Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome. - Wikidata - awgldk - TriplyDB

Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome.

Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome.

http://www.wikidata.org/entity/Q33842946

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From the genome to the phenome and back: linking genes with human brain function and structure using genetically informed neuroimaging Spatial representation across species: geometry, language, and maps Subjective experience of episodic memory and metacognition: a neurodevelopmental approach Challenging the use of adult neuropsychological models for explaining neurodevelopmental disorders: developed versus developing brains A dual comparative approach: integrating lines of evidence from human evolutionary neuroanatomy and neurodevelopmental disorders Auditory attraction: activation of visual cortex by music and sound in Williams syndrome.Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.The effect of intellectual ability on functional activation in a neurodevelopmental disorder: preliminary evidence from multiple fMRI studies in Williams syndrome 3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry.Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype.Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome 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.Neurodevelopmental disorders.Space and Language in Williams syndrome: Insights from typical development Impaired geometric reorientation caused by genetic defect.Rearrangements of the Williams-Beuren syndrome locus: molecular basis and implications for speech and language development.Altered microstructure within social-cognitive brain networks during childhood in Williams syndrome.Object recognition in Williams syndrome: uneven ventral stream activation.Neuropsychological components of intellectual disability: the contributions of immediate, working, and associative memory.Isolation and characterization of the TIGA genes, whose transcripts are induced by growth arrest LIMK1 regulates long-term memory and synaptic plasticity via the transcriptional factor CREB.Alterations in diffusion properties of white matter in Williams syndrome.The Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function.Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome Geometric and featural systems, separable and combined: Evidence from reorientation in people with Williams syndrome.Chronic cigarette smoking modulates injury and short-term recovery of the medial temporal lobe in alcoholics.Developmental regulation of expression of schizophrenia susceptibility genes in the primate hippocampal formation.Language abilities in Williams syndrome: a critical review.Neural phenotypes of common and rare genetic variants.Synaptic plasticity and spatial working memory are impaired in the CD mouse model of Williams-Beuren syndrome.A genetic model for understanding higher order visual processing: functional interactions of the ventral visual stream in Williams syndrome.Working memory impairment in people with Williams syndrome: effects of delay, task and stimuli.Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits.MRI assessment of superior temporal gyrus in Williams syndrome.Transcriptional profiling of GBM invasion genes identifies effective inhibitors of the LIM kinase-Cofilin pathway.Spatial Impairment and Memory in Genetic Disorders: Insights from Mouse Models.Handedness and corpus callosal morphology in Williams syndrome.Genetics of the hippocampal transcriptome in mouse: a systematic survey and online neurogenomics resource.More than the sum of its parts: new mouse models for dissecting the genetic complexities of Williams-Beuren syndrome.

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Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome.

http://www.wikidata.org/entity/Q33842946

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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Functional, structural, and me ...... ormation in Williams syndrome.

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Functional, structural, and me ...... ormation in Williams syndrome.

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Functional, structural, and me ...... ormation in Williams syndrome.

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Carolyn B Mervis

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Deepak Sarpal

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Karen Faith Berman

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Paul Koch

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Philip Kohn

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Saumitra Das

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Shane Kippenhan

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Sonya Steele

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Stefano Marenco

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Venkata S Mattay

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P2860

The DNA sequence of human chromosome 7

A synaptic model of memory: long-term potentiation in the hippocampus

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

Navigation-related structural change in the hippocampi of taxi drivers

The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat

A cortical representation of the local visual environment

The medial temporal lobe

Proton MR spectroscopic imaging without water suppression.

The neural basis of object perception.

Prevalence estimation of Williams syndrome.

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10.1172/JCI24892

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7

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115

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Daniel R. Weinberger

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