Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations.
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DYX1C1 is required for axonemal dynein assembly and ciliary motilityThe 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 sampleMutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in miceDevelopmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.Genetic factors contributing to human primary ciliary dyskinesia and male infertilityDyslexia 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.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 ratsNeocortical 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 genesPersistent 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 dyslexiaForced 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 languageImaging 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 ratA common variant associated with dyslexia reduces expression of the KIAA0319 geneGenome 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 scenesThe 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.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 childrenTwo Chronic Stress Models Based on Movement Restriction in Rats Respond Selectively to Antidepressant Drugs: Aldolase C As a Potential BiomarkerAtypical 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.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 11 January 2007
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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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
P2093
P2860
P356
P1433
P1476
Disruption of neuronal migrati ...... and hippocampal malformations.
@en
P2093
Albert M Galaburda
Christopher G Fiondella
Joseph J LoTurco
Steven W Threlkeld
P2860
P304
P356
10.1093/CERCOR/BHL162
P577
2007-01-11T00:00:00Z