28 research outputs found

    Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

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    We carried out a trans-ancestry genome-wide association and replication study of blood pressure phenotypes among up to 320,251 individuals of East Asian, European and South Asian ancestry. We find genetic variants at 12 new loci to be associated with blood pressure (P = 3.9 × 10-11 to 5.0 × 10-21). The sentinel blood pressure SNPs are enriched for association with DNA methylation at multiple nearby CpG sites, suggesting that, at some of the loci identified, DNA methylation may lie on the regulatory pathway linking sequence variation to blood pressure. The sentinel SNPs at the 12 new loci point to genes involved in vascular smooth muscle (IGFBP3, KCNK3, PDE3A and PRDM6) and renal (ARHGAP24, OSR1, SLC22A7 and TBX2) function. The new and known genetic variants predict increased left ventricular mass, circulating levels of NT-proBNP, and cardiovascular and all-cause mortality (P = 0.04 to 8.6 × 10-6). Our results provide new evidence for the role of DNA methylation in blood pressure regulation

    Enzymatic hydrolysis of sago starch in a twin-screw extruder

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    Journal of Food Engineering324403-426JFOE

    High moisture twin-screw extrusion of sago starch: 1. Influence on granule morphology and structure

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    10.1016/S0144-8617(96)00024-0Carbohydrate Polymers304275-286CAPO

    Influence of extrusion variables on subsequent saccharification behaviour of sage starch

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    10.1016/0308-8146(95)00049-OFood Chemistry543289-296FOCH
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