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Martin H Berryer

Showing results (1-10 of 9) with videos related to

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Elife|December 7, 2019
Fly model sheds light on brain diseaseMartin H Berryer, Sara G Kosmaczewski, Lindy E Barrett
Eneuro|April 18, 2023
<i>Syngap1</i> Disruption Induced by Recombination between Inverted loxP Sites Is Associated with Hippocampal Interneuron DysfunctionAbdessattar Khlaifia, Vidya Jadhav, Marc Danik, et al.
Cell Reports|September 7, 2022
Molecular convergence between Down syndrome and fragile X syndrome identified using human pluripotent stem cell modelsSara G Susco, Sulagna Ghosh, Patrizia Mazzucato, et al.
Nature Communications|November 10, 2016
Decrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive functionMartin H Berryer, Bidisha Chattopadhyaya, Paul Xing, et al.
Iscience|August 3, 2023
Robust induction of functional astrocytes using NGN2 expression in human pluripotent stem cellsMartin H Berryer, Matthew Tegtmeyer, Loïc Binan, et al.
Elife|April 21, 2023
High-content synaptic phenotyping in human cellular models reveals a role for BET proteins in synapse assemblyMartin H Berryer, Gizem Rizki, Anna Nathanson, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 3, 2017
Antenatal Suppression of IL-1 Protects against Inflammation-Induced Fetal Injury and Improves Neonatal and Developmental Outcomes in MiceMathieu Nadeau-Vallée, Peck-Yin Chin, Lydia Belarbi, et al.
Autophagy|July 8, 2025
Activation of endogenous PRKN by structural derepression is linked to increased turnover of the E3 ubiquitin ligaseFabienne C Fiesel, Bernardo A Bustillos, Jens O Watzlawik, et al.
Human Mutation|November 20, 2012
Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiencyMartin H Berryer, Fadi F Hamdan, Laura L Klitten, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Elife|December 7, 2019
Fly model sheds light on brain diseaseMartin H Berryer, Sara G Kosmaczewski, Lindy E Barrett
Eneuro|April 18, 2023
<i>Syngap1</i> Disruption Induced by Recombination between Inverted loxP Sites Is Associated with Hippocampal Interneuron DysfunctionAbdessattar Khlaifia, Vidya Jadhav, Marc Danik, et al.
Cell Reports|September 7, 2022
Molecular convergence between Down syndrome and fragile X syndrome identified using human pluripotent stem cell modelsSara G Susco, Sulagna Ghosh, Patrizia Mazzucato, et al.
Nature Communications|November 10, 2016
Decrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive functionMartin H Berryer, Bidisha Chattopadhyaya, Paul Xing, et al.
Iscience|August 3, 2023
Robust induction of functional astrocytes using NGN2 expression in human pluripotent stem cellsMartin H Berryer, Matthew Tegtmeyer, Loïc Binan, et al.
Elife|April 21, 2023
High-content synaptic phenotyping in human cellular models reveals a role for BET proteins in synapse assemblyMartin H Berryer, Gizem Rizki, Anna Nathanson, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 3, 2017
Antenatal Suppression of IL-1 Protects against Inflammation-Induced Fetal Injury and Improves Neonatal and Developmental Outcomes in MiceMathieu Nadeau-Vallée, Peck-Yin Chin, Lydia Belarbi, et al.
Autophagy|July 8, 2025
Activation of endogenous PRKN by structural derepression is linked to increased turnover of the E3 ubiquitin ligaseFabienne C Fiesel, Bernardo A Bustillos, Jens O Watzlawik, et al.
Human Mutation|November 20, 2012
Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiencyMartin H Berryer, Fadi F Hamdan, Laura L Klitten, et al.
Pageof 1