Similar articles for PMID: 28520345

Year	Number of Results
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2022	9

1

Methylenetetrahydrofolate Reductase Deficiency.

Dean L. Dean L. 2012 Mar 8 [updated 2016 Oct 27]. In: Pratt VM, Scott SA, Pirmohamed M, Esquivel B, Kane MS, Kattman BL, Malheiro AJ, editors. Medical Genetics Summaries [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2012–. 2012 Mar 8 [updated 2016 Oct 27]. In: Pratt VM, Scott SA, Pirmohamed M, Esquivel B, Kane MS, Kattman BL, Malheiro AJ, editors. Medical Genetics Summaries [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2012–. PMID: 28520345 Free Books & Documents. Review.

2

Methionine synthase reductase 66A->G polymorphism is associated with increased plasma homocysteine concentration when combined with the homozygous methylenetetrahydrofolate reductase 677C->T variant.

Vaughn JD, Bailey LB, Shelnutt KP, Dunwoody KM, Maneval DR, Davis SR, Quinlivan EP, Gregory JF 3rd, Theriaque DW, Kauwell GP. Vaughn JD, et al. J Nutr. 2004 Nov;134(11):2985-90. doi: 10.1093/jn/134.11.2985. J Nutr. 2004. PMID: 15514263

3

Genetic determinants of hyperhomocysteinaemia: the roles of cystathionine beta-synthase and 5,10-methylenetetrahydrofolate reductase.

Blom HJ. Blom HJ. Eur J Pediatr. 2000 Dec;159 Suppl 3:S208-12. doi: 10.1007/pl00014405. Eur J Pediatr. 2000. PMID: 11216902 Review.

4

Homozygous cystathionine beta-synthase deficiency, combined with factor V Leiden or thermolabile methylenetetrahydrofolate reductase in the risk of venous thrombosis.

Kluijtmans LA, Boers GH, Verbruggen B, Trijbels FJ, Novakova IR, Blom HJ. Kluijtmans LA, et al. Blood. 1998 Mar 15;91(6):2015-8. Blood. 1998. PMID: 9490685 Free article.

5

5,10-Methylenetetrahydrofolate reductase 677C-->T and 1298A-->C mutations are genetic determinants of elevated homocysteine.

Castro R, Rivera I, Ravasco P, Jakobs C, Blom HJ, Camilo ME, de Almeida IT. Castro R, et al. QJM. 2003 Apr;96(4):297-303. doi: 10.1093/qjmed/hcg039. QJM. 2003. PMID: 12651974

6

The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population.

Shane B, Pangilinan F, Mills JL, Fan R, Gong T, Cropp CD, Kim Y, Ueland PM, Bailey-Wilson JE, Wilson AF, Brody LC, Molloy AM. Shane B, et al. Am J Clin Nutr. 2018 Dec 1;108(6):1334-1341. doi: 10.1093/ajcn/nqy209. Am J Clin Nutr. 2018. PMID: 30339177 Free PMC article.

7

Effect of MTHFR 677C>T on plasma total homocysteine levels in renal graft recipients.

Födinger M, Wölfl G, Fischer G, Rasoul-Rockenschaub S, Schmid R, Hörl WH, Sunder-Plassmann G. Födinger M, et al. Kidney Int. 1999 Mar;55(3):1072-80. doi: 10.1046/j.1523-1755.1999.0550031072.x. Kidney Int. 1999. PMID: 10027946 Free article.

8

MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis.

Klerk M, Verhoef P, Clarke R, Blom HJ, Kok FJ, Schouten EG; MTHFR Studies Collaboration Group. Klerk M, et al. JAMA. 2002 Oct 23-30;288(16):2023-31. doi: 10.1001/jama.288.16.2023. JAMA. 2002. PMID: 12387655

9

Prevalence and effects of gene-gene and gene-nutrient interactions on serum folate and serum total homocysteine concentrations in the United States: findings from the third National Health and Nutrition Examination Survey DNA Bank.

Yang QH, Botto LD, Gallagher M, Friedman JM, Sanders CL, Koontz D, Nikolova S, Erickson JD, Steinberg K. Yang QH, et al. Am J Clin Nutr. 2008 Jul;88(1):232-46. doi: 10.1093/ajcn/88.1.232. Am J Clin Nutr. 2008. PMID: 18614746

10

Rate of T alleles and TT genotype at MTHFR 677C->T locus or C alleles and CC genotype at MTHFR 1298A->C locus among healthy subjects in Turkey: impact on homocysteine and folic acid status and reference intervals.

Ozarda Y, Sucu DK, Hizli B, Aslan D. Ozarda Y, et al. Cell Biochem Funct. 2009 Dec;27(8):568-77. doi: 10.1002/cbf.1610. Cell Biochem Funct. 2009. PMID: 19764044

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