Meta-Analysis of the Association of the C677T Polymorphism of the Methylenetetrahydrofolate Reductase Gene with Hyperuricemia
Author:
Publisher
S. Karger AG
Subject
Nutrition and Dietetics,Medicine (miscellaneous)
Reference37 articles.
1. High Prevalence of the Thermolabile Methylenetetrahydrofolate Reductase Variant in Mexico: A Country with a Very High Prevalence of Neural Tube Defects
2. Association of homocysteinemia with high concentrations of serum insulin and uric acid in Brazilian subjects with metabolic syndrome genotyped for C677T polymorphism in the methylenetetrahydrofolate reductase gene
3. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
4. Common Mutation in Methylenetetrahydrofolate Reductase
5. The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia
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1. Mild methylenetetrahydrofolate reductase deficiency accelerates liver triacylglycerol and uric acid accumulation in fructose-fed mice;Nutrition Research;2022-12
2. The Different Relationship between Homocysteine and Uric Acid Levels with Respect to the MTHFR C677T Polymorphism According to Gender in Patients with Cognitive Impairment;Nutrients;2020-04-19
3. Hyper-homocysteinemia Inducing Hyperuricemia: What are the Mechanisms?;Journal of Rheumatic Diseases;2017
4. AB0811 MTHFR C677T Polymorphism Is Associated with Increase in Homocysteine but Not with Uric Acid;Annals of the Rheumatic Diseases;2016-06
5. Transcobalamin II (TCN267A>G andTCN2776C>G) and Transcobalamin II Receptor (TCblR1104C>T) Polymorphisms in Korean Patients with Idiopathic Recurrent Spontaneous Abortion;American Journal of Reproductive Immunology;2014-04-18
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