The DLX1and DLX2 genes and susceptibility to autism spectrum disorders - Wikidata - awgldk - TriplyDB

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

http://www.wikidata.org/entity/Q34325623

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Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain Molecular underpinnings of prefrontal cortex development in rodents provide insights into the etiology of neurodevelopmental disorders Autism severity is associated with child and maternal MAOA genotypes Osteogenesis and neurogenesis: a robust link also for language evolution Approaching motor and language deficits in autism from below: a biolinguistic perspective The shape of the human language-ready brain The germinal zones of the basal ganglia but not the septum generate GABAergic interneurons for the cortex Genome-wide association study of the child behavior checklist dysregulation profile Brain plasticity and disease: a matter of inhibition.Novel primate miRNAs coevolved with ancient target genes in germinal zone-specific expression patterns Modulation 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 ASD Population- 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 disorders Refinement 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 response Epilepsy as a neurodevelopmental disorder.Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder Interneuron 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 suicide 2p15-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.

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

http://www.wikidata.org/entity/Q34325623

description

2008 nî lūn-bûn

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2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի օգոստոսին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

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type

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

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European Journal of Human Genetics

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The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

@en

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Albert E Chudley

http://www.w3.org/2001/XMLSchema#string

Ami Wang

http://www.w3.org/2001/XMLSchema#string

Cynthia J Forster-Gibson

http://www.w3.org/2001/XMLSchema#string

Ira L Cohen

http://www.w3.org/2001/XMLSchema#string

Jeanette J A Holden

http://www.w3.org/2001/XMLSchema#string

Melissa L Hudson

http://www.w3.org/2001/XMLSchema#string

Natalia Novosedlik

http://www.w3.org/2001/XMLSchema#string

Suzanne M E Lewis

http://www.w3.org/2001/XMLSchema#string

Xudong Liu

http://www.w3.org/2001/XMLSchema#string

P2860

Analysis of four DLX homeobox genes in autistic probands

Broader autism phenotype: evidence from a family history study of multiple-incidence autism families

Origin of GABAergic neurons in the human neocortex

The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

Haploview: analysis and visualization of LD and haplotype maps

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

Towards a cognitive phenotype for autism: increased prevalence of executive dysfunction and superior spatial span amongst siblings of children with autism

No association between single nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism

Developmental functions of the Distal-less/Dlx homeobox genes

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228-235

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scholarly article

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10.1038/EJHG.2008.148

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2

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17

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2008-08-27T00:00:00Z

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23195344

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18728693

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Autism spectrum

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2986060

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