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  • Epigenetic profiling in CD4+ and CD8+ T cells from Graves’ disease patients reveals changes in genes associated with T cell receptor signaling
  • Identification of susceptibility SNPs in IL10 and IL23R-IL12RB2 for Behçet’s disease in Han Chinese
  • Human Leukocyte Antigen-G Polymorphisms Association With Cancer Post-Heart Transplantation
  • Human leukocyte antigen G single-nucleotide polymorphism -201 (CC–CC) donor–recipient genotype matching as a predictor of severe cardiac allograft vasculopathy
  • Juvenile Chinook Salmon abundance in the northern Bering Sea: Implications for future returns and fisheries in the Yukon River
  • Evaluation of the iPLEX® ADME PGx Pro Panel and allele frequencies of pharmacogenetic markers in Danes
  • Epigenetic modification of OXT and human sociability
  • Development and verification of SNP arrays to monitor hybridization between two host-associated strains of knotweed psyllid, Aphalara itadori
  • Genetic and epigenetic methylation defects and implication of the ERMN gene in autism spectrum disorders
  • Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant
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