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    Results: 1 to 20 of 34

    1.

    A haplotype map of the human genome.

    International HapMap Consortium.

    Nature. 2005 Oct 27;437(7063):1299-320.PMID: 16255080 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    DNA methylation in epigenetic control of gene expression.

    Razin A, Kantor B.

    Prog Mol Subcell Biol. 2005;38:151-67. Review.PMID: 15881894 [PubMed - indexed for MEDLINE]Related articles

    3.

    Single nucleotide polymorphism genotyping by two colour melting curve analysis using the MGB Eclipse Probe System in challenging sequence environment.

    Belousov YS, Welch RA, Sanders S, Mills A, Kulchenko A, Dempcy R, Afonina IA, Walburger DK, Glaser CL, Yadavalli S, Vermeulen NM, Mahoney W.

    Hum Genomics. 2004 Mar;1(3):209-17.PMID: 15588480 [PubMed - indexed for MEDLINE]Related articles

    4.

    A mathematical model of the folate cycle: new insights into folate homeostasis.

    Nijhout HF, Reed MC, Budu P, Ulrich CM.

    J Biol Chem. 2004 Dec 31;279(53):55008-16. Epub 2004 Oct 20.PMID: 15496403 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    A mathematical model of the methionine cycle.

    Reed MC, Nijhout HF, Sparks R, Ulrich CM.

    J Theor Biol. 2004 Jan 7;226(1):33-43.PMID: 14637052 [PubMed - indexed for MEDLINE]Related articles

    6.

    Accounting for linkage in family-based tests of association with missing parental genotypes.

    Martin ER, Bass MP, Hauser ER, Kaplan NL.

    Am J Hum Genet. 2003 Nov;73(5):1016-26. Epub 2003 Oct 9.PMID: 14551902 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Transposable elements: targets for early nutritional effects on epigenetic gene regulation.

    Waterland RA, Jirtle RL.

    Mol Cell Biol. 2003 Aug;23(15):5293-300.PMID: 12861015 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Investigations of a common genetic variant in betaine-homocysteine methyltransferase (BHMT) in coronary artery disease.

    Weisberg IS, Park E, Ballman KV, Berger P, Nunn M, Suh DS, Breksa AP 3rd, Garrow TA, Rozen R.

    Atherosclerosis. 2003 Apr;167(2):205-14.PMID: 12818402 [PubMed - indexed for MEDLINE]Related articles

    9.

    Transcobalamin and methionine synthase reductase mutated polymorphisms aggravate the risk of neural tube defects in humans.

    Guéant-Rodriguez RM, Rendeli C, Namour B, Venuti L, Romano A, Anello G, Bosco P, Debard R, Gérard P, Viola M, Salvaggio E, Guéant JL.

    Neurosci Lett. 2003 Jul 3;344(3):189-92.PMID: 12812837 [PubMed - indexed for MEDLINE]Related articles

    11.

    Frequency of the thermolabile variant C677T in the MTHFR gene and lack of association with neural tube defects in the State of Yucatan, Mexico.

    González-Herrera L, García-Escalante G, Castillo-Zapata I, Canto-Herrera J, Ceballos-Quintal J, Pinto-Escalante D, Díaz-Rubio F, Del Angel RM, Orozco-Orozco L.

    Clin Genet. 2002 Nov;62(5):394-8.PMID: 12431255 [PubMed - indexed for MEDLINE]Related articles

    12.

    Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population.

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

    J Hum Genet. 2002;47(6):319-24.PMID: 12111380 [PubMed - indexed for MEDLINE]Related articles

    13.

    Genes, folate and homocysteine in embryonic development.

    Rosenquist TH, Finnell RH.

    Proc Nutr Soc. 2001 Feb;60(1):53-61. Review.PMID: 11310424 [PubMed - indexed for MEDLINE]Related articles

    14.

    GOLD--graphical overview of linkage disequilibrium.

    Abecasis GR, Cookson WO.

    Bioinformatics. 2000 Feb;16(2):182-3.PMID: 10842743 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    A test for linkage and association in general pedigrees: the pedigree disequilibrium test.

    Martin ER, Monks SA, Warren LL, Kaplan NL.

    Am J Hum Genet. 2000 Jul;67(1):146-54. Epub 2000 May 23.PMID: 10825280 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD).

    Stegmann K, Ziegler A, Ngo ET, Kohlschmidt N, Schröter B, Ermert A, Koch MC.

    Am J Med Genet. 1999 Nov 5;87(1):23-9.PMID: 10528242 [PubMed - indexed for MEDLINE]Related articles

    17.

    Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative Group.

    Speer MC, Nye J, McLone D, Worley G, Melvin EC, Viles KD, Franklin A, Drake C, Mackey J, George TM.

    Clin Genet. 1999 Aug;56(2):142-4.PMID: 10517251 [PubMed - indexed for MEDLINE]Related articles

    18.

    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.PMID: 10444342 [PubMed - indexed for MEDLINE]Related articles

    19.

    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

    20.

    The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

    Shields DC, Kirke PN, Mills JL, Ramsbottom D, Molloy AM, Burke H, Weir DG, Scott JM, Whitehead AS.

    Am J Hum Genet. 1999 Apr;64(4):1045-55.PMID: 10090889 [PubMed - indexed for MEDLINE]Related articlesFree article

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