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303 related items for PubMed ID: 15259035

  • 1. Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern Brazil.
    Félix TM, Leistner S, Giugliani R.
    Birth Defects Res A Clin Mol Teratol; 2004 Jul; 70(7):459-63. PubMed ID: 15259035
    [Abstract] [Full Text] [Related]

  • 2. 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 22; 9(2):1197-203. PubMed ID: 20589617
    [Abstract] [Full Text] [Related]

  • 3. 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 22; 27(8):568-77. PubMed ID: 19764044
    [Abstract] [Full Text] [Related]

  • 4. 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 22; 91(9):848-56. PubMed ID: 21770021
    [Abstract] [Full Text] [Related]

  • 5. 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 22; 70(1):27-44. PubMed ID: 10833329
    [Abstract] [Full Text] [Related]

  • 6. The maternal homocysteine pathway is influenced by riboflavin intake and MTHFR polymorphisms without affecting the risk of orofacial clefts in the offspring.
    Vujkovic M, Steegers EA, van Meurs J, Yazdanpanah N, van Rooij IA, Uitterlinden AG, Steegers-Theunissen RP.
    Eur J Clin Nutr; 2010 Mar 22; 64(3):266-73. PubMed ID: 19935819
    [Abstract] [Full Text] [Related]

  • 7. Polymorphism C776G in the transcobalamin II gene and homocysteine, folate and vitamin B12 concentrations. Association with MTHFR C677T and A1298C and MTRR A66G polymorphisms in healthy children.
    Aléssio AC, Höehr NF, Siqueira LH, Bydlowski SP, Annichino-Bizzacchi JM.
    Thromb Res; 2007 Mar 22; 119(5):571-7. PubMed ID: 16820193
    [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 22; 11 Suppl 1():S14-7. PubMed ID: 11813127
    [Abstract] [Full Text] [Related]

  • 9. 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 Dec 22; 46(3):105-9. PubMed ID: 11310576
    [Abstract] [Full Text] [Related]

  • 10. [Relationship between folate, vitamin B12, total plasma homocysteine and mutation of reductase].
    Hao L, Liu M, Liu X, Chen X, Tang Y, Li Z.
    Zhonghua Yu Fang Yi Xue Za Zhi; 2000 Jan 22; 34(1):22-4. PubMed ID: 11860891
    [Abstract] [Full Text] [Related]

  • 11. Mild hyperhomocysteinemia and low folate concentrations as risk factors for cervical arterial dissection.
    Arauz A, Hoyos L, Cantú C, Jara A, Martínez L, García I, Fernández Mde L, Alonso E.
    Cerebrovasc Dis; 2007 Jan 22; 24(2-3):210-4. PubMed ID: 17596690
    [Abstract] [Full Text] [Related]

  • 12. 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 22; 20(1):9-15. PubMed ID: 20066615
    [Abstract] [Full Text] [Related]

  • 13. Effects of the interaction between the C677T 5,10-methylenetetrahydrofolate reductase polymorphism and serum B vitamins on homocysteine levels in pregnant women.
    Kim KN, Kim YJ, Chang N.
    Eur J Clin Nutr; 2004 Jan 22; 58(1):10-6. PubMed ID: 14679361
    [Abstract] [Full Text] [Related]

  • 14. Dietary and genetic determinants of homocysteine levels among Mexican women of reproductive age.
    Torres-Sánchez L, Chen J, Díaz-Sánchez Y, Palomeque C, Bottiglieri T, López-Cervantes M, López-Carrillo L.
    Eur J Clin Nutr; 2006 Jun 22; 60(6):691-7. PubMed ID: 16418743
    [Abstract] [Full Text] [Related]

  • 15. 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 Jun 22; 47(4):327-33. PubMed ID: 16363341
    [Abstract] [Full Text] [Related]

  • 16. 677TT polymorphism of methylenetetrahydrofolate reductase in combination with low serum vitamin B12 is associated with coronary in-stent restenosis.
    Chung SL, Chiou KR, Charng MJ.
    Catheter Cardiovasc Interv; 2006 Mar 22; 67(3):349-55. PubMed ID: 16489563
    [Abstract] [Full Text] [Related]

  • 17. Evaluation of the relationship between C677T variants of methylenetetrahydrofolate reductase gene and hyperhomocysteinemia in children receiving antiepileptic drug therapy.
    Vurucu S, Demirkaya E, Kul M, Unay B, Gul D, Akin R, Gokçay E.
    Prog Neuropsychopharmacol Biol Psychiatry; 2008 Apr 01; 32(3):844-8. PubMed ID: 18234410
    [Abstract] [Full Text] [Related]

  • 18. High plasma homocysteine is associated with the risk of coronary artery disease independent of methylenetetrahydrofolate reductase 677C-->T genotypes.
    Lin PT, Huang MC, Lee BJ, Cheng CH, Tsai TP, Huang YC.
    Asia Pac J Clin Nutr; 2008 Apr 01; 17(2):330-8. PubMed ID: 18586656
    [Abstract] [Full Text] [Related]

  • 19. Methylenetetrahydrofolate reductase and transcobalamin genetic polymorphisms in human spontaneous abortion: biological and clinical implications.
    Zetterberg H.
    Reprod Biol Endocrinol; 2004 Feb 17; 2():7. PubMed ID: 14969589
    [Abstract] [Full Text] [Related]

  • 20. Hyperhomocysteinemia and methylenetetrahydrofolate reductase 677C-->T and 1298A-->C mutations in patients with inflammatory bowel disease.
    Fernández-Miranda C, Martínez Prieto M, Casis Herce B, Sánchez Gómez F, Gómez González P, Martínez López J, Sáenz-López Pérez S, Gómez de la Cámara A.
    Rev Esp Enferm Dig; 2005 Jul 17; 97(7):497-504. PubMed ID: 16262529
    [Abstract] [Full Text] [Related]

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