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DYX1C1 encodes a tetratricopeptide repeat domain-containing protein. Additionally we are shipping DYX1C1 Proteins (4) and many more products for this protein.
Showing 10 out of 76 products:
Human Polyclonal DYX1C1 Primary Antibody for ELISA, WB - ABIN185356
Taipale, Kaminen, Nopola-Hemmi, Haltia, Myllyluoma, Lyytinen, Muller, Kaaranen, Lindsberg, Hannula-Jouppi, Kere: A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. in Proceedings of the National Academy of Sciences of the United States of America 2003
Show all 2 references for ABIN185356
Dog (Canine) Polyclonal DYX1C1 Primary Antibody for ELISA, WB - ABIN4306553
Fisher, Francks: Genes, cognition and dyslexia: learning to read the genome. in Trends in cognitive sciences 2006
Chicken Polyclonal DYX1C1 Primary Antibody for WB - ABIN2784979
Marino, Citterio, Giorda, Facoetti, Menozzi, Vanzin, Lorusso, Nobile, Molteni: Association of short-term memory with a variant within DYX1C1 in developmental dyslexia. in Genes, brain, and behavior 2007
Chimpanzee Polyclonal DYX1C1 Primary Antibody for WB - ABIN374525
Wang, Paramasivam, Thomas, Bai, Kaminen-Ahola, Kere, Voskuil, Rosen, Galaburda, Loturco: DYX1C1 functions in neuronal migration in developing neocortex. in Neuroscience 2006
Dog (Canine) Polyclonal DYX1C1 Primary Antibody for EIA, WB - ABIN374956
Hanson, Blank, Valenzuela, Garner, Madison: The functional nature of synaptic circuitry is altered in area CA3 of the hippocampus in a mouse model of Down's syndrome. in The Journal of physiology 2007
promoter SNP rs12899331 of DYX1C1 may contribute towards the manifestation of DD. This study supports the association of DYX1C1 with DD in an Indian population
results demonstrate that DYX1C1 can modulate the expression of genes involved in cell migration and nervous system development and associates with a number of cytoskeletal proteins.
DYX1C1 is required for axonemal dynein assembly and ciliary motility.
The results of this study do not provide evidence for association between the putatively functional single nucleotide polymorphisms -3G/A and 1249G/T in DYX1C1 and reading disabilities.
Gene-by-environment effects were found between some specified environmental moderators (i.e. maternal smoke during pregnancy, birth weight and socio-economic status) and the DYX1C1-1259C/G marker
results suggested that the 931C > T variant in KIAA0319 (show KIAA0319 Antibodies), but not the -3G > A in DYX1C1, was significantly associated with the risk of dyslexia
DYX1C1 influences reading development in the general Chinese population and supports a universal effect of this gene.
The results of this study found that DYX1C1 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.
Mutations in cilia co-expressed DCDC2 (show DCDC2 Antibodies), DYX1C1 and KIAA0319 (show KIAA0319 Antibodies) genes are associated with a cognitive neurological disorder, dyslexia.
the expression of DYX1C1 in breast cancer is associated with several clinicopathological parameters and that loss of DYX1C1 correlates with a more aggressive disease, in turn indicating that DYX1C1 is a potential prognostic biomarker in breast cancer.
In dyx1c1 morphants, cilia length is reduced in several organs including Kupffer's vesicle, pronephros, spinal canal and olfactory placode.
This gene encodes a tetratricopeptide repeat domain-containing protein. The encoded protein interacts with estrogen receptors and the heat shock proteins, Hsp70 and Hsp90. An homologous protein in rat has been shown to function in neuronal migration in the developing neocortex. A chromosomal translocation involving this gene is associated with a susceptibility to developmental dyslexia. Mutations in this gene are associated with deficits in reading and spelling. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream cell cycle progression 1 (CCPG1) gene.
dyslexia susceptibility 1 candidate 1
, dyslexia susceptibility 1 candidate gene 1 protein
, Dyslexia susceptibility 1 candidate gene 1 protein homolog
, dyslexia susceptibility 1 candidate 1 homolog
, dyslexia susceptibility 1 candidate gene 1 protein homolog