نتایج جستجو برای: c677t mutation

تعداد نتایج: 292722  

2016
Hamid Rouhi-Broujeni Batoul Pourgheysari Ali-Mohammad Hasheminia

BACKGROUND Venous thromboembolism (VTE) is a major cause of mortality. Factor V Leiden (FVL), methylenetetrahydrofolate reductase (MTHFR) C677T, and prothrombin (FII) G20210A polymorphisms are the main inherited risk factors for VTE. Since evidence is limited on homozygotes, the aim of this study was to investigate the association between homozygous variants of these polymorphisms and VTE in Sh...

2017
P.A. Abhinand M. Manikandan R. Mahalakshmi P.K. Ragunath

Ischemic stroke is a condition characterized by reduced blood supply to part of the brain, initiating the ischemic cascade, leading to dysfunction of the brain tissue in that area. It is one of the leading causes of death and disability and is estimated to cause around 5.7 million deaths worldwide. Methyl tetra hydro-folate reductase (MTHFR) is a rate limiting enzyme in the methyl cycle which c...

Journal: :International Journal of Medical Sciences 2004
Mohamed El-Sammak Mona Kandil Safaa El-Hifni Randa Hosni Mahmoud Ragab

This study aimed to evaluate the plasma homocysteine (tHcy) and folate levels as well as the methylenetetrahydrofolate reductase (MTHFR) C677T mutation in Egyptian subjects. Fasting total homocysteine (tHcy) and the (MTHFR) C677T mutation were evaluated in 50 healthy young control males (age 35-50 years, Gp1), 50 elderly males age ranged between 50-75 years without any cardiovascular diseases (...

2016
Wenfang Tang Ranwei Li Jingjin Tan Yaqin Yu Lijing Zhao Xingxing Li Shan Jiang Rihui Liu Ke Wang

Background: Conflicting results have been reported regarding the correlation of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and the risk of lung cancer as well as response to chemotherapy. Objective: To estimate the correlations of the MTHFR C677T polymorphism and risk of lung cancer as well as response to chemotherapy by conducting a meta-analysis. Methods: A comprehensi...

Journal: :Reproductive health of woman 2022

The objective: to study the genetic aspects of pathogenesis abnormal uterine bleeding during puberty (AUB PP) and evaluate effectiveness diagnostic measures taking into account presence or absence mutations in MTHFR C677T gene.Materials methods. Sixty girls with a history AUB PP were included main group 30 healthy without consisted control group. is divided three subgroups: 1st subgroup (n=20) ...

Journal: :Sao Paulo medical journal = Revista paulista de medicina 2002
Egle Couto Ricardo Barini Marcelo Luís Nomura Joyce Maria Annichino-Bizzacchi

CONTEXT High plasmatic homocysteine levels have been associated with arterial and venous thrombosis. The C677T methylene tetrahydrofolate reductase (MTHFR) gene mutation is one of the known causes for high homocysteine levels in plasma. Anticardiolipin antibody (ACA) is also associated with thrombosis and, along with other clinical complications such as recurrent abortion and stillbirth, is par...

2015
In Young Park Byoung Joo Do Jae Sung Ahn Jae Hyuk Lee Jun Ho Park Jin Gu Kang Bo Kyung Yang Hyoung Su Kim

Acute mesenteric venous thrombosis (MVT) is an uncommon form of intestinal ischemia with high mortality and usually occurs in the setting of preexisting comorbidities including thrombophilia and abdominal inflammatory conditions. Hyperhomocysteinemia has been known to be a risk factor for thromboembolism, often located on an unusual site. Considering that homocysteine metabolism is determined g...

2017
Noormohammad Noori Ebrahim Miri-Moghaddam Asieh Dejkam Yasman Garmie Ali Bazi

BACKGROUND The 5, 10-methyleneterahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) are two essential enzymes involved in folate metabolism. The relationship between genetic polymorphisms and congenital heart defects (CHDs) is inconsistent. Our aim was to investigate the association between two well-known polymorphisms of MTHFR and MTRR genes, C677T and A66G, respectively, ...

Journal: :African health sciences 2013
Z Ocak T Özlü O Ozyurt

BACKGROUND Recurrent pregnancy loss (RPL) which is generally known as >3 consecutive pregnancy losses before 20 weeks' gestation is seen in 0.5-2% of women. OBJECTIVE To evaluate the association of parental and fetal chromosomal abnormalities with recurrent pregnancy loss in our area and to analyze the frequency of three types of hereditary thrombophilia's; (MTHFR C677T polymorphisms, FV Leid...

Journal: :Gut 1999
N Mahmud A Molloy J McPartlin R Corbally A S Whitehead J M Scott D G Weir

BACKGROUND Inflammatory bowel disease (IBD) is associated with an increased incidence of thromboembolic disease. Hyperhomocysteinaemia (hyper-tHcy), a condition associated with the C677T variant of 5, 10-methylenetetrahydrofolate reductase (MTHFR), is linked with an increased incidence of thromboembolic disease. Hyper-tHcy has been reported in patients with IBD. AIMS To assess the prevalence ...

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