MTHFR , prothrombin and Factor V gene variants in Turkish patients with coronary artery stenosis

MTHFR , prothrombin and Factor V gene variants in Turkish patients with coronary artery stenosis

Many epidemiological studies have reported an association between hemostatic factors and risk of both coronary and peripheral artery diseases. Using polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) analysis, we investigated the association between coronary artery dis...

Full description

Bibliographic Details
Main Authors:	Müge Caner, Rifat Bircan, Deniz Sevinç, Fehime Benli, A. Ilter Güney, Nuri Kurtoglu
Format:	Article
Language:	English
Published:	Sociedade Brasileira de Genética 2008-01-01
Series:	Genetics and Molecular Biology
Subjects:	genetic polymorphism coronary disease MTHFR gene prothrombin gene Factor V gene
Online Access:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572008000500006

Similar Items

The 3’ End Prothrombin Gene Variants in Serbian Patients with Idiopathic Thrombophilia
by: Aradjanski M., et al.
Published: (2014-12-01)

Association of prothrombin, FV Leiden and MTHFR gene polymorphisms in the Montenegrin patients with venous thromboembolism
by: Teofilov Slađana, et al.
Published: (2021-01-01)

Association of The Mthfr C677t, Factor V (Leiden) G1961a and Prothrombin G20210a Gene Mutations with Recurrent Spontaneous Aboration (Rsa) in Duhok Province
by: Shaima S. Mohammed, et al.
Published: (2018-09-01)

Detection of MTHFR (A1298C) Gene Polymorphism in Women Suffer from Different Types of Abortion in Mosul City
by: Owayes Alhassani, et al.
Published: (2020-09-01)

Homozygous prothrombin gene mutation and ischemic cerebrovascular disease: A case report and review of literature
by: Mohammed AlSheef, et al.
Published: (2019-01-01)

The predictive value of factor V Leiden, prothrombin G20210A and MTHFR C677T Gene mutations on the location of venous thromboembolism
by: Muammer Bilici, et al.
Published: (2015-12-01)

Factor V Leiden, Prothrombin G20210A, and MTHFR C677T Polymorphisms in Cancer Patients with Venous Thromboembolism
by: Lattimore, Lois Eileen
Published: (2010)

The C20068T gene variant in the 3` end of the prothrombin gene and recurrent pregnancy loss: A pilot study
by: Pruner Iva, et al.
Published: (2015-01-01)

Clinical and laboratory manifestations of the prothrombin gene mutation in women of reproductive age
by: Momot AP, et al.
Published: (2019-08-01)

Prevalence of the prothrombin G20210A mutation among ischemic stroke patients
by: Salar A. Ahmed, et al.
Published: (2020-09-01)

Histological Analysis, Bioinformatics Profile, and Expression of Methylenetetrahydrofolate Reductase (MTHFR) in Bovine Testes
by: Seth Yaw Afedo, et al.
Published: (2020-09-01)

MTHFR gene polymorphism and associated nutritional deficiency in the etiology and pathogenesis of Down syndrome
by: Radhika Kedar, et al.
Published: (2019-09-01)

Possible influence of MTHFR C677T polymorphism on serum lipid levels in Serbian school children
by: Damnjanović Tatjana, et al.
Published: (2014-01-01)

Association study of MTHFR-c677t with male infertility and reporting new potential SNPS/ sequence variants as a sourse of population genetic markers
by: Pourborhanzadeh Amir, et al.
Published: (2020-01-01)

Relationship between genetic polymorphisms MTHFR (C677T, A1298C), MTR (A2756G) and MTRR (A66G) genes and multiple sclerosis: a case-control study
by: Suat Cakina, et al.
Published: (2019-03-01)

Role of methyltetrahydrofolate reductase (MTHFR) gene polymorphism in the development of ischemic stroke in the dwellers of the Kyrgyz Republic
by: N T Kudaĭbergenova, et al.
Published: (2012-10-01)

Do the MTHFR gene polymorphism and Down syndrome pregnancy association stands true? A case–control study of Indian population and meta-analysis
by: Srinivasan Muthuswamy, et al.
Published: (2016-01-01)

Frequency of 677C -> T and 1298A -> C polymorphisms in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene in Turner syndrome individuals
by: Kelly Santos, et al.
Published: (2006-01-01)

The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura
by: Sundholm James, et al.
Published: (2004-02-01)

