BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

374 related articles for article (PubMed ID: 12923861)

  • 1. 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]  

  • 2. [Folate gene polymorphism and the risk of Down syndrome pregnancies in young Chinese women].
    Liao YP; Bao MS; Liu CQ; Liu H; Zhang D
    Yi Chuan; 2010 May; 32(5):461-6. PubMed ID: 20466634
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Relationship between methionine synthase, methionine synthase reductase genetic polymorphisms and deep vein thrombosis among South Indians.
    Naushad SM; Jain Jamal MN; Prasad CK; Rama Devi AR
    Clin Chem Lab Med; 2008; 46(1):73-9. PubMed ID: 18034637
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Association of MTRRA66G polymorphism (but not of MTHFR C677T and A1298C, MTRA2756G, TCN C776G) with homocysteine and coronary artery disease in the French population.
    Guéant-Rodriguez RM; Juilliére Y; Candito M; Adjalla CE; Gibelin P; Herbeth B; Van Obberghen E; Gueánt JL
    Thromb Haemost; 2005 Sep; 94(3):510-5. PubMed ID: 16268464
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Effects of polymorphisms of methionine synthase and methionine synthase reductase on total plasma homocysteine in the NHLBI Family Heart Study.
    Jacques PF; Bostom AG; Selhub J; Rich S; Ellison RC; Eckfeldt JH; Gravel RA; Rozen R;
    Atherosclerosis; 2003 Jan; 166(1):49-55. PubMed ID: 12482550
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic polymorphisms in folate metabolism as risk for Down syndrome in the southern China.
    Jiajin L; Shuyan C; Ying W; Junxiao C; Xiudi W
    J Matern Fetal Neonatal Med; 2019 Jun; 32(12):2030-2035. PubMed ID: 29343135
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in Brazil.
    da Silva LR; Vergani N; Galdieri Lde C; Ribeiro Porto MP; Longhitano SB; Brunoni D; D'Almeida V; Alvarez Perez AB
    Am J Med Genet A; 2005 Jun; 135(3):263-7. PubMed ID: 15889417
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Polymorphisms of methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), and thymidylate synthase (TYMS) in multiple myeloma risk.
    Lima CS; Ortega MM; Ozelo MC; Araujo RC; De Souza CA; Lorand-Metze I; Annichino-Bizzacchi JM; Costa FF
    Leuk Res; 2008 Mar; 32(3):401-5. PubMed ID: 17655928
    [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. Association between decreased vitamin levels and MTHFR, MTR and MTRR gene polymorphisms as determinants for elevated total homocysteine concentrations in pregnant women.
    Barbosa PR; Stabler SP; Machado AL; Braga RC; Hirata RD; Hirata MH; Sampaio-Neto LF; Allen RH; Guerra-Shinohara EM
    Eur J Clin Nutr; 2008 Aug; 62(8):1010-21. PubMed ID: 17522601
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Are genetic variants of the methyl group metabolism enzymes risk factors predisposing to obesity?
    Terruzzi I; Senesi P; Fermo I; Lattuada G; Luzi L
    J Endocrinol Invest; 2007 Oct; 30(9):747-53. PubMed ID: 17993766
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MTRR and MTHFR polymorphism: link to Down syndrome?
    O'Leary VB; Parle-McDermott A; Molloy AM; Kirke PN; Johnson Z; Conley M; Scott JM; Mills JL
    Am J Med Genet; 2002 Jan; 107(2):151-5. PubMed ID: 11807890
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring.
    Coppedè F; Migheli F; Bargagna S; Siciliano G; Antonucci I; Stuppia L; Palka G; Migliore L
    Neurosci Lett; 2009 Jan; 449(1):15-9. PubMed ID: 18983896
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of homocysteine (but not of MTHFR 677 C>T, MTR 2756 A>G, MTRR 66 A>G and TCN2 776 C>G) with ischaemic cerebrovascular disease in Sicily.
    Bosco P; Guéant-Rodriguez RM; Anello G; Spada R; Romano A; Fajardo A; Caraci F; Ferri R; Guéant JL
    Thromb Haemost; 2006 Aug; 96(2):154-9. PubMed ID: 16894458
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Influence of methionine synthase (A2756G) and methionine synthase reductase (A66G) polymorphisms on plasma homocysteine levels and relation to risk of coronary artery disease.
    Laraqui A; Allami A; Carrié A; Coiffard AS; Benkouka F; Benjouad A; Bendriss A; Kadiri N; Bennouar N; Benomar A; Guedira A; Raisonnier A; Fellati S; Srairi JE; Benomar M
    Acta Cardiol; 2006 Feb; 61(1):51-61. PubMed ID: 16485733
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic polymorphisms involved in folate metabolism and elevated plasma concentrations of homocysteine: maternal risk factors for Down syndrome in Brazil.
    Biselli JM; Goloni-Bertollo EM; Zampieri BL; Haddad R; Eberlin MN; Pavarino-Bertelli EC
    Genet Mol Res; 2008 Jan; 7(1):33-42. PubMed ID: 18273817
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The MTRR 66A>G polymorphism and maternal risk of birth of a child with Down syndrome in Caucasian women: a case-control study and a meta-analysis.
    Coppedè F; Bosco P; Lorenzoni V; Denaro M; Anello G; Antonucci I; Barone C; Stuppia L; Romano C; Migliore L
    Mol Biol Rep; 2014 Sep; 41(9):5571-83. PubMed ID: 24965145
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gene polymorphisms as risk factors for predicting the cardiovascular manifestations in Marfan syndrome. Role of folic acid metabolism enzyme gene polymorphisms in Marfan syndrome.
    Benke K; Ágg B; Mátyás G; Szokolai V; Harsányi G; Szilveszter B; Odler B; Pólos M; Maurovich-Horvat P; Radovits T; Merkely B; Nagy ZB; Szabolcs Z
    Thromb Haemost; 2015 Oct; 114(4):748-56. PubMed ID: 26063524
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 5,10-Methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTRR), and methionine synthase reductase (MTR) gene polymorphisms and adult meningioma risk.
    Zhang J; Zhou YW; Shi HP; Wang YZ; Li GL; Yu HT; Xie XY
    J Neurooncol; 2013 Nov; 115(2):233-9. PubMed ID: 23959833
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MTR, MTRR, and MTHFR Gene Polymorphisms and Susceptibility to Nonsyndromic Cleft Lip With or Without Cleft Palate.
    Wang W; Jiao XH; Wang XP; Sun XY; Dong C
    Genet Test Mol Biomarkers; 2016 Jun; 20(6):297-303. PubMed ID: 27167580
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.