Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice
about
Molecular mechanisms in 22q11 deletion syndrome.Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit developmentAltered functional protein networks in the prefrontal cortex and amygdala of victims of suicidePersistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice.Animal models of gene-environment interaction in schizophrenia: A dimensional perspective.Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.Chronic overload of SEPT4, a parkin substrate that aggregates in Parkinson's disease, causes behavioral alterations but not neurodegeneration in miceGenetic models of sensorimotor gating: relevance to neuropsychiatric disorders.Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse modelThe 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in miceSeptin 14 is involved in cortical neuronal migration via interaction with Septin 4.Mouse Models of 22q11.2-Associated Autism Spectrum DisorderThree phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genesAvoiding mouse traps in schizophrenia genetics: lessons and promises from current and emerging mouse models.The emerging functions of septins in metazoansThe social brain: transcriptome assembly and characterization of the hippocampus from a social subterranean rodent, the colonial tuco-tuco (Ctenomys sociabilis)Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome.Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities.Septin functions in organ system physiology and pathology.Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brainSeptin 6 regulates the cytoarchitecture of neurons through localization at dendritic branch points and bases of protrusions.Functional Redundancy of Septin Homologs in Dendritic Branching.Application of in utero electroporation and live imaging in the analyses of neuronal migration during mouse brain development.Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation.The Mammalian Septin Interactome.Septins regulate developmental switching from microdomain to nanodomain coupling of Ca(2+) influx to neurotransmitter release at a central synapseExpression of sept3, sept5a and sept5b in the Developing and Adult Nervous System of the Zebrafish (Danio rerio).Critical Reappraisal of Mechanistic Links of Copy Number Variants to Dimensional Constructs of Neuropsychiatric Disorders in Mouse Models.Serotonergic, noradrenergic and dopaminergic markers are related to cognitive function in adults with 22q11 deletion syndrome.Septin9 is involved in T-cell development and CD8+ T-cell homeostasis.Evo Devo and cognitive science.Lethal phenotype of mice carrying a Sept11 null mutation.Further reducing on the map of synaptic autoimmunity
P2860
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P2860
Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice
description
2009 nî lūn-bûn
@nan
2009 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2009年の論文
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2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
name
Sept5 deficiency exerts pleiot ...... nd cognitive functions in mice
@ast
Sept5 deficiency exerts pleiot ...... nd cognitive functions in mice
@en
type
label
Sept5 deficiency exerts pleiot ...... nd cognitive functions in mice
@ast
Sept5 deficiency exerts pleiot ...... nd cognitive functions in mice
@en
prefLabel
Sept5 deficiency exerts pleiot ...... nd cognitive functions in mice
@ast
Sept5 deficiency exerts pleiot ...... nd cognitive functions in mice
@en
P2093
P2860
P356
P1476
Sept5 deficiency exerts pleiot ...... nd cognitive functions in mice
@en
P2093
Kenji Tanigaki
Mahalah Buell
Mark A Geyer
MoonSook Lee
Noboru Hiroi
Soh Agatsuma
Takehito Sawamura
Takeshi Hiramoto
William S Trimble
P2860
P304
P356
10.1093/HMG/DDP086
P577
2009-02-24T00:00:00Z