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Toplam kayıt 8, listelenen: 1-8
Crimean-Congo hemorrhagic fever virus in tortoises and Hyalomma aegyptium ticks in East Thrace, Turkey: Potential of a cryptic transmission cycle
(BioMed Central Ltd., 2020)
Background: Recent reports have demonstrated the presence of Crimean-Congo hemorrhagic fever virus (CCHFV) genomic material in Hyalomma aegyptium ticks feeding primarily on tortoises belonging to the genus Testudo. This ...
Çapraz bağlayıcı ve büyüme faktörü emdirilen hidrojel sistemlerinden kontrollü ilaç salımı: Sistematik inceleme
(2012)
Amaç: Bu çalışmada, dünya genelinde son 31 yılda yapılan çalışmalar içerisinde, kontrollü ilaç taşıma sistemi olan ve çapraz bağlayıcı ilavesi ile biodegradasyona uğratılmış büyüme faktörü emdirilen hidrojelin, kıkırdak ...
How Different Methodologies of Harvesting and Analysing the Samples Affect the Test Results in Determining Joint Mediators
(Hindawi Ltd, 2013)
Purpose. This study has researched the affect of different methodologies of harvesting and analysing the samples in determining the mediators emerging after the rat articular cartilage injury. Materials and Methods. One ...
BRAF V600E mutation in papillary thyroid cancer is correlated with adverse clinicopathological features but not with iodine exposure
(Via Medica, 2019)
Introduction: BRAF(V600E) activating mutation is the most frequent genetic abnormality in the pathogenesis of papillary thyroid carcinoma. We aimed to evaluate the association between BRAF(V600E )mutation and well-established ...
Two siblings with familial subclinical hyperthyroidism with unknown etiology
(2017)
Subclinical hyperthyroidism is defined as low or undetectable concentration of serum thyrotrophin (TSH) with normal free triiodothyronine (FT3) and free thyroxine (FT4) levels. 1). Familial subclinical hyperthyroidism is ...
Is the TSHR D727E polymorphism a genetic predisposition for multinodular goiter in the Turkish population?
(Funpec-Editora, 2016)
The D727E germline polymorphism in the thyroid-stimulating hormone receptor gene (TSHR) may cause genetic susceptibility to the development of goiter. Therefore, in this study we investigated allele frequencies and genotype ...
Recurrent EZH1 mutations are a second hit in autonomous thyroid adenomas
(Amer Soc Clinical Investigation Inc, 2016)
Autonomous thyroid adenomas (ATAs) are a frequent cause of hyperthyroidism. Mutations in the genes encoding the TSH receptor (TSHR) or the Gs protein alpha subunit (GNAS) are found in approximately 70% of ATAs. The involvement ...
MTHFR, prothrombin and Factor V gene variants in Turkish patients with coronary artery stenosis
(Soc Brasil Genetica, 2008)
Many epidemiological studies have reported an association between hemostatic factors and risk of both coronary and peripheral artery diseases. Using polymerase chain reaction and restriction fragment length polymorphism ...