Results 71 to 80 of about 13,481 (184)

GENETIC POLIMORPHISMS OF ENZYMES INVOLVED IN FOLATE METABOLISM IN HEALTHY SLOVENIAN POPULATION

open access: yesZdravniški Vestnik, 2004
Background. Enzymes that play a major role in folate metabolism are 5,10-methylenetetrahydrofolate reductase (MTHFR), thymidilate synthase (TS), methionine synthase (MS) and methionine synthase reductase (MTRR). Polymorphisms in their corresponding genes
Petra Bohanec, Vita Dolžan
doaj  

The MTHFR C677T polymorphism and global DNA methylation in oral epithelial cells

open access: yesGenetics and Molecular Biology, 2013
DNA methylation is mediated by DNA methyltransferases (DNMTs) that add a methyl group to the 5'-carbon of cytosine. The enzyme methylenetetrahydrofolate reductase (MTHFR) catalyzes the reduction of 5,10-methylenetetrahydrofolate to 5 ...
Isabela Tatiana Sales de Arruda   +2 more
doaj  

Methylenetetrahydrofolate reductase polymorphisms in acute deep vein thrombosis

open access: yesTurkish Journal of Vascular Surgery, 2019
Objectives: In this study, we aimed to investigate the effectiveness of methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C gene polymorphisms in acute deep vein thrombosis (DVT).
Sefa Şenol, Kurşat Kargun
doaj  

Relationship between methylenetetrahydrofolate reductase C677T gene polymorphism and neutrophil gelatinase-associated lipocalin in early renal injury in H-type hypertension

open access: yesBMC Cardiovascular Disorders
Objective To analyse the relationship between the polymorphisms of the H-type hypertensive methylenetetrahydrofolate reductase (MTHFR) C677T gene and neutrophil gelatinase-associated lipocalin (NGAL) in early kidney injury.
Chi Zhang   +6 more
doaj   +1 more source

Recurrent Placental Abruption with Methylenetetrahydrofolate Reductase C667t Heterozygosity: A Case Report

open access: yesGynecology Obstetrics & Reproductive Medicine, 2007
Placental abruption although uncommon, can result in high rate of maternal and fetal morbidity and mortality. Several studies suggest abnormal placental vasculature, thrombosis and reduced placental perfusion in pathophysiology.
Ilgın Türkçüoğlu   +2 more
doaj  

C677T methylenetetrahydrofolate reductase (MTHFR) gene polymorphism in Schizophrenia and Bipolar disorder: An association study in Iranian population [PDF]

open access: yesIranian Journal of Psychiatry, 2011
"n Objective: The methylenetetrahydrofolate reductase (MTHFR) gene polymorphism C677T is suspected to be a risk factor for psychiatric disorders, but it remains inconclusive whether the MTHFR polymorphism C677T is imputed to vulnerability to ...
Bagher Larijani   +5 more
doaj  

HYPERHOMOCYSTEINEMIA AND DIABETIC NEPHROPATHY: THE INFLUENCE OF GENETIC FACTORS, CLINICAL AND PATHOGENIC INTERRELATIONS WITH INFLAMMATION AND ANEMIA

open access: yesJuvenis Scientia, 2016
The article is focused on the pathogenic factors and clinical significance of hyperhomocysteinemia in patients with diabetic nephropathy. We summarize the data on the role of methylenetetrahydrofolate reductase gene polymorphism in the development and ...
I. Yu. Pchelin   +3 more
doaj  

The Headaches and Polymorphisms of the Methylenetetrahydrofolate Reductase

open access: yesJournal of Headache & Pain Management, 2017
The headaches are a heterogeneous clinical manifestations characterized not only by pain but also by a severe multifactorial disabilities. Numerous studies showed the association between the enzyme MTHFR mutations, the T allele and genotype TT and migraine, particularly migraine with aura.
openaire   +2 more sources

Анализ полиморфных вариантов С677Т и А1298С гена MTHFR у больных псориазом

open access: yesФактори експериментальної еволюції організмів, 2015
Aim. Analysis of DNA samples for the study of psoriasis patients SNP C677T and A1298C gene methylenetetrahydrofolate reductase (MTHFR). Methods. Genealogical analysis of 201 probands and relatives was carried out. Genomic DNA of 201 patients was analyzed
А. М. Федота   +3 more
doaj  

Home - About - Disclaimer - Privacy