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 *

98 related articles for article (PubMed ID: 10083027)

  • 1. C677T gene mutation in methylenetetrahydrofolate reductase as a risk factor for cardiac allograft vasculopathy.
    Elstein E; Huan C; Fitchett D; Cantarovitch M; Marpole D
    Transplant Proc; 1999; 31(1-2):99. PubMed ID: 10083027
    [No Abstract]   [Full Text] [Related]  

  • 2. Cardiac allograft vascular disease after orthotopic heart transplantation: methylenetetrahydrofolate reductase gene polymorphism C677T does not account for rapidly progressive forms.
    Pethig K; Hoffmann A; Heublein B; Timke A; Gross G; Haverich A
    Transplantation; 2000 Feb; 69(3):442-5. PubMed ID: 10706059
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hyperhomocysteinemia, MTHFR C677T genotype and low folate levels: a risk combination for acute coronary disease in a Portuguese population.
    Araújo F; Lopes M; Gonçalves L; Maciel MJ; Cunha-Ribeiro LM
    Thromb Haemost; 2000 Mar; 83(3):517-8. PubMed ID: 10744169
    [No Abstract]   [Full Text] [Related]  

  • 4. [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]  

  • 5. The (Ala-Val) mutation of methylenetetrahydrofolate reductase as a genetic risk factor for vascular disease in non-insulin-dependent diabetic patients.
    Brulhart MC; Dussoix P; Ruiz J; Passa P; Froguel P; James RW
    Am J Hum Genet; 1997 Jan; 60(1):228-9. PubMed ID: 8981966
    [No Abstract]   [Full Text] [Related]  

  • 6. A common mutation in the methylenetetrahydrofolate reductase gene and risk of coronary heart disease: results among U.S. men.
    Verhoef P; Rimm EB; Hunter DJ; Chen J; Willett WC; Kelsey K; Stampfer MJ
    J Am Coll Cardiol; 1998 Aug; 32(2):353-9. PubMed ID: 9708460
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Homocyst(e)ine and the C677T mutation of methylenetetrahydrofolate reductase in survivors of premature myocardial infarction.
    Virgos C; Joven J; Simó JM; Vilella E; Camps J; Arcelus R; Blanco-Vaca F; Figuera L; Martorell L
    Clin Biochem; 2000 Aug; 33(6):509-12. PubMed ID: 11074245
    [No Abstract]   [Full Text] [Related]  

  • 8. Methylenetetrahydrofolate reductase mutation and coronary artery disease.
    Narang R; Callaghan G; Haider AW; Davies GJ; Tuddenham EG
    Circulation; 1996 Nov; 94(9):2322-3. PubMed ID: 8901706
    [No Abstract]   [Full Text] [Related]  

  • 9. [Relationship between methylenetetrahydrofolate reductase gene polymorphism and coronary heart disease].
    Chen B; Wang X; Yu J; Zhang G; Chen F; Den J; Fu S; Li P; Cao W; Yu H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Oct; 15(5):300-2. PubMed ID: 9758879
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Homocysteine, methylenetetrahydrofolate reductase/C677T genotype and risk for coronary heart disease. The AtheroGene study].
    Blankenberg S; Rupprecht HJ; Peetz D; Bickel C; Hofman KP; Tiret L; Meyer J
    Dtsch Med Wochenschr; 2002 Apr; 127(14):729-35. PubMed ID: 11935469
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Methylenetetrahydrofolate reductase mutation and coronary artery disease.
    Samani NJ
    Circulation; 1998 Dec 22-29; 98(25):2932-3. PubMed ID: 9860798
    [No Abstract]   [Full Text] [Related]  

  • 13. The 677 C-->T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in five Chinese ethnic groups.
    Yu J; Chen B; Zhang G; Fu S; Li P
    Hum Hered; 2000; 50(4):268-70. PubMed ID: 10782023
    [No Abstract]   [Full Text] [Related]  

  • 14. Heterogeneity in world distribution of the thermolabile C677T mutation in 5,10-methylenetetrahydrofolate reductase.
    Pepe G; Camacho Vanegas O; Giusti B; Brunelli T; Marcucci R; Attanasio M; Rickards O; De Stefano GF; Prisco D; Gensini GF; Abbate R
    Am J Hum Genet; 1998 Sep; 63(3):917-20. PubMed ID: 9718345
    [No Abstract]   [Full Text] [Related]  

  • 15. Methylenetetrahydrofolate reductase gene polymorphism and coronary artery disease in Taiwan Chinese.
    Chen TY; Chen JH; Tsao CJ
    Haematologica; 2000 Apr; 85(4):445-6. PubMed ID: 10756383
    [No Abstract]   [Full Text] [Related]  

  • 16. Homocysteine and coronary heart disease: how great is the hazard?
    Wilson PW
    JAMA; 2002 Oct 23-30; 288(16):2042-3. PubMed ID: 12387658
    [No Abstract]   [Full Text] [Related]  

  • 17. Recurrent coronary events are not increased in postinfarction patients with methylenetetrahydrofolate reductase gene C677T polymorphism.
    Vulapalli R; Liang C; Zareba W; Moss AJ
    Am J Cardiol; 2001 Jun; 87(11):1289-92. PubMed ID: 11377358
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Hyperhomocyst(e)inemia, MTHFR 677C-->T polymorphism and folate status in acute coronary disease.
    Kelly PJ; Furie KL
    Thromb Haemost; 2000 Oct; 84(4):737-8. PubMed ID: 11057888
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.