uehara, et al.
Page
of 1