The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
about
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brainMolecular underpinnings of prefrontal cortex development in rodents provide insights into the etiology of neurodevelopmental disordersAutism severity is associated with child and maternal MAOA genotypesOsteogenesis and neurogenesis: a robust link also for language evolutionApproaching motor and language deficits in autism from below: a biolinguistic perspectiveThe shape of the human language-ready brainThe germinal zones of the basal ganglia but not the septum generate GABAergic interneurons for the cortexGenome-wide association study of the child behavior checklist dysregulation profileBrain plasticity and disease: a matter of inhibition.Novel primate miRNAs coevolved with ancient target genes in germinal zone-specific expression patternsModulation of GABAergic transmission in development and neurodevelopmental disorders: investigating physiology and pathology to gain therapeutic perspectives.Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism.Bio-collections in autism research.Transcriptional dysregulation of neocortical circuit assembly in ASDPopulation- and family-based studies associate the MTHFR gene with idiopathic autism in simplex families.Common genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disorders.Genetics and function of neocortical GABAergic interneurons in neurodevelopmental disordersRefinement of the Region for Split Hand/Foot Malformation 5 on 2q31.1.Homeobox gene distal-less is required for neuronal differentiation and neurite outgrowth in the Drosophila olfactory system.Maternal immune activation by LPS selectively alters specific gene expression profiles of interneuron migration and oxidative stress in the fetus without triggering a fetal immune responseEpilepsy as a neurodevelopmental disorder.Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorderInterneuron development and epilepsy: early genetic defects cause long-term consequences in seizures and susceptibility.VARPRISM: incorporating variant prioritization in tests of de novo mutation association.The role of GABAergic system in neurodevelopmental disorders: a focus on autism and epilepsy.Chromatin-based epigenetics of adult subventricular zone neural stem cells.GABAergic dysfunction in pediatric neuro-developmental disorders.An SNP in an ultraconserved regulatory element affects Dlx5/Dlx6 regulation in the forebrain.Regulation of neuronal migration, an emerging topic in autism spectrum disorders.Methylomic profiling of cortex samples from completed suicide cases implicates a role for PSORS1C3 in major depression and suicide2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders.Identification of direct downstream targets of Dlx5 during early inner ear development.CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.Hierarchical temporal processing deficit model of reality distortion and psychoses.Dopamine receptor D4 gene variation predicts preschoolers' developing theory of mind.Association of GTF2i in the Williams-Beuren syndrome critical region with autism spectrum disorders.Peptide Sharing Between Viruses and DLX Proteins: A Potential Cross-Reactivity Pathway to Neuropsychiatric Disorders.Common Ribs of Inhibitory Synaptic Dysfunction in the Umbrella of Neurodevelopmental Disorders.
P2860
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P2860
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
description
2008 nî lūn-bûn
@nan
2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
@ast
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
@en
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
@nl
type
label
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
@ast
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
@en
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
@nl
prefLabel
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
@ast
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
@en
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
@nl
P2093
P2860
P356
P1476
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
@en
P2093
Albert E Chudley
Cynthia J Forster-Gibson
Ira L Cohen
Jeanette J A Holden
Melissa L Hudson
Natalia Novosedlik
Suzanne M E Lewis
Xudong Liu
P2860
P2888
P304
P356
10.1038/EJHG.2008.148
P577
2008-08-27T00:00:00Z