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Kistik Fibrozisli Hastalarda Anaerop Bakterilerin Rolünün Araştırılması
(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. ...
Allelik Heterojenitenin Gözlendiği Kas Distrofilerinin Biyoenformatik Araçlar Kullanılarak Araştırılması
(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 ...
Mikrodizilim Gen İfade Çalışmalarında Genelleştirme Yöntemlerinin Regresyon Modelleri Üzerine Etkisi.
(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 ...
Demir Birikimine Bağlı Yetmezlik Gelişen Endokrin Organların T2 Ve T2* Değerlerinin Belirlenmesi
(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 ...
Karaciğer Metastazlarinda Düşük Dozlu Perfüzyon BT'nin Değişkenliği ve Tekrarlanabilirliği
(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 ...
Desmin Geni C.1289-2a>G Mutasyonunun Desmin Proteinine Etkisinin İncelenmesi
(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 ...
Frontonasal Displazi Tip 3 Ailelerinde Malformasyondan Sorumlu Genin Araştırılması
(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, ...
Şizofrenide Mevcut Tedaviye Yardımcı Olarak Rastgele, Çift Kör, Çapraz Geçişli, Plasebo Kontrollü L-Arjinin Eklenmesi
(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 ...
İzole Edilmiş Sıçan Pankreas Adacık Hücrelerine in Vitro Trombospondinin Etkisi
(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 ...
Biyotinidaz Enzim Eksikliğinin Değerlendirilmesinde Spektrofotometrik ve Florometrik Yöntemlerin Karşılaştırılması
(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 ...