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KIAA0319 encodes a transmembrane protein that contains a large extracellular domain with multiple polycystic kidney disease (PKD) domains. Zusätzlich bieten wir Ihnen KIAA0319 Proteine (5) und viele weitere Produktgruppen zu diesem Protein an.
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Mouse (Murine) Polyclonal KIAA0319 Primary Antibody für IHC (p), IHC - ABIN408727
Paracchini, Thomas, Castro, Lai, Paramasivam, Wang, Keating, Taylor, Hacking, Scerri, Francks, Richardson, Wade-Martins, Stein, Knight, Copp, Loturco, Monaco: The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. in Human molecular genetics 2006
Show all 2 Pubmed References
Missense variant in DYX2 gene is associated with reading disability.
Two SNPs in the KIAA0319 gene were nominally associated with rapid naming, and these associations were stable across different ages in longitudinal data set from the Dutch Dyslexia Program.
Study establishes KIAA0319 as a novel player in axon growth and regeneration with the ability to repress the intrinsic growth potential of axons; describes a novel regulatory mechanism operating during peripheral nervous system and central nervous system axon growth, and offers novel targets for the development of effective therapies to promote axon regeneration
This study indicated that genetic polymorphisms of KIAA0319 are associated with an increased risk of DD in the Uyghur population.
The KIAA0319 gene is associated with both reading ability and general cognition, but in different ways. The effect on IQ appears to occur earlier in development and is transient, whereas the effect of reading ability occurs later and is moderated by antenatal maternal stress.
Markers in DYX2 genes KIAA0319 and FAM65B (zeige FAM65B Antikörper) were associated with cortical thickness in the left developing orbitofrontal region and global fractional anisotropy, respectively. KIAA0319 and ACOT13 (zeige ACOT13 Antikörper) were suggestively associated with overall fractional anisotropy and left pars (zeige EPRS Antikörper) opercularis cortical thickness, respectively.
These results indicate that KIAA0319L (zeige KIAA0319L Antikörper) is the fourth of four candidate dyslexia susceptibility genes that is involved in neuronal migration, which supports the association of abnormal neuronal migration with developmental dyslexia.
the association of DCDC2 (zeige DCDC2 Antikörper) and KIAA0319 with Developmental dyslexia in Chinese population should be further validated
our findings suggest that KIAA0319 is associated with a reading-related cognitive skill
KIAA0319 and ROBO1 (zeige ROBO1 Antikörper) genes, and developmental dyslexia (DD), related neuropsychological phenotypes and comorbid language and mathematical (dis)abilities in a large cohort of 493 Italian nuclear families ascertained through a proband with a diagnosis of DD.
This gene encodes a transmembrane protein that contains a large extracellular domain with multiple polycystic kidney disease (PKD) domains. The encoded protein may play a role in the development of the cerebral cortex by regulating neuronal migration and cell adhesion. Single nucleotide polymorphisms in this gene are associated with dyslexia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
, dyslexia susceptibility 2
, dyslexia-associated protein KIAA0319
, dyslexia-associated protein KIAA0319 homolog