Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319. - Wikidata - thesis-toulmin - TriplyDB

Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319.

Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319.

http://www.wikidata.org/entity/Q30454040

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Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.Neurobiology of dyslexia.Early neural disruption and auditory processing outcomes in rodent models: implications for developmental language disability Opposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the Study Population.Speech sound processing deficits and training-induced neural plasticity in rats with dyslexia gene knockdown Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children 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.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 cortex 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.The genetics of reading disabilities: from phenotypes to candidate genes Reading and language disorders: the importance of both quantity and quality.Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms KIAA0319 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.Embryonic disruption of the candidate dyslexia susceptibility gene homolog Kiaa0319-like results in neuronal migration disorders.Insights into the genetic foundations of human communication.Study of Genetic Association With DCDC2 and Developmental Dyslexia in Hong Kong Chinese Children.Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis.Knockout Mice for Dyslexia Susceptibility Gene Homologs KIAA0319 and KIAA0319L have Unaffected Neuronal Migration but Display Abnormal Auditory Processing.An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia.KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia.

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P2860

Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319.

http://www.wikidata.org/entity/Q30454040

description

2012 nî lūn-bûn

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2012 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2012 թվականի փետրվարին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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Neocortical disruption and beh ...... e dyslexia risk gene Kiaa0319.

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Neocortical disruption and beh ...... e dyslexia risk gene Kiaa0319.

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Neocortical disruption and beh ...... e dyslexia risk gene Kiaa0319.

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Neocortical disruption and beh ...... e dyslexia risk gene Kiaa0319.

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Neocortical disruption and beh ...... e dyslexia risk gene Kiaa0319.

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J.IJDEVNEU.2012.01.009

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International Journal of Developmental Neuroscience

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Neocortical disruption and beh ...... e dyslexia risk gene Kiaa0319.

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Albert M Galaburda

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Caitlin E Szalkowski

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Christopher G Fiondella

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Joseph J Loturco

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R Holly Fitch

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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

The effect of variation in expression of the candidate dyslexia susceptibility gene homolog Kiaa0319 on neuronal migration and dendritic morphology in the rat.

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.

At the height of fashion: what genetics can teach us about neurodevelopmental disabilities

Genes, cognition, and communication: insights from neurodevelopmental disorders

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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