Expression of the KIAA0319 gene from a haplotype associated with developmental dyslexia

Expression of the KIAA0319 gene from a haplotype associated with developmental dyslexia

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Dennis, M, Paracchini, S, Wade-Martins, R, Velayos-Baeza, A, Green, E, Monaco, A
التنسيق:	Conference item
منشور في:	2006

مواد مشابهة

Alternative splicing in the dyslexia-associated gene KIAA0319.
حسب: Velayos-Baeza, A, وآخرون
منشور في: (2007)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
حسب: Dennis, M, وآخرون
منشور في: (2009)

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.
حسب: Velayos-Baeza, A, وآخرون
منشور في: (2008)

Further evidence that KIAA0319 is associated with developmental dyslexia
حسب: Harold, D, وآخرون
منشور في: (2006)

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
حسب: Harold, D, وآخرون
منشور في: (2006)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
حسب: Megan Y Dennis, وآخرون
منشور في: (2009-03-01)

Knockout mice for dyslexia susceptibility gene homologs KIAA0319 and KIAA0319L have unaffected neuronal migration but display abnormal auditory processing
حسب: Guidi, L, وآخرون
منشور في: (2017)

Functional characterisation of dyslexia-susceptibility candidate genes KIAA0319 and KIAA0319L
حسب: Guidi, L
منشور في: (2017)

Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia
حسب: Harold, D, وآخرون
منشور في: (2006)

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
حسب: Paracchini, S, وآخرون
منشور في: (2008)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
حسب: Paracchini, S, وآخرون
منشور في: (2006)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
حسب: Paracchini, S, وآخرون
منشور في: (2006)

The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.
حسب: Velayos-Baeza, A, وآخرون
منشور في: (2010)

The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway.
حسب: Levecque, C, وآخرون
منشور في: (2009)

The Dyslexia-susceptibility protein KIAA0319 inhibits axon growth through Smad2 signaling.
حسب: Franquinho, F, وآخرون
منشور في: (2017)

Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.
حسب: Martinez-Garay, I, وآخرون
منشور في: (2016)

DCDC2, KIAA0319 and CMIP are associated with reading-related traits
حسب: Scerri, T, وآخرون
منشور في: (2011)

DCDC2, KIAA0319 and CMIP are associated with reading-related traits.
حسب: Scerri, T, وآخرون
منشور في: (2011)

Dyslexia associated gene KIAA0319 regulates cell cycle during human neuroepithelial cell development
حسب: Steven Paniagua, وآخرون
منشور في: (2022-08-01)

KIAA0319 influences cilia length, cell migration and mechanical cell–substrate interaction
حسب: Rebeca Diaz, وآخرون
منشور في: (2022-01-01)

The neuronal migration hypothesis of dyslexia: a critical evaluation 30 years on
حسب: Guidi, L, وآخرون
منشور في: (2018)

The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on
حسب: Guidi, LG, وآخرون
منشور في: (2018)

The genetic lexicon of dyslexia.
حسب: Paracchini, S, وآخرون
منشور في: (2007)

Cumulative genetic score of KIAA0319 affects reading ability in Chinese children: moderation by parental education and mediation by rapid automatized naming
حسب: Jingjing Zhao, وآخرون
منشور في: (2023-06-01)

Haplotype-specific expression of exon 10 at the human MAPT locus
حسب: Caffrey, T, وآخرون
منشور في: (2006)

Haplotype-specific expression of exon 10 at the human MAPT locus.
حسب: Caffrey, T, وآخرون
منشور في: (2006)

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population
حسب: Paracchini, S, وآخرون
منشور في: (2011)

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.
حسب: Paracchini, S, وآخرون
منشور في: (2011)

Developmental Dyslexia
حسب: Guinevere F. Eden, وآخرون
منشور في: (2019-08-01)

Developmental dyslexia
حسب: Snowling, M
منشور في: (2001)

PCSK6 is associated with handedness in individuals with dyslexia
حسب: Richardson, A, وآخرون
منشور في: (2011)

PCSK6 is associated with handedness in individuals with dyslexia.
حسب: Scerri, T, وآخرون
منشور في: (2011)

Identification of candidate genes for dyslexia susceptibility on chromosome 18
حسب: Richardson, A, وآخرون
منشور في: (2010)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
حسب: Scerri, T, وآخرون
منشور في: (2010)

Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18.
حسب: Scerri, T, وآخرون
منشور في: (2010)

What is Developmental Dyslexia?
حسب: Stein, J
منشور في: (2018)

Neuropathology of Developmental Dyslexia
حسب: J Gordon Millichap
منشور في: (1991-01-01)

What is Developmental Dyslexia?
حسب: John Stein
منشور في: (2018-02-01)

Cerebellar morphology in developmental dyslexia.
حسب: Rae, C, وآخرون
منشور في: (2002)

Transcriptional and epigenetic regulation of KIAA1199 gene expression in human breast cancer.
حسب: Cem Kuscu, وآخرون
منشور في: (2012-01-01)