نتایج جستجو برای: ژن mthfr

تعداد نتایج: 18761  

2007
Ok Joon Kim Sun Pyo Hong Jung Yong Ahn Seung Ho Hong Tae Sun Hwang Soo Ok Kim Wangdon Yoo Doyeun Oh Nam Keun Kim

PURPOSE Methionine synthase (MTR) and 5,10-methylenetetrahydrofolate reductase (MTHFR) are the main regulatory enzymes for homocysteine metabolism. The present case- control study was conducted to determine whether there is an association between the MTR 2756A > G or MTHFR 677C > T polymorphism and plasma homocysteine concentration in Korean subjects with ischemic stroke. MATERIALS AND METHOD...

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: :Genetics and molecular research : GMR 2014
S-S Li J Li Z Xiao A-G Ren L Jin

The aim of this study was to explore the relationship between 2 genetic polymorphisms of the methylenetetrahydrofolate reductase gene (MTHFR), C677T and A1298C, and determine the long-term reproductive outcome in infertile men. This was a prospective study conducted in an andrology clinic. Men with a 1-year history of infertility were assessed for the MTHFR polymorphisms at a 5-year follow-up. ...

Journal: :Toxicology and applied pharmacology 2014
Bogdan J Wlodarczyk Huiping Zhu Richard H Finnell

BACKGROUND In utero exposure to arsenic is known to adversely affect reproductive outcomes. Evidence of arsenic teratogenicity varies widely and depends on individual genotypic differences in sensitivity to As. In this study, we investigated the potential interaction between 5,10-methylenetetrahydrofolate reductase (Mthfr) genotype and arsenic embryotoxicity using the Mthfr knockout mouse model...

ژورنال: :فصلنامه پژوهشی خون 0
امین خالق پرست a. khaleghparast دانشکده علوم پایه دانشگاه آزاد اسلامی ـ واحد علوم و تحقیقات تهران سعید مروتی s. morovvati دانشگاه علوم پزشکی بقیه اله)عج(سازمان اصلی تایید شده: دانشگاه آزاد اسلامی علوم و تحقیقات (islamic azad university science and research branch) زهرا نورمحمدی z. noormohammadi استادیار دانشکده علوم پایه دانشگاه آزاد اسالمی ـ واحد علوم و تحقیقات تهرانسازمان اصلی تایید شده: دانشگاه علوم پزشکی بقیه الله (baqiyatallah university of medical sciences)

چکید ه   سابقه و هدف   یکی از فاکتورهای مطرح در ایجاد ترومبوفیلی در زنان مبتلا به سقط مکرر، پلی مورفیسم های a1298c و c677t در ژن mthfr است. هدف از این تحقیق، بررسی ارتباط این دو پلی مورفیسم با سندروم سقط مکرر به عنوان یکی از عوامل خطر ژنتیکی برای این سندروم بود.   مواد و روش ها   در یک مطالعه مورد شاهدی از میان مراجعین بیمارستان بقیه اله و مرکز ناباروری ابن سینا، 30 زن با سابقه سقط مکرر خود به ...

2016
Seh Hyun Kim

Neonatal cerebral sinovenous thrombosis (CSVT) is a rare disease with severe neu­ rological sequelae. Methylenetetrahydrofolate reductase (MTHFR) is a key enzyme in the folate cycle, and mutations in MTHFR are associated with vascular diseases. Here, we report the case of a newborn with MTHFR mutation­associated CSVT. Analysis of MTHFR in the patient detected heterozygous C677T (677CT) and A129...

Journal: :Croatian medical journal 2008
Igor Spiroski Sashko Kedev Slobodan Antov Todor Arsov Marija Krstevska Sloboda Dzhekova-Stojkova Stojanka Kostovska Dejan Trajkov Aleksandar Petlichkovski Ana Strezova Olivija Efinska-Mladenovska Mirko Spiroski

AIM To analyze the association of methylenetetrahydrofolate reductase polymorphisms (MTHFR-677 and MTHFR-1298) with occlusive artery disease and deep venous thrombosis in Macedonians. METHODS We examined 83 healthy respondents, 76 patients with occlusive artery disease, and 67 patients with deep venous thrombosis. Blood samples were collected and DNA was isolated from peripheral blood leukocy...

Fatehmanesh P Keyhanee M Khazamipour N Noruzinia M Pujol P

Background: MTHFR promoter hypermethylation in testicular biopsies of patients with non-obstructive azoospermia: the role of epigenetics in male infertility. Materials and Methods: DNA from peripheral blood (PB) samples of 50 patients with NOA and 50 fertile men (controls) as well as DNA from testicular biopsies of 32 patients with NOA and five patients with obstructive azoospemia, but normal s...

سازگار, حسین, سنبلستان, الهام, ضیاء, نوشا, محمدی فارسانی, فرزانه,

زمینه و هدف: ژن متیلن تتراهیدروفولات ردوکتاز به‌عنوان یکی از عوامل ژنتیکی مؤثر بر ناباروری، آنزیم متیل هیدروفولات ردوکتاز را کد می­کند که عملکرد آن کمک به تنظیم سطح هموسیستئین در بدن است. ﺟﻬﺶ در ژن ﮐﺪ ﮐﻨﻨﺪه ایﻦ آﻧﺰیﻢ سبب ﮐﺎﻫﺶ ﻓﻌﺎﻟﯿﺖ آن ﻣﯽ­گردد که این امر نیز به‌نوبه‌ی خود منجر به افزایش سطح ﻫﻤﻮﺳﯿﺴﺘﺌﯿﻦ ﺧﻮن شده و می­تواند باعث ایجاد ناباروری شود. هدف از این مطالعه بررسی ارتباط پلی­مورفیسم C677T ژ...

2013
Khuram Shahzad Abdul Hai Asifa Ahmed Nadeem Kizilbash Jamal Alruwaili

The structure of human Methylenetetrahydrofolate Reductase (MTHFR) is not known either by NMR or by X-ray methods. Phosphorylation seems to play an important role in the functioning of this flavoprotein. MTHFR catalyzes an irreversible reaction in homocysteine metabolism. Phosphorylation decreases the activity of MTHFR by enhancing the sensitivity of the enzyme to SAdenosylmethione. Two common ...

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