نتایج جستجو برای: a1298c
تعداد نتایج: 565 فیلتر نتایج به سال:
Frequently an inherited predisposition to thrombosis remains clinically silent until an additional environmental factor intervenes. The present study aimed to assess distribution of inherited risk factors of venous thrombosis in patients with venous thromboembolism (VTE). The prevalences of factor V Leiden (FV Leiden), prothrombin factor II G20210A (FII G20210A), C677T and A1298C of methylenete...
High-resolution melting (HRM) shows great promise for high-throughput, rapid genotyping of individual polymorphic loci. We have developed HRM assays for genotyping single nucleotide polymorphisms (SNP) in several key genes that are involved in methyl metabolism and may directly or indirectly affect the methylation status of the DNA. The SNPs are in the 5,10-methylenetetrahydrofolate reductase (...
BACKGROUND The aim of the study was to assess the association of single nucleotide polymorphisms (SNPs) C677T and A1298C in the methylenetetrahydrofolate reductase gene with colorectal, esophageal/gastric and pancreatic cancer in a cohort of Italian patients. METHODS A total of 790 cancer patients and 202 healthy controls were genotyped and distributions in genotype and allele frequencies wer...
BACKGROUND Leber hereditary optic neuropathy (LHON) is an inherited form of bilateral optic atrophy leading to the loss of central vision. The primary cause of vision loss is mutation in the mitochondrial DNA (mtDNA), however, unknown secondary genetic and/or epigenetic risk factors are suggested to influence its neuropathology. In this study folate gene polymorphisms were examined as a possibl...
We aimed to explore the correlation between unexplained recurrent spontaneous abortion and polymorphisms in the methylene tetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) genes. A case control study was conducted in 118 patients with unexplained recurrent spontaneous abortion (abortion group) and 174 healthy women (control group). The genetic material was extracted fr...
Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and gastric cancer susceptibility
Studies have indicated that thrombophilic genes polymorphisms are associated with recurrent pregnancy loss (RPL) in the Iranian population. We aimed to evaluate the precise association between thrombophilic genes polymorphisms (MTHFR C677T, MTHFR A1298C, Prothrombin G20210A, FVL G1691A, and PAI-1 4G/5G) and RPL risk in the Iranian population. PubMed, Web of Science, Google Scholar, an...
براساس مطالعات سال های اخیر جهش های ژنی منجر به اختلالات ترومبوفیلیک? در بروز سقط های مکرر خود به خودی دخالت دارند. جهش های c677t و a1298c در ژن آنزیم متیل تترا هیدروفولات ردوکتاز? جهش g20210a در ژن پروترومبین و جهش g1691a در ژن فاکتور انعقادی 5 به عنوان شایع ترین جهش های ژنی اختلالات ترومبوفیلیک گزارش شده اند. در این مطالعه فراوانی این جهش های ژنی بین 50 زن با سابقه حداقل دو سقط مکرر به عنوان ...
زمینه و هدف:علت ایجادناهنجاریشکاف لب با یا بدون شکاف کام غیر سندرمی پیچیده است. وقوع آن می تواند ناشی از بر هم کنش عوامل مختلف ژنتیکی و محیطی باشد. اخیرا مشخص شده است که پلیمورفیسم های ژن متیلن تترا هیدروفولات ردوکتاز(mthfr) خطر این ناهنجاری را افزایش می دهد. با این حال، این یافته ها هنوز مورد بحث است و نیاز به بررسی های بیشتر در این زمینه احساس می شود. هدف از اینمطالعه، بررسی پلی مورفیسم های...
Hyperhomocysteinemia (hHcy) has been associated with an increased risk of cardiovascular disease and stroke. Essential hypertension (EH), a polygenic condition, has also been associated with increased risk of cardiovascular related disorders. To investigate the role of the homocysteine (Hcy) metabolism pathway in hypertension we conducted a case-control association study of Hcy pathway gene var...
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