ORCID "0000-0001-7639-1122" Makale Koleksiyonu için listeleme
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Angiotensin converting enzyme gene insertion/deletion variant and familial Mediterranean fever-related amyloidosis
Nursal, Ayşe Feyda; Türkmen, Ercan; Uzun Kaya, Süheyla; Tekcan, Akın; Sezer, Özlem; Çelik, Sümeyya Deniz; Yiğit, Serbülent (Iranian Society of Nephrology, 2018)Introduction. The most important complication of familial Mediterranean fever (FMF) is secondary amyloidosis, which can lead to kidney failure. Genetic variability in the genes of various components of the renin-angiotensin ... -
Association of the TNF-α, IL-2, and IL-2RB gene variants with susceptibility to psoriasis in a Turkish cohort
Gülel, Aslıhan; İnaloz, Hüseyin Serhat; Nursal, Ayşe Feyda; Sever, Tuğçe; Pehlivan, Sacide (Termedia Publishing House Ltd., 2018)Aim of the study: The aim of this study was to investigate the role TNF-α, IL -2, and IL -2RB variants in psoriasis (Ps) and to evaluate the association between these variants and clinical features. Material and methods: ... -
Association of XRCC1 and XPD functional gene variants with nicotine dependence and/or schizophrenia: a case-control study and in silico analysis
Pehlivan, Sacide; Aydın, Nizamettin; Nursal, Ayşe Feyda; Uysal, Mehmet Atilla; Pehlivan, Mustafa; Tekcan, Akın; Yavuz, Fatih Kasım; Sever, Ülgen; Yavuzlar, Hazal; Kurnaz, Selin; Uysal, Seda; Çetinay Aydın, Pınar (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 ... -
CYP2A6 gene variants may explain smoking status in a Turkish cohort
Pehlivan, Sacide; Uysal, Mehmet Atilla; Çağatay, Tülin; Nursal, Ayşe Feyda; Kekik Çınar, Çiğdem; Erkan, Feyza; Sever, Ülgen; Bingöl, Züleyha; Pehlivan, Mustafa; Pençe, Sadrettin (Taylor and Francis Ltd., 2018)OBJECTIVE: Nicotine is the main addictive agent present in tobacco and is principally metabolized by a cytochrome P450-mediated oxidation process. While smoking patterns differ widely among smokers, the metabolization rate ... -
Cytokine gene variants/expressions and non-syndromic microtia – Is there a link?
Nursal, Ayşe Feyda; Bekerecioğlu, Mehmet; Pehlivan, Sacide; Sever, Tuğçe; Büyükgüral, Berker (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 ... -
Dopamine D4 Receptor Gene Exon III VNTR Variant influences smoking status in Turkish population
Uysal, Mehmet Atilla; Sever, Ülgen; Nursal, Ayşe Feyda; Yedikule Smoking Cessation Study Group; Pehlivan, Sacide (Turkish Neuropsychiatric Society, 2019)Introduction: Dopaminergic gene variants may affect nicotine dependence through their possible impact on the dopamine reward pathway. The purpose of this study is to investigate the relationship between the variable number ... -
Effect of a functional variant of tumor necrosis factor-β gene in temporomandibular disorders: a pilot study
Yerliyurt, Kaan; Nursal, Ayşe Feyda; Tekcan, Akın; Karakuş, Nevin; Tümer, Mehmet Kemal; Yiğit, Serbülent (John Wiley and Sons Inc., 2019)Background: Temporomandibular disorders (TMD) are a group of conditions that cause chronic orofacial pain. The tumor necrosis factor ? (TNF-?) is a proinflammatory cytokine that is involved in the various aspects of the ... -
Effect of monoamine oxidase B A644G variant on nicotine dependence and/or schizophrenia risk
Pehlivan, Sacide; Çetinay Aydın, Pınar; Uysal, Mehmet Atilla; Şentürk Çiftçi, Hayriye; Sever, Ülgen; Yavuz, Fatih Kasım; Aydın, Nazan; Nursal, Ayşe Feyda (Universidade de Sao Paulo, 2019)Objectives Schizophrenia (Sch) is a severe and chronic mental illness. Smoking prevalence is higher in patients with Sch than general population. We aimed to investigate the effects of MAOB gene A644G variant on nicotine ... -
The endothelial nitric oxide synthase gene variants as a risk factor for chronic lymphocytic leukemia
Pehlivan, Mustafa; Tomatır, Ayşe G.; Nursal, Ayşe Feyda; Şahin, Handan H.; Pehlivan, Sacide (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 ... -
The IL-1Ra gene variable number tandem repeat variant is associated with susceptibility to temporomandibular disorders in Turkish population
