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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 9502183)

  • 41. C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease.
    Hanson NQ; Aras O; Yang F; Tsai MY
    Clin Chem; 2001 Apr; 47(4):661-6. PubMed ID: 11274015
    [TBL] [Abstract][Full Text] [Related]  

  • 42. The TT genotype of the methylenetetrahydrofolate reductase C677T gene polymorphism is associated with the extent of coronary atherosclerosis in patients at high risk for coronary artery disease.
    Gardemann A; Weidemann H; Philipp M; Katz N; Tillmanns H; Hehrlein FW; Haberbosch W
    Eur Heart J; 1999 Apr; 20(8):584-92. PubMed ID: 10337543
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 5,10-Methylenetetrahydrofolate reductase polymorphism and early organ damage in primary hypertension.
    Ravera M; Viazzi F; Berruti V; Leoncini G; Zagami P; Bezante GP; Rosatto N; Ravazzolo R; Pontremoli R; Deferrari G
    Am J Hypertens; 2001 Apr; 14(4 Pt 1):371-6. PubMed ID: 11336184
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Thermolabile methylenetetrahydrofolate reductase, homocysteine, and cardiovascular disease risk: the European Concerted Action Project.
    Meleady R; Ueland PM; Blom H; Whitehead AS; Refsum H; Daly LE; Vollset SE; Donohue C; Giesendorf B; Graham IM; Ulvik A; Zhang Y; Bjorke Monsen AL;
    Am J Clin Nutr; 2003 Jan; 77(1):63-70. PubMed ID: 12499324
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Methylene tetrahydrofolate reductase (MTHFR) and nitric oxide synthase (ecNOS) genes and risks of peripheral arterial disease and coronary heart disease: Edinburgh Artery Study.
    Fowkes FG; Lee AJ; Hau CM; Cooke A; Connor JM; Lowe GD
    Atherosclerosis; 2000 May; 150(1):179-85. PubMed ID: 10781649
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Identification of six methylenetetrahydrofolate reductase (MTHFR) genotypes resulting from common polymorphisms: impact on plasma homocysteine levels and development of coronary artery disease.
    Meisel C; Cascorbi I; Gerloff T; Stangl V; Laule M; Müller JM; Wernecke KD; Baumann G; Roots I; Stangl K
    Atherosclerosis; 2001 Feb; 154(3):651-8. PubMed ID: 11257266
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Genetic variation of the methylenetetrahydrofolate reductase and cystathionine beta-synthase genes in Korean patients with coronary artery disease and a new polymorphism in intron 7.
    Hong SH; Song J; Kim JQ
    Mol Cell Probes; 2001 Apr; 15(2):119-23. PubMed ID: 11292330
    [TBL] [Abstract][Full Text] [Related]  

  • 49. The role of hyperhomocysteinemia and methylenetetrahydrofolate reductase (MTHFR) C677T mutation in patients with retinal artery occlusion.
    Weger M; Stanger O; Deutschmann H; Leitner FJ; Renner W; Schmut O; Semmelrock J; Haas A
    Am J Ophthalmol; 2002 Jul; 134(1):57-61. PubMed ID: 12095808
    [TBL] [Abstract][Full Text] [Related]  

  • 50. C677T (thermolabile alanine/valine) polymorphism in methylenetetrahydrofolate reductase (MTHFR): its frequency and impact on plasma homocysteine concentration in different European populations. EARS group.
    Gudnason V; Stansbie D; Scott J; Bowron A; Nicaud V; Humphries S
    Atherosclerosis; 1998 Feb; 136(2):347-54. PubMed ID: 9543106
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The relation between erythrocyte volume and folate levels is influenced by a common mutation in the methylenetetrahydrofolate reductase (MTHFR) gene (C677T).
    Lalouschek W; Aull S; Serles W; Wolfsberger M; Deecke L; Pabinger-Fasching I; Mannhalter C
    J Investig Med; 2000 Jan; 48(1):14-20. PubMed ID: 10695265
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Methylenetetrahydrofolate reductase (MTHFR) mutation, homocyst(e)ine, and coronary artery disease.
    Wilcken DE; Wang XL; Wilcken B
    Circulation; 1997 Oct; 96(8):2738-40. PubMed ID: 9355925
    [No Abstract]   [Full Text] [Related]  

  • 53. The C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene and vascular dementia.
    Pollak RD; Pollak A; Idelson M; Bejarano-Achache I; Doron D; Blumenfeld A
    J Am Geriatr Soc; 2000 Jun; 48(6):664-8. PubMed ID: 10855603
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Methylenetetrahydrofolate reductase (MTHFR) C677T mutation in Turkish patients with thrombosis.
    Balta G; Gürgey A
    Turk J Pediatr; 1999; 41(2):197-9. PubMed ID: 10770658
    [TBL] [Abstract][Full Text] [Related]  

  • 55. MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis.
    Klerk M; Verhoef P; Clarke R; Blom HJ; Kok FJ; Schouten EG;
    JAMA; 2002 Oct 23-30; 288(16):2023-31. PubMed ID: 12387655
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Methylenetetrahydrofolate reductase gene mutation and hyperhomocysteinemia as a risk factor for coronary heart disease in the Indian population.
    Nair KG; Nair SR; Ashavaid TF; Dalal JJ; Eghlim FF
    J Assoc Physicians India; 2002 May; 50 Suppl():9-15. PubMed ID: 12186157
    [TBL] [Abstract][Full Text] [Related]  

  • 57. The C677T mutation of the methylenetetrahydrofolate reductase gene is not associated with the risk of coronary artery disease or venous thrombosis among Chinese in Taiwan.
    Hsu LA; Ko YL; Wang SM; Chang CJ; Hsu TS; Chiang CW; Lee YS
    Hum Hered; 2001; 51(1-2):41-5. PubMed ID: 11096270
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Impact of plasma homocysteine and prothrombin G20210 A on primary antiphospholipid syndrome.
    Ames PR; Margaglione M; Tommasino C; Bossone A; Iannaccone L; Brancaccio V
    Blood Coagul Fibrinolysis; 2001 Dec; 12(8):699-704. PubMed ID: 11734671
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease.
    Kang SS; Passen EL; Ruggie N; Wong PW; Sora H
    Circulation; 1993 Oct; 88(4 Pt 1):1463-9. PubMed ID: 8403293
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis.
    Brattström L; Wilcken DE; Ohrvik J; Brudin L
    Circulation; 1998 Dec; 98(23):2520-6. PubMed ID: 9843457
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.