نتایج جستجو برای: mthfr c677t

تعداد نتایج: 3382  

امجدی, ام البنین, علیزاده نوایی, رضا, عمرانی نوا, ورسا, محمود بابویی, محمد, مخبری, وحید, هدایتی زاده عمران, اکبر, گلچین, سهیلا,

Background and purpose: Coronary artery disease (CAD) is a complex disease that is caused by both environmental and genetic factors. Methylenetetrahydrofolate (MTHFR) enzyme is associated with metabolism of homocysteine and its impaired function is considered as a risk factor for developing CAD. Some variants are involved in decreased activity of MTHFR and its deficiency. The polymorphism of C6...

Journal: :the journal of tehran university heart center 0
ahmad aleyasin national research center for genetic engineering and biotechnology, tehran, iran. mahboobeh ghaedi national research center for genetic engineering and biotechnology, tehran, iran. saeed davoodi tehran heart center, tehran university of medical sciences, tehran, iran. seyed hesameddin abassi tehran heart center, tehran university of medical sciences, tehran, iran. manouchehr madani tehran heart center, tehran university of medical sciences, tehran, iran.

background: several studies showed that elevated plasma homocysteine level is a risk factor for coronary artery disease (cad). a common polymorphism c677t of methylenetetrahydrofolate reductase (mthfr) gene is reported to be associated with decreased enzyme activity and increased blood homocysteine level. methods: this study evaluated the association between c677t polymorphism and blood homocys...

2012
Mohsin Yakub Naushad Moti Siddiqa Parveen Bushra Chaudhry Iqbal Azam Mohammad Perwaiz Iqbal

BACKGROUND Hyperhomocysteinemia (>15 µmol/L) is highly prevalent in South Asian populations including Pakistan. In order to investigate the genetic determinants of this condition, we studied 6 polymorphisms in genes of 3 enzymes--methylenetetrahydrofolate reductase (MTHFR; C677T; A1298C), methionine synthase (MS; A2756G), cystathionine-β-synthase (CBS; T833C/844ins68, G919A) involved in homocys...

2014
Rinki Kumari Aruna Agrawal

Methylenetetrahydrofolate reductase, (MTHFR) is a key enzyme that is required to metabolize folate and is essential for normal development of central nervous system. Mutation in the MTHFR gene may result in elevated plasma homocysteine level. MTHFR C677T is most common polymorphism associated with impairment of cognitive function. In the present study, we examined the relationship between 677C>...

ژورنال: کومش 2016
تفویضی, فرزانه, حاج اسمعیلی, موگه, سرمدی, سهیلا,

سابقه و هدف: سرطان دهانه رحم یکی از سرطان‌های شایع در زنان می‌باشد. فاکتورهای متعددی در ابتلا به این سرطان نقش دارند که می‌توان به عفونت پاپیلوما ویروس (HPV)، تغییرات اپی‌ژنتیکی از جمله متیلاسیون غیرطبیعی پروموتر ژن متیلن تتراهیدروفولات ردوکتاز (MTHFR) و برخی پلی‌مورفیسم‌ها از جمله، پلی‌مورفیسم MTHFR C677T اشاره کرد. MTHFR آنزیمی است که در تنظیم متابولیسم فولات و متیونین نقش دارد. هدف از این ت...

Journal: :Journal of the National Cancer Institute 2004
Kyoung-Jin Sohn Ruth Croxford Zoe Yates Mark Lucock Young-In Kim

BACKGROUND Although single nucleotide polymorphisms may be potentially important pharmacogenetic determinants of cancer therapy, functional evidence regarding their relevance is currently lacking. The C677T polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene is associated with changes in cellular composition of folates. We hypothesized that this polymorphism may modulate the cy...

2018
Mohaddeseh Salehi Mona Amin-Beidokhti Behnam Safarpour Lima Milad Gholami Gholam-Reza Javadi Reza Mirfakhraie

Introduction Migraine is a painful complex neurovascular disease characterized by recurrent moderate-to-severe headaches. Increased level of homocysteine is related to dilation of cerebral vessels and endothelial injury that could trigger migraine attacks. Functional polymorphisms in the MTHFR gene affect homocysteine metabolism and, therefore, play an important role in the etiology of the dise...

Journal: :Genetics and molecular research : GMR 2016
Y Yang Y Y Luo S Wu Y D Tang X D Rao L Xiong M Tan M Z Deng H Liu

Published studies on the association between the C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase (MTHFR) gene and male infertility risk are controversial. To obtain a more precise evaluation, we performed a meta-analysis based on published case-control studies. We conducted an electronic search of PubMed, EMBASE, the Cochrane Library, the Web of Science, and the China ...

Journal: :The journal of obstetrics and gynaecology research 2008
Venkatesan Vettriselvi Krishnaswami Vijayalakshmi Solomon F D Paul Perumal Venkatachalam

AIM To assess the association between polymorphisms in angiotensin converting enzyme and methylene tetrahydrofolate reductase genes and recurrent pregnancy loss by a case-control study in South Indian women. METHODS DNA was extracted from peripheral blood leukocytes of 104 women with Recurrent Pregnancy Loss (RPL) and 120 controls. Genotyping of ACE Insertion Deletion and MTHFR C677T polymorp...

2016
Qin Zhu Li Li Ting Wang Wei Jiang Jie Ding Minjuan Liu Yun Wang Haibo Li

Objective: Neural tube defect (NTD) incidence could be effectively reduced by folic acid supplementation before and during pregnancy. We studied single nucleotide polymorphisms (SNPs) involved in folate metabolism to explore genetic susceptibility to NTD. We studied the association between 12 SNPs involved in 11 folate metabolism genes and NTDs. Methods: We enrolled 76 children with NTD and 188...

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