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CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung disease
Acetylation of H2A.Z is a key epigenetic modification associated with gene deregulation and epigenetic remodeling in cancer
Late-replicating heterochromatin is characterized by decreased cytosine methylation in the human genome
Identification of improved IL28B SNPs and haplotypes for prediction of drug response in treatment of hepatitis C using massively parallel sequencing in a cross-sectional European cohort
DNA methylation is associated with downregulation of the organic cation transporter OCT1 (SLC22A1) in human hepatocellular carcinoma
Septin 9 isoform expression, localization and epigenetic changes during human and mouse breast cancer progression
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers
Common breast cancer susceptibility alleles are associated with tumor subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2
Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium
Homocysteine promotes human endothelial cell dysfunction via site-specific epigenetic regulation of p66shc