نتایج جستجو برای: mthfr
تعداد نتایج: 3045 فیلتر نتایج به سال:
Abstract Beyond well-assessed risk factors, cardiovascular events could be also associated with the presence of epigenetic and genetic alterations, such as methylenetetrahydrofolate-reductase (MTHFR) C677T polymorphism. This gene variant is related to increased circulating levels homocysteine (Hcy) risk. However, heterozygous carriers have an augmented accidents independently from normal Hcy le...
Altered expression of methylenetetrahydrofolate reductase modifies response to methotrexate in mice.
OBJECTIVE Folates provide one-carbon units for nucleotide synthesis and methylation reactions. A common polymorphism (677C-->T) in methylenetetrahydrofolate reductase (MTHFR) encodes an enzyme with reduced activity. Response to the antifolate methotrexate (MTX) may be modified in 677TT individuals because MTHFR converts nonmethylated folates, used for thymidine and purine synthesis, to 5-methyl...
OBJECTIVE We evaluated the effect of hyperhomocystinemia and angiotensin (Ang) II on vascular function and structure in methylenetetrahydrofolate reductase knockout mice (Mthfr+/-). METHODS AND RESULTS Mthfr+/- and controls (Mthfr+/+) received Ang II (400 ng/kg per min SC) or saline (14 days). Blood pressure, similar in Mthfr+/- and Mthfr+/+, was increased by Ang II. Acetylcholine- and bradyk...
Deficiency of methylenetetrahydrofolate reductase (MTHFR) predisposes to hyperhomocysteinemia and vascular disease. We tested the hypothesis that heterozygous disruption of the Mthfr gene sensitizes mice to diet-induced hyperhomocysteinemia and endothelial dysfunction. Mthfr / and Mthfr / mice were fed 1 of 4 diets: control, high methionine (HM), low folate (LF), or high methionine/low folate (...
اوتیسم یک زیر گروه از اختلالات طیف اوتیسم است که به عنوان یک اختلال عصبی طبقه بندی شده و در سه سال اول زندگی رخ می دهد. علت اوتیسم تا حد زیادی ناشناخته است اما اعتقاد بر این است که ممکن است عوامل محیطی و ژنتیکی مسئول این بیماری باشد. مطالعات اخیر نشان داده است که ژن های دخیل در مسیر فولات/ هوموسیستئین ممکن است از عوامل خطر برای کودکان مبتلا به اوتیسم باشد. یکی از ژن های مهم در اوتیسم، ژن mthfr ...
Methylenetetrahydrofolate reductase (MTHFR; EC 1.5.1.20) is the sole enzyme responsible for generation of 5-methyltetrahydrofolate, which is required for methionine synthesis and provision of methyl groups via S-adenosylmethionine. Genome analysis showed that Leishmania species, unlike Trypanosoma brucei and Trypanosoma cruzi, contain genes encoding MTHFR and two distinct methionine synthases. ...
Deficiency of methylenetetrahydrofolate reductase (MTHFR) predisposes to hyperhomocysteinemia and vascular disease. We tested the hypothesis that heterozygous disruption of the Mthfr gene sensitizes mice to diet-induced hyperhomocysteinemia and endothelial dysfunction. Mthfr(+/-) and Mthfr(+/+) mice were fed 1 of 4 diets: control, high methionine (HM), low folate (LF), or high methionine/low fo...
Introduction: Breast cancer is the most common malignancy in women worldwide. It also second leading cause of death among after lung cancer. Considering relationship plasma folate levels, level uracil, and DNA damage cell division, methyl tetrahydrofolate reductase (MTHFR) a suitable candidate for studies on susceptibility to cancer, including breast This study aimed investigate between two pol...
Methylenetetrahydrofolate reductase (MTHFR) plays an important role in folate metabolism and is involved in DNA synthesis, DNA repair and DNA methylation. The two common functional polymorphisms of MTHFR, C677T and A1298C have been associated with several diseases, including cancer. We made a case-control study to analyze a possible association of MTHFR gene polymorphisms C677T and A1298C ...
Background and objectivesMethylenetetrahydrofolate Reductase (MTHFR) is the critical enzyme in folate 1-carbon metabolism. MTHFR polymorphisms may result increased homocysteine levels, be associated with abnormal lipid metabolism liver. This study aims to explore association between gene of rs1801131 rs1801133 susceptibility nonalcoholic fatty liver disease (NAFLD) coronary artery (CAD).
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