… Among several cytokines, TNFα and IL-1 can regulate and stimulate PG endoperoxide H
synthase 2 expression and PG synthesis and may have a role in PTB. There are several …

Venous thromboembolism (VTE) is a universal health hazard. Inherited and acquired risk
factors increase the risk of VTE. We evaluated the relationship between factor V (G1691A, …

Obesity is associated with the changes of plasminogen activator inhibitor-1 (PAI-1), tumor
necrosis factor-alpha (TNFα) and transforming growth factor beta (TGFβ) levels. However, the …

Background. Chronic allograft dysfunction (CAD) is a complex phenomenon caused by
underlying kidney disease and superimposed environmental and genetic factors. We …

Introduction A mutation at nucleotide position 3435 in exon 26 of the multidrug resistance 1 (MDR1)
gene is the most frequently studied polymorphism in relation to multidrug resistance. …

The objective of the study was to determine the association between intron 4 variable number
of tandem repeats (VNTR), E298A and IVF 23+ 10 G/T polymorphisms of ec-NOS gene …

The prevalence of mutations in the precore and core promoter regions of hepatitis B virus
DNA and the association with the hepatitis B e antigen-negative phenotype vary in different …

The aim of this study was to evaluate the prevalence of factor V Leiden (FVL), prothrombin
G20210A, methylenetetrahydrofolate reductase (MTHFR) C677T gene mutations, and …

Bronchopulmonary dysplasia (BPD) is a multifactorial disease of preterm infants that is
characterized by airway injury, inflammation, and parenchymal remodeling. Extravascular fibrin …

A mutation in the methylenetetrahydrofolate reductase (MTHFR) gene is known as one of the
causes of hyperhomocyteinemia. The oxidation products of homocysteine can initiate lipid …