Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk.
about
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disordersNeurogenomics of speech and language disorders: the road aheadComplete or partial reduction of the Met receptor tyrosine kinase in distinct circuits differentially impacts mouse behaviorA familial heterozygous null mutation of MET in autism spectrum disorderMET receptor tyrosine kinase controls dendritic complexity, spine morphogenesis, and glutamatergic synapse maturation in the hippocampusAndrogen modulation of Foxp1 and Foxp2 in the developing rat brain: impact on sex specific vocalizationFoxp2 mediates sex differences in ultrasonic vocalization by rat pups and directs order of maternal retrieval.Recent Advances in the Genetics of Vocal LearningPossible functional links among brain- and skull-related genes selected in modern humansASD-relevant Animal Models of the Foxp Family of Transcription FactorsAutism-associated promoter variant in MET impacts functional and structural brain networks.Genome-wide gene amplification during differentiation of neural progenitor cells in vitro.Developmental heterochrony and the evolution of autistic perception, cognition and behaviorTranscriptional architecture of the primate neocortex.The autism-associated MET receptor tyrosine kinase engages early neuronal growth mechanism and controls glutamatergic circuits development in the forebrainReceptor Tyrosine Kinase MET Interactome and Neurodevelopmental Disorder Partners at the Developing Synapse.Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome.Foxp2 controls synaptic wiring of corticostriatal circuits and vocal communication by opposing Mef2c.Identifying essential cell types and circuits in autism spectrum disorders.The conundrums of understanding genetic risks for autism spectrum disordersSexual differentiation of the brain in man and animals: of relevance to Klinefelter syndrome?Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia.Modeling of autism genetic variations in mice: focusing on synaptic and microcircuit dysfunctions.A review of the evidence for the canonical Wnt pathway in autism spectrum disorders.Identifying early-risk markers and developmental trajectories for language impairment in neurodevelopmental disorders.MET receptor tyrosine kinase as an autism genetic risk factor.Developmental neurogenetics and multimodal neuroimaging of sex differences in autism.CNTNAP2 is a direct FoxP2 target in vitro and in vivo in zebra finches: complex regulation by age and activity.Involvement of Neuroinflammation during Brain Development in Social Cognitive Deficits in Autism Spectrum Disorder and Schizophrenia.The Pleiotropic MET Receptor Network: Circuit Development and the Neural-Medical Interface of Autism.Distinct intracellular signaling mediates C-MET regulation of dendritic growth and synaptogenesis.Modification of spectral features by nonhuman primatesDecoding the molecular evolution of human cognition using comparative genomics.Developmental Connectivity and Molecular Phenotypes of Unique Cortical Projection Neurons that Express a Synapse-Associated Receptor Tyrosine Kinase.Novel transcriptional networks regulated by CLOCK in human neurons.Mice lacking cyclin-dependent kinase-like 5 manifest autistic and ADHD-like behaviors.The sound of one hand clapping: overdetermination and the pansensory nature of communication.FOXP2 Expression in Frontotemporal Lobar Degeneration-Tau.Sociability and synapse subtype-specific defects in mice lacking SRPX2, a language-associated gene.The untold stories of the speech gene, the FOXP2 cancer gene.
P2860
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P2860
Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Regulation of MET by FOXP2, ge ...... e dysfunction and autism risk.
@en
type
label
Regulation of MET by FOXP2, ge ...... e dysfunction and autism risk.
@en
prefLabel
Regulation of MET by FOXP2, ge ...... e dysfunction and autism risk.
@en
P2093
P2860
P1476
Regulation of MET by FOXP2, ge ...... e dysfunction and autism risk.
@en
P2093
Eric Wexler
Gregory E Osborn
Hongmei Dong
Mica Y Bergman
Pat Levitt
Zohar Mukamel
P2860
P304
11437-11442
P356
10.1523/JNEUROSCI.0181-11.2011
P407
P577
2011-08-01T00:00:00Z