نتایج جستجو برای: methylenetetrahydrofolate reductase nadph2

تعداد نتایج: 44962  

Abeer Ismail, Basma El-Sayed Fotouh, Moataza Moataza Hassan Omran, Shimaa Shawki Ramadan, Wafaa Ghoneim Shousha,

Background: Breast Cancer (BC), the second leading cause of cancer mortality after lung cancer and varied across the world due to genetic and environmental factors. In this study, we evaluated the interaction between the polymorphisms in genes encoding enzymes of folate metabolism: methylenetetrahydrofolate reductase (MTHFR), methionine synthesis reductase (MTR) with the BC prognostic factors. ...

Journal: :Egyptian Journal of Medical Human Genetics 2022

Abstract Background Acute myocardial infarction (AMI) is a leading cause of death and morbidity around the world. Although association between thrombophilia AMI well-established, controversial data are present on thrombophilic polymorphisms AMI. The aim this study was to investigate three including factor V Leiden ( FVL ), MTHFRC677T (methylenetetrahydrofolate reductase), Coagulation XIIIVal34L...

Journal: :Acta Crystallographica Section A Foundations and Advances 2018

Journal: :Brain research bulletin 2006
Ali Sazci Emel Ergul Nese Tuncer Gurler Akpinar Ihsan Kara

Hyperhomocysteinemia is an independent risk factor for ischemic stroke. The enzyme methylenetetrahydrofolate reductase (MTHFR) plays a critical role in modulating the levels of plasma homocysteine. Two polymorphisms in the MTHFR gene, C677T, A1298C result in reduced enzyme activity. The mechanisms of ischemic and hemorrhagic stroke are not well understood. Although controversial, previous studi...

Journal: :The European respiratory journal 2003
E Nizankowska-Mogilnicka L Adamek P Grzanka T B Domagala M Sanak M Krzanowski A Szczeklik

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...

2012
Henry Cardona Serguei A. Castañeda Wálter Cardona Maya Leonor Alvarez Joaquín Gómez Jorge Gómez José Torres Luis Tobón Gabriel Bedoya Ángela P. Cadavid

Studies have shown an association between recurrent pregnancy loss and inherited thrombophilia in Caucasian populations, but there is insufficient knowledge concerning triethnic populations such as the Colombian. The aim of this study was to evaluate whether inherited thrombophilia is associated with recurrent pregnancy loss. Methods. We conducted a case-control study of 93 patients with recurr...

Journal: :Annals of the Academy of Medicine, Singapore 2011
Elsa Haniffah Mejia Mohamed Kay Sin Tan Johari Mohd Ali Zahurin Mohamed

INTRODUCTION The functional point mutation C677T in the methylenetetrahydrofolate reductase (MTHFR) gene, has been reported to contribute to hyperhomocysteinaemia which is a risk factor for atherothrombotic ischaemic strokes. This study evaluated the prevalence of the C677T polymorphism of the gene in Malaysian ischaemic stroke subjects of Malay, Chinese and Indian ethnicities, and its associat...

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