Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations. - Wikidata - awgldk - TriplyDB

Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations.

Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations.

http://www.wikidata.org/entity/Q37091458

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DYX1C1 is required for axonemal dynein assembly and ciliary motility The effect of variation in expression of the candidate dyslexia susceptibility gene homolog Kiaa0319 on neuronal migration and dendritic morphology in the rat.Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.Genetic factors contributing to human primary ciliary dyskinesia and male infertility Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation 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.Primary Cilia as a Possible Link between Left-Right Asymmetry and Neurodevelopmental Diseases.Disturbances in the positioning, proliferation and apoptosis of neural progenitors contribute to subcortical band heterotopia formation.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 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 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 dyslexia Forced G1-phase reduction alters mode of division, neuron number, and laminar phenotype in the cerebral cortex.The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language Imaging activity in astrocytes and neurons with genetically encoded calcium indicators following in utero electroporation.Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat A common variant associated with dyslexia reduces expression of the KIAA0319 gene Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.A theoretical molecular network for dyslexia: integrating available genetic findings.The dyslexia candidate gene DYX1C1 is a potential marker of poor survival in breast cancer.History of reading struggles linked to enhanced learning in low spatial frequency scenes 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 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.Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children.Genetic influences of resting state fMRI activity in language-related brain regions in healthy controls and schizophrenia patients: a pilot study.Spherical harmonic analysis of cortical complexity in autism and dyslexia.Gene-environment interaction on neural mechanisms of orthographic processing in Chinese children Two Chronic Stress Models Based on Movement Restriction in Rats Respond Selectively to Antidepressant Drugs: Aldolase C As a Potential Biomarker Atypical Sulcal Pattern in Children with Developmental Dyslexia and At-Risk Kindergarteners.Topological properties of large-scale structural brain networks in children with familial risk for reading difficulties.Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs.

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Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations.

http://www.wikidata.org/entity/Q37091458

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 11 January 2007

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Disruption of neuronal migrati ...... and hippocampal malformations.

@en

Disruption of neuronal migrati ...... and hippocampal malformations.

@nl

type

label

Disruption of neuronal migrati ...... and hippocampal malformations.

@en

Disruption of neuronal migrati ...... and hippocampal malformations.

@nl

prefLabel

Disruption of neuronal migrati ...... and hippocampal malformations.

@en

Disruption of neuronal migrati ...... and hippocampal malformations.

@nl

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Cerebral Cortex

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Disruption of neuronal migrati ...... and hippocampal malformations.

@en

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Albert M Galaburda

http://www.w3.org/2001/XMLSchema#string

Christopher G Fiondella

http://www.w3.org/2001/XMLSchema#string

Jilin Bai

http://www.w3.org/2001/XMLSchema#string

Joseph J LoTurco

http://www.w3.org/2001/XMLSchema#string

Steven W Threlkeld

http://www.w3.org/2001/XMLSchema#string

Yu Wang

http://www.w3.org/2001/XMLSchema#string

P2860

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

Slit2-Mediated chemorepulsion and collapse of developing forebrain axons

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

DYX1C1 functions in neuronal migration in developing neocortex

Robo1 and Robo2 are homophilic binding molecules that promote axonal growth

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.

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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2562-2572

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scholarly article

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10.1093/CERCOR/BHL162

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11

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17

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2007-01-11T00:00:00Z

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6584042

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P698

17218481

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3742088

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