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.
139 related articles for article (PubMed ID: 10517251)
1. Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative Group. Speer MC; Nye J; McLone D; Worley G; Melvin EC; Viles KD; Franklin A; Drake C; Mackey J; George TM Clin Genet; 1999 Aug; 56(2):142-4. PubMed ID: 10517251 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria. Houcher B; Bourouba R; Djabi F; Yilmaz E; Eğin Y; Akar N Pediatr Neurosurg; 2009; 45(6):472-7. PubMed ID: 20160465 [TBL] [Abstract][Full Text] [Related]
4. Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects. Rampersaud E; Melvin EC; Siegel D; Mehltretter L; Dickerson ME; George TM; Enterline D; Nye JS; Speer MC; Clin Genet; 2003 Mar; 63(3):210-4. PubMed ID: 12694231 [TBL] [Abstract][Full Text] [Related]
5. Exploring gene-gene interactions in the etiology of neural tube defects. Botto LD; Mastroiacovo P Clin Genet; 1998 Jun; 53(6):456-9. PubMed ID: 9712534 [TBL] [Abstract][Full Text] [Related]
6. The thermolabile variant of methylenetetrahydrofolate reductase (MTHFR) is not a major risk factor for neural tube defect in American Caucasians. The NTD Collaborative Group. Speer MC; Worley G; Mackey JF; Melvin E; Oakes WJ; George TM Neurogenetics; 1997 Sep; 1(2):149-50. PubMed ID: 10732818 [TBL] [Abstract][Full Text] [Related]
7. Are common mutations of cystathionine beta-synthase involved in the aetiology of neural tube defects? Ramsbottom D; Scott JM; Molloy A; Weir DG; Kirke PN; Mills JL; Gallagher PM; Whitehead AS Clin Genet; 1997 Jan; 51(1):39-42. PubMed ID: 9084933 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Human T and risk for neural tube defects. Richter B; Schultealbert AH; Koch MC J Med Genet; 2002 Mar; 39(3):E14. PubMed ID: 11897834 [No Abstract] [Full Text] [Related]
10. High prevalence of the thermolabile methylenetetrahydrofolate reductase variant in Mexico: a country with a very high prevalence of neural tube defects. Mutchinick OM; López MA; Luna L; Waxman J; Babinsky VE Mol Genet Metab; 1999 Dec; 68(4):461-7. PubMed ID: 10607475 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother. Shields DC; Kirke PN; Mills JL; Ramsbottom D; Molloy AM; Burke H; Weir DG; Scott JM; Whitehead AS Am J Hum Genet; 1999 Apr; 64(4):1045-55. PubMed ID: 10090889 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Genetic variation of the methylenetetrahydrofolate reductase and cystathionine beta-synthase genes in Korean patients with coronary artery disease and a new polymorphism in intron 7. Hong SH; Song J; Kim JQ Mol Cell Probes; 2001 Apr; 15(2):119-23. PubMed ID: 11292330 [TBL] [Abstract][Full Text] [Related]
15. [Prevalence of methylenetetrahydrofolate reductase (MTHFR) gene polymorphism (C677T) in the Hungarian population]. Czeizel E; Tímár L; Botto L Orv Hetil; 2001 Jun; 142(23):1227-9. PubMed ID: 11433922 [TBL] [Abstract][Full Text] [Related]
16. The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations. Dávalos IP; Olivares N; Castillo MT; Cantú JM; Ibarra B; Sandoval L; Morán MC; Gallegos MP; Chakraborty R; Rivas F Ann Genet; 2000; 43(2):89-92. PubMed ID: 10998450 [TBL] [Abstract][Full Text] [Related]
17. Genetic basis of neural tube defects. II. Genes correlated with folate and methionine metabolism. Gos M; Szpecht-Potocka A J Appl Genet; 2002; 43(4):511-24. PubMed ID: 12441636 [TBL] [Abstract][Full Text] [Related]
18. Gene-gene interaction between the cystathionine beta-synthase 31 base pair variable number of tandem repeats and the methylenetetrahydrofolate reductase 677C > T polymorphism on homocysteine levels and risk for neural tube defects. Afman LA; Lievers KJ; Kluijtmans LA; Trijbels FJ; Blom HJ Mol Genet Metab; 2003 Mar; 78(3):211-5. PubMed ID: 12649066 [TBL] [Abstract][Full Text] [Related]
19. Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects. Mornet E; Muller F; Lenvoisé-Furet A; Delezoide AL; Col JY; Simon-Bouy B; Serre JL Hum Genet; 1997 Oct; 100(5-6):512-4. PubMed ID: 9341863 [TBL] [Abstract][Full Text] [Related]
20. [Genetic risk factors of neural tube defects]. Sliwerska E; Szpecht-Potocka A Med Wieku Rozwoj; 2002; 6(4):349-70. PubMed ID: 12810987 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]