1064 related articles for article (PubMed ID: 20589617)
21. 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]
22. Rate of T alleles and TT genotype at MTHFR 677C->T locus or C alleles and CC genotype at MTHFR 1298A->C locus among healthy subjects in Turkey: impact on homocysteine and folic acid status and reference intervals.
Ozarda Y; Sucu DK; Hizli B; Aslan D
Cell Biochem Funct; 2009 Dec; 27(8):568-77. PubMed ID: 19764044
[TBL] [Abstract][Full Text] [Related]
23. The relation between erythrocyte volume and folate levels is influenced by a common mutation in the methylenetetrahydrofolate reductase (MTHFR) gene (C677T).
Lalouschek W; Aull S; Serles W; Wolfsberger M; Deecke L; Pabinger-Fasching I; Mannhalter C
J Investig Med; 2000 Jan; 48(1):14-20. PubMed ID: 10695265
[TBL] [Abstract][Full Text] [Related]
24. Physiologic changes in homocysteine metabolism in pregnancy: a longitudinal study in Spain.
Ubeda N; Reyes L; González-Medina A; Alonso-Aperte E; Varela-Moreiras G
Nutrition; 2011 Sep; 27(9):925-30. PubMed ID: 21367581
[TBL] [Abstract][Full Text] [Related]
25. MTHFR C677T polymorphism as a risk factor of neural tube defects in Malay: a case control study.
Hayati AR; Zainal AI; Tan GC; Ong LC; Khoo TB
Med J Malaysia; 2008 Dec; 63(5):379-83. PubMed ID: 19803295
[TBL] [Abstract][Full Text] [Related]
26. [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]
27. The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease.
Kadziela J; Janas J; Dzielińska Z; Szperl M; Gaździk D; Chotkowska E; Piotrowski W; Ruzyłło W
Kardiol Pol; 2003 Jul; 59(7):17-26; discussion 26. PubMed ID: 14560345
[TBL] [Abstract][Full Text] [Related]
28. Association of MTHFR and RFC1 gene polymorphism with hyperhomocysteinemia and its modulation by vitamin B12 and folic acid in an Indian population.
Sukla KK; Raman R
Eur J Clin Nutr; 2012 Jan; 66(1):111-8. PubMed ID: 21878957
[TBL] [Abstract][Full Text] [Related]
29. The relationship between homocysteine and genes of folate-related enzymes in migraine patients.
Oterino A; Toriello M; Valle N; Castillo J; Alonso-Arranz A; Bravo Y; Ruiz-Alegria C; Quintela E; Pascual J
Headache; 2010 Jan; 50(1):99-168. PubMed ID: 19619240
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects.
Brouns R; Ursem N; Lindemans J; Hop W; Pluijm S; Steegers E; Steegers-Theunissen R
Prenat Diagn; 2008 Jun; 28(6):485-93. PubMed ID: 18435414
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Association between the MTHFR C677T polymorphism, blood folate and vitamin B12 deficiency, and elevated serum total homocysteine in healthy individuals in Yunnan Province, China.
Ni J; Zhang L; Zhou T; Xu WJ; Xue JL; Cao N; Wang X
J Chin Med Assoc; 2017 Mar; 80(3):147-153. PubMed ID: 28094233
[TBL] [Abstract][Full Text] [Related]
34. Effect of folate, vitamin B6, and vitamin B12 intake and MTHFR C677T polymorphism on homocysteine concentrations of renal transplant recipients.
Biselli PM; Sanches de Alvarenga MP; Abbud-Filho M; Ferreira-Baptista MA; Galbiatti AL; Goto MT; Cardoso MA; Eberlin MN; Haddad R; Goloni-Bertollo EM; Pavarino-Bertelli EC
Transplant Proc; 2007 Dec; 39(10):3163-5. PubMed ID: 18089344
[TBL] [Abstract][Full Text] [Related]
35. Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population.
Boduroğlu K; Alanay Y; Alikaşifoğlu M; Aktaş D; Tunçbilek E
Turk J Pediatr; 2005; 47(4):327-33. PubMed ID: 16363341
[TBL] [Abstract][Full Text] [Related]
36. Methylenetetrahydrofolate reductase gene polymorphisms and neural tube defects epidemiology in the Slovak population.
Behunova J; Klimcakova L; Zavadilikova E; Potocekova D; Sykora P; Podracka L
Birth Defects Res A Clin Mol Teratol; 2010 Aug; 88(8):695-700. PubMed ID: 20672355
[TBL] [Abstract][Full Text] [Related]
37. 677C>T and 1298A>C polymorphisms of methylenetetrahydropholate reductase gene and biochemical parameters in Turkish population with spina bifida occulta.
Eser B; Cosar M; Eser O; Erdogan MO; Aslan A; Yildiz H; Boyaci G; Buyukbas S; Solak M
Turk Neurosurg; 2010 Jan; 20(1):9-15. PubMed ID: 20066615
[TBL] [Abstract][Full Text] [Related]
38. Association of homocysteine, vitamin B12, folic acid, and MTHFR C677T in patients with a thrombotic event or recurrent fetal loss.
Nadir Y; Hoffman R; Brenner B
Ann Hematol; 2007 Jan; 86(1):35-40. PubMed ID: 17043779
[TBL] [Abstract][Full Text] [Related]
39. C677t polymorphism of MTHFR and G80A polymorphism of RFC genes and their relation with homocysteine levels in obese Tunisian children.
Gara S; Ochi H; Chango A; Najjar L; Feki M; B'chir F; Kaabachi N; Ben Becher S; Boukthir S; Abdennebi M
Tunis Med; 2011 Jun; 89(6):565-8. PubMed ID: 21681722
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]