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86 related items for PubMed ID: 10456448

  • 1. Genetic polymorphism of 5,10-MTHFR reductase gene in offspring of patients with myocardial infarction.
    Margaglione M, Colaizzo D, Cappucci G, del Popolo A, Vecchione G, Grandone E, Di Minno G.
    Thromb Haemost; 1999 Jul; 82(1):19-23. PubMed ID: 10456448
    [Abstract] [Full Text] [Related]

  • 2. C677T substitution in the methylenetetrahydrofolate reductase gene as a risk factor for venous thrombosis and arterial disease in selected patients.
    Gemmati D, Serino ML, Trivellato C, Fiorini S, Scapoli GL.
    Haematologica; 1999 Sep; 84(9):824-8. PubMed ID: 10477457
    [Abstract] [Full Text] [Related]

  • 3. The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation.
    Margaglione M, D'Andrea G, d'Addedda M, Giuliani N, Cappucci G, Iannaccone L, Vecchione G, Grandone E, Brancaccio V, Di Minno G.
    Thromb Haemost; 1998 May; 79(5):907-11. PubMed ID: 9609218
    [Abstract] [Full Text] [Related]

  • 4. An association of 5,10-methylenetetrahydrofolate reductase (MTHFR) gene polymorphism and common carotid atherosclerosis.
    Kawamoto R, Kohara K, Tabara Y, Miki T, Doi T, Tokunaga H, Konishi I.
    J Hum Genet; 2001 May; 46(9):506-10. PubMed ID: 11558898
    [Abstract] [Full Text] [Related]

  • 5. [Polymorphism of genes coding for angiotensin I converting enzyme and methylenetetrahydrofolate reductase in patients with ischemic heart disease].
    Goracy I.
    Ann Acad Med Stetin; 2000 May; 46():97-108. PubMed ID: 11712321
    [Abstract] [Full Text] [Related]

  • 6. Hyperhomocysteinemia and the MTHFR C677T mutation in Budd-Chiari syndrome.
    Li XM, Wei YF, Hao HL, Hao YB, He LS, Li JD, Mei B, Wang SY, Wang C, Wang JX, Zhu JZ, Liang JQ.
    Am J Hematol; 2002 Sep; 71(1):11-4. PubMed ID: 12221667
    [Abstract] [Full Text] [Related]

  • 7. [Association of genetic polymorphisms in plasminogen activator inhibitor-1 gene and 5,10-methylenetetrahydrofolate reductase gene with recurrent early spontaneous abortion].
    Guan LX, Du XY, Wang JX, Gao L, Wang RL, Li HB, Wang SX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):330-3. PubMed ID: 15952129
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. The relationship of mutations in the MTHFR, prothrombin, and PAI-1 genes to plasma levels of homocysteine, prothrombin, and PAI-1 in children and adults.
    Balasa VV, Gruppo RA, Glueck CJ, Stroop D, Becker A, Pillow A, Wang P.
    Thromb Haemost; 1999 May; 81(5):739-44. PubMed ID: 10365747
    [Abstract] [Full Text] [Related]

  • 10. Methylenetetrahydrofolate reductase polymorphisms increase risk of esophageal squamous cell carcinoma in a Chinese population.
    Song C, Xing D, Tan W, Wei Q, Lin D.
    Cancer Res; 2001 Apr 15; 61(8):3272-5. PubMed ID: 11309278
    [Abstract] [Full Text] [Related]

  • 11. Association of methylenetetrahydrofolate reductase polymorphism C677T and dietary folate with the risk of cervical dysplasia.
    Goodman MT, McDuffie K, Hernandez B, Wilkens LR, Bertram CC, Killeen J, Le Marchand L, Selhub J, Murphy S, Donlon TA.
    Cancer Epidemiol Biomarkers Prev; 2001 Dec 15; 10(12):1275-80. PubMed ID: 11751445
    [Abstract] [Full Text] [Related]

  • 12. The 4G/4G polymorphism of the hypofibrinolytic plasminogen activator inhibitor type 1 gene: an independent risk factor for serious pregnancy complications.
    Glueck CJ, Phillips H, Cameron D, Wang P, Fontaine RN, Moore SK, Sieve-Smith L, Tracy T.
    Metabolism; 2000 Jul 15; 49(7):845-52. PubMed ID: 10909993
    [Abstract] [Full Text] [Related]

  • 13. 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 15; 70(1):27-44. PubMed ID: 10833329
    [Abstract] [Full Text] [Related]

  • 14. Increased risk of the abdominal aortic aneurysm in carriers of the MTHFR 677T allele.
    Strauss E, Waliszewski K, Gabriel M, Zapalski S, Pawlak AL.
    J Appl Genet; 2003 May 15; 44(1):85-93. PubMed ID: 12590185
    [Abstract] [Full Text] [Related]

  • 15. [The relationship of methylenetetrahydrofolate reductase gene polymorphism and plasma homocysteine levels in type 2 diabetes mellitus patients with diabetic retinopathy].
    Sun J, Xu Y, Zhu Y, Lu H, Deng H, Fan Y, Sun S, Zhang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr 15; 20(2):131-4. PubMed ID: 12673582
    [Abstract] [Full Text] [Related]

  • 16. Methylenetetrahydrofolate reductase gene polymorphism and ischemic stroke: sex difference in Japanese.
    Wu Y, Tomon M, Sumino K.
    Kobe J Med Sci; 2001 Dec 15; 47(6):255-62. PubMed ID: 11870335
    [Abstract] [Full Text] [Related]

  • 17. Gene--nutrition interactions in coronary artery disease: correlation between the MTHFR C677T polymorphism and folate and homocysteine status in a Korean population.
    Huh HJ, Chi HS, Shim EH, Jang S, Park CJ.
    Thromb Res; 2006 Dec 15; 117(5):501-6. PubMed ID: 15935452
    [Abstract] [Full Text] [Related]

  • 18. The methylenetetrahydrofolate reductase 677C-->T polymorphism and distal colorectal adenoma risk.
    Levine AJ, Siegmund KD, Ervin CM, Diep A, Lee ER, Frankl HD, Haile RW.
    Cancer Epidemiol Biomarkers Prev; 2000 Jul 15; 9(7):657-63. PubMed ID: 10919734
    [Abstract] [Full Text] [Related]

  • 19. Methylenetetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12, and DNA damage in coronary artery disease.
    Andreassi MG, Botto N, Cocci F, Battaglia D, Antonioli E, Masetti S, Manfredi S, Colombo MG, Biagini A, Clerico A.
    Hum Genet; 2003 Feb 15; 112(2):171-7. PubMed ID: 12522558
    [Abstract] [Full Text] [Related]

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