497 related articles for article (PubMed ID: 20160465)
1. 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]
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. Concerning the article by Houcher et al., Pediatr Neurosurg 2009;45:472-477.
George TM
Pediatr Neurosurg; 2009; 45(6):478. PubMed ID: 20164651
[No Abstract] [Full Text] [Related]
4. 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]
5. Association of methylenetetrahydrofolate reductase C677T and cystathionine β-synthase polymorphisms in cardiovascular disease in the algerian population.
Houcher B; Houcher Z; Touabti A; Begag S; Torun D; Eğin Y; Akar N; Kadour F
Genet Test Mol Biomarkers; 2010 Dec; 14(6):775-80. PubMed ID: 20939734
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. MTHFR 677C-->T and 1298A-->C polymorphisms: evaluation of maternal genotypic risk and association with level of neural tube defect.
Dalal A; Pradhan M; Tiwari D; Behari S; Singh U; Mallik GK; Das V; Agarwal S
Gynecol Obstet Invest; 2007; 63(3):146-50. PubMed ID: 17085942
[TBL] [Abstract][Full Text] [Related]
14. [Study on the association of polymorphisms in homocysteine metabolism related enzymes with deep venous thrombosis].
Yu HD; Zheng H; Qi H; Lian JH; He Y; Dong ZM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Dec; 23(6):635-9. PubMed ID: 17160942
[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. 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]
17. [Frequency of C677T polymorphism of 5, 10-methylenetetrahydrofolate reductase (MTHFR) in Chilean mothers of spina bifida cases and controls ].
Nitsche F; Alliende MA; Santos JL; Pérez F; Santa María L; Hertrampf E; Cortés F
Rev Med Chil; 2003 Dec; 131(12):1399-404. PubMed ID: 15022402
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Association between MTHFR C677T polymorphism and neural tube defect risks: A comprehensive evaluation in three groups of NTD patients, mothers, and fathers.
Yang Y; Chen J; Wang B; Ding C; Liu H
Birth Defects Res A Clin Mol Teratol; 2015 Jun; 103(6):488-500. PubMed ID: 25808073
[TBL] [Abstract][Full Text] [Related]
20. [A case-control study on congenital heart diseases with methylenetetrahydrofolate reductase gene, cystathionine beta-synthase gene, and environmental factors].
Qiu XQ; Zhong QA; Zeng XY; Li YH; Nie SF
Zhonghua Liu Xing Bing Xue Za Zhi; 2006 Mar; 27(3):260-3. PubMed ID: 16792904
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]