Yazar "Kara, Murat" için listeleme
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The relationship between attention deficit hyperactivity disorder and reelin gene polymorphicms in Turkish population
Kara, Bilge; Sahin, Nilfer; Kara, Murat; Cetin, Esin Sakalli; Topal, Hatice (Taylor & Francis Ltd, 2018)PURPOSE: Although attention deficit hyperactivity disorder (ADHD) is one of the most frequently seen psychiatric disorders in childhood, its etiology and pathophysiology are not fully elucidated. The aim of the present ... -
The relationship between gestational diabetes mellitus and selenoprotein-P plasma 1 (SEPP1) gene polymorphisms
Akbaba, Gülhan; Akbaba, Eren; Şahin, Cem; Kara, Murat (Taylor & Francis Ltd, 2018)Our aim is to demonstrate any correlation between gestational diabetes mellitus (GDM) and polymorphism of the selenoprotein P (SEPP1) gene encoding the SEPP1 protein, having a role in the insulin resistance in GDM. Forty ... -
The rs3768777-G allele of ITGAV gene is associated with rheumatoid arthritis
Koca, Suleyman Serdar; Kara, Murat; Ozgen, Metin; Dagli, Mustafa Necati; Gozel, Nevzat; Yolbas, Servet; Isik, Ahmet (Springer Heidelberg, 2014)Integrin alpha v beta 3 (vitronectin receptor) plays a prominent role in angiogenesis, a key pathogenic feature of rheumatoid arthritis (RA). Moreover, integrin alpha(V) (ITGAV) subunit gene has been associated with a ... -
Serum adropin level and ENHO gene expression in systemic sclerosis
Yolbaş, Servet; Kara, Murat; Yılmaz, Musa; Aydın, Süleyman; Koca, Süleyman Serdar (Springer London Ltd, 2016)Adropin, a secreted protein, is encoded by the energy homeostasis associated (ENHO) gene. It has been implicated in the several physiological and pathological processes such as angiogenesis and apoptosis. Therefore, the ... -
Serum IL-33 level and IL-33 gene polymorphisms in Behcet's disease
Koca, Süleyman Serdar; Kara, Murat; Deniz, Fırat; Özgen, Metin; Demir, Caner Feyzi; İlhan, Nevin; Isık, Ahmet (Springer Heidelberg, 2015)Beh double dagger et's disease (BD) is a chronic inflammatory disease. Increased productions of cytokines including interleukin (IL)-1 beta and IL-18 are documented, and IL-1 alpha and beta gene polymorphisms are associated ... -
Sirtuin gene polymorphisms are associated with chronic obstructive pulmonary disease in patients in Mugla province
Kalemci, Serdar; Edgunlu, Tuba Gokdogan; Kara, Murat; Turkcu, Ummuhani Ozel; Cetin, Esin Sakalli; Zeybek, Arife (Termedia Publishing House Ltd, 2014)Introduction: Chronic obstructive pulmonary disease (COPD) is an irreversible progressive chronic inflammatory disease that causes shortness of breath in consequence of a decrease in pulmonary functions. The pulmonary ... -
Tip 2 Diabetes Mellitus Hastalarında Sirtuin 1 Gen Expresyonu ve Gen Polimorfizminin Rolünün İncelenmesi
Amaç:Diabetes Mellitus (DM); İnsülin hormon sekresyonu ve insülin etkisinin azlığı sonucu karbonhidrat, protein ve yağ metabolizmasında bozukluklara yol açan kronik metabolizma hastalığıdır. Sirtuin1 (SIRT-1) geni, ... -
Upregulation of SIRT1 gene in gastric adenocarcinoma
Özcan, Önder; Belli, Ahmet Korkut; Çetin, Esin Sakallı; Kara, Murat; Çelik, Özgur İlhan; Kaplan, Mehmet; Polat, Murat (Aves, 2019)Background/Aims: SIRT1 gene overexpression is reportedly associated with cancer development, via the triggering of DNA repair impairment, and cell proliferation. The study aimed to investigate SIRT1 expression in patients ...