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Harrison W Gabel

Showing results (31-40 of 43) with videos related to

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Nature Communications|September 30, 2021
CHARGE syndrome protein CHD7 regulates epigenomic activation of enhancers in granule cell precursors and gyrification of the cerebellumNaveen C Reddy, Shahriyar P Majidi, Lingchun Kong, et al.
Neuron|October 11, 2011
Genome-wide activity-dependent MeCP2 phosphorylation regulates nervous system development and functionSonia Cohen, Harrison W Gabel, Martin Hemberg, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 15, 2018
The Transcriptional Regulator SnoN Promotes the Proliferation of Cerebellar Granule Neuron Precursors in the Postnatal Mouse BrainXiaoying Chen, Ayan Chanda, Yoshiho Ikeuchi, et al.
Cell Reports|November 25, 2020
DNMT3A Haploinsufficiency Results in Behavioral Deficits and Global Epigenomic Dysregulation Shared across Neurodevelopmental DisordersDiana L Christian, Dennis Y Wu, Jenna R Martin, et al.
Immunity|January 8, 2026
State-specific enhancer landscapes govern microglial plasticityNicole Hamagami, Dvita Kapadia, Kia M Barclay, et al.
Cell Stem Cell|September 22, 2020
Deconstructing Stepwise Fate Conversion of Human Fibroblasts to Neurons by MicroRNAsKitra Cates, Matthew J McCoy, Ji-Sun Kwon, et al.
Neuron|October 6, 2021
A MYT1L syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturationJiayang Chen, Mary E Lambo, Xia Ge, et al.
Neuron|June 21, 2024
A MYT1L syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturationJiayang Chen, Mary E Lambo, Xia Ge, et al.
Biorxiv : the Preprint Server for Biology|March 13, 2023
Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional deficitsDiana C Beard, Xiyun Zhang, Dennis Y Wu, et al.
Nature Communications|July 28, 2021
Functional and epigenetic phenotypes of humans and mice with DNMT3A Overgrowth SyndromeAmanda M Smith, Taylor A LaValle, Marwan Shinawi, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Nature Communications|September 30, 2021
CHARGE syndrome protein CHD7 regulates epigenomic activation of enhancers in granule cell precursors and gyrification of the cerebellumNaveen C Reddy, Shahriyar P Majidi, Lingchun Kong, et al.
Neuron|October 11, 2011
Genome-wide activity-dependent MeCP2 phosphorylation regulates nervous system development and functionSonia Cohen, Harrison W Gabel, Martin Hemberg, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 15, 2018
The Transcriptional Regulator SnoN Promotes the Proliferation of Cerebellar Granule Neuron Precursors in the Postnatal Mouse BrainXiaoying Chen, Ayan Chanda, Yoshiho Ikeuchi, et al.
Cell Reports|November 25, 2020
DNMT3A Haploinsufficiency Results in Behavioral Deficits and Global Epigenomic Dysregulation Shared across Neurodevelopmental DisordersDiana L Christian, Dennis Y Wu, Jenna R Martin, et al.
Immunity|January 8, 2026
State-specific enhancer landscapes govern microglial plasticityNicole Hamagami, Dvita Kapadia, Kia M Barclay, et al.
Cell Stem Cell|September 22, 2020
Deconstructing Stepwise Fate Conversion of Human Fibroblasts to Neurons by MicroRNAsKitra Cates, Matthew J McCoy, Ji-Sun Kwon, et al.
Neuron|October 6, 2021
A MYT1L syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturationJiayang Chen, Mary E Lambo, Xia Ge, et al.
Neuron|June 21, 2024
A MYT1L syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturationJiayang Chen, Mary E Lambo, Xia Ge, et al.
Biorxiv : the Preprint Server for Biology|March 13, 2023
Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional deficitsDiana C Beard, Xiyun Zhang, Dennis Y Wu, et al.
Nature Communications|July 28, 2021
Functional and epigenetic phenotypes of humans and mice with DNMT3A Overgrowth SyndromeAmanda M Smith, Taylor A LaValle, Marwan Shinawi, et al.
Pageof 5