Further evidence for the role of MET in autism susceptibility.
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Complete or partial reduction of the Met receptor tyrosine kinase in distinct circuits differentially impacts mouse behaviorCircuit-specific intracortical hyperconnectivity in mice with deletion of the autism-associated Met receptor tyrosine kinaseA new synaptic player leading to autism risk: Met receptor tyrosine kinaseA familial heterozygous null mutation of MET in autism spectrum disorderMET receptor tyrosine kinase controls dendritic complexity, spine morphogenesis, and glutamatergic synapse maturation in the hippocampusAutism-associated promoter variant in MET impacts functional and structural brain networks.Replication of the association of a MET variant with autism in a Chinese Han population.MET and AKT genetic influence on facial emotion perception.Synaptic microcircuit dysfunction in genetic models of neurodevelopmental disorders: focus on Mecp2 and Met.NTRK2 expression levels are reduced in laser captured pyramidal neurons from the anterior cingulate cortex in males with autism spectrum disorder.Links between genetics and pathophysiology in the autism spectrum disorders.Autism risk gene MET variation and cortical thickness in typically developing children and adolescents.Insulin-Independent GABAA Receptor-Mediated Response in the Barrel Cortex of Mice with Impaired Met Activity.Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorderThe autism-associated MET receptor tyrosine kinase engages early neuronal growth mechanism and controls glutamatergic circuits development in the forebrainAge dependent forebrain structural changes in mice deficient in the autism associated gene Met tyrosine kinase.Receptor Tyrosine Kinase MET Interactome and Neurodevelopmental Disorder Partners at the Developing Synapse.Hepatocyte Growth Factor Modulates MET Receptor Tyrosine Kinase and β-Catenin Functional Interactions to Enhance Synapse Formation.Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome.Modeling of autism genetic variations in mice: focusing on synaptic and microcircuit dysfunctions.MET receptor tyrosine kinase as an autism genetic risk factor.Distinct projection targets define subpopulations of mouse brainstem vagal neurons that express the autism-associated MET receptor tyrosine kinase.The Pleiotropic MET Receptor Network: Circuit Development and the Neural-Medical Interface of Autism.Autoimmunity, Autoantibodies, and Autism Spectrum Disorder.Common and rare variants of microRNA genes in autism spectrum disorders.Imaging genetics in neurodevelopmental psychopathology
P2860
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P2860
Further evidence for the role of MET in autism susceptibility.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Further evidence for the role of MET in autism susceptibility.
@en
Further evidence for the role of MET in autism susceptibility.
@nl
type
label
Further evidence for the role of MET in autism susceptibility.
@en
Further evidence for the role of MET in autism susceptibility.
@nl
prefLabel
Further evidence for the role of MET in autism susceptibility.
@en
Further evidence for the role of MET in autism susceptibility.
@nl
P2093
P50
P1476
Further evidence for the role of MET in autism susceptibility
@en
P2093
Ayyappan Anitha
Eiji Hattori
Gen-Ichi Sugihara
Hironobu Ichikawa
Ismail Thanseem
Kaori Matsumoto
Kazuhiko Nakamura
Kazuo Yamada
Kiyokazu Takebayashi
Masatsugu Tsujii
P304
P356
10.1016/J.NEURES.2010.06.014
P577
2010-07-06T00:00:00Z