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Background The nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) signaling pathway plays a key role in the regulatory network of inflammation.The deletion variant allele of the NFKB 1-94 ins/del ATTG promoter polymorphism leads to lower transcription levels of the p50 subunit,and the variant allele has been associated with several inflammatory diseases as well as CAD with inflammation as an important part of the pathogenesis.The aim of the present study was to assess the association between the human NFKB1 gene polymorphism and CAD in a Han and Uygur population of China.