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Journal Abstract Search

340 related items for PubMed ID: 17024475

  • 1. The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida.
    van der Linden IJ, den Heijer M, Afman LA, Gellekink H, Vermeulen SH, Kluijtmans LA, Blom HJ.
    J Mol Med (Berl); 2006 Dec; 84(12):1047-54. PubMed ID: 17024475
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  • 2. MTRR 66A>G polymorphism in relation to congenital heart defects.
    van Beynum IM, Kouwenberg M, Kapusta L, den Heijer M, van der Linden IJ, Daniels O, Blom HJ.
    Clin Chem Lab Med; 2006 Dec; 44(11):1317-23. PubMed ID: 17087642
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  • 3. 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
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  • 4. [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
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  • 5. 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 May; 46(1):73-9. PubMed ID: 18034637
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  • 11. Methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) gene polymorphisms as risk factors for hepatocellular carcinoma in a Korean population.
    Kwak SY, Kim UK, Cho HJ, Lee HK, Kim HJ, Kim NK, Hwang SG.
    Anticancer Res; 2008 May; 28(5A):2807-11. PubMed ID: 19035314
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  • 12. Methionine synthase reductase 66A->G polymorphism is associated with increased plasma homocysteine concentration when combined with the homozygous methylenetetrahydrofolate reductase 677C->T variant.
    Vaughn JD, Bailey LB, Shelnutt KP, Dunwoody KM, Maneval DR, Davis SR, Quinlivan EP, Gregory JF, Theriaque DW, Kauwell GP.
    J Nutr; 2004 Nov; 134(11):2985-90. PubMed ID: 15514263
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  • 13. 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
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  • 14. The polymorphisms of methionine synthase (MTR) and methionine synthase reductase (MTRR) genes in pathogenesis of preeclampsia.
    Seremak-Mrozikiewicz A, Bogacz A, Deka-Pawlik D, Klejewski A, Wolski H, Drews K, Karasiewicz M, Czerny B.
    J Matern Fetal Neonatal Med; 2017 Oct; 30(20):2498-2504. PubMed ID: 27806663
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  • 15. [Allelic polymorphism of MTHFR, MTR and MTRR genes in patients with cleft lip and/or palate and their mothers].
    Chorna LB, Akopian HR, Makukh HV, Fedoryk IM.
    Tsitol Genet; 2011 Oct; 45(3):51-6. PubMed ID: 21774403
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  • 16. Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida.
    Doolin MT, Barbaux S, McDonnell M, Hoess K, Whitehead AS, Mitchell LE.
    Am J Hum Genet; 2002 Nov; 71(5):1222-6. PubMed ID: 12375236
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  • 17. Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome.
    Hobbs CA, Sherman SL, Yi P, Hopkins SE, Torfs CP, Hine RJ, Pogribna M, Rozen R, James SJ.
    Am J Hum Genet; 2000 Sep; 67(3):623-30. PubMed ID: 10930360
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  • 18. 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
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  • 19. Common Polymorphisms That Affect Folate Transport or Metabolism Modify the Effect of the MTHFR 677C > T Polymorphism on Folate Status.
    Bueno O, Molloy AM, Fernandez-Ballart JD, García-Minguillán CJ, Ceruelo S, Ríos L, Ueland PM, Meyer K, Murphy MM.
    J Nutr; 2016 Jan; 146(1):1-8. PubMed ID: 26561410
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  • 20. Risk of congenital heart defects is influenced by genetic variation in folate metabolism.
    Christensen KE, Zada YF, Rohlicek CV, Andelfinger GU, Michaud JL, Bigras JL, Richter A, Dubé MP, Rozen R.
    Cardiol Young; 2013 Feb; 23(1):89-98. PubMed ID: 22475273
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