Human FMS-like tyrosine kinase 3 receptor,Flt-3R ELISA Kit
- Known as:
- Human FMS-like tyrosine phosphorylation catalyst 3 receptor,Flt-3R Enzyme-linked immunosorbent assay test Kit
- Catalog number:
- YHB1225Hu
- Product Quantity:
- 48T
- Category:
- Elisa Kits
- Supplier:
- yehua
- Gene target:
- Human FMS-like tyrosine kinase 3 receptor Flt-3R ELISA Kit
Related genes to: Human FMS-like tyrosine kinase 3 receptor,Flt-3R ELISA Kit
- Gene:
- ANKK1 NIH gene
- Name:
- ankyrin repeat and kinase domain containing 1
- Previous symbol:
- -
- Synonyms:
- X-kinase
- Chromosome:
- 11q23.2
- Locus Type:
- gene with protein product
- Date approved:
- 2003-05-13
- Date modifiied:
- 2013-01-10
Related products to: Human FMS-like tyrosine kinase 3 receptor,Flt-3R ELISA Kit
Related articles to: Human FMS-like tyrosine kinase 3 receptor,Flt-3R ELISA Kit
- Numerous studies have established associations between single nucleotide polymorphisms (SNPs) and various behavioral and neurodevelopmental conditions. This study explores the links between SNPs in candidate genes involved in central nervous system (CNS) physiology and their implications for the behavioral and emotional aspects in children and teenagers. A total of 590 participants, aged 7-15 years, from the Early Life Exposures In Mexico To Environmental Toxicants (ELEMENT) cohort study in Mexico City, underwent genotyping for at least one of 15 CNS gene-related SNPs at different timepoints. We employed multiple linear regression models to assess the potential impact of genetic variations on behavioral and cognitive traits, as measured by the Behavioral Assessment System for Children (BASC) and Conners parent rating scales. Significant associations were observed, including the rs1800497 TC genotype (ANKK1) with the Cognitive Problems/Inattention variable (p value = 0.003), the rs1800955 CT genotype (DDR4) with the Emotional Lability Global index variable (p value = 0.01), and the rs10492138 GA and rs7970177 TC genotypes (GRIN2B) with the Depression variable (p values 0.007 and 0.012, respectively). These finds suggest potential genetic profiles associated with "risk" and "protective" behaviors for these SNPs. Our results provide valuable insights into the role of genetic variations in neurobehavior and highlight the need for further research in the early identification and intervention in individuals at risk for these conditions. - Source: PubMed
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