نتایج جستجو برای: il1β
تعداد نتایج: 533 فیلتر نتایج به سال:
Diabetic Retinopathy (DR) is a complication of diabetes associated with irreversible loss of blindness. Various types of DR have been reported like mild non-proliferative retinopathy, moderate non-proliferative retinopathy, severe non-proliferative retinopathy and proliferative retinopathy. A number of signaling mechanisms like nuclear factor kappa-B (NF-κB), cyclo-oxygenase (COX), intracellula...
Abstract Background and Aims Glomerular injury in Anti-Neutrophil Cytoplasmic Antibodies (ANCA)-associated glomerulonephritis (AGN) is associated with macrophage infiltration. To date, their role origin remain to be fully elucidated. Activated blood monocytes likely transmigrate differentiate into kidney macrophages depending on the local microenvironment. Even remission, some studies indicate ...
Objective(s): Current acute myeloid leukemia (AML) therapeutic strategies have irreversible side-effects. Berberine (BBR) is an isoquinoline alkaloid, which has been known as an aryl hydrocarbon receptor (AhR) ligand. AhR is a cytoplasmic receptor, which is involved in the regulation of cellular and immune responses. Here, we investigated the expression profile of genes involved in the cell cyc...
اهداف: بالابودن غلظت سایتوکینهای پیشالتهابی اینترلوکین-1 بتا (IL-1β) و عامل نکروزدهنده تومور آلفا (TNF-α)، از عوامل خطر مهم برای ایجاد بیماری قلبی- عروقی بهشمار میرود. هدف پژوهش حاضر، بررسی اثر همزمان تمرین تناوبی شدید و مصرف مکمل روغن بذر کتان با دوزهای مختلف بر سطوح سرمی TNF-α و IL1β موشهای صحرایی بود. مواد و روشها: در این مطالعه تجربی، 30 سر موش صحرایی نژاد ویستار بهصورت تصادفی به ش...
Lysinuric protein intolerance (LPI) is a recessively inherited aminoaciduria caused by mutations of SLC7A7, the gene encoding y+LAT1 light chain of system y+L for cationic amino acid transport. The pathogenesis of LPI is still unknown. In this study, we have utilized a gene silencing approach in macrophages and airway epithelial cells to investigate whether complications affecting lung and immu...
Hereditary predisposition is one of the aetiopathogenetic factors in development gastric ulcer and duodenal ulcer. The analysis literature materials allows us to identify a number candidate genes that play role formation peptic ulcer: PSCA, ABO, IL1β, IL1RN, TNFα, HSP70-1, GSR, TLR4, TLR2, TLR9, MMP-1, MMP-3, MMP- 9, TIMP-3, PGC, MIF, MPO, COX-1. Considering most studies were carried out abroad...
Background: Osteoarthritis (OA) incidence has skyrocketed in the last decade and yet a definitive treatment still to be found. This worldwide disease is depriving our society from their life quality become grave economic burden. Research on anti-inflammatory tools been done traditional Asian medicine. Boswellic acid plant-derived molecule Boswellia species that shown prevent cartilage loss an O...
BACKGROUND Osteoarthritis (OA) is a degenerative joint disease characterised by cartilage degradation and chondrocyte hypertrophy. A recent study showed that Rac1 promoted expression of MMP13 and chondrocyte hypertrophy within the growth plate. These findings warrant further investigations on the roles of Rac1 in OA development and therapy in animal models. OBJECTIVE To investigate the role a...
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