CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
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Chd8 Mutation Leads to Autistic-like Behaviors and Impaired Striatal CircuitsUsing Animal Models to Study the Role of the Gut-Brain Axis in Autism.Arid1b haploinsufficient mice reveal neuropsychiatric phenotypes and reversible causes of growth impairment.Epigenetic Mistakes in Neurodevelopmental Disorders.Transcribing the connectome: roles for transcription factors and chromatin regulators in activity-dependent synapse development.Autism spectrum disorder: neuropathology and animal models.Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in MiceToward a conceptual framework for early brain and behavior development in autism.Decreased Brain pH as a Shared Endophenotype of Psychiatric Disorders.Genomic Patterns of De Novo Mutation in Simplex Autism.When size matters: CHD8 in autism.Early postnatal vocalizations predict sociability and spatial memory in C57BL/6J mice: Individual differences in behavioral traits emerge early in development.Germline Chd8 haploinsufficiency alters brain development in mouse.Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.Fundamental Elements in Autism: From Neurogenesis and Neurite Growth to Synaptic Plasticity.Nervous system development and disease: A focus on trithorax related proteins and chromatin remodelers.Whither the genotype-phenotype relationship? An historical and methodological appraisal.Translating genetic and preclinical findings into autism therapies.Lineage specific transcription factors and epigenetic regulators mediate TGFβ-dependent enhancer activation.Epigenetic Modifications: Insight into Oligodendrocyte Lineage Progression, Regeneration and Disease.ATP-Dependent Chromatin Remodeling During Cortical Neurogenesis.Degradation of the endoplasmic reticulum-anchored transcription factor MyRF by the ubiquitin ligase SCFFbxw7 in a manner dependent on the kinase GSK-3.Altered Neocortical Gene Expression, Brain Overgrowth and Functional Over-Connectivity in Chd8 Haploinsufficient Mice.Behavioral and neuroanatomical approaches in models of neurodevelopmental disorders: opportunities for translation.Dual Requirement of CHD8 for Chromatin Landscape Establishment and Histone Methyltransferase Recruitment to Promote CNS Myelination and RepairSertraline, chlorprothixene, and chlorpromazine characteristically interact with the REST-binding site of the corepressor mSin3, showing medulloblastoma cell growth inhibitory activitiesOligodendrocyte precursor survival and differentiation requires chromatin remodeling by Chd7 and Chd8Sex-specific Behavioral Features of Rodent Models of Autism Spectrum DisorderConnexin 30 Deficiency Attenuates Chronic but Not Acute Phases of Experimental Autoimmune Encephalomyelitis Through Induction of Neuroprotective Microglia
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P2860
CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh-hant
name
CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
@en
CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
@nl
type
label
CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
@en
CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
@nl
prefLabel
CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
@en
CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
@nl
P2093
P2860
P921
P356
P1433
P1476
CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
@en
P2093
Atsuki Kawamura
Hirotaka Shoji
Keiichi I Nakayama
Masaaki Nishiyama
Mikita Suyama
Tetsuya Sato
Toru Takumi
Tsuyoshi Miyakawa
Yuta Katayama
P2860
P2888
P304
P356
10.1038/NATURE19357
P407
P577
2016-09-07T00:00:00Z
P6179
1002336951