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 *

198 related articles for article (PubMed ID: 9102178)

  • 1. Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease.
    Christensen B; Frosst P; Lussier-Cacan S; Selhub J; Goyette P; Rosenblatt DS; Genest J; Rozen R
    Arterioscler Thromb Vasc Biol; 1997 Mar; 17(3):569-73. PubMed ID: 9102178
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Thermolabile methylenetetrahydrofolate reductase in coronary artery disease.
    Kluijtmans LA; Kastelein JJ; Lindemans J; Boers GH; Heil SG; Bruschke AV; Jukema JW; van den Heuvel LP; Trijbels FJ; Boerma GJ; Verheugt FW; Willems F; Blom HJ
    Circulation; 1997 Oct; 96(8):2573-7. PubMed ID: 9355896
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.
    Jacques PF; Bostom AG; Williams RR; Ellison RC; Eckfeldt JH; Rosenberg IH; Selhub J; Rozen R
    Circulation; 1996 Jan; 93(1):7-9. PubMed ID: 8616944
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Relation of a common mutation in methylenetetrahydrofolate reductase to plasma homocysteine and early onset coronary artery disease.
    Dunn J; Title LM; Bata I; Johnstone DE; Kirkland SA; O'Neill BJ; Zayed E; MacDonald MC; Dempsey G; Nassar B
    Clin Biochem; 1998 Mar; 31(2):95-100. PubMed ID: 9622772
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The methylenetetrahydrofolate reductase gene polymorphism in Koreans with coronary artery disease.
    Kim CH; Hwang KY; Choi TM; Shin WY; Hong SY
    Int J Cardiol; 2001 Mar; 78(1):13-7. PubMed ID: 11259808
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians.
    Ma J; Stampfer MJ; Hennekens CH; Frosst P; Selhub J; Horsford J; Malinow MR; Willett WC; Rozen R
    Circulation; 1996 Nov; 94(10):2410-6. PubMed ID: 8921781
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases.
    Tsai MY; Welge BG; Hanson NQ; Bignell MK; Vessey J; Schwichtenberg K; Yang F; Bullemer FE; Rasmussen R; Graham KJ
    Atherosclerosis; 1999 Mar; 143(1):163-70. PubMed ID: 10208491
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Methylenetetrahydrofolate reductase 677 C-->T mutation and coronary heart disease risk in UK Indian Asians.
    Chambers JC; Ireland H; Thompson E; Reilly P; Obeid OA; Refsum H; Ueland P; Lane DA; Kooner JS
    Arterioscler Thromb Vasc Biol; 2000 Nov; 20(11):2448-52. PubMed ID: 11073851
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The effect of a common methylenetetrahydrofolate reductase mutation on levels of homocysteine, folate, vitamin B12 and on the risk of premature atherosclerosis.
    Verhoeff BJ; Trip MD; Prins MH; Kastelein JJ; Reitsma PH
    Atherosclerosis; 1998 Nov; 141(1):161-6. PubMed ID: 9863549
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Methylenetetrahydrofolate reductase C677T mutation, plasma homocysteine, and folate in subjects from northern Italy with or without angiographically documented severe coronary atherosclerotic disease: evidence for an important genetic-environmental interaction.
    Girelli D; Friso S; Trabetti E; Olivieri O; Russo C; Pessotto R; Faccini G; Pignatti PF; Mazzucco A; Corrocher R
    Blood; 1998 Jun; 91(11):4158-63. PubMed ID: 9596662
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Effects of serum B vitamins on elevated plasma homocysteine levels associated with the mutation of methylenetetrahydrofolate reductase gene in Japanese.
    Moriyama Y; Okamura T; Kajinami K; Iso H; Inazu A; Kawashiri M; Mizuno M; Takeda Y; Sakamoto Y; Kimura H; Suzuki H; Mabuchi H
    Atherosclerosis; 2002 Oct; 164(2):321-8. PubMed ID: 12204804
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Methylenetetrahydrofolate reductase gene and coronary artery disease.
    van Bockxmeer FM; Mamotte CD; Vasikaran SD; Taylor RR
    Circulation; 1997 Jan; 95(1):21-3. PubMed ID: 8994411
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events.
    D'Angelo A; Coppola A; Madonna P; Fermo I; Pagano A; Mazzola G; Galli L; Cerbone AM
    Thromb Haemost; 2000 Apr; 83(4):563-70. PubMed ID: 10780318
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Plasma homocysteine levels related to interactions between folate status and methylenetetrahydrofolate reductase: a study in 52 healthy subjects.
    Zittoun J; Tonetti C; Bories D; Pignon JM; Tulliez M
    Metabolism; 1998 Nov; 47(11):1413-8. PubMed ID: 9826223
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation.
    Gallagher PM; Meleady R; Shields DC; Tan KS; McMaster D; Rozen R; Evans A; Graham IM; Whitehead AS
    Circulation; 1996 Nov; 94(9):2154-8. PubMed ID: 8901666
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients.
    Födinger M; Mannhalter C; Wölfl G; Pabinger I; Müller E; Schmid R; Hörl WH; Sunder-Plassmann G
    Kidney Int; 1997 Aug; 52(2):517-23. PubMed ID: 9264011
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Plasma homocysteine, methylenetetrahydrofolate reductase genotypes, and age at onset of symptoms of myocardial ischemia.
    Mager A; Battler A; Birnbaum Y; Magal N; Shohat M
    Am J Cardiol; 2002 Apr; 89(8):919-23. PubMed ID: 11950428
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.