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Adherence to Mediterranean nutrition pattern in patients with non-alcoholic fatty liver disease: Relationship with metabolic risk factors and -UCP2-866G/A gene polymorphisms
(2016)
The current study evaluated the association between major components of Mediterranean dietary regimen with metabolic biomarkers and uncoupling protein-2 (UCP2)-866G/A gene polymorphism in patients with non-alcoholic fatty ...
Association of UCP2 -866G>A polymorphism with nonalcoholic fatty liver disease in patients from North-West of Iran
(2017)
Objective: To investigate the association of uncoupling protein-2 (UCP2) -866G>A gene polymorphism (rs659366) with nonalcoholic fatty liver disease (NAFLD). Methods: We performed a case-control study with a cohort of 75 ...
Association study of CTLA-4 +49A/G gene polymorphism with recurrent pregnancy loss in the Iranian Azeri Turkish ethnic group
(2017)
Background/aim: Recurrent pregnancy loss (RPL) is defined as two or more pregnancy losses. T-regulatory cells play an important role in the feto-maternal interface. Cytotoxic-T-lymphocyte antigen-4 (CTLA-4) is a molecule ...
Association of endothelial nitric oxide synthase gene variants (-786 T>C, intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A case-control study with haplotype and in silico analysis
(2017)
Objective(s) Many lines of evidence suggest that reduced production of nitric oxide (NO) due to single nucleotide polymorphisms in endothelial nitric oxide synthase (eNOS) gene may affect the implantation and maintenance ...
Association of cystathionine beta-synthase polymorphisms and aneurysmal subarachnoid hemorrhage
(2018)
OBJECTIVE Cystathionine b-synthase (CBS) is involved in homocysteine and hydrogen sulfide (H2S) metabolism. Both products have been implicated in the pathophysiology of cerebrovascular diseases. The impact of CBS polymorphisms ...
Association of P53 (?16ins-Pro) Haplotype with the Decreased Risk of Differentiated Thyroid Carcinoma in Iranian-Azeri Patients
(2015)
Association of P53 polymorphisms with the increased risk of various cancers has been investigated in numerous studies. However, the results were conflicting and no polymorphism has been determined as a definite risk factor. ...
A single nucleotide polymorphism in the FOXP3 gene associated wit] behcet's disease in an Iranian population
(2015)
Background: Behcet's Disease (BD) is a rare autoimmune disease that involves the dysfunction of regulatory T cells. FOXP3 is a key transcription factor in the development and function of Treg cells. Recent studies have ...
Association of CCND1 Gene c.870G>A Polymorphism with Breast Cancer Risk: A Case-ControlStudy and a Meta-Analysis
(2017)
Cyclin D1 (CCND1) plays an essential role in regulating the progress of the cell cycle from G1 to S phase. There is a common c.870G>A polymorphism in the CCND1 gene. The aim of this study was to investigate the association ...
Association of ABO blood grouping with recurrent aphthous stomatitis
(2017)
This study aimed to investigate Association of ABO blood grouping in patients with recurrent aphthous stomatitis referring to Oral Medicine department of Tabriz Dental Faculty. In this cross sectional study blood group ...
Analysis of CTLA-4 + 49A/G gene polymorphism in cases with leprosy of Azerbaijan, Northwest Iran
(2018)
Leprosy, which is developed by the obligate intracellular Mycobacterium leprae (ML); has different manifestations, associated with the host immune responses. The protective immune response against ML includes T-cell-mediated ...