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Toplam kayıt 31, listelenen: 1-10
Association of XRCC1 and XPD functional gene variants with nicotine dependence and/or schizophrenia: a case-control study and in silico analysis
(Taylor and Francis Ltd., 2019)
OBJECTIVE: The role of DNA repair mechanisms has received attention recently in schizophrenia (Sch). Sch patients show an increased prevalence of nicotine dependence (ND). This study aimed to find out whether functional ...
Possible association between DNA repair gene variants and cannabis dependence in a Turkish cohort: a pilot study
(Taylor and Francis Ltd., 2018)
OBJECTIVE: Substance use disorder (SUD) has important effects on health and well-being. It is well known that genetic factors play a role in SUD. The purpose of this research was to investigate whether functional variants ...
Importance of anaplastic lymphoma kinase gene re-arrangements on non-small cell lung cancer
(Kafkas Üniversitesi Tıp Fakültesi, 2017)
Despite all improvements in treatment modalities, lung cancer
is the leading cause of death related to cancers worldwide.
Environmental, occupational and genetic factors, as well as smoking
play role in the etiology. ...
Cytokine gene variants/expressions and non-syndromic microtia – Is there a link?
(Continuing Education, and Scientific Research Association (CESRA), 2017)
Sitokin gen varyantları/ekspresyonları ve non-sendromik mikrotia - Bir ilişki var mıdır?Amaç: Mikrotianın etyopatogenezinde birçok genetik ve çevreselfaktörler araştırılmasına rağmen hala belirsizlik vardır. Bu çalışmadabir ...
Interleukin-1 gene variants and the risk of non-syndromic microtia
(Pamukkale Üniversitesi, 2018)
Purpose: Microtia is a congenital anomaly, manifested by a small and disfigured auricle. Interleukin (IL) 1 is an
important mediator of inflammation and cartilage destruction, This study is aimed at investigating association ...
The roles of endothelial nitric oxide synthase (eNOS) and myeloperoxidase (MPO) genes in microtia
(Deomed Publishing, 2016)
Objective:The aim of this study was to determine the relationshipbetween polymorphisms of endothelial nitric oxide synthase (eNOS)and myeloperoxidase (MPO) genes and development of microtia. Methods:Nineteen (11 males, 8 ...
eNOS and XRCC4 VNTR variants contribute to formation of nicotine dependence and/or schizophrenia
(Comenius University, 2017)
BACKGROUND: This study aimed to evaluate whether VNTR variants in the Endothelial Nitric Oxide Synthase (eNOS) and the XRCC4 gene play any role in nicotine dependence (ND) and/or Schizophrenia+ND (Sch+ND) ethiopathogenesis. ...
The endothelial nitric oxide synthase gene variants as a risk factor for chronic lymphocytic leukemia
(Akademi Doktorlar Yayınevi, 2017)
Nitric oxide (NO) plays complicated roles in carcinogenesis. Endothelial nitric oxide synthase (eNOS) gene is responsible for most of the NO produced. For this reason, it was considered that the eNOS gene variants is ...
Significance of IL-1Ra and IL-6 gene variants in Turkish patients with Crimean-Congo hemorrhagic fever
(Wolters Kluwer Medknow Publications, 2019)
Objective: To investigate the association between IL-1Ra variable number of tandem repeat (rs2234663), IL-6 -597GA (rs1800797), IL-6 -572GC (rs1800796) and the risk of Crimean-Congo hemorrhagic fever (CCHF) in the Turkish ...
Macrophage migration inhibitory factor -173GC variant might increase the risk of behçet's disease
(S. Karger AG, 2018)
Objective: The aim of the present study was to investigate any possible association between the macrophage migration inhibitory factor (MIF) -173GC variant and Behçet's disease (BD) in a group of Turkish patients. Subjects ...