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 *

153 related articles for article (PubMed ID: 12108010)

  • 1. [Hyperhomocysteinemia and C677T mutation of methylenetetrahydrofolate reductase].
    Grasa Ullrich JM; Torres Gómez M; Sánchez Marín B; Calvo Martín MT; García Erce JA; Giralt Raichs M
    An Med Interna; 2002 May; 19(5):269. PubMed ID: 12108010
    [No Abstract]   [Full Text] [Related]  

  • 2. Heterozygous methylene tetrahydrofolate reductase mutation with mild hyperhomocysteinemia associated with deep vein thrombosis.
    Pathare A; al Kindi S; al Belushi T; Bayoumi R; Dennison D; Murlitharan S
    Haematologia (Budap); 2002; 32(4):551-6. PubMed ID: 12803132
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic basis of hyperhomocysteinemia.
    Medina MA; Amores-Sánchez MI
    Mol Genet Metab; 2000 Nov; 71(3):478-80. PubMed ID: 11073715
    [No Abstract]   [Full Text] [Related]  

  • 4. [Role of polymorphic variants of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene in the pathogenesis of cardiovascular diseases].
    Spiridonova MG; Stepanov VA; Puzyrev VP
    Klin Med (Mosk); 2001; 79(2):10-6. PubMed ID: 11419077
    [No Abstract]   [Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Is there a role for genetic polymorphism of C677T methylenetetrahydrofolate reductase (MTHFR) in Buerger's disease?
    Kawasaki T; Fujimura H; Kakinoki E; Uemichi A; Miyata T
    Thromb Haemost; 2000 Oct; 84(4):736-7. PubMed ID: 11057887
    [No Abstract]   [Full Text] [Related]  

  • 7. Factor V G1691A, apo E4 allele, hyperhomocysteinemia and MTHFR C677T in a young patient with myocardial infarction.
    Assanelli D; Ferrari R; Bollani G; Ettori F; Bonetti P; Bersatti F; Archetti S; Ruggeri G; Bonanome A; Martini G
    Thromb Haemost; 1999 Sep; 82(3):1196. PubMed ID: 10494787
    [No Abstract]   [Full Text] [Related]  

  • 8. Prevalence of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation in patients with varicose veins of lower limbs.
    Sverdlova AM; Bubnova NA; Baranovskaya SS; Vasina VI; Avitisjan AO; Schwartz EI
    Mol Genet Metab; 1998 Jan; 63(1):35-6. PubMed ID: 9538515
    [No Abstract]   [Full Text] [Related]  

  • 9. High frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in Northern Italy.
    Sacchi E; Tagliabue L; Duca F; Mannucci PM
    Thromb Haemost; 1997 Aug; 78(2):963-4. PubMed ID: 9268207
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Common mutation in the methylenetetrahydrofolate reductase gene offers no support for mild hyperhomocysteinemia being a causal risk factor for cardiovascular disease.
    Brattström L
    Circulation; 1997 Nov; 96(10):3805-7. PubMed ID: 9396508
    [No Abstract]   [Full Text] [Related]  

  • 12. Hyperhomocysteinemia but not MTHFR genotype is associated with young-onset essential hypertension.
    Garfunkel VA; Porto PI; Garcia SI; Dieuzeide G; Kirszner T; Plotquin Y; Spataro RJ; Gonzalez C; Pirola CJ
    J Hum Hypertens; 2003 May; 17(5):361-4. PubMed ID: 12756410
    [No Abstract]   [Full Text] [Related]  

  • 13. The mutation C677T in the methylene tetrahydrofolate reductase gene as a risk factor for myocardial infarction in the Portuguese population.
    Ferrer-Antunes C; Palmeiro A; Morais J; Lourenço M; Freitas M; Providência L
    Thromb Haemost; 1998 Sep; 80(3):521-2. PubMed ID: 9759639
    [No Abstract]   [Full Text] [Related]  

  • 14. The 677C-->T mutation of the methylene-tetrahydrofolate reductase gene in the pathogenesis of osteonecrosis of the femoral head.
    Zalavras CG; Malizos KN; Dokou E; Vartholomatos G
    Haematologica; 2002 Jan; 87(1):111-2. PubMed ID: 11801474
    [No Abstract]   [Full Text] [Related]  

  • 15. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two mutations in the MTHFR gene associated with mild hyperhomocysteinaemia.
    Tikly M; Zannettou N; Traub B
    S Afr Med J; 2003 Mar; 93(3):161-2. PubMed ID: 12768933
    [No Abstract]   [Full Text] [Related]  

  • 17. Hyperhomocysteinemia: another independent vascular risk factor.
    Deleu D
    Saudi Med J; 2000 Aug; 21(8):787-8. PubMed ID: 11423902
    [No Abstract]   [Full Text] [Related]  

  • 18. Homozygous methylenetetrahydrofolate reductase C677T mutation and male infertility.
    Bezold G; Lange M; Peter RU
    N Engl J Med; 2001 Apr; 344(15):1172-3. PubMed ID: 11302150
    [No Abstract]   [Full Text] [Related]  

  • 19. Comment on 'increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos'.
    Isotalo PA; Donnelly JG
    Eur J Hum Genet; 2002 Oct; 10(10):578-9; author reply 579-82. PubMed ID: 12357326
    [No Abstract]   [Full Text] [Related]  

  • 20. The methylenetetrahydrofolate reductase gene C677T mutant and ischemic stroke in sickle cell disease.
    Driscoll MC; Prauner R
    Thromb Haemost; 1999 Dec; 82(6):1780-1. PubMed ID: 10613678
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.