Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1. - Wikidata - awgldk - TriplyDB

Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

http://www.wikidata.org/entity/Q30469964

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Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice Deficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1 Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability.Knockdown of the candidate dyslexia susceptibility gene homolog dyx1c1 in rodents: effects on auditory processing, visual attention, and cortical and thalamic anatomy.The effects of Kiaa0319 knockdown on cortical and subcortical anatomy in male rats Effects of test experience and neocortical microgyria on spatial and non-spatial learning in rats A behavioral evaluation of sex differences in a mouse model of severe neuronal migration disorder.Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319.The genetics of reading disabilities: from phenotypes to candidate genes Use of an eight-arm radial water maze to assess working and reference memory following neonatal brain injury.Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes.Embryonic disruption of the candidate dyslexia susceptibility gene homolog Kiaa0319-like results in neuronal migration disorders.A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia.Genus Spondias: A Phytochemical and Pharmacological Review.

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Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

http://www.wikidata.org/entity/Q30469964

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2010 nî lūn-bûn

@nan

2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

@ast

Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

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type

label

Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

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Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

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prefLabel

Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

@ast

Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

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J.1601-183X.2010.00662.X

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Genes, Brain and Behavior

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Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.

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A LePack

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C E Szalkowski

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G D Rosen

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J J Chrobak

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J J LoTurco

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J R Hinman

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R H Fitch

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S W Threlkeld

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Y Wang

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P2860

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia

DCDC2 is associated with reading disability and modulates neuronal development in the brain.

DYX1C1 functions in neuronal migration in developing neocortex

Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.

Evidence for aberrant auditory anatomy in developmental dyslexia

Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

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244-252

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