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Molecular Brain|April 5, 2022
CTCF in parvalbumin-expressing neurons regulates motor, anxiety and social behavior and neuronal identityLiron Davis, Prudhvi Raj Rayi, Dmitriy Getselter, et al.
Cells|February 9, 2024
Molecular Insights into Transcranial Direct Current Stimulation Effects: Metabolomics and Transcriptomics AnalysesBhanumita Agrawal, Soad Boulos, Soliman Khatib, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 2, 2011
Alterations in intrinsic membrane properties and the axon initial segment in a mouse model of Angelman syndromeHanoch Kaphzan, Shelly A Buffington, Joo In Jung, et al.
Plos One|January 6, 2007
NMDA and dopamine converge on the NMDA-receptor to induce ERK activation and synaptic depression in mature hippocampusHanoch Kaphzan, Kenneth J O'Riordan, Kile P Mangan, et al.
Frontiers in Molecular Neuroscience|August 8, 2014
Dopamine-induced tyrosine phosphorylation of NR2B (Tyr1472) is essential for ERK1/2 activation and processing of novel taste informationOrit David, Iliana Barrera, Adaikkan Chinnakkaruppan, et al.
Journal of Neuroscience Research|February 12, 2016
Calmodulin activity regulates group I metabotropic glutamate receptor-mediated signal transduction and synaptic depressionFerzin Sethna, Ming Zhang, Hanoch Kaphzan, et al.
Molecular Neurobiology|February 2, 2019
Sex-Dependent Sensory Phenotypes and Related Transcriptomic Expression Profiles Are Differentially Affected by Angelman SyndromeLee Koyavski, Julia Panov, Lilach Simchi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 15, 2015
Mitochondrial Superoxide Contributes to Hippocampal Synaptic Dysfunction and Memory Deficits in Angelman Syndrome Model MiceEmanuela Santini, Kathryn L Turner, Akila B Ramaraj, et al.
Cell Reports|July 21, 2012
Brain-specific disruption of the eIF2α kinase PERK decreases ATF4 expression and impairs behavioral flexibilityMimi A Trinh, Hanoch Kaphzan, Ronald C Wek, et al.
Neuron|October 23, 2012
Genetic removal of p70 S6 kinase 1 corrects molecular, synaptic, and behavioral phenotypes in fragile X syndrome miceAditi Bhattacharya, Hanoch Kaphzan, Amanda C Alvarez-Dieppa, et al.
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