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Search Results for: Hereditary Genetics

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  • Cortical mediation of relationships between dopamine receptor D2 and cognition is absent in youth at risk of bipolar disorder
  • A regulatory variant at 3q21. 1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density
  • Evaluation of the relationship between VRK2, rs4380187 polymorphisms, and genetic susceptibility to schizophrenia in the Chinese Han population
  • EphA2, vascular endothelial growth factor, and vascular endothelial growth factor correlate with adverse outcomes and poor survival in patients with glioma
  • Regulation of the acute sickness response by the P2X7 receptor
  • IP6K3 and IPMK variations in LOAD and longevity: evidence for a multifaceted signaling network at the crossroad between neurodegeneration and survival
  • Serum uric acid levels, but not rs7442295 polymorphism of SCL2A9 gene, predict mortality in clinically stable coronary artery disease
  • Associations of Genetic Variants Contributing to Gut Microbiota Composition in Immunoglobin A Nephropathy
  • Association Between Single Nucleotide Polymorphisms in CDKAL1 and HHEX and Type 2 Diabetes in Chinese Population
  • Immune-related genes STIM1, ITPKC and PELI1 polymorphisms are associated with risk of colorectal cancer
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