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Toplam kayıt 59, listelenen: 1-10
Sutura Sphenovomeralıs' ın Endoskopik Transsphenoidal ve Radyolojik Yöntemlerle Incelenmesi
(Tıp Fakültesi, 2013)
Rostrum of sphenoid bone articulates with ala of vomer forming schindylesis type of joint. The circumference of this joint is called sphenovomerine suture (SSV). Although this suture is mentioned in Terminologia Anatomica, ...
Mikroarray Gen Ekspresyon Veri Setlerinde Random Forest Ve Naıve Bayes Sınıflama Yöntemleri Yaklaşım
(Sağlık Bilimleri Enstitüsü, 2013)
Two classification methods,Random Forest and Naive Bayes,were compared about various types of cancer
Ankara Bölgesinde Batı Nil Virusu ve Toskana Virus Vektörlerinin Araştırılması
(Sağlık Bilimleri Enstitüsü, 2013)
West Nile Virus (WNV) and Toscana virus (TOSV) may cause febrile diseases and central nervous system infections and even severe meningoencephalitis in susceptible individuals. Major transmission route is via blood sucking ...
Mycobacterium Tuberculosis Klinik İzolatlarında İlaç Direncinin Multipleks Real-Time Pcr Yöntemiyle Saptanması
(Sağlık Bilimleri Enstitüsü, 2013)
Tuberculosis (TB) is stil one of the most serious threats to human health around the world. Increasing of the drug resistance is one of the main cause of this state. Early diagnosis of drug-resistant TB cases is urgently ...
Hukuki ve Etik Yönleri ile Biyotıp Araştırmalarında Biyobankalar
(Sağlık Bilimleri Enstitüsü, 2013)
Biobanks are the organizations where biological materials and associated personal information are collected, stored, processed and distributed in a particular systematic. Biobanks provide opportunity to easily obtain enough ...
Spinal Müsküler Atrofi Patogenezinde Rol Alan Genetik Düzenleyicilerin İfade Analizi
(Sağlık Bilimleri Enstitüsü, 2013)
Childhood- onset spinal muscular atrophy (SMA) is an autosomal recessive disorder, which leads to alpha motor neuron degeneration. Although 95-98 % of the patients have homozygous deletions in exon 7 and 8 SMN1 gene, ...
Lizozomal Depo Hastalığı Olan Gaucher Hastalığında Otofaji Mekanizmasının Moleküler Düzeyde İncelenmesi
(Sağlık Bilimleri Enstitüsü, 2013)
Lysosomes are the most important degradation organelles of the cell. The functions of the lysosomes depend upon the harmonious coordination between the lysosomal hydrolases and the lysosomal membrane proteins existing in ...
New Approach to Unsupervised Based Classification on Microarray Data
(Sağlık Bilimleri Enstitüsü, 2013)
Genetic studies have been an important part of medical researches in recent years. These studies have become essential for the development of personalized treatment options and discovery of new drugs. The majority of these ...
Nörofibromatozis Tip 1 ile İlişkili Tümörlerde C-X-C Kemokin Reseptör Tip 4 Gen İfade Düzeyinin Belirlenmesi
(Sağlık Bilimleri Enstitüsü, 2013)
Neurofibromatosis type 1 (NF1) is a common genetic disorder that affects skin
and nervous system that is inherited in autosomal dominant trait. It occurs due to the
mutations in NF1 gene. The most common Schwann cell ...
Metakromatik Lökodistrofi: Üç Arilsülfataz A Mutasyonunun (P.307Glu→Lys, P.318Trp→Cys Ve C.1165G Delesyonu) Arilsülfataz A Aktivitesi ve Arilsülfataz A Proteini Üzerine Etkisinin Tanımlanması
(Tıp Fakültesi, 2013)
Metachromatic leukodystrophy (MLD) is an autosomal recessively inherited sphingolipid storage disease that occurs as a result of a lack of lysosomal enzyme Arylsulfatase A (ASA) or its activator protein. In this study, two ...