Yazar "Kırıkkale Üniversitesi" için Tıbbi Genetik Anabilim Dalı listeleme
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Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction
Jenkins, Dagan; Caubit, Xavier; Dimovski, Aleksandar; Matevska, Nadica; Lye, Claire M.; Cabuk, Feryal; Woolf, Adrian S. (Oxford Univ Press, 2010)Methods. Given the phenotype of Tshz3 mutant mice, we considered that Teashirt genes, which code for a family of transcription factors, might represent candidate genes for human PUJO. To evaluate this possibility, we used ... -
CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
Demirkan, Serkan; Sayin, Derya Beyza; Gunduz, Ozgur (Termedia Publishing House Ltd, 2019)Introduction: Acne vulgaris (AV) is a multifactorial, inflammatory disease of the pilosebaceous unit. Hormones play a major role in the pathogenesis of acne. In cases of hyperandrogenism; hirsutism, acne, seborrhoea and ... -
The effect of the angiotensin-converting enzyme gene polymorphism on the depression and anxiety levels
Ozen, Nurper Erberk; Kocak, Orhan Murat; Dogru, Tolga; Sayin, D. Beyza (Cumhuriyet Univ Tip Fak Psikiyatri Anabilim Dali, 2009)Objective: We aimed to investigate the relationship between the angiotensin-converting enzyme (ACE) gene insertion (I) and deletion (D) polymorphism and the levels of anxiety and depression. Methods: This is a cross-sectional ... -
The frequency of Familial Mediterranean fever gene mutations and genotypes at Kirikkale and comparison with the mean of regional MEFV mutation frequency of Turkey
Kocakap, Derya Beyza Sayin; Gunel-Ozcan, Aysen; Cabuk, Feryal; Ensari, Cuneyt (Springer, 2014)In this study we have retrospectively analysed the mutation spectrum of the 351 Familial Mediterranean fever patients referred to KA +/- rA +/- kkale University Faculty of Medicine, Department of Medical Genetics Laboratory ... -
Hereditary haemochromatosis gene (HFE) H63D mutation shows an association with abnormal sperm motility
Gunel-Ozcan, Aysen; Basar, M. Murad; Kisa, Ucler; Ankarali, Handan C. (Springer, 2009)The aim of this study was to screen infertile men for HFE H63D mutation in correlation with clinical characteristics of infertile men (sperm concentration, sperm motility, morphology, testicular volume, Follicle Stimulating ... -
Interleukin (IL)-17F (H161R) and IL-23R (R381Q) Gene Polymorphisms in Turkish Population with Periodontitis
Erdemir, Ebru Olgun; Hendek, Meltem Karsiyaka; Kocakap, Derya Beyza Sayin; Ozkan, Serdar Yucel (Amber Publication, 2015)Background: Periodontitis is triggered by periodontal pathogens and influenced by environmental and genetic factors. Genes encoding molecules related to the immune response are the main candidates for polymorphisms analysis ... -
MEFV gene mutations in Henoch- Schonlein purpura
Altug, Umut; Ensari, Cuneyt; Sayin, Derya B.; Ensari, Arzu (Wiley, 2013)AimCoexistence of familial Mediterranean fever (FMF) with various systemic vasculitides, including Henoch-Schonlein purpura (HSP) and other inflammatory disorders has been reported and the MEFV gene has been suggested to ...