Successful living donor kidney transplantation in a patient with prothrombin gene mutation: Case report and literature review
by: Edward Shen, et al.
Published: (2014-01-01)

<i>MTHFR</i> Gene Mutations Correlate with White Matter Disease Burden and Predict Cerebrovascular Disease and Dementia
by: Christian E. Cajavilca, et al.
Published: (2019-08-01)

Study of genotype–phenotype correlation of methylene tetrahydrofolate reductase (MTHFR) gene polymorphisms in a sample of Egyptian autistic children
by: Rabah M. Shawky, et al.
Published: (2014-10-01)

Superior Mesenteric and Splenic Vein Thromboembolism due to PAI-1 SERPINE 4, MTHFR 1298 CC and Factor II Prothrombin 2021GA Mutations: A Case Report
by: Ahmet Can Sarı, et al.
Published: (2019-12-01)

Thrombophilia genetic testing in Romanian young women with acute thrombotic events: role of Factor V Leiden, Prothrombin G20210A, MTHFR C677T and A1298C polymorphisms / Evaluarea genetică a trombofiliilor la femei tinere din România cu evenimente acute trombotice: rolul Factorului V Leiden, Protrombinei G20210A, polimorfismelor MTHFR C677T și A1298C
by: Daraban Ana Maria, et al.
Published: (2016-09-01)

Correlations between plasma homocysteine and MTHFR gene polymorphism and white matter lesions
by: Min Li, et al.
Published: (2018-12-01)

Association Study of MTHFR C677T Polymorphism and Birth Body Mass With Risk of Autism in Chinese Han Population
by: Jishui Zhang, et al.
Published: (2021-02-01)

A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene
by: Eman M. Mansory, et al.
Published: (2021-05-01)

Combined effect of GSTM1 gene deletion, GSTT1 gene deletion and MTHFR C677T mutation in male infertility
by: Đorđević Valentina, et al.
Published: (2010-01-01)

REMODELING OF CARDIOVASCULAR SYSTEM AND DEVELOPMENT OF CHRONIC KIDNEY DISEASE IN PATIENTS WITH METABOLIC SYNDROME AND OBESITY: ROLE OF GENES ENOS, SUBUNIT P22-PHOX OF NADPH-OXIDASE AND MTHFR
by: E A Saginova, et al.
Published: (2012-06-01)

Polymorphism study of MTHFR 677C→T and its correlation with oxidative stress and their influence on female infertility in Erbil – Iraq
by: Muthanna A. Thabit, et al.
Published: (2017-10-01)

Polymorphism study of MTHFR 677C?T and its correlation with oxidative stress and their influence on female infertility in Erbil – Iraq
by: Baghdad Science Journal
Published: (2017-09-01)

Association between MTHFR C677T polymorphism and non-traumatic osteonecrosis of the femoral head: An update meta-analysis
by: Zhang Tao, et al.
Published: (2020-03-01)

<i>DPYD</i>, <i>TYMS</i> and <i>MTHFR</i> Genes Polymorphism Frequencies in a Series of Turkish Colorectal Cancer Patients
by: Arsalan Amirfallah, et al.
Published: (2018-12-01)

Prothrombin Gene G20210A Variant in Angiographically Documented Patients with Coronary Artery Stenosis
by: Leyla Pourgholi, et al.
Published: (2019-10-01)

STANDARDIZATION OF PROTHROMBIN TIME TEST AND EVALUATION OF QUALITY OF PATIENT MANAGEMENT WITH WARFARIN
by: A.H ZARGARZADEH, et al.
Published: (2000-12-01)

Prevalence of hereditary risk factors for thrombophilia in Belém, Brazilian Amazon
by: France Keiko Nascimento Yoshioka, et al.
Published: (2006-01-01)

Study of some genetic predisposition in pulmonary embolism
by: Gehan Elassal, et al.
Published: (2014-10-01)

Comparative evaluation of genetic risk models of reproductive disorders caused by MTHFR, MTRR, MTR1 gene polymorphism.
by: Z. І. Rossokha, et al.
Published: (2018-06-01)

Evaluation of c677t and a1298c polymorphism of the methylenetetrahydrofolate reductase gene as a maternal risk factor for trisomy 21 (a monocentric study)
by: Bucerzan Simona, et al.
Published: (2017-03-01)

Prothrombin expression in cancer-derived cell lines
by: Dunjić Sofija, et al.
Published: (2019-01-01)