Browsing by Author "Ozdemir O."
Now showing items 1-8 of 8
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Atherosclerosis in Behçet's Syndrome
Seyahi E.; Ugurlu S.; Cumali R.; Balci H.; Ozdemir O.; Melikoglu M.; Hatemi G.; Fresko I.; Hamuryudan V.; Yurdakul S.; Yazici H. (2008)Objectives: We had the impression and preliminary evidence that atherosclerosis was not much increased in Behçet's syndrome (BS). Thus, we evaluated the presence of subclinical atherosclerosis in a sizeable group of patients ... -
Epidemiology and distribution of interstitial lung diseases in Turkey
Musellim B.; Okumus G.; Uzaslan E.; Akgün M.; Cetinkaya E.; Turan O.; Akkoclu A.; Hazar A.; Kokturk N.; Calisir H.C.; Sever F.; Kiter G.; Celik G.; Bilgin S.; Kurutepe M.; Uzun O.; Tabak L.; Ozdemir O.; Turker H.; Ogus C.; Kiral N.; Ozkan M.; Yalniz E.; Camsari G.; Dogan T.; Yilmaz U.; Cildag O.; Yildiz F.; Hanta I.; Oztuna F.; Arik D.; Goktalay T.; Kanmaz D.; Yilmaz V.; Altiay G.; Komurcuoglu B.; Ozkan G.; Erbaycu A.; Dogrul M.I.; Ongen G.; Tuncay E.; Dabak G.; Sakar A.; Bircan A.; Uzel I.; Kalpaklioglu F.; Gülbay B; Bulbul Y.; Gulbanu H.; Havlucu Y.; Ekici Z.; Zamani A.; Caglayan B.; Kayacan O.; Dursunoglu N. (2014)Introduction: There is very few data on the epidemiological features of interstitial lung diseases (ILD) in the literature. These studies on this subject suffer from limited number of patients. Objective: The goal of this ... -
[Genetic constitution analysis of idiopathic sudden hearing loss]. [Idyopatik ani işitme kayipli olgularin genetik yapilarinin analizi.]
Bora A.; Altuntaş E.E.; Ozdemir O.; Uysal I.O.; Müderris S. (2010)The purpose of this research is to understand the etiology of sudden hearing loss due to genetic factors in Turkish people. Determination of these genetic factors and better understanding of molecular pathogenesis may guide ... -
K-Ras mutation in transitional cell carcinoma of urinary bladder
Ayan S.; Gokce G.; Kilicarslan H.; Ozdemir O.; Yildiz E.; Gultekin E.Y. (2001)In the present study it was aimed to investigate the frequency of K-RAS mutation in the human bladder transitional cell carcinoma. For this purpose, tissue specimens obtained from the patients with bladder tumors. Genomic ... -
Karyometric analysis of nasal polyps.
Yildirim A.; Ozdemir O.; Gül E.; Yildirim B.; Elagöz S.; Kunt T. (2006)OBJECTIVES: Nuclear characteristics of epithelial cells in nasal polyps were analyzed. PATIENTS AND METHODS: The slides of 35 patients who underwent surgery for nasal polyposis and 18 slides of normal mucosa were examined. ... -
The relationship between CYP2C9 gene polymorphisms and upper gastrointestinal bleeding in patients who used warfarin
Ucar M.; Alagozlu H.; Sahin S.; Ozdemir O. (2013)Aim Oral anticoagulants are the most common used substance for treatment and prophylaxis of warfarin venous and arterial thromboembolic disorders in the world. Therapeutic index of warfarin is narrow. CYP2C9 is a hepatic ... -
Underorganisation of chromatin structure in human metaphase chromosomes by induction of 5-aza-2'-deoxycytidine (Decitabine) [Baz analogu 5-aza-2'-deoksisitidin (Desitabin) in insan kromozomlarinda neden oldugu kromatin organizasyon bozukluklari]
Ozdemir O.; Sezgin I.; Colak A. (Gulhane Askeri Tip Akademisi, 1998)Human metaphase chromosomes were exposed to different concentrations (10-8-10-2 M) of 5-aza-2'-deoxycytidine, a DNA methyl inhibitor, in order to determine the in vivo effect of the agent on chromosome packaging. It has ... -
Variable R.Msp1 fragmentation in genomic DNA due to DNA hypomethylation in CRF patients with MTHFR C677Tgene polymorphism: From genetics to epigenetics
Ozdemir O.; Silan F.; Urfali U.; Uludag A.; Ari E.; Kayatas M. (2014)The role of inflammation, hyperhomocysteinemia, germ-line genetic markers and epimutations haven't been understood completely in chronic renal failure (CRF). DNA methylation is a postreplicative modification mechanism that ...