These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

300 related items for PubMed ID: 22475273

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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 Feb; 28(5A):2807-11. PubMed ID: 19035314
    [Abstract] [Full Text] [Related]

  • 3. Genetic variation in folate metabolism is associated with the risk of conotruncal heart defects in a Chinese population.
    Wang X, Wei H, Tian Y, Wu Y, Luo L.
    BMC Pediatr; 2018 Aug 30; 18(1):287. PubMed ID: 30165839
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects.
    Brouns R, Ursem N, Lindemans J, Hop W, Pluijm S, Steegers E, Steegers-Theunissen R.
    Prenat Diagn; 2008 Jun 30; 28(6):485-93. PubMed ID: 18435414
    [Abstract] [Full Text] [Related]

  • 6. Association of COMT, MTHFR, and SLC19A1(RFC-1) polymorphisms with homocysteine blood levels and cognitive impairment in Parkinson's disease.
    Białecka M, Kurzawski M, Roszmann A, Robowski P, Sitek EJ, Honczarenko K, Gorzkowska A, Budrewicz S, Mak M, Jarosz M, Gołąb-Janowska M, Koziorowska-Gawron E, Droździk M, Sławek J.
    Pharmacogenet Genomics; 2012 Oct 30; 22(10):716-24. PubMed ID: 22890010
    [Abstract] [Full Text] [Related]

  • 7. Folate pathway gene polymorphisms and risk of childhood brain tumors: results from an Australian case-control study.
    Greenop KR, Scott RJ, Attia J, Bower C, de Klerk NH, Norris MD, Haber M, Jamieson SE, van Bockxmeer FM, Gottardo NG, Ashton LJ, Armstrong BK, Milne E.
    Cancer Epidemiol Biomarkers Prev; 2015 Jun 30; 24(6):931-7. PubMed ID: 25809864
    [Abstract] [Full Text] [Related]

  • 8. Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring.
    Coppedè F, Migheli F, Bargagna S, Siciliano G, Antonucci I, Stuppia L, Palka G, Migliore L.
    Neurosci Lett; 2009 Jan 02; 449(1):15-9. PubMed ID: 18983896
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Methylenetetrahydrofolate reductase C677T and reduced folate carrier 80 G>A polymorphisms are associated with an increased risk of conotruncal heart defects.
    Gong D, Gu H, Zhang Y, Gong J, Nie Y, Wang J, Zhang H, Liu R, Hu S, Zhang H.
    Clin Chem Lab Med; 2012 Feb 04; 50(8):1455-61. PubMed ID: 22868813
    [Abstract] [Full Text] [Related]

  • 11. Methylenetetrahydrofolate reductase and methionine synthase reductase gene polymorphisms and protection from microvascular complications in adolescents with type 1 diabetes.
    Wiltshire EJ, Mohsin F, Chan A, Donaghue KC.
    Pediatr Diabetes; 2008 Aug 04; 9(4 Pt 2):348-53. PubMed ID: 18774994
    [Abstract] [Full Text] [Related]

  • 12. [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 04; 32(5):461-6. PubMed ID: 20466634
    [Abstract] [Full Text] [Related]

  • 13. Functional polymorphisms in folate metabolism genes influence the risk of meningioma and glioma.
    Bethke L, Webb E, Murray A, Schoemaker M, Feychting M, Lönn S, Ahlbom A, Malmer B, Henriksson R, Auvinen A, Kiuru A, Salminen T, Johansen C, Christensen HC, Muir K, McKinney P, Hepworth S, Dimitropoulou P, Lophatananon A, Swerdlow A, Houlston R.
    Cancer Epidemiol Biomarkers Prev; 2008 May 04; 17(5):1195-202. PubMed ID: 18483342
    [Abstract] [Full Text] [Related]

  • 14. 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 May 04; 44(11):1317-23. PubMed ID: 17087642
    [Abstract] [Full Text] [Related]

  • 15. 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 04; 70(1):27-44. PubMed ID: 10833329
    [Abstract] [Full Text] [Related]

  • 16. 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 04; 27(8):981-7. PubMed ID: 16524890
    [Abstract] [Full Text] [Related]

  • 17. Variants c.677 C>T, c.1298 A>C in MTHFR, and c.66 A>G in MTRR Affect the Occurrence of Recurrent Pregnancy Loss in Chinese Women.
    Zhang Y, Zhan W, Du Q, Wu L, Ding H, Liu F, Yin A.
    Genet Test Mol Biomarkers; 2020 Nov 04; 24(11):717-722. PubMed ID: 33121283
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. 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 04; 67(3):623-30. PubMed ID: 10930360
    [Abstract] [Full Text] [Related]

  • 20. Association between folate-metabolizing pathway polymorphism and non-Hodgkin lymphoma.
    Kim HN, Lee IK, Kim YK, Tran HT, Yang DH, Lee JJ, Shin MH, Park KS, Shin MG, Choi JS, Kim HJ.
    Br J Haematol; 2008 Feb 04; 140(3):287-94. PubMed ID: 18042267
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.