Evidence supporting WNT2 as an autism susceptibility gene. - Wikidata - awgldk - TriplyDB

Evidence supporting WNT2 as an autism susceptibility gene.

Evidence supporting WNT2 as an autism susceptibility gene.

http://www.wikidata.org/entity/Q48810402

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The genetics of autistic disorders and its clinical relevance: a review of the literature Constitutional downregulation of SEMA5A expression in autism Birth defects, season of conception, and sex of children born to pesticide applicators living in the Red River Valley of Minnesota, USA Synaptic Wnt/GSK3β Signaling Hub in Autism Wnt signaling in neuropsychiatric disorders: ties with adult hippocampal neurogenesis and behavior Frizzled-9 is activated by Wnt-2 and functions in Wnt/beta -catenin signaling The ups and downs of Wnt signaling in prevalent neurological disorders Gene expression profiling of lymphoblasts from autistic and nonaffected sib pairs: altered pathways in neuronal development and steroid biosynthesis Activation of Wnt signaling rescues neurodegeneration and behavioral impairments induced by beta-amyloid fibrils Mouse behavioral tasks relevant to autism: phenotypes of 10 inbred strains Neurodevelopment in schizophrenia: the role of the wnt pathways.Annual Research Review: Transgenic mouse models of childhood-onset psychiatric disorders.Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction Genetic and neurodevelopmental influences in autistic disorder.No association between polymorphisms of WNT2 and schizophrenia in a Korean population Increased activities of Na+/K+-ATPase and Ca2+/Mg2+-ATPase in the frontal cortex and cerebellum of autistic individuals Association of specific language impairment (SLI) to the region of 7q31.Autism and cancer risk.Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment Wnt signaling and the control of human stem cell fate.Disease susceptibility genes for autism.Autism-associated gene expression in peripheral leucocytes commonly observed between subjects with autism and healthy women having autistic children Synaptic Wnt signaling-a contributor to major psychiatric disorders?Molecular genetics of autism spectrum disorder.An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males.Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism.Alteration of astrocytes and Wnt/β-catenin signaling in the frontal cortex of autistic subjects.Triggers for autism: genetic and environmental factors.Pathophysiology of early onset schizophrenia.Advances in behavioral genetics: mouse models of autism.Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses.Modeling human neurodevelopmental disorders in the Xenopus tadpole: from mechanisms to therapeutic targets.A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation.Presence of large deletions in kindreds with autism.Effect of activation of canonical Wnt signaling by the Wnt-3a protein on the susceptibility of PC12 cells to oxidative and apoptotic insults.The best-laid plans go oft awry: synaptogenic growth factor signaling in neuropsychiatric disease.The neurobiology of lipid metabolism in autism spectrum disorders.A review of the evidence for the canonical Wnt pathway in autism spectrum disorders.Genomic and proteomic advances in autism research.Functional annotation of genes overlapping copy number variants in autistic patients: focus on axon pathfinding.

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Evidence supporting WNT2 as an autism susceptibility gene.

http://www.wikidata.org/entity/Q48810402

description

2001 nî lūn-bûn

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2001年の論文

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2001年学术文章

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2001年学术文章

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2001年学术文章

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2001年学术文章

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2001年学术文章

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2001年学术文章

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2001年學術文章

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2001年學術文章

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name

Evidence supporting WNT2 as an autism susceptibility gene.

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Evidence supporting WNT2 as an autism susceptibility gene.

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type

label

Evidence supporting WNT2 as an autism susceptibility gene.

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Evidence supporting WNT2 as an autism susceptibility gene.

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prefLabel

Evidence supporting WNT2 as an autism susceptibility gene.

@en

Evidence supporting WNT2 as an autism susceptibility gene.

@nl

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P1433

American Journal of Medical Genetics Part A

P1476

Evidence supporting WNT2 as an autism susceptibility gene

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P2093

G Beck

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

J L Haines

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J Pietila

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J Piven

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R E Swiderski

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S E Folstein

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T Braun

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V J Vieland

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P2860

Chromosome 7q: where autism meets language disorder?

Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual.

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder

A genomic screen of autism: evidence for a multilocus etiology.

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

Genetic studies of autistic disorder and chromosome 7

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

Wnt signaling: a common theme in animal development

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5

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105

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Thomas H Wassink

Val C Sheffield

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2001-07-01T00:00:00Z

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11449391

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