BACKGROUND One of the promises of human genetics is individualized therapy. Therefore, we evaluated the impact of CYP3A5 gene polymorphism on the effectiveness of simvastatin (a HMG-CoA reductase inhibitor). METHODS Patients (n = 191) with hypercholesterolemia were treated with simvastatin for at least 6 months and were genotyped for the CYP3A5 polymorphism. RESULTS The frequency of CYP3A5 ...

background: pre-eclampsia (pe) is one of the most important and life-threatening pregnancy disorders that affect at least 3-5% of all pregnancies. imbalance in helper t cell functions may play a role in predisposing to pe or severity of the disease. elevated frequencies of th17 cells in the peripheral blood of pe patients have been reported. several single nucleotide polymorphisms (snp) within ...

background: β-thalassemia as a hereditary disease is defined as defective synthesis of   β-globin chains, resulting in erythropoiesis abnormalities and severe anemia. different studies have shown that cytokines and cytokine gene polymorphisms play a major role in the pathogenesis of   β-thalassemia. single nucleotide polymorphisms (snps) within the promoter region or other regulatory sequences ...

Objective(s): Asthma, the most frequent chronic respiratory disease, results from a complex interaction between multiple genes and environmental factors. To date, more than 100 candidate genes and single nucleotide polymorphisms (SNPs) have been reported to be associated with asthma. One of the discovered genes related to asthma is ADAM33. However, the relationship between ADAM33 gene polymorph...

background: multiple sclerosis (ms) is an autoimmune disease of the central nervous system (cns) caused by autoreactive t cells against myelin antigens. t-cell immunoglobulin mucin -3 (tim-3) is a negative regulator glycoprotein expressed by a range of immune cells, including, th1 cells, activated cd8+ t cells and in a lower level on th17 cells. a defect in tim-3 regulation has been shown in mu...

Cystic fibrosis (CF) is the most common severe autosomal recessive disorder caused by a wide spectrum of mutations in the gene encoding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The frequencies, types and distributions of mutations vary widely between different populations and ethnic groups. The aim of this study was to perform a comprehensive analysis of the C...

Abstract Background: Single nucleotide polymorphisms (SNPs) in some genes which are involving in sperm maturation, are considered as one of the main reason for male infertility. Any changes in protamine genes may cause abnormal histone-protamine replacement during spermiogenesis and have been indicated to cause sperm DNA damage and infertility. Objective: The aim of present case-control study w...

Background & Aims: Lipoprotein lipase (LPL) is one of the key enzymes regulating the metabolism of triglycerides (TG) and HDL cholesterol. The lipoprotein lipase (LPL) gene polymorphisms are possibly involved in the pathophysiology of dyslipidemia. Hind III polymorphism is one of the most common polymorphisms in LPL gene. In some studies, association of Hind III polymorphism with dyslipidemia h...

Background: β-thalassemia as a hereditary disease is defined as defective synthesis of   β-globin chains, resulting in erythropoiesis abnormalities and severe anemia. Different studies have shown that cytokines and cytokine gene polymorphisms play a major role in the pathogenesis of   β-thalassemia. Single nucleotide polymorphisms (SNPs) within the promoter region or other regulatory sequences ...

background: increased levels of interleukin-8 (il-8) and interleukin-6 (il-6) in acute human brucellosis have been reported. previous studies have shown that the production and level of il-6 and il-8 cytokines are associated with the polymorphism of the encoding genes. objective: to investigate the probable association between il-6 (-174 c/g) and il-8 (-251 a/t) gene polymorphisms and susceptib...