BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 18435414)

  • 1. 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]  

  • 2. 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]  

  • 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. Polymorphisms of folate metabolic genes and susceptibility to bladder cancer: a case-control study.
    Lin J; Spitz MR; Wang Y; Schabath MB; Gorlov IP; Hernandez LM; Pillow PC; Grossman HB; Wu X
    Carcinogenesis; 2004 Sep; 25(9):1639-47. PubMed ID: 15117811
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Effects of folic acid fortification and multivitamin therapy on homocysteine and vitamin B(12) status in cardiac transplant recipients.
    Miriuka SG; Langman LJ; Keren ES; Miner SE; Mamer OA; Delgado DH; Evrovski J; Ross HJ; Cole DE
    J Heart Lung Transplant; 2004 Apr; 23(4):405-12. PubMed ID: 15063399
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. Neural-tube defects are associated with low concentrations of cobalamin (vitamin B12) in amniotic fluid.
    Steen MT; Boddie AM; Fisher AJ; Macmahon W; Saxe D; Sullivan KM; Dembure PP; Elsas LJ
    Prenat Diagn; 1998 Jun; 18(6):545-55. PubMed ID: 9664599
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome?
    Guéant JL; Guéant-Rodriguez RM; Anello G; Bosco P; Brunaud L; Romano C; Ferri R; Romano A; Candito M; Namour B
    Clin Chem Lab Med; 2003 Nov; 41(11):1473-7. PubMed ID: 14656028
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic basis of neural tube defects. II. Genes correlated with folate and methionine metabolism.
    Gos M; Szpecht-Potocka A
    J Appl Genet; 2002; 43(4):511-24. PubMed ID: 12441636
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults.
    Kluijtmans LA; Young IS; Boreham CA; Murray L; McMaster D; McNulty H; Strain JJ; McPartlin J; Scott JM; Whitehead AS
    Blood; 2003 Apr; 101(7):2483-8. PubMed ID: 12642343
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage.
    Botto N; Andreassi MG; Manfredi S; Masetti S; Cocci F; Colombo MG; Storti S; Rizza A; Biagini A
    Eur J Hum Genet; 2003 Sep; 11(9):671-8. PubMed ID: 12939653
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interaction between common folate polymorphisms and B-vitamin nutritional status modulates homocysteine and risk for a thrombotic event.
    Yates Z; Lucock M
    Mol Genet Metab; 2003 Jul; 79(3):201-13. PubMed ID: 12855226
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome.
    Bosco P; Guéant-Rodriguez RM; Anello G; Barone C; Namour F; Caraci F; Romano A; Romano C; Guéant JL
    Am J Med Genet A; 2003 Sep; 121A(3):219-24. PubMed ID: 12923861
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic evidence that nitric oxide modulates homocysteine: the NOS3 894TT genotype is a risk factor for hyperhomocystenemia.
    Brown KS; Kluijtmans LA; Young IS; Woodside J; Yarnell JW; McMaster D; Murray L; Evans AE; Boreham CA; McNulty H; Strain JJ; Mitchell LE; Whitehead AS
    Arterioscler Thromb Vasc Biol; 2003 Jun; 23(6):1014-20. PubMed ID: 12689917
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Effect of TCN2 776C>G on vitamin B12 cellular availability in end-stage renal disease patients.
    Födinger M; Veitl M; Skoupy S; Wojcik J; Röhrer C; Hagen W; Puttinger H; Hauser AC; Vychytil A; Sunder-Plassmann G
    Kidney Int; 2003 Sep; 64(3):1095-100. PubMed ID: 12911562
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gene polymorphism and folate metabolism: a maternal risk factor for Down syndrome.
    Sheth JJ; Sheth FJ
    Indian Pediatr; 2003 Feb; 40(2):115-23. PubMed ID: 12626825
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Transcobalamin and methionine synthase reductase mutated polymorphisms aggravate the risk of neural tube defects in humans.
    Guéant-Rodriguez RM; Rendeli C; Namour B; Venuti L; Romano A; Anello G; Bosco P; Debard R; Gérard P; Viola M; Salvaggio E; Guéant JL
    Neurosci Lett; 2003 Jul; 344(3):189-92. PubMed ID: 12812837
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Folate status, metabolic genotype, and biomarkers of genotoxicity in healthy subjects.
    Zijno A; Andreoli C; Leopardi P; Marcon F; Rossi S; Caiola S; Verdina A; Galati R; Cafolla A; Crebelli R
    Carcinogenesis; 2003 Jun; 24(6):1097-103. PubMed ID: 12807760
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.