Yazar "Gunes, S." için listeleme
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Association between promoter methylation of MLH1 and MSH2 and reactive oxygen species in oligozoospermic menA pilot study
Gunes, S.; Agarwal, A.; Henkel, R.; Mahmutoglu, A. M.; Sharma, R.; Esteves, S. C.; Sabanegh, E. (Wiley, 2018)MLH1 and MSH2 are important genes for DNA mismatch repair and crossing over during meiosis and are implicated in male infertility. Therefore, the methylation patterns of the DNA mismatch repair genes MLH1 and MSH2 in ... -
Genetic and Molecular Mechanisms in Bladder Cancer Development
Gunes, S.; Buyukalpelli, R.; Yegin, Z. (Nova Science Publishers, Inc, 2010)Bladder cancer is the second most common malignancy of the urinary system and the fourth leading cause of cancer. Development and progression of bladder cancer is a multistage process and involves molecular (cell cycle ... -
Lack of association between leptin G2548A gene polymorphism and Behcet's disease
Aydin, F.; Kara, N.; Senturk, N.; Gunes, S.; Canturk, M. T.; Bagci, H.; Turanli, A. Y. (Wiley, 2007)Background Behcet's disease is a chronic, multisystem, inflammatory disease characterized by the predominance of T-helper 1 cytokines. The disease is also characterized by infiltration of lymphocytes and neutrophils into ... -
Methylation Profile of Cat Gene in Infertile Males Exhibiting Oxidative Stress.
Gunes, S.; Agarwal, A.; Sharma, R.; Sabanegh, E. S. (Elsevier Science Inc, 2015)… -
DE NOVO 18q DELETION WITH MITRAL VALVE INSUFFICIENCY
Gunes, S.; Okten, G.; Kara, N.; Saglam, Y.; Tasdemir, H. A.; Kayacik, O. Eroglu; Tural, S. (Medecine Et Hygiene, 2008)De novo 18q deletion with mitral valve insufficiency: We report all IS year-old Turkish girl with all 18q- deletion and abnormalities of face, mental and growth retardation, mitral deficiency and hypothyroidism. Mitral ... -
TWO CASES OF 9p DELETION SYNDROME AND A CASE OF PARTIAL TRISOMY 8 AND PARTIAL MONOSOMY 9p
Okten, G.; Sezer, O.; Gunes, S.; Kucukoduk, S.; Ogur, G. (Medecine Et Hygiene, 2009)Two cases of 9p deletion syndrome and a case of partial trisomy, 8 and partial monosomy 9p: We report 3 girls with mental retardation (MR), distinctive malformations of the skull and facial region, including trigonocephaly, ...