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  • Association of TGFB1 rs1800469 and BCMO1 rs6564851 with coronary heart disease and IL1B rs16944 with all-cause mortality in men from the Northern Ireland PRIME study
  • The antileukemic activity of decitabine upon PML/RARA-negative AML blasts is supported by all-trans retinoic acid: in vitro and in vivo evidence for cooperation
  • Genetic variation of ERN1 and susceptibility to type 2 diabetes
  • Genetic Variation in the HSD17B1 Gene and Risk of Prostate Cancer
  • Sex-specific DNA methylation: impact on human health and development
  • Loss of ALK hotspot mutations in relapsed neuroblastoma
  • Study on the Correlation between the Prevalence of Venous Thromboembolism in Kazak Pregnant and Lying-In Women in Xinjiang
  • Interaction between manganese and SLC6A3 genetic polymorphisms in relation to dyslexia
  • Sex Differences in Clopidogrel Effects Among Young Patients with Acute Coronary Syndrome: A Role for Genetics?
  • Non‐genetic and genetic predictors of haemodynamic instability induced by propofol and opioids: a retrospective clinical study
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