PVT participants: MTHFR CC n=36, MTHFR CT n=53, MTHFR TT n=19; age, sex, age at PVT, Child-Pugh score, rs1799963 PT polymorphisms (G→A 20,210 transition), plasma HC and natural anticoagulants available for all
> Section > Chapter Ortega, E.; Dicenta, F. Scientia Horticulturae 109(3): 288-292 2006 ISSN/ISBN:0304-4238 10.1016/j.scienta.2006.04.017 004525453 Full-Text Article emailed within 0-6 h Buy Now for$19.90 Payments are secure & encrypted ...
reductase (MTHFR) rs1801133 (C→T667 transition) on age at first idiopathic portal vein thrombosis (PVT) and to identify clinical and/or laboratory variables influencing age at first PVT, including plasma homocysteine and the prothrombin rs1799963 PT (G→A transition at position 20210) (PT) ...
A common C677T transition in the MTHFR gene results in a variant with a lower specific activity and a greater sensitivity to heat than the normal enzyme, as measured in vitro. This study was undertaken to determine the capacity of homozygotes for the MTHFR C677T transition to convert 5-...
Background and Aim Age at portal vein thrombosis (PVT) in liver cirrhosis (LC) carriers of the methylene tetrahydrofolate reductase (MTHFR) rs1801133 (C?→?T667 transition) polymorphism has never been addressed; we compared age at PVT in LC patients genotyped for the MTHFR and explored the ...
Hermans M, Gala JL, Buysschaert M (2006) The MTHFR C677T polymorphism confers a high risk for stroke in both homozygous and heterozygous T allele carriers with Type 2 diabetes. Diabetic medicine 23: 529-536.Hermans M, Gala JL, Buysschaert M (2006) The MTHFR C677T polymorphism confers ...
miR-199a-5p is a marker of blood pressure in premature cardiovascular disease patients homozygous for the MTHFR C677T polymorphism.Seodhna LynchMary WardHelene McNultyG HoriganJJ StrainJohn purvisMike tackettDeclan McKennaSpringer
The gene for methylenetetrahydrofolate reductase (MTHFR) has shown polymorphism in the general human population. In its homozygous form, a C677T mutation occurs in more than 5% of the grown-up population and produces a thermolabile variant which reduces the overall enzyme activity to less than ...
A diagnosis of combined CRVO and nasal CLRAO with homozygosity for the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene and elevated levels of serum homocysteine was made. The patient was prescribed folic and acetylsalicylic acid and subsequent follow-up demonstrated gradual ...
MTHFR C677T homo- zygous as risk factor for complications after OLT for cryptogenic cirrhosis. Clin Transplant 2006;20:796-798.Pasta L, Marrone C, D'Amico M et al. MTHFR C677T homozygous as risk factor for complications after OLT for cryptogenic cirrhosis. Clin Transplant 2006; 20: 796- ...