BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

241 related articles for article (PubMed ID: 10528242)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Distribution of alleles of the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in familial spina bifida.
    Johnson WG; Stenroos ES; Heath SC; Chen Y; Carroll R; McKoy VV; Chatkupt S; Lehner T
    Am J Med Genet; 1999 Dec; 87(5):407-12. PubMed ID: 10594879
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. A second common variant in the methylenetetrahydrofolate reductase (MTHFR) gene and its relationship to MTHFR enzyme activity, homocysteine, and cardiovascular disease risk.
    Lievers KJ; Boers GH; Verhoef P; den Heijer M; Kluijtmans LA; van der Put NM; Trijbels FJ; Blom HJ
    J Mol Med (Berl); 2001 Sep; 79(9):522-8. PubMed ID: 11692165
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 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. 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]  

  • 12. Association of total plasma homocysteine with methylenetetrahydrofolate reductase genotypes 677C>T, 1298A>C, and 1793G>A and the corresponding haplotypes in Swedish children and adolescents.
    Böttiger AK; Hurtig-Wennlöf A; Sjöström M; Yngve A; Nilsson TK
    Int J Mol Med; 2007 Apr; 19(4):659-65. PubMed ID: 17334642
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lack of evidence of association between MTHFR C677T polymorphism and congenital heart disease in a TDT study design.
    Pereira AC; Xavier-Neto J; Mesquita SM; Mota GF; Lopes AA; Krieger JE
    Int J Cardiol; 2005 Oct; 105(1):15-8. PubMed ID: 16207540
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Genotype and haplotype distributions of MTHFR677C>T and 1298A>C single nucleotide polymorphisms: a meta-analysis.
    Ogino S; Wilson RB
    J Hum Genet; 2003; 48(1):1-7. PubMed ID: 12560871
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.