Zobrazeno 1 - 10
of 149
pro vyhledávání: '"Tepeli E"'
Publikováno v:
Balkan Journal of Medical Genetics, Vol 22, Iss 1, Pp 21-28 (2019)
Pentraxin 3 (PTX3), a prototypical member of the long pentraxin subfamily, is a evolutionarily conserved multimeric pattern recognition receptor involved in the humoral component of the innate immune system. Pentraxin 3 is released when tissue is str
Externí odkaz:
https://doaj.org/article/92d4075ddcde41cdae7e3aad94763f2d
Purpose Plasminogen activator inhibitor 1 (PAI-1) is a critical enzyme that regulates coagulation and fibrinolytic systems. The aim of this study was to determine the role of PAI-1 4G/5G polymorphism in nontraumatic avascular necrosis of the lunate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::9afc298adb19f02df69e8bdabeefe9ba
Pentraxin 3 (PTX3), a prototypical member of the long pentraxin subfamily, is a evolutionarily conserved multimeric pattern recognition receptor involved in the humoral component of the innate immune system. Pentraxin 3 is released when tissue is str
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::64595c0d15bebc1c3c9ecd26764de37b
Attention-deficit/hyperactivity disorder (ADHD) is a prevalent neurodevelopmental disorder. Its etiology is not clearly understood yet, but neurobiological, genetic and environmental factors are shown to play a role. The relationship between ADHD and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::066a29bb26bc61db703e52cbb42fc712
BackgroundGout is a clinical syndrome that occurs as an inflammatory response to increased concentration of uric acid and monosodium urate crystals. Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease with autosomal recessive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::8e68cd7e9e7819e09506656b9e859944
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/24630
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/24630
Background: Synaptosomal-associated protein 25 (SNAP-25) may be contribute to the pathogenesis of fibromyalgia Syndrome (FMS) by affecting the release of neurotransmitters. Objectives: We aimed to investigate the relationship between the SNAP-25 gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::58722e1882e382d365c9552782ab5ef8
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/24378
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/24378
Background/aim: Midkine (MK), a heparin-binding growth factor, has an important role in cancer progression. The aim of this study was to determine MK expression in breast tissue and the preoperative and postoperative serum levels of patients with bre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0f1903a8ea9e9e7bbf848f4475a8b244
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/15596
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/15596
OBJECTIVE: The effects of certain genetic alterations in the brain function of patients with attention deficit hyperactivity disorder (ADHD) remain unclear and, in fact, there is a limited amount of data in this field. For example, the relationship b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::5dfa67981808cbacdff5f14f6ac432bb
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/23121
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/23121
Autor:
Cetin, GO, Baris, IC, Caner, V, Sarikepe, B, Sen Turk, N, Tepeli, E, Hacioglu, S, Sari, I, Bagci, G, Keskin, A
OBJECTIVE: We aimed to determine the hot spot mutational frequencies of Enhancer of Zeste homolog 2 (EZH2) and cluster of differentiation 79B (CD79B) genes in a cohort of mature B-cell non-Hodgkin's lymphomas.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::ede2c475c174c8d1dfd726262c08da13
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/23258
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/23258
Neonatal Bartter syndrome (NBS) is a rare autosomal recessive renal tubular disorder. This disease is characterized by hypokalemia, hypochloremia, and metabolic alkalosis that is often associated with failure to thrive and recurrent episodes of dehyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::2a7e0fab73ebe75fa98df84eface955b