Güncel Gönderiler: Yayın Koleksiyonu
Toplam kayıt 28, listelenen: 21-28
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Interleukin-1Ra rs2234663 and Interleukin-4 rs79071878 Polymorphisms in Familial Mediterranean Fever
(ELSEVIER SCIENCE BV, 2016)Objective: Familial Mediterranean Fever (FMF) is an autosomal recessively inherited auto inflammatory disorder. MEFV gene, causing FMF, encodes pyrin that is associated with the interleukin-1 (IL-1) related inflammation ... -
The IL-1Ra gene variable number tandem repeat variant is associated with susceptibility to temporomandibular disorders in Turkish population
(WILEY, 2018)BackgroundTemporomandibular joint disorders (TMD) are a group of disorders involving temporomandibular joint and related structures. Interleukine-1 receptor antagonist (IL-1Ra) is an important anti-inflammatory molecule ... -
Macrophage Migration Inhibitory Factor-173GC Variant Might Increase the Risk of Behcet's Disease
(KARGER, 2018)Objective: The aim of the present study was to investigate any possible association between the macrophage migration inhibitory factor (MIF) -173GC variant and Behcet's disease (BD) in a group of Turkish patients. Subjects ... -
The investigation of association between IL-1Ra and ACE I/D polymorphisms in carpal tunnel syndrome
(WILEY, 2018)BackgroundCarpal tunnel syndrome (CTS) is a common neurologic impairment caused by injury on the median nerve in the wrist, characterized by pain and loss of sensory. CTS usually occurs through three factors, such as a ... -
Angiotensin Converting Enzyme Gene Insertion/Deletion Variant and Familial Mediterranean Fever-related Amyloidosis
(IRANIAN SOC NEPHROLGY, 2018)Introduction. The most important complication of familial Mediterranean fever (FMF) is secondary amyloidosis, which can lead to kidney failure. Genetic variability in the genes of various components of the renin-angiotensin ... -
Importance of NPC1 Gene 644 A -> G Mutation in Coronary Artery Disease
(KAMLA-RAJ ENTERPRISES, 2017)Coronary artery disease (CAD) is the most prominent cause of mortality worldwide. The basis of CAD pathogenesis is the occlusion of coroner vessels progressively due to atherosclerotic plaques. NPCI gene plays a critical ... -
Effect of a functional variant of tumor necrosis factor-beta gene in temporomandibular disorders: A pilot study
(WILEY, 2019)Background Temporomandibular disorders (TMD) are a group of conditions that cause chronic orofacial pain. The tumor necrosis factor beta (TNF-beta) is a proinflammatory cytokine that is involved in the various aspects of ... -
Association of XRCC1 and XPD functional gene variants with nicotine dependence and/or schizophrenia: a case-control study and in silico analysis
(TAYLOR & FRANCIS LTD, 2019)OBJECTIVE: The role of DNA repair mechanisms has received attention recently in schizophrenia (Sch). Sch patients show an increased prevalence of nicotine dependence (ND). This study aimed to find out whether functional ...
