Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Müjgan CENGİZ"'
Autor:
Berk Arapi, Burcu Bayoğlu, Müjgan Cengiz, Ahmet Dirican, Serkan Burç Deser, Yerik Junusbekov, Caner Arslan
Publikováno v:
Balkan Medical Journal, Vol 35, Iss 3, Pp 250-255 (2018)
Background: Carotid artery stenosis is the atherosclerotic narrowing of the proximal internal carotid artery and one of the primary causes of stroke. Elevated expression of the pleiotropic proinflammatory cytokine interleukin-18 has been demonstrated
Externí odkaz:
https://doaj.org/article/02e793e6c5a04015bcdb1b0fa370f1b0
Autor:
Burcu BAYOĞLU, Müjgan CENGİZ
Publikováno v:
Bezmiâlem Science, Vol 5, Iss 2, Pp 74-79 (2017)
For many years, proteins have been known be the major regulators in biological processes such as transcription and translation. However, in recent years, with the advent of high-throughput sequencing technology, a high-resolution map of the human tra
Externí odkaz:
https://doaj.org/article/af2204a309c04b12aaf9ab2cbb67c814
Autor:
Saadet Busra Aksoyer Sezgin, Burcu Bayoglu, Feyzullah Ersoz, Murat Sarici, Mutlu Niyazoglu, Ahmet Dirican, Müjgan Cengiz
Publikováno v:
Turkish Journal of Biochemistry. 47:425-433
Objectives Adipose tissue mediates various bioactive molecules and cytokine discharge. The anti-inflammatory cytokine, interleukin-10 (IL-10), has roles in systemic inflammation. Matrix metalloproteinases (MMPs) are endopeptidases implicating in tiss
Autor:
Burcu Bayoglu, T. Eseroglu Soylemez, Gul Karacetin, Türkay Demir, Çağatay Ermiş, S.B. Aksoyer Sezgin, M. Topal, E. Bulanik Koc, M. Elagoz Yuksel, Müjgan Cengiz, M. Tekden, E.S. Ercan, M. Erkiran
Background and Objectives: To investigate the clinical characteristics of adolescents with early-onset full psychotic disorders either with Brain-derived neurotrophic factor (BDNF) Val66Met (rs6265) or DRD2/ANKK1 Taq1A (rs1800497) polymorphisms. Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15b9c9e8a5f78f6a4aaca0980068041d
https://avesis.deu.edu.tr/publication/details/59017f46-9ac2-440b-9eb4-deddf6aa3c41/oai
https://avesis.deu.edu.tr/publication/details/59017f46-9ac2-440b-9eb4-deddf6aa3c41/oai
Publikováno v:
Irish Journal of Medical Science (1971 -). 189:885-894
Peripheral arterial diseases (PAD) refer to the arterial diseases other than coronary arteries and the aorta. Atherosclerosis is the major cause of PAD. Renin angiotensin aldosterone system (RAAS)-related genes were associated with cardiovascular dis
Autor:
Müjgan Cengiz, Ahmet Dirican, Burcu Bayoglu, Vilson Karaj, Nese Kocabasoglu, Gokcen Gozubatik-Celik
Publikováno v:
International Journal of Psychiatry in Clinical Practice. 23:114-121
Objective: Orexins (hypocretins) are neuropeptides expressed in hypothalamic neurons and have regulatory roles in feeding/drinking behaviours, endocrine functions and sleep/wakefulness state. Major...
Autor:
Müjgan Cengiz, Nese Kocabasoglu, Emel Hulya Yukseloglu, Irmak Sah, Burcu Bayoglu, Emre Cirakoglu
Publikováno v:
Molecular biology reports. 48(1)
Antisocial personality disorder (ASPD) is a cluster B personality disorder characterized by a disposition for criminal behaviors. It has been determined by previous studies that ASPD may have a genetic origin and the human serotonin transporter gene
Publikováno v:
Experimental and Therapeutic Medicine. 13:1160-1168
Oxidized low-density lipoprotein receptor 1 (OLR1) and interleukin 17A (IL17A) have pro-inflammatory roles in the development of cardiovascular disorders. The present study evaluated the association of OLR1 and IL17A and their polymorphisms with the
Publikováno v:
Indian Journal of Psychiatry
15th National Medical Biology and Genetics Congress -- OCT 26-29, 2017 -- Mugla, TURKEY Cengiz, Mujgan/0000-0003-1030-5425; KOCABASOGLU, NESE/0000-0002-8328-4736; Bayoglu, Burcu/0000-0001-6568-6398; Asliyuksek, Hizir/0000-0001-6845-3717 WOS:000468922
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d05984022704b1cd2772e70c9b4f8c33
https://hdl.handle.net/20.500.12831/912
https://hdl.handle.net/20.500.12831/912
Publikováno v:
Clinical Biochemistry. 49:821-827
Objectives Hypertension (HT) is a complex disorder influenced by both genetic and environmental factors. Recent genome-wide association studies have identified a major risk locus for atherosclerosis on chromosome 9p21.3. SNPs within the coding sequen