VI. Genome structure and cognitive map of Williams syndrome. - Wikidata - wikimedia - TriplyDB

VI. Genome structure and cognitive map of Williams syndrome.

VI. Genome structure and cognitive map of Williams syndrome.

http://www.wikidata.org/entity/Q30909238

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Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes CNV and nervous system diseases--what's new?Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase Amygdala response to faces parallels social behavior in Williams syndrome Extracellular Release and Signaling by Heat Shock Protein 27: Role in Modifying Vascular Inflammation Promoting social plasticity in developmental disorders with non-invasive brain stimulation techniques Resting-State Functional Connectivity in Individuals with Down Syndrome and Williams Syndrome Compared with Typically Developing Controls Neurobiology of social behavior abnormalities in autism and Williams syndrome A human neurodevelopmental model for Williams syndrome Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23 Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndrome RETRACTED: Distinct function of 2 chromatin remodeling complexes that share a common subunit, Williams syndrome transcription factor (WSTF)Cortical Folding of the Primate Brain: An Interdisciplinary Examination of the Genetic Architecture, Modularity, and Evolvability of a Significant Neurological Trait in Pedigreed Baboons (Genus Papio)Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism Musicality Correlates With Sociability and Emotionality in Williams Syndrome Cross-modal influences of affect across social and non-social domains in individuals with Williams syndrome.Oxytocin and vasopressin are dysregulated in Williams Syndrome, a genetic disorder affecting social behavior Sensitivity of the autonomic nervous system to visual and auditory affect across social and non-social domains in williams syndrome Perception of emotion in musical performance in adolescents with autism spectrum disorders Atypical hemispheric asymmetry in the perception of negative human vocalizations in individuals with Williams syndrome.3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry.Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour.Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.Emotions in action through the looking glass.Differences in age-related effects on brain volume in Down syndrome as compared to Williams syndrome and typical development.Abnormal structure or function of the amygdala is a common component of neurodevelopmental disorders.Toward a deeper characterization of the social phenotype of Williams syndrome: The association between personality and social drive Affiliative behavior in Williams syndrome: social perception and real-life social behavior Characterizing associations and dissociations between anxiety, social, and cognitive phenotypes of Williams syndrome.Nature and nurture: Williams syndrome across cultures.Mapping genetically controlled neural circuits of social behavior and visuo-motor integration by a preliminary examination of atypical deletions with Williams syndrome Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome.A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders Contrasting patterns of language-associated brain activity in autism and Williams syndrome.Effect of nonrigid registration algorithms on deformation-based morphometry: a comparative study with control and Williams syndrome subjects.Frontal asymmetry index in Williams syndrome: Evidence for altered emotional brain circuitry?A multimeasure approach to investigating affective appraisal of social information in Williams syndrome

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VI. Genome structure and cognitive map of Williams syndrome.

http://www.wikidata.org/entity/Q30909238

description

2000 nî lūn-bûn

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2000 թվականի հունվարին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年论文

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name

VI. Genome structure and cognitive map of Williams syndrome.

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VI. Genome structure and cognitive map of Williams syndrome.

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VI. Genome structure and cognitive map of Williams syndrome.

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VI. Genome structure and cognitive map of Williams syndrome.

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VI. Genome structure and cognitive map of Williams syndrome.

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Journal of Cognitive Neuroscience

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VI. Genome structure and cognitive map of Williams syndrome.

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Bellugi U

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Burian D

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Chen XN

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Hirota H

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Korenberg JR

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Lai Z

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Matsuoka R

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P2860

The murine CYLN2 gene: genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region

Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease

Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome

A novel human gene FKBP6 is deleted in Williams syndrome

A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK

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89-107

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12 Suppl 1

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12368215

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10953236

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