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 *

141 related articles for article (PubMed ID: 9538515)

  • 21. 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]  

  • 22. Hyperhomocyst(e)inemia and MTHFR C677T genotypes in patients with central retinal vein occlusion.
    Weger M; Stanger O; Deutschmann H; Temmel W; Renner W; Schmut O; Semmelrock J; Haas A
    Graefes Arch Clin Exp Ophthalmol; 2002 Apr; 240(4):286-90. PubMed ID: 11981642
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The high prevalence of thermolabile 5-10 methylenetetrahydrofolate reductase (MTHFR) in Italians is not associated to an increased risk for coronary artery disease (CAD).
    Abbate R; Sardi I; Pepe G; Marcucci R; Brunelli T; Prisco D; Fatini C; Capanni M; Simonetti I; Gensini GF
    Thromb Haemost; 1998 Apr; 79(4):727-30. PubMed ID: 9569181
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The C677T mutation in the methylene tetrahydrofolate reductase gene increases serum uric acid in elderly men.
    Zuo M; Nishio H; Lee MJ; Maejima K; Mimura S; Sumino K
    J Hum Genet; 2000; 45(4):257-62. PubMed ID: 10944859
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [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]  

  • 26. [The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans].
    Guo C; Guo Q; Gong Y; Chen B; Liu Q; Li J; Gao G; Zhou H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):295-7. PubMed ID: 12170465
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Superficial venous thrombosis: prevalence of common genetic risk factors and their role on spreading to deep veins.
    Milio G; Siragusa S; Minà C; Amato C; Corrado E; Grimaudo S; Novo S
    Thromb Res; 2008; 123(2):194-9. PubMed ID: 18387654
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [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]  

  • 31. 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]  

  • 32. 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]  

  • 33. The mutation C677-->T in the methylene tetrahydrofolate reductase gene and stroke.
    Reuner KH; Ruf A; Kaps M; Druschky KF; Patscheke H
    Thromb Haemost; 1998 Feb; 79(2):450-1. PubMed ID: 9493611
    [No Abstract]   [Full Text] [Related]  

  • 34. 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]  

  • 35. Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects.
    Mornet E; Muller F; Lenvoisé-Furet A; Delezoide AL; Col JY; Simon-Bouy B; Serre JL
    Hum Genet; 1997 Oct; 100(5-6):512-4. PubMed ID: 9341863
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and risk of nonsyndromic cleft lip.
    Wyszynski DF; Diehl SR
    Am J Med Genet; 2000 May; 92(1):79-80. PubMed ID: 10797428
    [No Abstract]   [Full Text] [Related]  

  • 37. The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease.
    Brunelli T; Bagnoli S; Giusti B; Nacmias B; Pepe G; Sorbi S; Abbate R
    Neurosci Lett; 2001 Nov; 315(1-2):103-5. PubMed ID: 11711225
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Methylene tetrahydrofolate reductase C677T genotype and stroke.
    Salooja N; Catto A; Carter A; Tudenham EG; Grant PJ
    Clin Lab Haematol; 1998 Dec; 20(6):357-61. PubMed ID: 9951581
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Human methylenetetrahydrofolate reductase: isolation of cDNA mapping and mutation identification.
    Goyette P; Sumner JS; Milos R; Duncan AM; Rosenblatt DS; Matthews RG; Rozen R
    Nat Genet; 1994 Aug; 7(4):551. PubMed ID: 7951330
    [No Abstract]   [Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.