نتایج جستجو برای: .c677t

تعداد نتایج: 1675  

Journal: :Anticancer research 2011
Chia-Wen Tsai Chia-Fang Hsu Ming-Hsui Tsai Yung-An Tsou Chun-Hung Hua Wen-Shin Chang Cheng-Chieh Lin Da-Tian Bau

The aim of this study was to evaluate the association and interaction of genotypic polymorphism in methylenetetrahydrofolate reductase (MTHFR) with smoking habits and oral cancer in Taiwan. Two well-known polymorphic variants of MTHFR, C677T (rs1801133) and A1298C (rs1801131), were analyzed in association with oral cancer risk, and their joint effects with individual smoking habits on oral canc...

Journal: :Pathophysiology of haemostasis and thrombosis 2008
Anna L Soares Ana P Fernandes Jarbas E Cardoso Marinez O Sousa Marcelo C Lasmar Bethânia A Novelli Geralda F Lages Luci M Dusse Lauro M Vieira Bashir A Lwaleed Maria G Carvalho

BACKGROUND Thrombotic episodes account for approximately 80% of deaths in type 2 diabetic patients. Hyperhomocysteinaemia is a well recognized independent risk factor for atherosclerosis and thromboembolism. Increased homocysteine levels may occur due to a number of factors including inherited gene polymorphism of methylenetetrahydrofolate reductase (MTHFR) C677T. Here, we evaluate plas- ma tot...

2011
So-Young Lee Hoe-Young Kim Kyung Mi Park Stephen Yon Gu Lee Seong Geun Hong Hyung-Jong Kim Dong Ho Yang

Polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T is one of the suggested risk factors for atherosclerosis. However, few studies have reported on the relationship between MTHFR C677T polymorphism and vascular calcification (VC) in chronic hemodialysis patients. We investigated the relationship between the MTHFR C677T polymorphism and VC in 152 chronic hemodialysis patients....

Journal: :acta medica iranica 0
navid nilforoushan department of ophthalmology, eye research center of rasoul hospital, tehran university of medical sciences, tehran, iran. sevil aghapour department of ophthalmology, eye research center of rasoul hospital, tehran university of medical sciences, tehran, iran. and department of medical genetics, tehran university of medical sciences, tehran, iran. reza raoofian department of medical genetics, tehran university of medical sciences, tehran, iran. samira saee rad department of medical genetics, tehran university of medical sciences, tehran, iran. wayne k. greene school of veterinary and biomedical sciences, faculty of health sciences, murdoch university, perth wa 6150, australia. ghasem fakhraie eye research center, farabi eye hospital, tehran university of medical sciences, tehran, iran.

glaucoma is a major cause of blindness worldwide. a single nucleotide polymorphism of the mthfr gene (c677t) has been associated with susceptibility to this disease, although this is controversial in the last decade. in this study, the possible association between the mthfr c677t polymorphism and the risk of developing primary open angle (poag) and pseudoexfoliation glaucoma (pexg) was investig...

Journal: :Cell biochemistry and function 2005
Ali Sazci Emel Ergul Guner Kaya Ihsan Kara

The polymorphic methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms C677T and A1298C cause mild hyperhomocysteinemia, not only in homozygotes for C677T, but also in compound heterozygotes for C677T/A1298C. The aim of this study was to determine allelic frequencies of the polymorphic MTHFR gene C677T, A1298C. In this regard, we have investigated the allelic frequencies of C677T and A1...

2016
Xin Hu Chuanyuan Tao Zhiyi Xie Yunke Li Jun Zheng Yuan Fang Sen Lin Hao Li Chao You

BACKGROUND Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism has been speculated to be and extensively investigated as a risk factor for various vascular diseases, including intracerebral hemorrhage (ICH). However, results from published studies regarding the role of C677T polymorphism in ICH risk in Chinese populations were contradictory rather than conclusive. MATERIAL/METHODS ...

Journal: :American journal of epidemiology 2000
L D Botto Q Yang

The enzyme 5,10-methylenetetrahydrofolate reductase (MTHFR) is involved in folate metabolism. The MTHFR gene is located on chromosome 1 (1p36.3), and two common alleles, the C677T (thermolabile) allele and the A1298C allele, have been described. The population frequency of C677T homozygosity ranges from 1% or less among Blacks from Africa and the United States to 20% or more among Italians and ...

2008
Cynara Gomes Barbosa Claudio Lima Souza José Pereira de Moura Neto Maria da Glória Bomfim Arruda José Henrique Barreto Mitermayer Galvão Reis Marilda Souza Goncalves Edgard Santos

Methylenetetrahydrofolate reductase (MTHFR: EC 1.5.1.20) polymorphisms are associated to acute lymphoid leukemia in different populations. We used the polymerase chain reaction and the restriction fragment length polymorphism method (PCR-RFLP) to investigate MTHFR C677T and A1298C polymorphism frequencies in 67 patients with chronic myeloid leukemia (CML), 27 with acute myeloid leukemia FAB sub...

2017
Di Wang Liwei Bai Qianqian Zhai Yan Li Meng Cao Jie Hai Qinggui Zhang

Type 2 diabetic nephropathy is a major cause of end-stage renal disease. MTHFR plays a vital role in folate metabolism, DNA methylation, and RNA synthesis. The aim of this study was to investigate the association between MTHFR C677T and A1298C genomic polymorphisms and development of type 2 diabetic nephropathy in a Chinese population. A hospital-based case-control study was performed. A total ...

2013
Serbulent Yigit Nevin Karakus Ahmet Inanir

PURPOSE Diabetic peripheral neuropathy (DPN) is one of the most common diabetic chronic complications. Methylenetetrahydrofolate reductase (MTHFR) gene variants have been associated with vasculopathy that has been linked to diabetic neuropathy. The aim of the present study was to investigate the possible association between MTHFR gene C677T mutation and DPN and evaluate if there is an associati...

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