نتایج جستجو برای: c677t mutation

تعداد نتایج: 292722  

2017
Meral Ekim Hasan Ekim

Objectives. Coronary artery disease (CAD) is the leading cause of mortality in the world. It is a complex disorder resulting from the interaction between environmental risk factors and hereditary predisposition. The role of the factor V Leiden (FVL), protrombin gene (PT G20210A) and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms in the development of CAD is controversial. In th...

2010
Eleni N. Evagelidou Vasileios I. Giapros Anna S. Challa Vasileios K. Cholevas Georgios A. Vartholomatos Ekaterini C. Siomou Nikolaos I. Kolaitis Eleni T. Bairaktari Styliani K. Andronikou

OBJECTIVE To evaluate metabolic syndrome and cardiovascular disease risk factors in prepubertal children born large for gestational age (LGA) to nondiabetic, nonobese mothers. RESEARCH DESIGN AND METHODS At 6-7 years of age, the comparison of various factors was made between 31 LGA and 34 appropriate-for-gestational-age (AGA) children: fibrinogen, antithrombin III, protein C and S, fasting in...

Journal: :Journal of gastrointestinal and liver diseases : JGLD 2009
Gelu Osian Lucia Procopciuc Liviu Vlad Cornel Iancu Teodora Mocan Lucian Mocan

BACKGROUND AND AIMS Our preliminary results laboratory have shown some association between C677T and A1298C MTHFR mutations and factors influencing survival in colorectal cancer. We studied the survival of patients with colorectal cancer depending on the initial Dukes-MAC stage of the disease at the time of diagnosis and the MTHFR mutation present. METHODS We randomly selected 69 patients wit...

Journal: :Revista Brasileira de Ginecologia e Obstetrícia / RBGO Gynecology and Obstetrics 2017

Journal: :Arteriosclerosis, thrombosis, and vascular biology 1998
K Demuth N Moatti O Hanon M O Benoit M Safar X Girerd

Studies of symptomatic patients have identified hyperhomocysteinemia as an independent risk factor for vascular disease. In case-control studies, a point mutation (C677T) in the gene encoding 5,10-methylenetetrahydrofolate reductase (MTHFR) has also been linked to an increased risk of vascular disease through its effect on homocysteinemia. Our aim was to extend these observations to asymptomati...

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...

Journal: :Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2008
Vaibhav S Banait M S Sandeep Shrimati Shetty Mukta R Bapat Pravin M Rathi Kanjaksha Ghosh Dipika Mohanty Philip Abraham

BACKGROUND Previous reports on hypercoagulable factors in inflammatory bowel diseases involve heterogeneous populations and patients on various medications. AIMS To determine the frequency of thrombotic complications in ulcerative colitis (UC); to evaluate for hyperhomocysteinemia and its relationship to vitamin B12 and folate levels and methylene tetrahydrofolate reductase (MTHFR) mutation; ...

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