https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Methylation diet and methyl group genetics in risk for adenomatous polyp occurrence https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:28251 Wed 11 Apr 2018 14:22:59 AEST ]]> Vitamin D receptor polymorphisms relate to risk of adenomatous polyps in a sex-specific manner https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:26534 Wed 06 Apr 2022 14:04:50 AEST ]]> Folate nutritional genetics and risk for hypertension in an elderly population sample https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:6997 T-MTHFR, 1298A>C-MTHFR, 80G>A-RFC, 2756A>G-MS, 66A>G- MSR, 19bpDHFR and 1561C>T-GCPII), only 677C>T-MTHFR was a significant risk for hypertension: OR 1.89; 95% CI 1.07–3.32 (χ² p = 0.038). Additionally, hypertensive subjects had a significantly lower intake of dietary folate than normotensive individuals (p = 0.0221), although this did not markedly alter blood metabolite levels. Several significant linear associations between dietary folate and related blood metabolites were found in normotensive subjects (p<0.001 for Hcy, red cell and serum folate) and were as predicted on an a priori basis – generally weaker associations existed in hypertensive subjects (p<0.05 for serum folate). This was true for data examined collectively or by genotype. Multiple regression analysis for diastolic or systolic blood pressure showed significant interaction for gender and folate intake (p = 0.014 and 0.019, respectively). In both cases this interaction occurred only in females, with higher folate intake associated with decreased blood pressure. Regressing diastolic blood pressure and 677C>T-MTHFR genotype showed significance (males; p = 0.032) and borderline significance (all subjects). Conclusion: Dietary folate and 677C>T-MTHFR genotype may modify blood pressure.]]> Sat 24 Mar 2018 08:37:49 AEDT ]]> G80A reduced folate carrier SNP influences the absorption and cellular translocation of dietary folate and its association with blood pressure in an elderly population https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:1162 Sat 24 Mar 2018 08:28:43 AEDT ]]> Vitamin C-related nutrient-nutrient and nutrient-gene interactions that modify folate status https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:17304 Sat 24 Mar 2018 08:01:49 AEDT ]]> TAS2R38 bitter taste genetics, dietary vitamin C, and both natural and synthetic dietary folic acid predict folate status, a key micronutrient in the pathoaetiology of adenomatous polyps https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:17921 Sat 24 Mar 2018 07:56:14 AEDT ]]> Preliminary evidence for genetic selection of 677T→MTHFR by natural annual cycle of folate abundance https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:4945 Sat 24 Mar 2018 07:48:07 AEDT ]]> Physicochemical effect of pH and antioxidants on mono- and triglutamate forms of 5-methyltetrahydrofolate, and evaluation of vitamin stability in human gastric juice: implications for folate bioavailability https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:4942 Sat 24 Mar 2018 07:48:04 AEDT ]]> Folic acid: An essential nutrient with added health benefits https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:319 Sat 24 Mar 2018 07:42:42 AEDT ]]> Genetic variation in glutamate carboxypeptidase II and interaction with dietary natural vitamin C may predict risk for adenomatous polyp occurrence https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:28911 Sat 24 Mar 2018 07:26:00 AEDT ]]> Gene-nutrient interaction between folate and dihydrofolate reductase in risk for adenomatous polyp occurrence: a preliminary report https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:23349 Sat 24 Mar 2018 07:13:33 AEDT ]]>