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149 related items for PubMed ID: 12576444

  • 21. Study on homocysteine levels and methylenetetrahydrofolate reductase gene variant (C677T) in a population of Buenos Aires City.
    Fridman O, Porcile R, Vanasco V, Junco MN, Gariglio L, Potenzoni MA, Bañes I, Morales A.
    Clin Exp Hypertens; 2008 Oct; 30(7):574-84. PubMed ID: 18855261
    [Abstract] [Full Text] [Related]

  • 22. No association between methylenetetrahydrofolate reductase C677T polymorphism and breast cancer.
    Hekim N, Ergen A, Yaylim I, Yilmaz H, Zeybek U, Oztürk O, Isbir T.
    Cell Biochem Funct; 2007 Oct; 25(1):115-7. PubMed ID: 16134079
    [Abstract] [Full Text] [Related]

  • 23. Maternal and offspring MTHFR gene C677T polymorphism as predictors of congenital atrial septal defect and patent ductus arteriosus.
    Zhu WL, Li Y, Yan L, Dao J, Li S.
    Mol Hum Reprod; 2006 Jan; 12(1):51-4. PubMed ID: 16373366
    [Abstract] [Full Text] [Related]

  • 24. Polymorphisms in the methylenetetrahydrofolate reductase gene are determinant for vascular complications after liver transplantation.
    Akoglu B, Kindl P, Weber N, Trojan J, Caspary WF, Faust D.
    Eur J Clin Nutr; 2008 Mar; 62(3):430-5. PubMed ID: 17311050
    [Abstract] [Full Text] [Related]

  • 25. [The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans].
    Guo C, Guo Q, Gong Y, Chen B, Liu Q, Li J, Gao G, Zhou H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):295-7. PubMed ID: 12170465
    [Abstract] [Full Text] [Related]

  • 26. The methylentetrahydrofolate reductase C677T point mutation is a risk factor for vascular access thrombosis in hemodialysis patients.
    Fukasawa M, Matsushita K, Kamiyama M, Mikami Y, Araki I, Yamagata Z, Takeda M.
    Am J Kidney Dis; 2003 Mar; 41(3):637-42. PubMed ID: 12612987
    [Abstract] [Full Text] [Related]

  • 27. Methylenetetrahydrofolate reductase polymorphism is associated with folate pool in gastrointestinal cancer tissue.
    Kawakami K, Omura K, Kanehira E, Watanabe G.
    Anticancer Res; 2001 Mar; 21(1A):285-9. PubMed ID: 11299748
    [Abstract] [Full Text] [Related]

  • 28. The thermolabile variant 677C-->T can further reduce activity when expressed in cis with severe mutations for human methylenetetrahydrofolate reductase.
    Goyette P, Rozen R.
    Hum Mutat; 2000 Mar; 16(2):132-8. PubMed ID: 10923034
    [Abstract] [Full Text] [Related]

  • 29. MTHFR C677T polymorphism and risk of HCC in patients with liver cirrhosis: role of male gender and alcohol consumption.
    Fabris C, Toniutto P, Falleti E, Fontanini E, Cussigh A, Bitetto D, Fornasiere E, Fumolo E, Avellini C, Minisini R, Pirisi M.
    Alcohol Clin Exp Res; 2009 Jan; 33(1):102-7. PubMed ID: 18945219
    [Abstract] [Full Text] [Related]

  • 30. [677T mutation of the MTHFR gene in adenomas and colorectal cancer in a population sample from the Northeastern Mexico. Preliminary results].
    Delgado-Enciso I, Martínez-Garza SG, Rojas-Martínez A, Ortiz-López R, Bosques-Padilla F, Calderón-Garcidueñas AL, Zárate-Gómez M, Barrera-Saldaña HA.
    Rev Gastroenterol Mex; 2001 Jan; 66(1):32-7. PubMed ID: 11464627
    [Abstract] [Full Text] [Related]

  • 31. Methylenetetrahydrofolate reductase genotype association with the risk of follicular lymphoma.
    Ismail SI, Ababneh NA, Khader Y, Abu-Khader AA, Awidi A.
    Cancer Genet Cytogenet; 2009 Dec; 195(2):120-4. PubMed ID: 19963111
    [Abstract] [Full Text] [Related]

  • 32. 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; 67(3):154-7. PubMed ID: 12797455
    [Abstract] [Full Text] [Related]

  • 33. [C677T genetic polymorphism of methylenetetrahydrofolate reductase in premature coronary heart disease].
    Xu H, Chen Z, Tang J, Zhu D, Zhang C.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1999 Apr; 21(2):118-21. PubMed ID: 12569666
    [Abstract] [Full Text] [Related]

  • 34. Impact of methylenetetrahydrofolate reductase (MTHFR) codon (677) and methionine synthase (MS) codon (2756) on risk of cervical carcinogenesis in North Indian population.
    Shekari M, Sobti RC, Kordi Tamandani DM, Suri V.
    Arch Gynecol Obstet; 2008 Dec; 278(6):517-24. PubMed ID: 18351371
    [Abstract] [Full Text] [Related]

  • 35. Genetic polymorphisms of the methylenetetrahydrofolate reductase gene, plasma folate levels and breast cancer susceptibility: a case-control study in Taiwan.
    Chou YC, Wu MH, Yu JC, Lee MS, Yang T, Shih HL, Wu TY, Sun CA.
    Carcinogenesis; 2006 Nov; 27(11):2295-300. PubMed ID: 16777985
    [Abstract] [Full Text] [Related]

  • 36. No association between the common MTHFR 677C->T polymorphism and venous thrombosis: results from the MEGA study.
    Bezemer ID, Doggen CJ, Vos HL, Rosendaal FR.
    Arch Intern Med; 2007 Mar 12; 167(5):497-501. PubMed ID: 17353498
    [Abstract] [Full Text] [Related]

  • 37. The relationship between MTHFR gene polymorphisms, plasma homocysteine levels and diabetic retinopathy in type 2 diabetes mellitus.
    Sun J, Xu Y, Zhu Y, Lu H, Deng H, Fan Y, Sun S, Zhang Y.
    Chin Med J (Engl); 2003 Jan 12; 116(1):145-7. PubMed ID: 12667409
    [Abstract] [Full Text] [Related]

  • 38. The MTHFR C677T polymorphism and colorectal cancer: the multiethnic cohort study.
    Le Marchand L, Wilkens LR, Kolonel LN, Henderson BE.
    Cancer Epidemiol Biomarkers Prev; 2005 May 12; 14(5):1198-203. PubMed ID: 15894672
    [Abstract] [Full Text] [Related]

  • 39. High prevalence of the thermolabile methylenetetrahydrofolate reductase variant in Mexico: a country with a very high prevalence of neural tube defects.
    Mutchinick OM, López MA, Luna L, Waxman J, Babinsky VE.
    Mol Genet Metab; 1999 Dec 12; 68(4):461-7. PubMed ID: 10607475
    [Abstract] [Full Text] [Related]

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