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Journal Abstract Search
217 related items for PubMed ID: 24014284
1. The association between plasma homocysteine and coronary heart disease is modified by the MTHFR 677C>T polymorphism. Mehlig K, Leander K, de Faire U, Nyberg F, Berg C, Rosengren A, Björck L, Zetterberg H, Blennow K, Tognon G, Torén K, Strandhagen E, Lissner L, Thelle D. Heart; 2013 Dec; 99(23):1761-5. PubMed ID: 24014284 [Abstract] [Full Text] [Related]
2. Association of total plasma homocysteine with methylenetetrahydrofolate reductase genotypes 677C>T, 1298A>C, and 1793G>A and the corresponding haplotypes in Swedish children and adolescents. Böttiger AK, Hurtig-Wennlöf A, Sjöström M, Yngve A, Nilsson TK. Int J Mol Med; 2007 Apr; 19(4):659-65. PubMed ID: 17334642 [Abstract] [Full Text] [Related]
3. MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis. Klerk M, Verhoef P, Clarke R, Blom HJ, Kok FJ, Schouten EG, MTHFR Studies Collaboration Group. JAMA; 2007 Apr; 288(16):2023-31. PubMed ID: 12387655 [Abstract] [Full Text] [Related]
5. The maternal homocysteine pathway is influenced by riboflavin intake and MTHFR polymorphisms without affecting the risk of orofacial clefts in the offspring. Vujkovic M, Steegers EA, van Meurs J, Yazdanpanah N, van Rooij IA, Uitterlinden AG, Steegers-Theunissen RP. Eur J Clin Nutr; 2010 Mar; 64(3):266-73. PubMed ID: 19935819 [Abstract] [Full Text] [Related]
7. Hyperhomocysteinemia is a risk factor of recurrent coronary event in young patients irrespective to the MTHFR C677T polymorphism. Gonzalez-Porras JR, Martin-Herrero F, Garcia-Sanz R, Lopez ML, Balanzategui A, Mateos MV, Pavon P, Gonzalez M, Alberca I, San Miguel JF. Thromb Res; 2007 Mar; 119(6):691-8. PubMed ID: 17005242 [Abstract] [Full Text] [Related]
8. Prospective study of first stroke in relation to plasma homocysteine and MTHFR 677C>T and 1298A>C genotypes and haplotypes - evidence for an association with hemorrhagic stroke. Hultdin J, Van Guelpen B, Winkvist A, Hallmans G, Weinehall L, Stegmayr B, Nilsson TK. Clin Chem Lab Med; 2011 Sep; 49(9):1555-62. PubMed ID: 21631392 [Abstract] [Full Text] [Related]
9. Homocysteine levels in children and adolescents are associated with the methylenetetrahydrofolate reductase 677C>T genotype, but not with physical activity, fitness or fatness: the European Youth Heart Study. Ruiz JR, Hurtig-Wennlöf A, Ortega FB, Patterson E, Nilsson TK, Castillo MJ, Sjöström M. Br J Nutr; 2007 Feb; 97(2):255-62. PubMed ID: 17298693 [Abstract] [Full Text] [Related]
10. High plasma homocysteine is associated with the risk of coronary artery disease independent of methylenetetrahydrofolate reductase 677C-->T genotypes. Lin PT, Huang MC, Lee BJ, Cheng CH, Tsai TP, Huang YC. Asia Pac J Clin Nutr; 2008 Feb; 17(2):330-8. PubMed ID: 18586656 [Abstract] [Full Text] [Related]
11. Serum folate, total homocysteine levels and methylenetetrahydrofolate reductase 677C>T polymorphism in young healthy female Japanese. Taguchi T, Mori H, Hamada A, Yamori Y, Mori M. Asia Pac J Clin Nutr; 2012 Feb; 21(2):291-5. PubMed ID: 22507617 [Abstract] [Full Text] [Related]
