نتایج جستجو برای: hla
تعداد نتایج: 40049 فیلتر نتایج به سال:
مالتیپل اسکلروزیس یکی از معمول ترین بیماری های التهابی و تحلیل برنده دستگاه عصبی مرکزی است و مجموعه ای از عوامل ژنتیکی و محیطی در ایجاد آن نقش دارند. ناحیه کد کننده آنتی ژن گلبول های سفید انسانی(hla) مهمترین ناحیه ای است که با استعداد ابتلا به بیماری ارتباط دارد. تاکنون درمان قطعی برای این بیماری یافت نشده است و اثرات بیماری به کمک داروهای تعدیل کننده بیماری کنترل می شود. یکی از متداول ترین این...
Objective(s): Juvenile idiopathic arthritis (JIA) is one of the most common chronic rheumatic diseases in children. The complex nature of this immune-mediated disease owes itself to several predisposing genes and environmental factors affecting its pathogenesis. Conducted in Iran, this study was originally intended to investigate every possible association between HLA DRB1 alleles and a suscept...
Background: Multiple sclerosis (MS), as a multifactorial autoimmune disease with complex genetic basis, causes demyelination in the central nervous system via cytokine responses to myelin antigens. Myelin basic protein (MBP) is the main protein component of the myelin sheath. HLA-DRB (human leukocyte antigen-DR beta) alleles, particularly HLA-DRB1*1501, may be of significance in the pathogenesi...
Background and purpose: Alopecia areata (AA), also known as spot baldness, is an autoimmune disease in which hair is lost from some or all areas of the body. Genetic factors are known to play a role in the onset of this disease. The HLA complex genes are primarily involved in AA. In present study, effect of HLA-DQA2 allele frequency was analyzed in Iranian AA patients and control samples. Mate...
Background and purpose: Preeclampsia is a pregnancy complication with multiorgan involvement caused by the loss of mother's immune tolerance to the placenta and fetus antigen or the wrong adjustment. HLA-G is an immune-modulatory molecule and this study aimed at investigating the levels of HLA-G and its association with incidence and severity of preeclampsia in pregnant women in third trimester...
The current coronavirus disease 2019 (COVID-19) pandemic that is caused by the severe acute respiratory syndrome 2 (SARS-CoV-2) has a significant threat to public health. Although vaccines based on mRNA of SARS-CoV-2 spike protein have been developed induce both cellular and humoral immunity against SARS-CoV-2, there some concerns raised about their high cost, particularly in developing countri...
objective: this study aimed to investigate the association between hla alleles and visceral leishmaniasis (vl) in a sample of iraqi patients. methods: a total of 30 patients were studied, in addition to 20 age, gender and ethnicity matched controls. all subjects were genotyped by polymerase chain reaction-sequence specific primers (pcr-ssp) method. results: for hla-class i region (a and b loci)...
introduction systemic lupus erythematosus (sle) is a complex autoimmune and inflammatory disease. many studies show hla alleles can be associated with sle. the aim of this study was to determine the association of hla-drb1 alleles with juvenile- onset in iranian children. materials and methods at a case – control study, 31 children with systemic lupus erythematosus (case group) who referred to ...
Papillon Lefevre Syndrome (PLS) is a rare disease, associated with the early onset periodontal break down in deciduous and permanent dentition.The etiology of PLS is not exactly determined but recently, mutation in catespin C gene, as a genetic basis for the disease, has been established. The aim of this study was to investigate the HLA status in patients affected with PLS. In this research, th...
background: a common human leukocyte antigen (hla) class ii allele, dqβ1*03:01, seems to be associated with bullous pemphigoid (bp) in caucasians whereas previous studies in other ethnic groups showed other hla class ii alleles as genetic predisposing factors for bp. objective: to investigate the association of hla class ii alleles and haplotypes with bp in iranian population. methods: fifty pa...
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