Knockout mice for dyslexia susceptibility gene homologs KIAA0319 and
KIAA0319L have unaffected neuronal migration but display abnormal
auditory processing

Knockout mice for dyslexia susceptibility gene homologs KIAA0319 and KIAA0319L have unaffected neuronal migration but display abnormal auditory processing

Developmental dyslexia is a neurodevelopmental disorder that affects reading ability caused by genetic and non-genetic factors. Amongst the susceptibility genes identified to date, KIAA0319 is a prime candidate. RNA-interference experiments in rats suggested its involvement in cortical mi...

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Manylion Llyfryddiaeth
Prif Awduron:	Guidi, L, Mattley, J, Martinez-Garay, I, Monaco, A, Linden, J, Velayos Baeza, A, Molnar, Z
Fformat:	Journal article
Cyhoeddwyd:	Oxford University Press 2017

Eitemau Tebyg

Functional characterisation of dyslexia-susceptibility candidate genes KIAA0319 and KIAA0319L
gan: Guidi, L
Cyhoeddwyd: (2017)

Alternative splicing in the dyslexia-associated gene KIAA0319.
gan: Velayos-Baeza, A, et al.
Cyhoeddwyd: (2007)

Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.
gan: Martinez-Garay, I, et al.
Cyhoeddwyd: (2016)

Expression of the KIAA0319 gene from a haplotype associated with developmental dyslexia
gan: Dennis, M, et al.
Cyhoeddwyd: (2006)

Further evidence that KIAA0319 is associated with developmental dyslexia
gan: Harold, D, et al.
Cyhoeddwyd: (2006)

The Dyslexia-susceptibility protein KIAA0319 inhibits axon growth through Smad2 signaling.
gan: Franquinho, F, et al.
Cyhoeddwyd: (2017)

The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.
gan: Velayos-Baeza, A, et al.
Cyhoeddwyd: (2010)

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
gan: Harold, D, et al.
Cyhoeddwyd: (2006)

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.
gan: Velayos-Baeza, A, et al.
Cyhoeddwyd: (2008)

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
gan: Paracchini, S, et al.
Cyhoeddwyd: (2008)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
gan: Dennis, M, et al.
Cyhoeddwyd: (2009)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
gan: Megan Y Dennis, et al.
Cyhoeddwyd: (2009-03-01)

The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway.
gan: Levecque, C, et al.
Cyhoeddwyd: (2009)

DCDC2, KIAA0319 and CMIP are associated with reading-related traits
gan: Scerri, T, et al.
Cyhoeddwyd: (2011)

DCDC2, KIAA0319 and CMIP are associated with reading-related traits.
gan: Scerri, T, et al.
Cyhoeddwyd: (2011)

Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia
gan: Harold, D, et al.
Cyhoeddwyd: (2006)

Dyslexia associated gene KIAA0319 regulates cell cycle during human neuroepithelial cell development
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Cyhoeddwyd: (2022-08-01)

KIAA0319 influences cilia length, cell migration and mechanical cell–substrate interaction
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Cyhoeddwyd: (2022-01-01)

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

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

Cumulative genetic score of KIAA0319 affects reading ability in Chinese children: moderation by parental education and mediation by rapid automatized naming
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New recombinant T. pallidum antigens Tp0453 and Tp0319 in the diagnostics of syphilis
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Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia
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0319 Transparent Paper as a Medium of Copying and Design in the Early Modern Architectural Workshop
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Preparation of monoclonal antibody against human KIAA0100 protein and Northern blot analysis of human KIAA0100 gene
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Photometric Solutions of W UMa Type Stars: GSC2576-0319 and GSC2584-1731
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CRISPR-Cas9 knockout screening identifies KIAA1429 as an essential gene in Ewing sarcoma
gan: Kezhe Tan, et al.
Cyhoeddwyd: (2023-09-01)

Bioinformatic prediction and functional characterization of human KIAA0100 gene
gan: He Cui, et al.
Cyhoeddwyd: (2017-02-01)

KIAA0101 is overexpressed, and promotes growth and invasion in adrenal cancer.
gan: Meenu Jain, et al.
Cyhoeddwyd: (2011-01-01)

The neuronal migration hypothesis of dyslexia: a critical evaluation 30 years on
gan: Guidi, L, et al.
Cyhoeddwyd: (2018)

The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on
gan: Guidi, LG, et al.
Cyhoeddwyd: (2018)

Potential mechanism of circKIAA1429 accelerating the progression of hepatocellular carcinoma
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Cyhoeddwyd: (2025-03-01)

KIAA0753 promotes glucose and energy metabolism in osteoblasts inhibited by diabetes
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Cyhoeddwyd: (2024-10-01)

Endosomal trafficking defects in patient cells with KIAA1109 biallelic variants
gan: Megan S. Kane, et al.
Cyhoeddwyd: (2019-03-01)

KIAA1109 variants are associated with a severe disorder of brain development and arthrogryposis
gan: Roechert, Bernd, et al.
Cyhoeddwyd: (2019)

Targeting pyroptosis reverses KIAA1199-mediated immunotherapy resistance in colorectal cancer
gan: Tao Zhang, et al.
Cyhoeddwyd: (2025-02-01)

Overexpression of KIAA1199 is an independent prognostic marker in laryngeal squamous cell carcinoma
gan: Meixiang Huang, et al.
Cyhoeddwyd: (2020-09-01)

KIAA1363—A Multifunctional Enzyme in Xenobiotic Detoxification and Lipid Ester Hydrolysis
gan: Carina Wagner, et al.
Cyhoeddwyd: (2022-06-01)

Comprehensive analysis of the prognostic impact and immune implication of KIAA1429 in lung adenocarcinoma
gan: Lei Guo, et al.
Cyhoeddwyd: (2022-12-01)

Deregulation of miR-183 and KIAA0101 in aggressive and malignant pituitary tumours
gan: Magali eRoche, et al.
Cyhoeddwyd: (2015-08-01)