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Now showing items 11-20 of 26
Sulfotransferase 1A1 (SULT1A1) polymorphism and susceptibility to primary brain tumors
(SPRINGER, 2008)
Purpose Sulfotransferase 1A1 is a member of sulfotransferase family that plays an important role in the biotransformation of numerous carcinogenic and mutagenic compounds through sulfation. The present study has investigated ...
Polymorphisms of CYP1A1, GSTM1, GSTT1, and prostate cancer risk in Turkish population
(TAYLOR & FRANCIS INC, 2006)
Prostate cancer is the most common cancer among men in many countries. Although the etiology of prostate cancer largely is unknown, both genetic and environmental factors may be involved. Advanced age, androgen metabolism, ...
Is There Any Relationship Between Toll-Like Receptor 3 c.1377C/T and-7C/A Polymorphisms and Susceptibility to Crimean Congo Hemorrhagic Fever?
(WILEY-BLACKWELL, 2016)
Crimean-Congo hemorrhagic fever (CCHF) is an infectious disease that is caused by CCHF virus. A family of transmembrane receptors called as Toll-like receptors (TLRs) selectively acts in recognizing a wide range of microbial ...
Polymorphisms of selected genes related to increased cardiovascular risk in patients with acute coronary syndromes and their relation to the severity of coronary artery disease
(TERMEDIA PUBLISHING HOUSE LTD, 2012)
Background: beta-Fibrinogen 455G/A, factor V 1691G/A, 1299H/A and glycoprotein Ilb/IIla PL A1/A2 polymorphisms are tought to be related to arterial thrombotic disorders, especially coronary artery disease (CAD) and myocardial ...
The Association of MYNN and TERC Gene Polymorphisms and Bladder Cancer in a Turkish Population
(UROL & NEPHROL RES CTR-UNRC, 2019)
Purpose: Researchers reported that, MYNN rs10936599 polymorphism is in strong or moderate linkage disequilibrium with SNPs within the 3q26.2 chromosomal regions that also include the TERC gene. In addition, it has been ...
Studying the Association between Sudden Hearing Loss and DNA N-Methyltransferase 1 (DNMT1) Genetic Polymorphism
(AVES, 2017)
OBJECTIVE: The aim of the present study was to investigate whether there was any relationship between some DNA N-methyltransferase 1 (DNMT1) polymorphisms and susceptibility to idiopathic sudden sensorineural hearing loss ...
Effect of tumour necrosis factor-alpha and interleukin-6 promoter polymorphisms on course of Crimean-Congo hemorrhagic fever in Turkish patients
(WOLTERS KLUWER MEDKNOW PUBLICATIONS, 2015)
Objective: In this case-control study, we investigated whether IL-6 (-174G/C) and TNF-alpha (-308G/A) gene polymorphisms affect the clinical course and outcome of CCHF. Methods: Total 150 patients with CCHF and 170 controls ...
Microsomal epoxide hydrolase polymorphisms
(SPANDIDOS PUBL LTD, 2010)
Microsomal epoxide hydrolase plays a dual role in the activation and detoxification of carcinogenic compounds. Two polymorphic sites have been described in exons 3 and 4 of the microsomal epoxide hydrolase gene that change ...
Multiple Inherited Thrombophilic Gene Polymorphisms in Spontaneous Abortions in Turkish Population
(CELLULAR & MOLECULAR BIOLOGY RESEARCH CENTER, 2015)
The aim of this study was to investigate the possible role of multiple inherited thrombophilic gene variations in women with unexplained spontaneous abortions. For this purpose, the Factor V Leiden (FVL) (rs6025), Prothrombin ...
Glutathione-S-Transferase Variants are not Associated With Increased Carotid Intima-Media Thickness in Turkish Familial Mediterranean Fever Patients
(TURKISH LEAGUE AGAINST RHEUMATISM, 2016)
Objectives: This study aims to evaluate the carotid intima-media thickness (CIMT) in patients diagnosed with familial Mediterranean fever (FMF) and investigate whether there is a relationship between glutathione-S-transferase ...