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Journal Abstract Search

163 related items for PubMed ID: 17349292

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  • 6. Influence of combined methylenetetrahydrofolate reductase (MTHFR) and thymidylate synthase enhancer region (TSER) polymorphisms to plasma homocysteine levels in Korean patients with recurrent spontaneous abortion.
    Kim NK, Choi YK, Kang MS, Choi DH, Cha SH, An MO, Lee S, Jeung M, Ko JJ, Oh D.
    Thromb Res; 2006; 117(6):653-8. PubMed ID: 15985285
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  • 8. Methylenetetrahydrofolate reductase deficiency and low dietary folate increase embryonic delay and placental abnormalities in mice.
    Pickell L, Li D, Brown K, Mikael LG, Wang XL, Wu Q, Luo L, Jerome-Majewska L, Rozen R.
    Birth Defects Res A Clin Mol Teratol; 2009 Jun; 85(6):531-41. PubMed ID: 19215022
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  • 9. MTHFR: Addressing Genetic Counseling Dilemmas Using Evidence-Based Literature.
    Levin BL, Varga E.
    J Genet Couns; 2016 Oct; 25(5):901-11. PubMed ID: 27130656
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  • 11. [Population study of frequency of methylenetetrahydrofolate reductase C677T gene polymorphism in Yakutia].
    Spiridonova MG, Stepanov VA, Maksimova NR, Puzyrev VP.
    Genetika; 2004 May; 40(5):704-8. PubMed ID: 15272569
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  • 13. [The genetic polymorphism of MTHFR gene in schizophrenia].
    Mavros M, Chiriţă V, Popescu O, Ferencz B.
    Rev Med Chir Soc Med Nat Iasi; 2008 May; 112(1):76-82. PubMed ID: 18677906
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  • 14. 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. PubMed ID: 11813127
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  • 15. Functional characterization of missense mutations in severe methylenetetrahydrofolate reductase deficiency using a human expression system.
    Burda P, Suormala T, Heuberger D, Schäfer A, Fowler B, Froese DS, Baumgartner MR.
    J Inherit Metab Dis; 2017 Mar; 40(2):297-306. PubMed ID: 27743313
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  • 16. Evaluation of the relationship between C677T variants of methylenetetrahydrofolate reductase gene and hyperhomocysteinemia in children receiving antiepileptic drug therapy.
    Vurucu S, Demirkaya E, Kul M, Unay B, Gul D, Akin R, Gokçay E.
    Prog Neuropsychopharmacol Biol Psychiatry; 2008 Apr 01; 32(3):844-8. PubMed ID: 18234410
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  • 17. Increased resistance to malaria in mice with methylenetetrahydrofolate reductase (Mthfr) deficiency suggests a mechanism for selection of the MTHFR 677C>T (c.665C>T) variant.
    Meadows DN, Pyzik M, Wu Q, Torre S, Gros P, Vidal SM, Rozen R.
    Hum Mutat; 2014 May 01; 35(5):594-600. PubMed ID: 24616178
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  • 18. A proteomic approach for the characterization of C677T mutation of the human gene methylenetetrahydrofolate reductase.
    Greco M, Chiriacò F, Del Boccio P, Tagliaferro L, Acierno R, Menegazzi P, Pinca E, Pignatelli F, Storelli C, Federici G, Urbani A, Maffia M.
    Proteomics; 2006 Oct 01; 6(19):5350-61. PubMed ID: 16955529
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  • 19. 5,10-methylenetetrahydrofolate reductase common mutations, folate status and plasma homocysteine in healthy French adults of the Supplementation en Vitamines et Mineraux Antioxydants (SU.VI.MAX) cohort.
    Chango A, Potier De Courcy G, Boisson F, Guilland JC, Barbé F, Perrin MO, Christidès JP, Rabhi K, Pfister M, Galan P, Hercberg S, Nicolas JP.
    Br J Nutr; 2000 Dec 01; 84(6):891-6. PubMed ID: 11177206
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  • 20. [Relationship between hyperhomocysteinemia and C677T polymorphism of methylene tetrahydrofolate reductase gene in a healthy Algerian population].
    Hambaba L, Abdessemed S, Yahia M, Laroui S, Rouabah F.
    Ann Biol Clin (Paris); 2008 Dec 01; 66(6):637-41. PubMed ID: 19091662
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