Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.
about
Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in miceEarly neural disruption and auditory processing outcomes in rodent models: implications for developmental language disabilitySpeech sound processing deficits and training-induced neural plasticity in rats with dyslexia gene knockdownTranscriptional program of ciliated epithelial cells reveals new cilium and centrosome components and links to human diseaseDyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutationDeficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.Defining the genetic architecture of human developmental language impairment.Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.Knockdown of Dyslexia-Gene Dcdc2 Interferes with Speech Sound Discrimination in Continuous Streams.Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability.Knockdown of the dyslexia-associated gene Kiaa0319 impairs temporal responses to speech stimuli in rat primary auditory cortexKnockdown of the candidate dyslexia susceptibility gene homolog dyx1c1 in rodents: effects on auditory processing, visual attention, and cortical and thalamic anatomy.Bilateral subcortical heterotopia with partial callosal agenesis in a mouse mutantThe effects of Kiaa0319 knockdown on cortical and subcortical anatomy in male ratsReprint of "Early testosterone modulated sex differences in behavioral outcome following neonatal hypoxia ischemia in rats"Early acoustic discrimination experience ameliorates auditory processing deficits in male rats with cortical developmental disruptionEffects of test experience and neocortical microgyria on spatial and non-spatial learning in ratsA behavioral evaluation of sex differences in a mouse model of severe neuronal migration disorder.Inhibition of X-linked inhibitor of apoptosis with embelin differentially affects male versus female behavioral outcome following neonatal hypoxia-ischemia in rats.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 genesCortical activity patterns predict robust speech discrimination ability in noise.Early testosterone modulated sex differences in behavioral outcome following neonatal hypoxia ischemia in ratsDiscrimination of brief speech sounds is impaired in rats with auditory cortex lesions.Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.Developmental learning impairments in a rodent model of nodular heterotopia.Progress towards a cellular neurobiology of reading disability.The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexiaPersistent spatial working memory deficits in rats with bilateral cortical microgyria.The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and languagePostnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the ratA common variant associated with dyslexia reduces expression of the KIAA0319 geneThe rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation.A theoretical molecular network for dyslexia: integrating available genetic findings.The effects of embryonic knockdown of the candidate dyslexia susceptibility gene homologue Dyx1c1 on the distribution of GABAergic neurons in the cerebral cortex.Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanismsThe zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and functionPosition of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes.Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children.
P2860
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P2860
Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.
description
2006 nî lūn-bûn
@nan
2006 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
name
Developmental disruptions and ...... lowing in utero RNAi of Dyx1c1
@nl
Developmental disruptions and ...... owing in utero RNAi of Dyx1c1.
@ast
Developmental disruptions and ...... owing in utero RNAi of Dyx1c1.
@en
type
label
Developmental disruptions and ...... lowing in utero RNAi of Dyx1c1
@nl
Developmental disruptions and ...... owing in utero RNAi of Dyx1c1.
@ast
Developmental disruptions and ...... owing in utero RNAi of Dyx1c1.
@en
prefLabel
Developmental disruptions and ...... lowing in utero RNAi of Dyx1c1
@nl
Developmental disruptions and ...... owing in utero RNAi of Dyx1c1.
@ast
Developmental disruptions and ...... owing in utero RNAi of Dyx1c1.
@en
P2093
P2860
P1476
Developmental disruptions and ...... owing in utero RNAi of Dyx1c1.
@en
P2093
Joe J LoTurco
Melissa M McClure
R Holly Fitch
Steven W Threlkeld
P2860
P304
P356
10.1016/J.BRAINRESBULL.2006.11.005
P407
P577
2006-12-05T00:00:00Z