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Toplam kayıt 61, listelenen: 11-20
Pigmentli ve Pigmentsiz Pseudomonas Aeruginosa Suşlarının Virulans Faktörlerinin Fenotipik ve Genotipik Olarak Karşılaştırılması
(Tıp Fakültesi, 2014)
Pseudomonas aeruginosa is an aerobic, motile, non-spore forming, straight or slightly curved, gram-negative bacilli and it can grow at 42 °C. The incidence of P. aeruginosa has been increased in recent years and its virulence ...
Cloning and Determination of Tissue Specific Expression Pattern of Astacus Leptodactylus Na+ Ca 2+ Exchanger Gene
(Sağlık Bilimleri Enstitüsü, 2014)
Cytosolic Ca2+ plays an essential role in various cellular functions. Changes in cytosolic Ca2+
concentration is important for different cellular activities like muscle contraction and
neurotransmitter release. A set of ...
Otozomal Resesif Limb-Girdle Kas Distrofisi Tanısı Alan Ailelerde Yeni Gen Araştırılması
(Sağlık Bilimleri Enstitüsü, 2014)
Limb-girdle muscular dystrophies (LGMD) are a clinically and genetically heterogeneous group of hereditary muscle disorders characterized by symmetric, proximal and progressive muscular weakness. In this thesis, four ...
Development And Evaluation Of The Evidence-Based Medicine Program In Surgery: A Spiral Approach
(2014)
Background Evidence-based medicine (EBM) aims to provide skills that help physicians answer clinically important questions, determine new evidence, and incorporate the acquired knowledge in practice. EBM skills are necessary ...
Mersin İli Kan Donörlerinde Flavivirus Seroepidemiyolojisi
(Ankara Microbiology Soc, 2014)
Among the vector-borne flaviviruses, West Nile virus (WNV), tick-borne encephalitis virus (TBEV) and Dengue virus (DENV) constitute the most frequently-observed pathogens with significant public health impact in endemic ...
Evidence For The Control Of Aggrecanases By Insulin And Glucose In Alzheimer'S Disease
(Kure Iletisim Grubu A S, 2014)
Objective: Alzheimer's disease (AD) is a progressive and irreversible central nervous system disease, which slowly destroys cognitive skills and memory, and eventually even the ability to handle the simplest tasks. The ...
Mutation In Tor1Aip1 Encoding Lap1B In A Form Of Muscular Dystrophy: A Novel Gene Related To Nuclear Envelopathies
(Pergamon-Elsevier Science Ltd, 2014)
We performed genome-wide homozygosity mapping and mapped a novel myopathic phenotype to chromosomal region 1q25 in a consanguineous family with three affected individuals manifesting proximal and distal weakness and atrophy, ...