546 related articles for article (PubMed ID: 11813127)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population.
De Marco P; Calevo MG; Moroni A; Arata L; Merello E; Finnell RH; Zhu H; Andreussi L; Cama A; Capra V
J Hum Genet; 2002; 47(6):319-24. PubMed ID: 12111380
[TBL] [Abstract][Full Text] [Related]
7. A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida.
Wilson A; Platt R; Wu Q; Leclerc D; Christensen B; Yang H; Gravel RA; Rozen R
Mol Genet Metab; 1999 Aug; 67(4):317-23. PubMed ID: 10444342
[TBL] [Abstract][Full Text] [Related]
8. Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor.
Molloy AM; Mills JL; Kirke PN; Ramsbottom D; McPartlin JM; Burke H; Conley M; Whitehead AS; Weir DG; Scott JM
Am J Med Genet; 1998 Jun; 78(2):155-9. PubMed ID: 9674907
[TBL] [Abstract][Full Text] [Related]
9. C677T polymorphism of the methylenetetrahydrofolate reductase gene does not affect folic acid, vitamin B12, and homocysteine serum levels in Turkish children with neural tube defects.
Erdogan MO; Yildiz SH; Solak M; Eser O; Cosar E; Eser B; Koken R; Buyukbas S
Genet Mol Res; 2010 Jun; 9(2):1197-203. PubMed ID: 20589617
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. A1298C polymorphism of the MTHFR gene and neural tube defects in the state of Yucatan, Mexico.
Gonzalez-Herrera L; Castillo-Zapata I; Garcia-Escalante G; Pinto-Escalante D
Birth Defects Res A Clin Mol Teratol; 2007 Aug; 79(8):622-6. PubMed ID: 17621650
[TBL] [Abstract][Full Text] [Related]
13. Impact of 5,10-methylenetetrahydrofolate reductase gene polymorphism on neural tube defects.
Harisha PN; Devi BI; Christopher R; Kruthika-Vinod TP
J Neurosurg Pediatr; 2010 Oct; 6(4):364-7. PubMed ID: 20887110
[TBL] [Abstract][Full Text] [Related]
14. Low erythrocyte folate status and polymorphic variation in folate-related genes are associated with risk of neural tube defect pregnancy.
Relton CL; Wilding CS; Laffling AJ; Jonas PA; Burgess T; Binks K; Tawn EJ; Burn J
Mol Genet Metab; 2004 Apr; 81(4):273-81. PubMed ID: 15059614
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects.
Whitehead AS; Gallagher P; Mills JL; Kirke PN; Burke H; Molloy AM; Weir DG; Shields DC; Scott JM
QJM; 1995 Nov; 88(11):763-6. PubMed ID: 8542260
[TBL] [Abstract][Full Text] [Related]
17. Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India.
Godbole K; Gayathri P; Ghule S; Sasirekha BV; Kanitkar-Damle A; Memane N; Suresh S; Sheth J; Chandak GR; Yajnik CS
Birth Defects Res A Clin Mol Teratol; 2011 Sep; 91(9):848-56. PubMed ID: 21770021
[TBL] [Abstract][Full Text] [Related]
18. Interaction between maternal periconceptional supplementation of folic acid and reduced folate carrier gene polymorphism of neural tube defects.
Pei LJ; Zhu HP; Li ZW; Zhang W; Ren AG; Zhu JH; Li Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):284-7. PubMed ID: 15952116
[TBL] [Abstract][Full Text] [Related]
19. Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?
Heil SG; Van der Put NM; Waas ET; den Heijer M; Trijbels FJ; Blom HJ
Mol Genet Metab; 2001 Jun; 73(2):164-72. PubMed ID: 11386852
[TBL] [Abstract][Full Text] [Related]
20. Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects.
Volcik KA; Shaw GM; Lammer EJ; Zhu H; Finnell RH
Birth Defects Res A Clin Mol Teratol; 2003 Mar; 67(3):154-7. PubMed ID: 12797455
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
