A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism. - Wikidata - wikimedia - TriplyDB

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism.

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism.

http://www.wikidata.org/entity/Q34557745

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A multi-platform draft de novo genome assembly and comparative analysis for the Scarlet Macaw (Ara macao)In Sickness and in Health: Perineuronal Nets and Synaptic Plasticity in Psychiatric Disorders Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathology Insulin-Like Growth Factor 1 and Related Compounds in the Treatment of Childhood-Onset Neurodevelopmental Disorders A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Infant siblings and the investigation of autism risk factors Dab2ip regulates neuronal migration and neurite outgrowth in the developing neocortex TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons.Impairment of translation in neurons as a putative causative factor for autism Protein interaction networks reveal novel autism risk genes within GWAS statistical noise Individual common variants exert weak effects on the risk for autism spectrum disorders The draft genome of a socially polymorphic halictid bee, Lasioglossum albipes.Medial prefrontal cortex: genes linked to bipolar disorder and schizophrenia have altered expression in the highly social maternal phenotype.Steroids as external temporal codes act via microRNAs and cooperate with cytokines in differential neurogenesis Bio-collections in autism research.Comparative analysis of methods for detecting interacting loci.The oxytocin receptor gene (OXTR) is associated with autism spectrum disorder: a meta-analysis.Development of a versatile enrichment analysis tool reveals associations between the maternal brain and mental health disorders, including autism Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants.Links between genetics and pathophysiology in the autism spectrum disorders.Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways Altered balance of proteolytic isoforms of pro-brain-derived neurotrophic factor in autism The IgLON Family Member Negr1 Promotes Neuronal Arborization Acting as Soluble Factor via FGFR2.Support for calcium channel gene defects in autism spectrum disorders.Drosophila Homolog of Human KIF22 at the Autism-Linked 16p11.2 Loci Influences Synaptic Connectivity at Larval Neuromuscular Junctions.Genome-wide identification of transcriptional targets of RORA reveals direct regulation of multiple genes associated with autism spectrum disorder.Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder Impaired thalamocortical connectivity in autism spectrum disorder: a study of functional and anatomical connectivity.SALM5 trans-synaptically interacts with LAR-RPTPs in a splicing-dependent manner to regulate synapse development AKAPs integrate genetic findings for autism spectrum disorders.Maternal exposure to carbamazepine at environmental concentrations can cross intestinal and placental barriers.N-cadherin regulates molecular organization of excitatory and inhibitory synaptic circuits in adult hippocampus in vivo Reduced subcortical glutamate/glutamine in adults with autism spectrum disorders: a [¹H]MRS study.GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis.Altered neural connectivity in excitatory and inhibitory cortical circuits in autism.Evidence for dysregulation of axonal growth and guidance in the etiology of ASD.Platelets of mice heterozygous for neurobeachin, a candidate gene for autism spectrum disorder, display protein changes related to aberrant protein kinase A activity RIM-binding protein 2 regulates release probability by fine-tuning calcium channel localization at murine hippocampal synapses.Casting a Wide Net: Role of Perineuronal Nets in Neural Plasticity.Genes showing altered expression in the medial preoptic area in the highly social maternal phenotype are related to autism and other disorders with social deficits

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A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism.

http://www.wikidata.org/entity/Q34557745

description

2011 nî lūn-bûn

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2011 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2011 թվականի հունվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

A noise-reduction GWAS analysi ...... growth and guidance in autism.

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A noise-reduction GWAS analysi ...... growth and guidance in autism.

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A noise-reduction GWAS analysi ...... growth and guidance in autism.

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A noise-reduction GWAS analysi ...... growth and guidance in autism.

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A noise-reduction GWAS analysi ...... growth and guidance in autism.

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A noise-reduction GWAS analysi ...... growth and guidance in autism.

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A noise-reduction GWAS analysi ...... growth and guidance in autism.

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A noise-reduction GWAS analysi ...... growth and guidance in autism.

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A noise-reduction GWAS analysi ...... growth and guidance in autism.

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Molecular Autism

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A noise-reduction GWAS analysi ...... growth and guidance in autism.

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Anthony J Griswold

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Deqiong Ma

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Eden R Martin

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Ioanna Konidari

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James M Jaworski

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John P Hussman

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John R Gilbert

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Michael L Cuccaro

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Patrice L Whitehead

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Ren-Hua Chung

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Population structure and eigenanalysis

Genetics of austim: complex aetiology for a heterogeneous disorder

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

Gene ontology: tool for the unification of biology

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

The semaphorin 4D-plexin-B signalling complex regulates dendritic and axonal complexity in developing neurons via diverse pathways

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

A novel and evolutionarily conserved PtdIns(3,4,5)P3-binding domain is necessary for DOCK180 signalling.

A Drosophila homolog of the polyglutamine disease gene SCA2 is a dosage-sensitive regulator of actin filament formation

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

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1

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scholarly article

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10.1186/2040-2392-2-1

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1

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2

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Margaret A. Pericak-Vance

Jeffery M. Vance

Daria Salyakina

Jonathan L Haines

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2011-01-19T00:00:00Z

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49767315

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1034005067

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21247446

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genome-wide association study

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3035032

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