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    Results: 1 to 20 of 279

    1.

    Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.

    Boyles AL, Billups AV, Deak KL, Siegel DG, Mehltretter L, Slifer SH, Bassuk AG, Kessler JA, Reed MC, Nijhout HF, George TM, Enterline DS, Gilbert JR, Speer MC; NTD Collaborative Group.

    Environ Health Perspect. 2006 Oct;114(10):1547-52.PMID: 17035141 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect population.

    Trembath D, Sherbondy AL, Vandyke DC, Shaw GM, Todoroff K, Lammer EJ, Finnell RH, Marker S, Lerner G, Murray JC.

    Teratology. 1999 May;59(5):331-41.PMID: 10332959 [PubMed - indexed for MEDLINE]Related articles

    3.

    Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population.

    Barber R, Shalat S, Hendricks K, Joggerst B, Larsen R, Suarez L, Finnell R.

    Mol Genet Metab. 2000 May;70(1):45-52.PMID: 10833330 [PubMed - indexed for MEDLINE]Related articles

    4.

    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.PMID: 11310576 [PubMed - indexed for MEDLINE]Related articles

    5.

    Polymorphisms in genes involved in folate metabolism as risk factors for NTDs.

    De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Cama A, Finnell RH, Andreussi L, Capra V.

    Eur J Pediatr Surg. 2001 Dec;11 Suppl 1:S14-7.PMID: 11813127 [PubMed - indexed for MEDLINE]Related articles

    6.

    Does prenatal screening for 5,10-methylenetetrahydrofolate reductase (MTHFR) mutations in high-risk neural tube defect pregnancies make sense?

    Finnell RH, Shaw GM, Lammer EJ, Volcik KA.

    Genet Test. 2002 Spring;6(1):47-52.PMID: 12180076 [PubMed - indexed for MEDLINE]Related articles

    7.

    Maternal MTHFR 677C>T is a risk factor for congenital heart defects: effect modification by periconceptional folate supplementation.

    van Beynum IM, Kapusta L, den Heijer M, Vermeulen SH, Kouwenberg M, Daniëls O, Blom HJ.

    Eur Heart J. 2006 Apr;27(8):981-7. Epub 2006 Mar 7.PMID: 16524890 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    MTHFR 677C-->T and 1298A-->C polymorphisms: evaluation of maternal genotypic risk and association with level of neural tube defect.

    Dalal A, Pradhan M, Tiwari D, Behari S, Singh U, Mallik GK, Das V, Agarwal S.

    Gynecol Obstet Invest. 2007;63(3):146-50. Epub 2006 Nov 2.PMID: 17085942 [PubMed - indexed for MEDLINE]Related articles

    9.

    Genetic basis of neural tube defects. II. Genes correlated with folate and methionine metabolism.

    Gos M Jr, Szpecht-Potocka A.

    J Appl Genet. 2002;43(4):511-24. Review.PMID: 12441636 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects.

    Rampersaud E, Melvin EC, Siegel D, Mehltretter L, Dickerson ME, George TM, Enterline D, Nye JS, Speer MC; NTD Collaborative Group.

    Clin Genet. 2003 Mar;63(3):210-4.PMID: 12694231 [PubMed - indexed for MEDLINE]Related articles

    11.

    118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.

    Shaw GM, Lu W, Zhu H, Yang W, Briggs FB, Carmichael SL, Barcellos LF, Lammer EJ, Finnell RH.

    BMC Med Genet. 2009 Jun 3;10:49.PMID: 19493349 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Genetic variation in genes of folate metabolism and neural-tube defect risk.

    van der Linden IJ, Afman LA, Heil SG, Blom HJ.

    Proc Nutr Soc. 2006 May;65(2):204-15. Review.PMID: 16672082 [PubMed - indexed for MEDLINE]Related articles

    13.

    Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population.

    Relton CL, Wilding CS, Pearce MS, Laffling AJ, Jonas PA, Lynch SA, Tawn EJ, Burn J.

    J Med Genet. 2004 Apr;41(4):256-60.PMID: 15060097 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts.

    Boyles AL, Wilcox AJ, Taylor JA, Meyer K, Fredriksen A, Ueland PM, Drevon CA, Vollset SE, Lie RT.

    Am J Med Genet A. 2008 Feb 15;146A(4):440-9.PMID: 18203168 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Analysis of seven maternal polymorphisms of genes involved in homocysteine/folate metabolism and risk of Down syndrome offspring.

    Scala I, Granese B, Sellitto M, Salomè S, Sammartino A, Pepe A, Mastroiacovo P, Sebastio G, Andria G.

    Genet Med. 2006 Jul;8(7):409-16.PMID: 16845273 [PubMed - indexed for MEDLINE]Related articles

    16.

    Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect.

    Al-Gazali LI, Padmanabhan R, Melnyk S, Yi P, Pogribny IP, Pogribna M, Bakir M, Hamid ZA, Abdulrazzaq Y, Dawodu A, James SJ.

    Am J Med Genet. 2001 Oct 1;103(2):128-32.PMID: 11568918 [PubMed - indexed for MEDLINE]Related articles

    17.

    High-level multiplex genotyping of polymorphisms involved in folate or homocysteine metabolism by matrix-assisted laser desorption/ionization mass spectrometry.

    Meyer K, Fredriksen A, Ueland PM.

    Clin Chem. 2004 Feb;50(2):391-402.PMID: 14752013 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Neural tube defects and a disturbed folate dependent homocysteine metabolism.

    van der Put NM, Blom HJ.

    Eur J Obstet Gynecol Reprod Biol. 2000 Sep;92(1):57-61. Review.PMID: 10986435 [PubMed - indexed for MEDLINE]Related articles

    19.

    Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population.

    Swanson DA, Pangilinan F, Mills JL, Kirke PN, Conley M, Weiler A, Frey T, Parle-McDermott A, O'Leary VB, Seltzer RR, Moynihan KA, Molloy AM, Burke H, Scott JM, Brody LC.

    Birth Defects Res A Clin Mol Teratol. 2005 Apr;73(4):239-44.PMID: 15782407 [PubMed - indexed for MEDLINE]Related articles

    20.

    The impact of folate pathway polymorphisms combined to nutritional deficiency as a maternal predisposition factor for Down syndrome.

    Santos-Rebouças CB, Corrêa JC, Bonomo A, Fintelman-Rodrigues N, Moura KC, Rodrigues CS, Santos JM, Pimentel MM.

    Dis Markers. 2008;25(3):149-57.PMID: 19096127 [PubMed - indexed for MEDLINE]Related articles

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