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4. C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease. Hanson NQ; Aras O; Yang F; Tsai MY Clin Chem; 2001 Apr; 47(4):661-6. PubMed ID: 11274015 [TBL] [Abstract][Full Text] [Related]
5. The common mutations C677T and A1298C in the human methylenetetrahydrofolate reductase gene are associated with hyperhomocysteinemia and cardiovascular disease in hemodialysis patients. Haviv YS; Shpichinetsky V; Goldschmidt N; Atta IA; Ben-Yehuda A; Friedman G Nephron; 2002 Sep; 92(1):120-6. PubMed ID: 12187094 [TBL] [Abstract][Full Text] [Related]
6. MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae. Parle-McDermott A; Mills JL; Kirke PN; Cox C; Signore CC; Kirke S; Molloy AM; O'Leary VB; Pangilinan FJ; O'Herlihy C; Brody LC; Scott JM Am J Med Genet A; 2005 Feb; 132A(4):365-8. PubMed ID: 15633187 [TBL] [Abstract][Full Text] [Related]
7. Association of MTHFR A1298C polymorphism (but not of MTHFR C677T) with elevated homocysteine levels and placental vasculopathies. Klai S; Fekih-Mrissa N; El Housaini S; Kaabechi N; Nsiri B; Rachdi R; Gritli N Blood Coagul Fibrinolysis; 2011 Jul; 22(5):374-8. PubMed ID: 21577095 [TBL] [Abstract][Full Text] [Related]
8. Association of MTHFR 677C>T polymorphism with IUGR and placental abruption risk: A systematic review and meta-analysis. Bahrami R; Schwartz DA; Asadian F; Karimi-Zarchi M; Dastgheib SA; Tabatabaie RS; Meibodi B; Neamatzadeh H Eur J Obstet Gynecol Reprod Biol; 2021 Jan; 256():130-139. PubMed ID: 33212322 [TBL] [Abstract][Full Text] [Related]
9. Placental genotyping of the factor V Leiden, prothrombin 20210A and the methylenetetrahydrofolate reductase (MTHFR) C677T alleles in IUGR pregnancies. Wisotzkey JD; Bayliss P; Rutherford E; Bell T Thromb Haemost; 1999 May; 81(5):844-5. PubMed ID: 10365762 [No Abstract] [Full Text] [Related]
10. A common mutation in the 5,10-methylenetetrahydrofolate reductase gene as a new risk factor for placental vasculopathy. van der Molen EF; Arends GE; Nelen WL; van der Put NJ; Heil SG; Eskes TK; Blom HJ Am J Obstet Gynecol; 2000 May; 182(5):1258-63. PubMed ID: 10819868 [TBL] [Abstract][Full Text] [Related]
11. Absence of association of thrombophilia polymorphisms with intrauterine growth restriction. Infante-Rivard C; Rivard GE; Yotov WV; Génin E; Guiguet M; Weinberg C; Gauthier R; Feoli-Fonseca JC N Engl J Med; 2002 Jul; 347(1):19-25. PubMed ID: 12097536 [TBL] [Abstract][Full Text] [Related]
12. [C677T and A1298C mutation of the methylenetetrahydrofolate reductase gene in unexplained recurrent spontaneous abortion]. Wang XP; Lin QD; Ma ZW; Zhao AM Zhonghua Fu Chan Ke Za Zhi; 2004 Apr; 39(4):238-41. PubMed ID: 15130349 [TBL] [Abstract][Full Text] [Related]
13. The influence of 5,10 methylenetetrahydrofolate reductase genotypes on enzyme activity in placental tissue. Daly SF; Molloy AM; Mills JL; Lee YJ; Conley M; Kirke PN; Weir DG; Scott JM Br J Obstet Gynaecol; 1999 Nov; 106(11):1214-8. PubMed ID: 10549970 [TBL] [Abstract][Full Text] [Related]
14. Methylenetetrahydrofolate reductase polymorphisms are not a risk factor for pre-eclampsia/eclampsia in Australian women. Kaiser T; Brennecke SP; Moses EK Gynecol Obstet Invest; 2000; 50(2):100-2. PubMed ID: 10965192 [TBL] [Abstract][Full Text] [Related]
15. Development of a highly accurate, rapid PCR-RFLP genotyping assay for the methylenetetrahydrofolate reductase gene. Sell SM; Lugemwa PR Genet Test; 1999; 3(3):287-9. PubMed ID: 10495928 [TBL] [Abstract][Full Text] [Related]
16. [C677T genetic polymorphism of methylenetetrahydrofolate reductase in premature coronary heart disease]. Xu H; Chen Z; Tang J; Zhu D; Zhang C Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1999 Apr; 21(2):118-21. PubMed ID: 12569666 [TBL] [Abstract][Full Text] [Related]
17. Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A. Rady PL; Szucs S; Grady J; Hudnall SD; Kellner LH; Nitowsky H; Tyring SK; Matalon RK Am J Med Genet; 2002 Jan; 107(2):162-8. PubMed ID: 11807892 [TBL] [Abstract][Full Text] [Related]
18. The silent T1317C mutation of methylenetetrahydrofolate reductase should not interfere with MboII restriction isotyping of the reported A1298C mutation. Donnelly JG Mol Genet Metab; 1999 Dec; 68(4):511-2. PubMed ID: 10607482 [No Abstract] [Full Text] [Related]
19. The 4G/4G polymorphism of the hypofibrinolytic plasminogen activator inhibitor type 1 gene: an independent risk factor for serious pregnancy complications. Glueck CJ; Phillips H; Cameron D; Wang P; Fontaine RN; Moore SK; Sieve-Smith L; Tracy T Metabolism; 2000 Jul; 49(7):845-52. PubMed ID: 10909993 [TBL] [Abstract][Full Text] [Related]
20. MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases. Zidan HE; Rezk NA; Mohammed D Gene; 2013 Oct; 529(1):119-24. PubMed ID: 23933414 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]