Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval
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Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.Frizzled Receptors in Development and DiseaseA human neurodevelopmental model for Williams syndromeSmad-interacting protein-1 (Zfhx1b) acts upstream of Wnt signaling in the mouse hippocampus and controls its formationLoss of Wnt8b has no overt effect on hippocampus development but leads to altered Wnt gene expression levels in dorsomedial telencephalonThe p53 transcriptional target gene wnt7b contributes to NGF-inducible neurite outgrowth in neuronal PC12 cellsControl of bone formation by the serpentine receptor Frizzled-9Frizzled-9 impairs acetylcholine receptor clustering in skeletal muscle cells.Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren SyndromeNeural 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.Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice.Wnt2 expression and signaling is increased by different classes of antidepressant treatments.Early natural stimulation through environmental enrichment accelerates neuronal development in the mouse dentate gyrus.Altered microstructure within social-cognitive brain networks during childhood in Williams syndrome.Williams syndrome as a model for elucidation of the pathway genes - the brain - cognitive functions: genetics and epigeneticsFrizzled-8 receptor is activated by the Wnt-2 ligand in non-small cell lung cancer.Neuropsychological components of intellectual disability: the contributions of immediate, working, and associative memory.Talampanel suppresses the acute and chronic effects of seizures in a rodent neonatal seizure model.Epigenetic regulation of neuronal dendrite and dendritic spine developmentUbiquitin ligase HUWE1 regulates axon branching through the Wnt/β-catenin pathway in a Drosophila model for intellectual disability.Alterations in diffusion properties of white matter in Williams syndrome.Can we safely target the WNT pathway?WNTs in synapse formation and neuronal circuitry.Sudden death in toddlers associated with developmental abnormalities of the hippocampus: a report of five cases.A role for WNT/β-catenin signaling in the neural mechanisms of behavior.Failure of neuronal homeostasis results in common neuropsychiatric phenotypes.Generation of Frizzled10-Cre transgenic mouse line: a useful tool for the study of dorsal telencephalic development.Wnt signaling in development and diseaseWNT/Frizzled signalling: receptor-ligand selectivity with focus on FZD-G protein signalling and its physiological relevance: IUPHAR Review 3Animal models of Williams syndrome.Wnt signaling during synaptic development and plasticityA review of the evidence for the canonical Wnt pathway in autism spectrum disorders.Hippocampal Wnt Signaling: Memory Regulation and Hormone Interactions.Canonical and noncanonical Wnt signaling in neural stem/progenitor cells.Wnt-5a/Frizzled9 Receptor Signaling through the Gαo-Gβγ Complex Regulates Dendritic Spine FormationWnt/β-catenin signaling plays an ever-expanding role in stem cell self-renewal, tumorigenesis and cancer chemoresistance.Modeling Williams syndrome with induced pluripotent stem cells.Role of G Protein-Coupled Receptors in the Regulation of Structural Plasticity and Cognitive Function.Trans-synaptic transmission of vesicular Wnt signals through Evi/Wntless.
P2860
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P2860
Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval
description
2005 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2005
@ast
im Juni 2005 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2005/06/01)
@sk
vědecký článek publikovaný v roce 2005
@cs
wetenschappelijk artikel (gepubliceerd op 2005/06/01)
@nl
наукова стаття, опублікована в червні 2005
@uk
مقالة علمية (نشرت في يونيو 2005)
@ar
name
Hippocampal and visuospatial l ...... ams syndrome deletion interval
@ast
Hippocampal and visuospatial l ...... ams syndrome deletion interval
@en
Hippocampal and visuospatial l ...... ams syndrome deletion interval
@nl
type
label
Hippocampal and visuospatial l ...... ams syndrome deletion interval
@ast
Hippocampal and visuospatial l ...... ams syndrome deletion interval
@en
Hippocampal and visuospatial l ...... ams syndrome deletion interval
@nl
prefLabel
Hippocampal and visuospatial l ...... ams syndrome deletion interval
@ast
Hippocampal and visuospatial l ...... ams syndrome deletion interval
@en
Hippocampal and visuospatial l ...... ams syndrome deletion interval
@nl
P2093
P356
P1433
P1476
Hippocampal and visuospatial l ...... ams syndrome deletion interval
@en
P2093
C Robert Almli
Carmen Avilés
Chunjie Zhao
Regina A Abel
Samuel J Pleasure
P304
P356
10.1242/DEV.01871
P407
P577
2005-06-01T00:00:00Z