BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

266 related articles for article (PubMed ID: 10833331)

  • 21. Methylenetetrahydrofolate reductase gene, homocysteine and coronary artery disease: the A1298C polymorphism does matter. Inferences from a case study (Madeira, Portugal).
    Freitas AI; Mendonça I; Guerra G; Brión M; Reis RP; Carracedo A; Brehm A
    Thromb Res; 2008; 122(5):648-56. PubMed ID: 18384842
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Influence of 699C-->T and 1080C-->T polymorphisms of the cystathionine beta-synthase gene on plasma homocysteine levels.
    Aras O; Hanson NQ; Yang F; Tsai MY
    Clin Genet; 2000 Dec; 58(6):455-9. PubMed ID: 11149614
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Intermediate and severe hyperhomocysteinemia with thrombosis: a study of genetic determinants.
    Gaustadnes M; Rüdiger N; Rasmussen K; Ingerslev J
    Thromb Haemost; 2000 Apr; 83(4):554-8. PubMed ID: 10780316
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Homocysteine, folate, methylene tetrahydrofolate reductase genotype and vascular morbidity in diabetic subjects.
    Kaye JM; Stanton KG; McCann VJ; Vasikaran SD; Burke V; Taylor RR; van Bockxmeer FM
    Clin Sci (Lond); 2002 Jun; 102(6):631-7. PubMed ID: 12049616
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Homocysteine concentrations in adults with trisomy 21: effect of B vitamins and genetic polymorphisms.
    Fillon-Emery N; Chango A; Mircher C; Barbé F; Bléhaut H; Herbeth B; Rosenblatt DS; Réthoré MO; Lambert D; Nicolas JP
    Am J Clin Nutr; 2004 Dec; 80(6):1551-7. PubMed ID: 15585767
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Methylenetetrahydrofolate reductase polymorphism determines the plasma homocysteine-lowering effect of large-dose folic acid supplementation in patients with cardiovascular disease.
    Liu CS; Chiang HC; Chen HW
    Nutrition; 2004; 20(11-12):974-8. PubMed ID: 15561486
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The effects of folic acid supplementation on plasma total homocysteine are modulated by multivitamin use and methylenetetrahydrofolate reductase genotypes.
    Malinow MR; Nieto FJ; Kruger WD; Duell PB; Hess DL; Gluckman RA; Block PC; Holzgang CR; Anderson PH; Seltzer D; Upson B; Lin QR
    Arterioscler Thromb Vasc Biol; 1997 Jun; 17(6):1157-62. PubMed ID: 9194768
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Vitamin B12 decreases, but does not normalize, homocysteine and methylmalonic acid in end-stage renal disease: a link with glycine metabolism and possible explanation of hyperhomocysteinemia in end-stage renal disease.
    Hyndman ME; Manns BJ; Snyder FF; Bridge PJ; Scott-Douglas NW; Fung E; Parsons HG
    Metabolism; 2003 Feb; 52(2):168-72. PubMed ID: 12601627
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Homocysteine, B-vitamins and CVD.
    McNulty H; Pentieva K; Hoey L; Ward M
    Proc Nutr Soc; 2008 May; 67(2):232-7. PubMed ID: 18412997
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Association between plasma homocysteine levels and coronary artery disease: a population-based study in northern Greece.
    Boufidou AI; Makedou AD; Adamidis DN; Karvounis HI; Gourassas JT; Kesidis HT; Makedou KG; Papadopoulos CE; Parharidis GE; Louridas GE
    Curr Med Res Opin; 2004; 20(2):175-80. PubMed ID: 15006011
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Levels of homocysteine and polymorphisms of homocysteine metabolism-related enzymes in patients with type 2 diabetes mellitus and coronary heart disease].
    Luo D; Yan S; Cheng X; Song Y
    Wei Sheng Yan Jiu; 2009 Jan; 38(1):39-42. PubMed ID: 19267073
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Susceptibility to spina bifida; an association study of five candidate genes.
    Morrison K; Papapetrou C; Hol FA; Mariman EC; Lynch SA; Burn J; Edwards YH
    Ann Hum Genet; 1998 Sep; 62(Pt 5):379-96. PubMed ID: 10088035
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Relation between plasma homocysteine concentration, the 844ins68 variant of the cystathionine beta-synthase gene, and pyridoxal-5'-phosphate concentration.
    Tsai MY; Yang F; Bignell M; Aras O; Hanson NQ
    Mol Genet Metab; 1999 Aug; 67(4):352-6. PubMed ID: 10444346
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Polymorphisms of key enzymes in homocysteine metabolism affect diet responsiveness of plasma homocysteine in healthy women.
    Silaste ML; Rantala M; Sämpi M; Alfthan G; Aro A; Kesäniemi YA
    J Nutr; 2001 Oct; 131(10):2643-7. PubMed ID: 11584084
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Polygenic influence on plasma homocysteine: association of two prevalent mutations, the 844ins68 of cystathionine beta-synthase and A(2756)G of methionine synthase, with lowered plasma homocysteine levels.
    Tsai MY; Bignell M; Yang F; Welge BG; Graham KJ; Hanson NQ
    Atherosclerosis; 2000 Mar; 149(1):131-7. PubMed ID: 10704624
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. [CBS gene variations and serum homocysteine level associated with congenital heart defects].
    Zhu W; Song X; Li M; Dao J
    Wei Sheng Yan Jiu; 2008 Jul; 37(4):463-7. PubMed ID: 18839533
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases.
    Tsai MY; Welge BG; Hanson NQ; Bignell MK; Vessey J; Schwichtenberg K; Yang F; Bullemer FE; Rasmussen R; Graham KJ
    Atherosclerosis; 1999 Mar; 143(1):163-70. PubMed ID: 10208491
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects.
    Whitehead AS; Gallagher P; Mills JL; Kirke PN; Burke H; Molloy AM; Weir DG; Shields DC; Scott JM
    QJM; 1995 Nov; 88(11):763-6. PubMed ID: 8542260
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.