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KIAA0319 encodes a transmembrane protein that contains a large extracellular domain with multiple polycystic kidney disease (PKD) domains. Additionally we are shipping KIAA0319 Proteins (5) and many more products for this protein.
Showing 10 out of 37 products:
Mouse (Murine) Polyclonal KIAA0319 Primary Antibody for 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 references for ABIN408727
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 (show FAM65B Antibodies) were associated with cortical thickness in the left developing orbitofrontal region and global fractional anisotropy, respectively. KIAA0319 and ACOT13 (show ACOT13 Antibodies) were suggestively associated with overall fractional anisotropy and left pars (show EPRS Antibodies) opercularis cortical thickness, respectively.
These results indicate that KIAA0319L (show KIAA0319L Antibodies) 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 (show DCDC2 Antibodies) 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 (show ROBO1 Antibodies) 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 study demonstrated the association of developmental dyslexia with rs4504469 of KIAA0319 and not with any single-nucleotide polymorphisms of DCDC2 (show DCDC2 Antibodies).
results suggested that the 931C > T variant in KIAA0319, but not the -3G > A in DYX1C1 (show DYX1C1 Antibodies), was significantly associated with the risk of dyslexia
The results of this study found that KIAA0319 gene contained polymorphisms that were significantly associated with white matter volume in the left temporo-parietal region and that white matter volume influenced reading ability.
Association study of a functional genetic variant in KIAA0319 in German dyslexics.
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