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Общее количество найденных документов : 70
Показаны документы с 1 по 20
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| Graham G.W. 5,10-Methylenetetrahydrofolate reductase (MTHFR) as a risk factor in neural tube defects: A study of a Scottisch population // Eur. J. Pediat. Surg., 2000. Vol. 10, прил. N 1.-С.61
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| Association between MTHFR 677C-T polymorphism and alcohol dependence according to Lesch and Babor typology // Addict. Biol., 2009. Vol. 14, N 4.-С.503-505
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| Association of methylenetetrahydrofolate reductase gene polymorphism with carotid arterial wall thickening and myocardial infarction risk in NIDDM // Diabetes, 1997. Vol. 46, N 12.-С.2102-2104
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| Zhang Association of plasma homocysteine level and N{5}, N{10} - methylenetetrahydrofolate reductase gene polymorphism with cerebral infarction // Chin. Med. Sci. J., 2002. Vol. 17, N 4.-С.231-235
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| Biochemical and genetic analysis of methylenetetrahydrofolate reductase in Leishmania metabolism and virulence // J. Biol. Chem., 2006. Vol. 281, N 50.-С.38150-38158
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| C677T methylentetrahydrofulate reductase and angiotensin converting enzyme gene polymorphisms in patients with Alzheimer's disease in Iranian population // Neurochem. Res., 2006. Vol. 31, N 8.-С.1079-1083
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| Cost-effectiveness analysis of MTHFR polymorphism screening by polymerase chain reaction in Korean patients with rheumatoid arthritis receiving methotrexate // J. Rheumatol., 2006. Vol. 33, N 7.-С.1266-1274
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| Differences in methylenetetrahydrofolate reductase genotype frequencies, between whites and blacks // Amer. J. Hum. Genet., 1997. Vol. 60, N 1.-С.229-230
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| Effects of serum B vitamins on elevated plasma homocysteine levels associated with the mutation of methylenetetrahydrofolate reductase gene in Japanese // Atherosclerosis, 2002. Vol. 164, N 2.-С.321-328
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| Evaluation of C677T and A1298C polymorphisms of the MTHFR gene as maternal risk factors for Down syndrome and congenital heart defects // Amer. J. Med. Genet. A, 2009. Vol. 149, N 10.-С.2080-2087
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11.
| Evidence for a haxaheteromeric methylenetetrahydrofolate reductase in Moorella thermoacetica // J. Bacteriol., 2014. Vol. 196, N 18.-С.3303-3314
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12.
| Genetic causes of mild hyperhomoysteinemia in patients with premature occlusive coronary artery diseases // Atherosclerosis, 1999. Vol. 143, N 1.-С.163-170
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| Cacoub Hyperhomocysteinemie: Nouveau facteur de risque d'atherome, de thrombose arterielle et de thrombose veineuse // Med. ther., 1999. Vol. 5, N 9.-С.738-742
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| Interaction of methylenetetrahydrofolate reductase genotype and smoking habit in Taiwanese lung cancer patients // Cancer Genom. and Proteom., 2009. Vol. 6, N 6.-С.325-329
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| Interaction of methylenetetrahydrofolate reductase genotype and smoking habit in Taiwanese lung cancer patients // Cancer Genom. and Proteom., 2009. Vol. 6, N 6.-С.325-329
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| Dodelson de Kremer R. Maternal mutation 677C>T in the methylenetetrahydrofolate reductase gene associated with severe brain injury in offspring // Clin. Genet., 2005. Vol. 67, N 1.-С.69-80
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| Methylenetetrahydrofolate reductase (MTHFR) polymorphisms and risk of moleculary defined subtypes of childhood acute leukemia // Proc. Nat. Acad. Sci. USA, 2001. Vol. 98, N 7.-С.4004-4009
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18.
| Methylenetetrahydrofolate reductase C677T mutation and nonalcoholic fatty liver disease // Dig. Diseases and Sci., 2007. Vol. 52, N 5.-С.1183-1186
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| Methylenetetrahydrofolate reductase polymorphisms in preeclampsia and the HELLP syndrome // Hypertens. Pregnancy, 2000. Vol. 19, N 3.-С.299-307
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| MTHFR C677T and A1298C genotypes in a portuguese population: Association with homocysteine, folate and vitamin B12 // Clin. Nutr., 2001. Vol. 20, прил. 3.-С.43
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