A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism.
about
Methylenetetrahydrofolate reductase and transcobalamin genetic polymorphisms in human spontaneous abortion: biological and clinical implicationsPharmacology of epigenetics in brain disordersThe screening power of methylenetetrahydrofolate reductase C677T polymorphism versus plasma homocysteine concentration in patients with stenosis of the internal carotid arteryCommon Mutations of the Methylenetetrahydrofolate Reductase (MTHFR) Gene in Non-Syndromic Cleft Lips and Palates Children in North-West of Iran.Plasmatic higher levels of homocysteine in non-alcoholic fatty liver disease (NAFLD)Increased DJ-1 expression under oxidative stress and in Alzheimer's disease brains.Polymorphisms of the methylenetetrahydrofolate reductase gene (C677T and A1298C) in nulliparous women complicated with preeclampsia.Polycystic ovary syndrome and the single nucleotide polymorphisms of methylenetetrahydrofolate reductase: a pilot observational study.A Structured-based Model for the Decreased Activity of Ala222Val and Glu429Ala Methylenetetrahydrofolate Reductase (MTHFR) Mutants.Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage.Detection of 677CT/1298AC "double variant" chromosomes: implications for interpretation of MTHFR genotyping results.5,10-Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms: genotype frequency and association with homocysteine and folate levels in middle-southern Italian adults.A common haplotype on methylenetetrahydrofolate reductase gene modifies the effect of angiotensin-converting enzyme inhibitor on blood pressure in essential hypertension patients--a family-based association study.Should the MTHFR 1298A>C polymorphism be considered in the clinical evaluation of patients at risk for thrombotic disease?Expression and activity of methionine cycle genes are altered following folate and vitamin E deficiency under oxidative challenge: modulation by apolipoprotein E-deficiency.Rapid cycling bipolar affective disorder and recurrent strokes secondary to high blood homocysteine.The methylenetetrahydrofolate reductase 677T-1298C haplotype is a risk factor for acute lymphoblastic leukemia in children.Association of the methylenetetrahydrofolate reductase A1298C but not the C677T single nucleotide polymorphism with sickle cell disease in Bahrain.
P2860
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P2860
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
A1298C methylenetetrahydrofola ...... omocysteine/folate metabolism.
@en
A1298C methylenetetrahydrofola ...... omocysteine/folate metabolism.
@nl
type
label
A1298C methylenetetrahydrofola ...... omocysteine/folate metabolism.
@en
A1298C methylenetetrahydrofola ...... omocysteine/folate metabolism.
@nl
prefLabel
A1298C methylenetetrahydrofola ...... omocysteine/folate metabolism.
@en
A1298C methylenetetrahydrofola ...... omocysteine/folate metabolism.
@nl
P2093
P356
P1476
A1298C methylenetetrahydrofola ...... homocysteine/folate metabolism
@en
P2093
C Stranieri
E Trabetti
N Martinelli
P F Pignatti
R Corrocher
P2888
P356
10.1007/S102380200001
P577
2002-05-01T00:00:00Z