A common variant associated with dyslexia reduces expression of the KIAA0319 gene.

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.

Numerous genetic association studies have implicated the KIAA0319 gene on human chromosome 6p22 in dyslexia susceptibility. The causative variant(s) remains unknown but may modulate gene expression, given that (1) a dyslexia-associated haplotype has been implicated in the reduced expression of KIAA0...

תיאור מלא

מידע ביבליוגרפי
Main Authors:	Dennis, M, Paracchini, S, Scerri, T, Prokunina-Olsson, L, Knight, J, Wade-Martins, R, Coggill, P, Beck, S, Green, E, Monaco, A
פורמט:	Journal article
שפה:	English
יצא לאור:	Public Library of Science 2009

פריטים דומים

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
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יצא לאור: (2009-03-01)

Expression of the KIAA0319 gene from a haplotype associated with developmental dyslexia
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יצא לאור: (2006)

Further evidence that KIAA0319 is associated with developmental dyslexia
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Alternative splicing in the dyslexia-associated gene KIAA0319.
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Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
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Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
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Functional characterisation of dyslexia-susceptibility candidate genes KIAA0319 and KIAA0319L
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Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia
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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
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יצא לאור: (2006)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
מאת: Paracchini, S, et al.
יצא לאור: (2006)

DCDC2, KIAA0319 and CMIP are associated with reading-related traits
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DCDC2, KIAA0319 and CMIP are associated with reading-related traits.
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The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.
מאת: Velayos-Baeza, A, et al.
יצא לאור: (2008)

Knockout mice for dyslexia susceptibility gene homologs KIAA0319 and KIAA0319L have unaffected neuronal migration but display abnormal auditory processing
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The Dyslexia-susceptibility protein KIAA0319 inhibits axon growth through Smad2 signaling.
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The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.
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The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway.
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Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.
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The genetic lexicon of dyslexia.
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Investigation of Dyslexia and SLI Risk Variants in Reading- and Language- Impaired Subjects
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PCSK6 is associated with handedness in individuals with dyslexia
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PCSK6 is associated with handedness in individuals with dyslexia.
מאת: Scerri, T, et al.
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Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18.
מאת: Scerri, T, et al.
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מאת: Richardson, A, et al.
יצא לאור: (2010)

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The DCDC2 deletion is not a risk factor for dyslexia
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יצא לאור: (2017)

Endosomal trafficking defects in patient cells with KIAA1109 biallelic variants
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Identification of candidate genes for dyslexia susceptibility on chromosome 18.
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יצא לאור: (2010-10-01)

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population
מאת: Paracchini, S, et al.
יצא לאור: (2011)

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.
מאת: Paracchini, S, et al.
יצא לאור: (2011)

Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.
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יצא לאור: (2010-01-01)

KIAA1109 variants are associated with a severe disorder of brain development and arthrogryposis
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New recombinant T. pallidum antigens Tp0453 and Tp0319 in the diagnostics of syphilis
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