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The Evidence for Association of ATP2B2 Polymorphisms with Autism in Chinese Han Population
Association study in Romanians confirms IL23A gene haplotype block rs2066808/rs11171806 as conferring risk to psoriatic arthritis
A Non-Synonymous Coding Variant (L616F) in the TLR5 Gene Is Potentially Associated with Crohn’s Disease and Influences Responses to Bacterial Flagellin
TNF-alpha promoter methylation in peripheral white blood cells: Relationship with circulating TNF?, truncal fat and n-6 PUFA intake in young women
Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder
Regulation of c-kit+ Progenitor Cells by Stromal Cell Derived Factor-1? in Adult Murine Heart:
Aberrant methylation of multiple imprinted genes in embryos of tamoxifen treated male rats:
Analyses in human urothelial cells identify methylation of miR-152, miR-200b and miR-10a genes as candidate bladder cancer biomarkers:
Association between PCSK9 and LDLR gene polymorphisms with coronary heart disease: Case-control study and meta-analysis
Methionine sulfoxide reductase A rs10903323 G/A polymorphism is associated with increased risk of coronary artery disease in a Chinese population
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