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 *

118 related articles for article (PubMed ID: 11377358)

  • 21. Association of methylenetetrahydrofolate reductase gene polymorphism with carotid arterial wall thickening and myocardial infarction risk in NIDDM.
    Arai K; Yamasaki Y; Kajimoto Y; Watada H; Umayahara Y; Kodama M; Sakamoto K; Hori M
    Diabetes; 1997 Dec; 46(12):2102-4. PubMed ID: 9392503
    [No Abstract]   [Full Text] [Related]  

  • 22. 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]  

  • 23. Evolution of genetic analysis strategies in coronary heart disease: a case of unnatural selection?
    Keavney B; Watkins H
    Eur Heart J; 2001 Feb; 22(4):271-3. PubMed ID: 11161941
    [No Abstract]   [Full Text] [Related]  

  • 24. Genetic coronary risk factors in conventionally low-risk patients.
    Morita H; Kurihara H; Imai Y; Yazaki Y; Nagai R
    Thromb Haemost; 2000 Jul; 84(1):137. PubMed ID: 10928484
    [No Abstract]   [Full Text] [Related]  

  • 25. Methylenetetrahydrofolate reductase gene and coronary artery disease.
    Mager A
    Circulation; 2000 Apr; 101(16):E172-3. PubMed ID: 10779474
    [No Abstract]   [Full Text] [Related]  

  • 26. 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]  

  • 27. Methylenetetrahydrofolate reductase gene polymorphism, hyperhomocysteinemia and occlusive retinal vascular disease in type 2 diabetic and non-diabetic subjects.
    Wirta V; Saransaari P; Wirta O; Rantalaiho V; Oja SS; Pasternack A; Koivula T; Lehtimäki T
    Clin Nephrol; 2002 Sep; 58(3):171-8. PubMed ID: 12356186
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [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]  

  • 29. [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]  

  • 30. 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]  

  • 31. [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]  

  • 32. 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]  

  • 33. [Study on the relationship between methylenetetrahydrofolate reductase gene C677T mutation and coronary heart disease].
    Wang X; Gu D; Sun F; Wu X; Yu Q; Jia X; Zhao J; Chen Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun; 18(3):206-8. PubMed ID: 11402451
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Role of the C677T polymorphism at the MTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: results from a case-control study in Brazil.
    Gaspar DA; Pavanello RC; Zatz M; Passos-Bueno MR; André M; Steman S; Wyszynski DF; Matiolli SR
    Am J Med Genet; 1999 Nov; 87(2):197-9. PubMed ID: 10533038
    [No Abstract]   [Full Text] [Related]  

  • 36. Methylenetetrahydrofolate reductase C677T genotype and venous thromboembolic disease.
    Couturaud F; Oger E; Abalain JH; Chenu E; Guias B; Floch HH; Mercier B; Mottier D; Leroyer C
    Respiration; 2000; 67(6):657-61. PubMed ID: 11124649
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Homocysteine, methylenetetrahydrofolate reductase C677T polymorphism and the B-vitamins: a facet of nature-nurture interplay.
    Herrmann W; Obeid R; Schorr H; Zarzour W; Geisel J
    Clin Chem Lab Med; 2003 Apr; 41(4):547-53. PubMed ID: 12747601
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Children with stroke: polymorphism of the MTHFR gene, mild hyperhomocysteinemia, and vitamin status.
    Cardo E; Monrós E; Colomé C; Artuch R; Campistol J; Pineda M; Vilaseca MA
    J Child Neurol; 2000 May; 15(5):295-8. PubMed ID: 10830195
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 6.