Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions. - Wikidata - wikimedia - TriplyDB

Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions.

Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions.

http://www.wikidata.org/entity/Q50312721

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Epigenetic Mechanisms in Developmental Alcohol-Induced Neurobehavioral Deficits Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice Neurobiology of social behavior abnormalities in autism and Williams syndrome GTF2IRD2 from the Williams-Beuren critical region encodes a mobile-element-derived fusion protein that antagonizes the action of its related family members Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization of TFII-I(1,2).Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome Mapping genetically controlled neural circuits of social behavior and visuo-motor integration by a preliminary examination of atypical deletions with Williams syndrome Williams syndrome as a model for elucidation of the pathway genes - the brain - cognitive functions: genetics and epigenetics Cognitive-behavioral phenotypes of Williams syndrome are associated with genetic variation in the GTF2I gene, in a healthy population.Behavioural and Brain Gene Expression Profiling in Pigs during Tail Biting Outbreaks - Evidence of a Tail Biting Resistant Phenotype Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders Genomic conflicts and sexual antagonism in human health: insights from oxytocin and testosterone Variation in the Williams syndrome GTF2I gene and anxiety proneness interactively affect prefrontal cortical response to aversive stimuli.Neural Androgen Receptors Modulate Gene Expression and Social Recognition But Not Social Investigation.Inverted low-copy repeats and genome instability--a genome-wide analysis Prenatal phenotype of Williams-Beuren syndrome and of the reciprocal duplication syndrome Structural variants in genes associated with human Williams-Beuren syndrome underlie stereotypical hypersociability in domestic dogs.Pathophysiology of TFII-I: Old Guard Wearing New Hats.Modeling Williams syndrome with induced pluripotent stem cells.Anxiety Disorders in Williams Syndrome Contrasted with Intellectual Disability and the General Population: A Systematic Review and Meta-Analysis.Role of Splice Variants of Gtf2i, a Transcription Factor Localizing at Postsynaptic Sites, and Its Relation to Neuropsychiatric Diseases.Behavioral impact of maternal allergic-asthma in two genetically distinct mouse strains.Novel splice variants in the 5'UTR of Gtf2i expressed in the rat brain: alternative 5'UTRs and differential expression in the neuronal dendrites.mmquant: how to count multi-mapping reads?Human induced pluripotent stem cell derived neurons as a model for Williams-Beuren syndrome.Multifactorial Origin of Neurodevelopmental Disorders: Approaches to Understanding Complex Etiologies.Haploinsufficiency of BAZ1B contributes to Williams syndrome through transcriptional dysregulation of neurodevelopmental pathways.Neuron density is decreased in the prefrontal cortex in Williams syndrome.A postmortem stereological study of the amygdala in Williams syndrome.The contribution of GTF2I haploinsufficiency to Williams syndrome.Dissociating intuitive physics from intuitive psychology: Evidence from Williams syndrome.A Common Polymorphism in a Williams Syndrome Gene Predicts Amygdala Reactivity and Extraversion in Healthy Adults.7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages.Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder.OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome.Generation of a mouse model for a conditional inactivation of Gtf2i allele.Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.Rare genomic rearrangement in a boy with Williams-Beuren syndrome associated to XYY syndrome and intriguing behavior.Consistent hypersocial behavior in mice carrying a deletion of Gtf2i but no evidence of hyposocial behavior with Gtf2i duplication: Implications for Williams-Beuren syndrome and autism spectrum disorder.

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P2860

Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions.

http://www.wikidata.org/entity/Q50312721

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2010 nî lūn-bûn

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Haploinsufficiency of Gtf2i, a ...... reases in social interactions.

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Haploinsufficiency of Gtf2i, a ...... reases in social interactions.

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Haploinsufficiency of Gtf2i, a ...... reases in social interactions.

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Haploinsufficiency of Gtf2i, a ...... reases in social interactions.

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Haploinsufficiency of Gtf2i, a ...... reases in social interactions.

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Haploinsufficiency of Gtf2i, a ...... reases in social interactions.

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Autism Research

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Haploinsufficiency of Gtf2i, a ...... reases in social interactions.

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P2093

Gregory A Elder

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

L Alison McInnes

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Nagahide Takahashi

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Nathan P Dorr

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Takeshi Sakurai

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P2860

Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex

Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.

GTF2IRD1 in craniofacial development of humans and mice

Mouse behavioral tasks relevant to autism: phenotypes of 10 inbred strains

Increased locomotor activity in mice lacking the low-density lipoprotein receptor

Slc25a12 disruption alters myelination and neurofilaments: a model for a hypomyelination syndrome and childhood neurodevelopmental disorders

Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice.

An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.

Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment.

Williams-Beuren syndrome.

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28-39

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1

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Joseph D. Buxbaum

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49843106

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21328569

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haploinsufficiency