The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities
about
Dyslexia-associated kiaa0319-like protein interacts with axon guidance receptor nogo receptor 1Imaging-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.Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexiaUnderstanding the complex etiologies of developmental disorders: behavioral and molecular genetic approaches.A theoretical molecular network for dyslexia: integrating available genetic findings.Etiologies and molecular mechanisms of communication disorders.Distinct and overlapping roles for AP-1 and GGAs revealed by the "knocksideways" systemPutative miRNAs for the diagnosis of dyslexia, dyspraxia, and specific language impairment.In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children.New insights into the genetic mechanism of IQ in autism spectrum disorders.Embryonic disruption of the candidate dyslexia susceptibility gene homolog Kiaa0319-like results in neuronal migration disorders.Molecular genetics of dyslexia: an overview.The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling.The Roles of Genes in the Neuronal Migration and Neurite Outgrowth Network in Developmental Dyslexia: Single- and Multiple-Risk Genetic Variants.Systemic Sclerosis is a Complex Disease Associated Mainly with Immune Regulatory and Inflammatory Genes.Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.Knockout Mice for Dyslexia Susceptibility Gene Homologs KIAA0319 and KIAA0319L have Unaffected Neuronal Migration but Display Abnormal Auditory Processing.Genetic and environmental risk factors for developmental dyslexia in children: systematic review of the last decade.AU040320 deficiency leads to disruption of acrosome biogenesis and infertility in homozygous mutant mice.The Influence of Dyslexia Candidate Genes on Reading Skill in Old Age
P2860
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P2860
The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
The KIAA0319-like (KIAA0319L) ...... idate for reading disabilities
@en
The KIAA0319-like
@nl
type
label
The KIAA0319-like (KIAA0319L) ...... idate for reading disabilities
@en
The KIAA0319-like
@nl
prefLabel
The KIAA0319-like (KIAA0319L) ...... idate for reading disabilities
@en
The KIAA0319-like
@nl
P2093
P2860
P1476
The KIAA0319-like (KIAA0319L) ...... idate for reading disabilities
@en
P2093
Barbara Anderson
Elizabeth N Kerr
Jennifer Archibald
Jillian M Couto
Karen Wigg
Lissette Gomez
Maureen W Lovett
Rosemary Tannock
Tasha Cate-Carter
Tom Humphries
P2860
P304
P356
10.1080/01677060802354328
P577
2008-01-01T00:00:00Z