These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
540 related articles for article (PubMed ID: 9545395)
1. A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? van der Put NM; Gabreëls F; Stevens EM; Smeitink JA; Trijbels FJ; Eskes TK; van den Heuvel LP; Blom HJ Am J Hum Genet; 1998 May; 62(5):1044-51. PubMed ID: 9545395 [TBL] [Abstract][Full Text] [Related]
2. [Methylene tetrahydrofolate reductase mutations as genetic risk factors for neural tube defects (NTF)]. Mierzejewska E Med Wieku Rozwoj; 1999; 3(4):521-7. PubMed ID: 10910677 [TBL] [Abstract][Full Text] [Related]
3. Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects. Christensen B; Arbour L; Tran P; Leclerc D; Sabbaghian N; Platt R; Gilfix BM; Rosenblatt DS; Gravel RA; Forbes P; Rozen R Am J Med Genet; 1999 May; 84(2):151-7. PubMed ID: 10323741 [TBL] [Abstract][Full Text] [Related]
4. Metabolic effects of C677T and A1298C mutations at the MTHFR gene in Brazilian children with neural tube defects. Cunha AL; Hirata MH; Kim CA; Guerra-Shinohara EM; Nonoyama K; Hirata RD Clin Chim Acta; 2002 Apr; 318(1-2):139-43. PubMed ID: 11880124 [TBL] [Abstract][Full Text] [Related]
5. Polymorphisms in genes involved in folate metabolism as risk factors for NTDs. De Marco P; Calevo MG; Moroni A; Arata L; Merello E; Cama A; Finnell RH; Andreussi L; Capra V Eur J Pediatr Surg; 2001 Dec; 11 Suppl 1():S14-7. PubMed ID: 11813127 [TBL] [Abstract][Full Text] [Related]
6. Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients. Födinger M; Mannhalter C; Wölfl G; Pabinger I; Müller E; Schmid R; Hörl WH; Sunder-Plassmann G Kidney Int; 1997 Aug; 52(2):517-23. PubMed ID: 9264011 [TBL] [Abstract][Full Text] [Related]
7. Plasma folate, vitamin B(12), and total homocysteine and homozygosity for the C677T mutation of the 5,10-methylene tetrahydrofolate reductase gene in patients with Alzheimer's dementia. A case-control study. Postiglione A; Milan G; Ruocco A; Gallotta G; Guiotto G; Di Minno G Gerontology; 2001; 47(6):324-9. PubMed ID: 11721146 [TBL] [Abstract][Full Text] [Related]
8. Folate levels and N(5),N(10)-methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case-control study. Martínez de Villarreal LE; Delgado-Enciso I; Valdéz-Leal R; Ortíz-López R; Rojas-Martínez A; Limón-Benavides C; Sánchez-Peña MA; Ancer-Rodríguez J; Barrera-Saldaña HA; Villarreal-Pérez JZ Arch Med Res; 2001; 32(4):277-82. PubMed ID: 11440783 [TBL] [Abstract][Full Text] [Related]
9. Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population. Barber R; Shalat S; Hendricks K; Joggerst B; Larsen R; Suarez L; Finnell R Mol Genet Metab; 2000 May; 70(1):45-52. PubMed ID: 10833330 [TBL] [Abstract][Full Text] [Related]
10. Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c --> t methylenetetrahydrofolate reductase and 2756a --> g methionine synthase genotypes. Lucock M; Daskalakis I; Briggs D; Yates Z; Levene M Mol Genet Metab; 2000 May; 70(1):27-44. PubMed ID: 10833329 [TBL] [Abstract][Full Text] [Related]
11. Reduced folate carrier polymorphism (80A-->G) and neural tube defects. De Marco P; Calevo MG; Moroni A; Merello E; Raso A; Finnell RH; Zhu H; Andreussi L; Cama A; Capra V Eur J Hum Genet; 2003 Mar; 11(3):245-52. PubMed ID: 12673279 [TBL] [Abstract][Full Text] [Related]
12. Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population. Richter B; Stegmann K; Röper B; Böddeker I; Ngo ET; Koch MC J Hum Genet; 2001; 46(3):105-9. PubMed ID: 11310576 [TBL] [Abstract][Full Text] [Related]
13. Folate, homocysteine and neural tube defects: an overview. van der Put NM; van Straaten HW; Trijbels FJ; Blom HJ Exp Biol Med (Maywood); 2001 Apr; 226(4):243-70. PubMed ID: 11368417 [TBL] [Abstract][Full Text] [Related]
14. The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events. D'Angelo A; Coppola A; Madonna P; Fermo I; Pagano A; Mazzola G; Galli L; Cerbone AM Thromb Haemost; 2000 Apr; 83(4):563-70. PubMed ID: 10780318 [TBL] [Abstract][Full Text] [Related]
15. Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect. Al-Gazali LI; Padmanabhan R; Melnyk S; Yi P; Pogribny IP; Pogribna M; Bakir M; Hamid ZA; Abdulrazzaq Y; Dawodu A; James SJ Am J Med Genet; 2001 Oct; 103(2):128-32. PubMed ID: 11568918 [TBL] [Abstract][Full Text] [Related]
16. Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD). Stegmann K; Ziegler A; Ngo ET; Kohlschmidt N; Schröter B; Ermert A; Koch MC Am J Med Genet; 1999 Nov; 87(1):23-9. PubMed ID: 10528242 [TBL] [Abstract][Full Text] [Related]
17. The influence of age, sex, vitamin B(12), folate levels and methylenetetrahydrofolate reductase C677T genetic mutations on plasma homocysteine in the Chinese population. Ho CH Haematologica; 2000 Oct; 85(10):1051-4. PubMed ID: 11025596 [TBL] [Abstract][Full Text] [Related]
18. Does prenatal screening for 5,10-methylenetetrahydrofolate reductase (MTHFR) mutations in high-risk neural tube defect pregnancies make sense? Finnell RH; Shaw GM; Lammer EJ; Volcik KA Genet Test; 2002; 6(1):47-52. PubMed ID: 12180076 [TBL] [Abstract][Full Text] [Related]
19. The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia. Harmon DL; Woodside JV; Yarnell JW; McMaster D; Young IS; McCrum EE; Gey KF; Whitehead AS; Evans AE QJM; 1996 Aug; 89(8):571-7. PubMed ID: 8935478 [TBL] [Abstract][Full Text] [Related]
20. Methylenetetrahydrofolate reductase 677 C-->T mutation and coronary heart disease risk in UK Indian Asians. Chambers JC; Ireland H; Thompson E; Reilly P; Obeid OA; Refsum H; Ueland P; Lane DA; Kooner JS Arterioscler Thromb Vasc Biol; 2000 Nov; 20(11):2448-52. PubMed ID: 11073851 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]