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Journal Abstract Search

232 related items for PubMed ID: 17184542

  • 1. CHKA and PCYT1A gene polymorphisms, choline intake and spina bifida risk in a California population.
    Enaw JO, Zhu H, Yang W, Lu W, Shaw GM, Lammer EJ, Finnell RH.
    BMC Med; 2006 Dec 21; 4():36. PubMed ID: 17184542
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  • 2. Polymorphic variants of genes involved in choline pathway and the risk of intrauterine fetal death.
    Drews K, Różycka A, Barlik M, Klejewski A, Kurzawińska G, Wolski H, Majchrzycki M, Gryszczyńska A, Kamiński A, Seremak-Mrozikiewicz A.
    Ginekol Pol; 2017 Dec 21; 88(4):205-211. PubMed ID: 28509322
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  • 3. Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida.
    Shaw GM, Rozen R, Finnell RH, Wasserman CR, Lammer EJ.
    Am J Epidemiol; 1998 Jul 01; 148(1):30-7. PubMed ID: 9663401
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  • 5. The NAT1 C1095A polymorphism, maternal multivitamin use and smoking, and the risk of spina bifida.
    Jensen LE, Hoess K, Whitehead AS, Mitchell LE.
    Birth Defects Res A Clin Mol Teratol; 2005 Jul 01; 73(7):512-6. PubMed ID: 15959877
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  • 8. Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects.
    Volcik KA, Shaw GM, Lammer EJ, Zhu H, Finnell RH.
    Birth Defects Res A Clin Mol Teratol; 2003 Mar 01; 67(3):154-7. PubMed ID: 12797455
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  • 9. Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts.
    Mostowska A, Hozyasz KK, Biedziak B, Misiak J, Jagodzinski PP.
    Eur J Oral Sci; 2010 Aug 01; 118(4):325-32. PubMed ID: 20662904
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  • 10. 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 01; 70(1):27-44. PubMed ID: 10833329
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  • 11. C677T mutation in methylenetetrahydrofolate reductase gene and neural tube defects: should Japanese women undergo gene screening before pregnancy?
    Kondo A, Fukuda H, Matsuo T, Shinozaki K, Okai I.
    Congenit Anom (Kyoto); 2014 Feb 01; 54(1):30-4. PubMed ID: 24588777
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  • 12. Risk factors for neural tube defects: associations between uncoupling protein 2 polymorphisms and spina bifida.
    Volcik KA, Shaw GM, Zhu H, Lammer EJ, Finnell RH.
    Birth Defects Res A Clin Mol Teratol; 2003 Mar 01; 67(3):158-61. PubMed ID: 12797456
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  • 17. Association between maternal COMT gene polymorphisms and fetal neural tube defects risk in a Chinese population.
    Liu J, Wang L, Fu Y, Li Z, Zhang Y, Zhang L, Jin L, Ye R, Ren A.
    Birth Defects Res A Clin Mol Teratol; 2014 Jan 01; 100(1):22-9. PubMed ID: 24382678
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  • 19. An association study of 45 folate-related genes in spina bifida: Involvement of cubilin (CUBN) and tRNA aspartic acid methyltransferase 1 (TRDMT1).
    Franke B, Vermeulen SH, Steegers-Theunissen RP, Coenen MJ, Schijvenaars MM, Scheffer H, den Heijer M, Blom HJ.
    Birth Defects Res A Clin Mol Teratol; 2009 Mar 01; 85(3):216-26. PubMed ID: 19161160
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