Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.
about
The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disordersConsensus paper: pathological role of the cerebellum in autismComplete or partial reduction of the Met receptor tyrosine kinase in distinct circuits differentially impacts mouse behaviorA new synaptic player leading to autism risk: Met receptor tyrosine kinaseA familial heterozygous null mutation of MET in autism spectrum disorderEvidence of cell-nonautonomous changes in dendrite and dendritic spine morphology in the met-signaling-deficient mouse forebrainRecent Advances in the Genetics of Vocal LearningRepetitive grooming and sensorimotor abnormalities in an ephrin-A knockout model for Autism Spectrum DisordersModeling an autism risk factor in mice leads to permanent immune dysregulation.Autism-associated promoter variant in MET impacts functional and structural brain networks.When linkage signal for autism MET candidate gene.Autism spectrum disorder: interaction of air pollution with the MET receptor tyrosine kinase gene.Hepatocyte growth factor (HGF) modulates GABAergic inhibition and seizure susceptibility.The genetics of autism: key issues, recent findings, and clinical implications.Association of genetic variation in the MET proto-oncogene with schizophrenia and general cognitive ability.Communication, interventions, and scientific advances in autism: a commentary.Bio-collections in autism research.Replication of the association of a MET variant with autism in a Chinese Han population.MET and AKT genetic influence on facial emotion perception.Prenatal polycyclic aromatic hydrocarbon exposure leads to behavioral deficits and downregulation of receptor tyrosine kinase, MET.Progranulin A-mediated MET signaling is essential for liver morphogenesis in zebrafish.Interneurons are necessary for coordinated activity during reversal learning in orbitofrontal cortex.Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder.Conserved subcortical and divergent cortical expression of proteins encoded by orthologs of the autism risk gene MET.Interaction between GSTT1 and GSTP1 allele variants as a risk modulating-factor for autism spectrum disorders.Reversal learning and attentional set-shifting in mice.Autism-associated gene expression in peripheral leucocytes commonly observed between subjects with autism and healthy women having autistic childrenGlutathione pathway gene variation and risk of autism spectrum disordersGenome-wide association study for endothelial growth factorsSimilarities in features of autism and asthma and a possible link to acetaminophen useAssociation of a MET genetic variant with autism-associated maternal autoantibodies to fetal brain proteins and cytokine expression.Links between genetics and pathophysiology in the autism spectrum disorders.Comparative two-dimensional polyacrylamide gel electrophoresis of the salivary proteome of children with autism spectrum disorder.Pregnancy at Advanced Maternal Age Affects Behavior and Hippocampal Gene Expression in Mouse Offspring.Altered gene expression in early postnatal monoamine oxidase A knockout mice.Autism risk gene MET variation and cortical thickness in typically developing children and adolescents.Maternal autoantibodies in autismThe autism risk genes MET and PLAUR differentially impact cortical developmentRegulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk.Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder
P2860
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P2860
Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
name
Genetic evidence implicating m ...... y in autism spectrum disorder.
@ast
Genetic evidence implicating m ...... y in autism spectrum disorder.
@en
type
label
Genetic evidence implicating m ...... y in autism spectrum disorder.
@ast
Genetic evidence implicating m ...... y in autism spectrum disorder.
@en
prefLabel
Genetic evidence implicating m ...... y in autism spectrum disorder.
@ast
Genetic evidence implicating m ...... y in autism spectrum disorder.
@en
P2093
P2860
P356
P1433
P1476
Genetic evidence implicating m ...... y in autism spectrum disorder.
@en
P2093
Daniel B Campbell
Pat Levitt
P2860
P304
P356
10.1002/AUR.27
P577
2008-06-01T00:00:00Z