Tümer, Mehmet Kemal; Nursal, Ayşe Feyda; Tekcan, Akın; Yerliyurt, Kaan; Geyko, Anastasia; Yiğit, Serbülent (John Wiley and Sons Inc., 2018)Background: Temporomandibular joint disorders (TMD) are a group of disorders involving temporomandibular joint and related structures. Interleukine-1 receptor antagonist (IL-1Ra) is an important anti-inflammatory molecule ... -
Il-1β and IL-1Ra variant profiles in Turkish patients with diabetic peripheral neuropathy
Nursal, Ayşe Feyda; İnanır, Ahmet; Rüstemoğlu, Aydın; Uzun, Süheyla; Şahin, Kübra; Yiğit, Serbülent (Bentham Science Publishers B.V., 2019)Background: Diabetic peripheral neuropathy (DPN) is one of the most common complications of Type 2 diabetes mellitus (T2DM). This study was conducted to investigate the possible association between interleukin-1β (IL-1β) ... -
Impact of glucocorticoid receptor gene Bcl-1 variant on temporomandibular disorders
Tümer, Mehmet Kemal; Yerliyurt, Kaan; Nursal, Ayşe Feyda; Karakuş, Nevin; Tekcan, Akın; Yiğit, Serbülent (Scientific Publishers of India, 2017)Objectives: Temporomandibular Disorders (TMD) constitute a heterogeneous group of disorders characterized by alterations in mandibular movement. The aim of this study was to investigate the association between the Bcl1 ... -
Interleukin-1 gene variants and the risk of non-syndromic microtia
Nursal, Ayşe Feyda; Bekerecioğlu, Mehmet; Büyükgüral, Berker; Pehlivan, Sacide (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 ... -
Küçük hücreli dışı akciğer kanserinde MET geninin güncel durumu
Nursal, Ayşe Feyda (Bozok Üniversitesi Tıp Fakültesi, 2016)Akciğer kanseri tüm dünyada kansere bağlı ölüm sebepleri içinde ilk sırada yer alır. Tedavi alanında tüm gelişmelere rağmen hala kötü prognoza sahiptir. Akciğer kanseri histolojik tipine göre küçük hücreli akciğer kanseri ... -
Macrophage migration inhibitory factor -173GC variant might increase the risk of behçet's disease
Nursal, Ayşe Feyda; Yiğit, Serbülent; Tural, Ercan; Kalkan, Göknur; Tümer, Mehmet Kemal; Tekcan, Akın (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 ... -
Possible association between DNA repair gene variants and cannabis dependence in a Turkish cohort: a pilot study
Pehlivan, Sacide; Yazıcı, Ahmet Bülent; Aydın, Nazan; Nursal, Ayşe Feyda; Kurnaz, Selin; Öngel Atar, Ayça; Sever, Ülgen; Kıncır, Zeliha; Pehlivan, Mustafa; Çetinay Aydın, Pınar (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 ... -
The possible role of CCR5Δ32 mutation in Crimean-Congo hemorrhagic fever infection
Rüstemoğlu, Aydın; Ekinci, Duygu; Nursal, Ayşe Feyda; Barut, Şener; Duygu, Fazilet; Günal, Özgür (John Wiley and Sons Inc., 2017)Crimean-Congo hemorrhagic fever infection (CCHF) is a viral zoonosis. The pathogenesis of this disease has not been established so far, however, cytokines account for its progression and outcome. The aim of the present ... -
The roles of endothelial nitric oxide synthase (eNOS) and myeloperoxidase (MPO) genes in microtia
Büyükgüral, Berker; Pehlivan, Sacide; Nursal, Ayşe Feyda; Bekerecioğlu, Mehmet (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 ... -
Significance of IL-1Ra and IL-6 gene variants in Turkish patients with Crimean-Congo hemorrhagic fever
Say Coşkun, Umut Safiye; Nursal, Ayşe Feyda; Güneş, Ferda; Rüstemoğlu, Aydın; Yaylı, Abdullah; Karakuş, Nevin; Barut, Hüseyin Şener; Yiğit, Serbülent (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 ... -
XRCC4 rs6869366 polymorphism is associated with susceptibility to both nicotine dependence and/or schizophrenia
Pehlivan, Sacide; Uysal, Metin Atilla; Aydın, Nazan; Nursal, Ayşe Feyda; Pehlivan, Mustafa; Yavuzlar, Hazal; Sever, Ülgen; Kurnaz, Selin; Yavuz, Fatih Kasım; Uysal, Suna; Çetinay Aydın, Pınar (Universidade de Sao Paulo, 2018)Background: Oxidative stress induced DNA damage has been assumed to contribute to the etiopathogenesis of schizophrenia (Sch). Smoking prevalence was more common in patients with Sch. The X-ray repair cross-complementation ...