Functional characterisation of dyslexia-susceptibility candidate genes KIAA0319 and KIAA0319L

Functional characterisation of dyslexia-susceptibility candidate genes KIAA0319 and KIAA0319L

<p>The capacity for language is one of the key features underlying human cognition and evolution. However, little is known about the neurobiological mechanisms underlying normal or impaired linguistic ability. Developmental dyslexia refers to a specific impairment in reading performance and it...

Detaylı Bibliyografya
Yazar:	Guidi, L
Diğer Yazarlar:	Molnar, Z
Materyal Türü:	Tez
Baskı/Yayın Bilgisi:	2017

Benzer Materyaller

Knockout mice for dyslexia susceptibility gene homologs KIAA0319 and KIAA0319L have unaffected neuronal migration but display abnormal auditory processing
Yazar:: Guidi, L, ve diğerleri
Baskı/Yayın Bilgisi: (2017)

Alternative splicing in the dyslexia-associated gene KIAA0319.
Yazar:: Velayos-Baeza, A, ve diğerleri
Baskı/Yayın Bilgisi: (2007)

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
Yazar:: Harold, D, ve diğerleri
Baskı/Yayın Bilgisi: (2006)

Further evidence that KIAA0319 is associated with developmental dyslexia
Yazar:: Harold, D, ve diğerleri
Baskı/Yayın Bilgisi: (2006)

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
Yazar:: Paracchini, S, ve diğerleri
Baskı/Yayın Bilgisi: (2008)

Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.
Yazar:: Martinez-Garay, I, ve diğerleri
Baskı/Yayın Bilgisi: (2016)

Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia
Yazar:: Harold, D, ve diğerleri
Baskı/Yayın Bilgisi: (2006)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
Yazar:: Dennis, M, ve diğerleri
Baskı/Yayın Bilgisi: (2009)

Expression of the KIAA0319 gene from a haplotype associated with developmental dyslexia
Yazar:: Dennis, M, ve diğerleri
Baskı/Yayın Bilgisi: (2006)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
Yazar:: Megan Y Dennis, ve diğerleri
Baskı/Yayın Bilgisi: (2009-03-01)

The Dyslexia-susceptibility protein KIAA0319 inhibits axon growth through Smad2 signaling.
Yazar:: Franquinho, F, ve diğerleri
Baskı/Yayın Bilgisi: (2017)

Dyslexia associated gene KIAA0319 regulates cell cycle during human neuroepithelial cell development
Yazar:: Steven Paniagua, ve diğerleri
Baskı/Yayın Bilgisi: (2022-08-01)

DCDC2, KIAA0319 and CMIP are associated with reading-related traits
Yazar:: Scerri, T, ve diğerleri
Baskı/Yayın Bilgisi: (2011)

DCDC2, KIAA0319 and CMIP are associated with reading-related traits.
Yazar:: Scerri, T, ve diğerleri
Baskı/Yayın Bilgisi: (2011)

The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.
Yazar:: Velayos-Baeza, A, ve diğerleri
Baskı/Yayın Bilgisi: (2010)

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.
Yazar:: Velayos-Baeza, A, ve diğerleri
Baskı/Yayın Bilgisi: (2008)

KIAA0319 influences cilia length, cell migration and mechanical cell–substrate interaction
Yazar:: Rebeca Diaz, ve diğerleri
Baskı/Yayın Bilgisi: (2022-01-01)

The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway.
Yazar:: Levecque, C, ve diğerleri
Baskı/Yayın Bilgisi: (2009)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
Yazar:: Paracchini, S, ve diğerleri
Baskı/Yayın Bilgisi: (2006)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
Yazar:: Paracchini, S, ve diğerleri
Baskı/Yayın Bilgisi: (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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Baskı/Yayın Bilgisi: (2023-06-01)

New recombinant T. pallidum antigens Tp0453 and Tp0319 in the diagnostics of syphilis
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Baskı/Yayın Bilgisi: (2017-08-01)

Preparation of monoclonal antibody against human KIAA0100 protein and Northern blot analysis of human KIAA0100 gene
Yazar:: He Cui, ve diğerleri
Baskı/Yayın Bilgisi: (2017-06-01)

Bioinformatic prediction and functional characterization of human KIAA0100 gene
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Baskı/Yayın Bilgisi: (2017-02-01)

Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia
Yazar:: Gawlik Micha, ve diğerleri
Baskı/Yayın Bilgisi: (2005-10-01)

Examination of <it>NRCAM</it>, <it>LRRN3</it>, KIAA0716, and <it>LAMB1 </it>as autism candidate genes
Yazar:: Santangelo Susan L, ve diğerleri
Baskı/Yayın Bilgisi: (2004-05-01)

0319 Transparent Paper as a Medium of Copying and Design in the Early Modern Architectural Workshop
Yazar:: Anna Bortolozzi
Baskı/Yayın Bilgisi: (2025-01-01)

Photometric Solutions of W UMa Type Stars: GSC2576-0319 and GSC2584-1731
Yazar:: Chung-Uk Lee, ve diğerleri
Baskı/Yayın Bilgisi: (2006-12-01)

High-resolution genomic profiling reveals KIAA1797/miR-491 as a novel candidate colorectal cancer susceptibility locus
Yazar:: Weren, R, ve diğerleri
Baskı/Yayın Bilgisi: (2012)

Transcriptional and epigenetic regulation of KIAA1199 gene expression in human breast cancer.
Yazar:: Cem Kuscu, ve diğerleri
Baskı/Yayın Bilgisi: (2012-01-01)

KIAA0101 is overexpressed, and promotes growth and invasion in adrenal cancer.
Yazar:: Meenu Jain, ve diğerleri
Baskı/Yayın Bilgisi: (2011-01-01)

Loss of KIAA1462, a coronary artery disease associated gene, decreases atherosclerosis
Yazar:: Douglas, G, ve diğerleri
Baskı/Yayın Bilgisi: (2018)

KIAA1462, a coronary artery disease associated gene, is a candidate gene for late onset Alzheimer disease in APOE carriers.
Yazar:: Deborah G Murdock, ve diğerleri
Baskı/Yayın Bilgisi: (2013-01-01)

KIAA1429 regulates alternative splicing events of cancer-related genes in hepatocellular carcinoma
Yazar:: Zhao-chen Liu, ve diğerleri
Baskı/Yayın Bilgisi: (2022-11-01)

Incidence of kiaa1549‐braf fusion gene in Egyptian pediatric low grade glioma
Yazar:: Hala Taha, ve diğerleri
Baskı/Yayın Bilgisi: (2015-12-01)

Potential mechanism of circKIAA1429 accelerating the progression of hepatocellular carcinoma
Yazar:: Yiting Yuan, ve diğerleri
Baskı/Yayın Bilgisi: (2025-03-01)

KIAA0753 promotes glucose and energy metabolism in osteoblasts inhibited by diabetes
Yazar:: LI Mengxue, ve diğerleri
Baskı/Yayın Bilgisi: (2024-10-01)

Endosomal trafficking defects in patient cells with KIAA1109 biallelic variants
Yazar:: Megan S. Kane, ve diğerleri
Baskı/Yayın Bilgisi: (2019-03-01)

CRISPR-Cas9 knockout screening identifies KIAA1429 as an essential gene in Ewing sarcoma
Yazar:: Kezhe Tan, ve diğerleri
Baskı/Yayın Bilgisi: (2023-09-01)

KIAA1109 gene mutation in surviving patients with Alkuraya-Kučinskas syndrome: a review of literature
Yazar:: Kishore Kumar, ve diğerleri
Baskı/Yayın Bilgisi: (2020-06-01)