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Kistik Fibrozisli Hastalarda Anaerop Bakterilerin Rolünün Araştırılması 

Doğan Ayçık, Özlem (Tıp Fakültesi, 2012)
Pseudomonas aeruginosa, Staphylococcus aureus, Haemophilus influenzae and Burkholderia cepacia complex are the most frequently isolated microorganisms from respiratory tract samples of the cystic fibrosis patients. ...
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Allelik Heterojenitenin Gözlendiği Kas Distrofilerinin Biyoenformatik Araçlar Kullanılarak Araştırılması 

Çalı Daylan, Ayşe Ece (Sağlık Bilimleri Enstitüsü, 2015)
Limb-girdle muscle dystrophy (LGMD) is a clinically and genetically heterogeneous group of inherited muscle disorders characterized by progressive muscle degeneration predominantly in proximal muscles of shoulder and pelvic ...
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Mikrodizilim Gen İfade Çalışmalarında Genelleştirme Yöntemlerinin Regresyon Modelleri Üzerine Etkisi. 

Yılmaz Işıkhan, Selen (Sağlık Bilimleri Enstitüsü, 2014)
The presence of thousands of gene data belonging to a few number of patients in genetic researches leads to problems in the use of classical statistical methods (linear regression analysis etc.). However, analysis of large ...
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Demir Birikimine Bağlı Yetmezlik Gelişen Endokrin Organların T2 Ve T2* Değerlerinin Belirlenmesi 

Yıldırım, Gökçe (Tıp Fakültesi, 2013)
The purpose of this study at first stage is to determine the normal R2/T2 for thyroid and pituitary gland, and R2*/T2* values for pancreas, and then at the second stage to evaluate if there is any difference between tl ...
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Karaciğer Metastazlarinda Düşük Dozlu Perfüzyon BT'nin Değişkenliği ve Tekrarlanabilirliği 

Topcuoğlu, Osman Melih (Tıp Fakültesi, 2014)
Hepatic perfusion CT enabling qualitative and quantitative assessment of the regional and global tumoral perfusion, have been used increasingly in recent years. However quite variability of the parameter measurements ...
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Desmin Geni C.1289-2a>G Mutasyonunun Desmin Proteinine Etkisinin İncelenmesi 

Çetin, Nilgün (Sağlık Bilimleri Enstitüsü, 2012)
Autosomal recessive limb girdle muscular dystrophy (LGMD2) is clinically and genetically heterogeneous group of diseases that are characterized by progressive atrophy and weakness of proximal muscles. Two siblings of a ...
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Frontonasal Displazi Tip 3 Ailelerinde Malformasyondan Sorumlu Genin Araştırılması 

Şahin, Yavuz (Tıp Fakültesi, 2015)
Frontonasal dysplasia type 3 (FND3, MIM 613456) is an autosomal recessive severe facial malformation characterized by biletaral extreme microphthalmia, bilateral oblique facial cleft, complete cleft palate, hypertelorism, ...
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Şizofrenide Mevcut Tedaviye Yardımcı Olarak Rastgele, Çift Kör, Çapraz Geçişli, Plasebo Kontrollü L-Arjinin Eklenmesi 

Koçyiğit, Yasemin (Tıp Fakültesi, 2013)
Schizophrenia is a disabling disorder which impairs social, occupational and individual functioning. Current drug treatments for schizophrenia are only partially effective and combination/augmentation strategies are commonly ...
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İzole Edilmiş Sıçan Pankreas Adacık Hücrelerine in Vitro Trombospondinin Etkisi 

Kurt, Şefika Nur (Sağlık Bilimleri Enstitüsü, 2013)
Pancreas islet cells are very sensitive to hypoxic stress because of having small amount of anti-oxidant enzyme. Loss of islet cell viability due to hipoxic damage decreases success of transplantation. Islet- endothelial ...
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Biyotinidaz Enzim Eksikliğinin Değerlendirilmesinde Spektrofotometrik ve Florometrik Yöntemlerin Karşılaştırılması 

Işeri Erten, Sevgin Özlem (Tıp Fakültesi, 2014)
Biotin, a water-soluble vitamin, is used as a co-factor by enzymes involved in carboxylation reactions. It functions as the carboxyl carrier for biotin-dependent carboxylases which catalyze gluconeogenesis, fatty acid ...
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