About: 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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About: Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	artículu científicu espublizáu en 2005 (ast) vědecký článek publikovaný v roce 2005 (cs) 2005 թուականի Յունիսին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в червні 2005 (uk) مقالة علمية (نشرت في يونيو 2005) (ar) 2005 թվականի հունիսին հրատարակված գիտական հոդված (hy) vedecký článok (publikovaný 2005/06/01) (sk) wetenschappelijk artikel (gepubliceerd op 2005/06/01) (nl) scientific journal article (en) im Juni 2005 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28509068-9F2C6126-558A-4F69-9778-EBEC831AFB11
publication date	2005-06-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28509068-A3213339-9030-4747-B8CD-D089C604C6F7
language of work or name	English
author name string	wds:Q28509068-0DFDAE39-6443-47D2-B82A-3C5DF826549C wds:Q28509068-1A03360D-A8EB-48EE-8D37-327F3323519D wds:Q28509068-347A5BDE-4A55-49D9-9BEB-B6E0011DB4D8 wds:Q28509068-76685CAB-58FD-4681-B3A5-2C0D023BEAB2 wds:Q28509068-F1AA6986-50AE-411D-BC4B-1F8486AD833A
author name string	Chunjie Zhao C Robert Almli Samuel J Pleasure Regina A Abel Carmen Avilés
rdfs:label	Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval (en) Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval (nl) Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval (ast)
skos:prefLabel	Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval (en) Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval (nl) Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval (ast)
name	Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval (en) Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval (nl) Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval (ast)
author	wds:Q28509068-EF9AF176-2A3A-4485-BFD9-4AC72076C2C0
author	Patrick S McQuillen
title	wds:Q28509068-55257723-CC27-4597-A79A-74CE16D6A495
title	Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval (en)
page(s)	wds:Q28509068-08137975-FEB2-47C8-94D4-A4DA9BAFBE71
page(s)	2917-2927
instance of	wds:Q28509068-444D33F5-3B87-41D9-9523-61FD7CBFA37F
instance of	scholarly article
main subject	wds:Q28509068-AF229B6E-E12A-48A2-A9EC-FDE3BCEE335F
main subject	Frizzled class receptor 9
PubMed ID	wds:Q28509068-1D5E80B4-67D3-4121-8799-C6DB80F6E994
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15930120
PubMed ID	15930120
published in	wds:Q28509068-3436A836-B196-48B8-8515-DB220E0978E4
published in	Development
issue	wds:Q28509068-6EE8B9B2-3FFD-43B3-99D7-D4D76E1ECE83
volume	wds:Q28509068-2FC8D2B6-23A9-4B1F-A214-DB9A4D57F70D
issue	12
volume	132
number of pages	wds:Q28509068-3AEC2B2A-9A58-4B8E-AD5B-369109E0677A
number of pages	11 (xsd:decimal)
DOI	wds:Q28509068-45D13D08-6B20-4A78-9322-85BBC4C3E624
DOI	http://dx.doi.org/10.1242/DEV.01871
DOI	10.1242/DEV.01871
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28509068
is cites work of	Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome Increased local gyrification mapped in Williams syndrome. Wnt-5a/Frizzled9 Receptor Signaling through the Gαo-Gβγ Complex Regulates Dendritic Spine Formation Control of bone formation by the serpentine receptor Frizzled-9 Frizzled-9 impairs acetylcholine receptor clustering in skeletal muscle cells Failure of neuronal homeostasis results in common neuropsychiatric phenotypes A human neurodevelopmental model for Williams syndrome Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior Can we safely target the WNT pathway? Smad-interacting protein-1 (Zfhx1b) acts upstream of Wnt signaling in the mouse hippocampus and controls its formation A review of the evidence for the canonical Wnt pathway in autism spectrum disorders Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour Ubiquitin ligase HUWE1 regulates axon branching through the Wnt/β-catenin pathway in a Drosophila model for intellectual disability WNT/Frizzled signalling: receptor-ligand selectivity with focus on FZD-G protein signalling and its physiological relevance: IUPHAR Review 3 Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice Dynamic temporal and cell type-specific expression of Wnt signaling components in the developing midbrain The role of Wnt signaling in neuronal dysfunction in Alzheimer's Disease Alterations in diffusion properties of white matter in Williams syndrome Trans-synaptic transmission of vesicular Wnt signals through Evi/Wntless Genetic regulation of dentate gyrus morphogenesis Wnt signaling during synaptic development and plasticity Wnt2 expression and signaling is increased by different classes of antidepressant treatments Hippocampal Wnt Signaling: Memory Regulation and Hormone Interactions. Wnt signaling in development and disease WNTs in synapse formation and neuronal circuitry Animal models of Williams syndrome Axonal growth and guidance defects in Frizzled3 knock-out mice: a comparison of diffusion tensor magnetic resonance imaging, neurofilament staining, and genetically directed cell labeling. FoxG1 haploinsufficiency results in impaired neurogenesis in the postnatal hippocampus and contextual memory deficits. Early natural stimulation through environmental enrichment accelerates neuronal development in the mouse dentate gyrus Talampanel suppresses the acute and chronic effects of seizures in a rodent neonatal seizure model The p53 transcriptional target gene wnt7b contributes to NGF-inducible neurite outgrowth in neuronal PC12 cells A role for WNT/β-catenin signaling in the neural mechanisms of behavior Sudden death in toddlers associated with developmental abnormalities of the hippocampus: a report of five cases Neuropsychological components of intellectual disability: the contributions of immediate, working, and associative memory Epigenetic regulation of neuronal dendrite and dendritic spine development Frizzled-8 receptor is activated by the Wnt-2 ligand in non-small cell lung cancer. Analyses of mental dysfunction-related ACSl4 in Drosophila reveal its requirement for Dpp/BMP production and visual wiring in the brain Canonical and noncanonical Wnt signaling in neural stem/progenitor cells. Role of Wnt1 and Fzd1 in the spinal cord pathogenesis of amyotrophic lateral sclerosis-transgenic mice Williams syndrome as a model for elucidation of the pathway genes - the brain - cognitive functions: genetics and epigenetics

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