Kaphzan, Hanoch

Genetic Removal of p70 S6 Kinase 1 Corrects Molecular, Synaptic, and Behavioral Phenotypes in Fragile X Syndrome Mice

Bhattacharya, A., Kaphzan, H., Alvarez-Dieppa, A. C., Murphy, J. P., Pierre, P., & Klann, E. (2012) · Neuron

Genetics and Neurodevelopmental DisordersRNA and protein synthesis mechanisms

Cited by 316

Macroautophagy deficiency mediates age-dependent neurodegeneration through a phospho-tau pathway

Inoue, K., Rispoli, J., Kaphzan, H., Klann, E., Chen, E. I., Kim, J., Komatsu, M., & Abeliovich, A. (2012) · Molecular Neurodegeneration

Alzheimer's disease research and treatmentsAutophagy in Disease and Therapy

Cited by 168

Neuronal CTCF Is Necessary for Basal and Experience-Dependent Gene Regulation, Memory Formation, and Genomic Structure of BDNF and Arc

Sams, D. S., Nardone, S., Getselter, D., Raz, D., Tal, M., Rayi, P. R., Kaphzan, H., Hakim, O., & Elliott, E. (2016) · Cell Reports

Memory and Neural MechanismsGenomics and Chromatin Dynamics

Cited by 92

Metabotropic glutamate receptor-dependent long-term depression is impaired due to elevated ERK signaling in the ΔRG mouse model of tuberous sclerosis complex

Chévere-Torres, I., Kaphzan, H., Bhattacharya, A., Kang, A., Maki, J. M., Gambello, M. J., Arbiser, J. L., Santini, E., & Klann, E. (2012) · Neurobiology of Disease

Tuberous Sclerosis Complex ResearchGenetics and Neurodevelopmental Disorders

Cited by 83

Dynamic shift in localization of UBE3A across developmental stages in an Angelman syndrome mouse model

Gupta, P. K., Feuermann, Y., & Kaphzan, H. (2025) · Neurobiology of Disease

Ubiquitin and proteasome pathwaysGenetic Syndromes and Imprinting

Cited by 5