12. 5,10-methylenetetrahydrofolate reductase common mutations, folate status and plasma homocysteine in healthy French adults of the Supplementation en Vitamines et Mineraux Antioxydants (SU.VI.MAX) cohort. Chango A, Potier De Courcy G, Boisson F, Guilland JC, Barbé F, Perrin MO, Christidès JP, Rabhi K, Pfister M, Galan P, Hercberg S, Nicolas JP. Br J Nutr; 2000 Dec; 84(6):891-6. PubMed ID: 11177206 [Abstract] [Full Text] [Related]
13. Role of methylenetetrahydrofolate reductase 677C->T polymorphism in the development of premature myocardial infarction. Rallidis LS, Gialeraki A, Komporozos C, Vavoulis P, Pavlakis G, Travlou A, Lekakis I, Kremastinos DT. Atherosclerosis; 2008 Sep; 200(1):115-20. PubMed ID: 18255072 [Abstract] [Full Text] [Related]
14. Interaction between plasma homocysteine and the MTHFR c.677C > T polymorphism is associated with site-specific changes in DNA methylation in humans. Nash AJ, Mandaviya PR, Dib MJ, Uitterlinden AG, van Meurs J, Heil SG, Andrew T, Ahmadi KR. FASEB J; 2019 Jan; 33(1):833-843. PubMed ID: 30080444 [Abstract] [Full Text] [Related]
15. Methylenetetrahydrofolate reductase (MTHFR-677 and MTHFR-1298) genotypes and haplotypes and plasma homocysteine levels in patients with occlusive artery disease and deep venous thrombosis. Spiroski I, Kedev S, Antov S, Arsov T, Krstevska M, Dzhekova-Stojkova S, Bosilkova G, Kostovska S, Trajkov D, Petlichkovski A, Strezova A, Efinska-Mladenovska O, Spiroski M. Acta Biochim Pol; 2008 Jan; 55(3):587-94. PubMed ID: 18800176 [Abstract] [Full Text] [Related]
16. Contribution of thermolabile methylenetetrahydrofolate reductase variant to total plasma homocysteine levels in healthy men and women. Inter99 (2). Husemoen LL, Thomsen TF, Fenger M, Jørgensen HL, Jørgensen T. Genet Epidemiol; 2003 May; 24(4):322-30. PubMed ID: 12687650 [Abstract] [Full Text] [Related]
17. Homocysteine, methylenetetrahydrofolate reductase C677T polymorphism, and risk of retinal vein occlusion: a meta-analysis. McGimpsey SJ, Woodside JV, Cardwell C, Cahill M, Chakravarthy U. Ophthalmology; 2009 Sep; 116(9):1778-1787.e1. PubMed ID: 19729099 [Abstract] [Full Text] [Related]
18. Association of COMT, MTHFR, and SLC19A1(RFC-1) polymorphisms with homocysteine blood levels and cognitive impairment in Parkinson's disease. Białecka M, Kurzawski M, Roszmann A, Robowski P, Sitek EJ, Honczarenko K, Gorzkowska A, Budrewicz S, Mak M, Jarosz M, Gołąb-Janowska M, Koziorowska-Gawron E, Droździk M, Sławek J. Pharmacogenet Genomics; 2012 Oct; 22(10):716-24. PubMed ID: 22890010 [Abstract] [Full Text] [Related]
19. The MTHFR CT polymorphism confers a high risk for stroke in both homozygous and heterozygous T allele carriers with Type 2 diabetes. Hermans MP, Gala JL, Buysschaert M. Diabet Med; 2006 May; 23(5):529-36. PubMed ID: 16681562 [Abstract] [Full Text] [Related]
20. No association between the common MTHFR 677C->T polymorphism and venous thrombosis: results from the MEGA study. Bezemer ID, Doggen CJ, Vos HL, Rosendaal FR. Arch Intern Med; 2007 Mar 12; 167(5):497-501. PubMed ID: 17353498 [Abstract] [Full Text] [Related] Page: [Next] [New Search]