نتایج جستجو برای: ovar drb1

تعداد نتایج: 3166  

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...

Journal: :Joint Bone Spine 2021

To investigate the human leukocyte antigen (HLA) association with anti-synthetase syndrome (ASSD). We conducted largest immunogenetic HLA-DRB1 and HLA-B study to date in a homogeneous cohort of 168 Caucasian patients ASSD 486 ethnically matched healthy controls by sequencing-based-typing. A statistically significant increase HLA-DRB1*03:01 HLA-B*08:01 alleles compared was disclosed (26.2% versu...

Journal: :Bratislavske lekarske listy 2013
M Dzurilla M Vrlík M Homolová M Buc

109 patients (62 boys/men and 47 girls/women) suffering from bronchial asthma induced by pollen allergens were typed for HLA-DRB1 and -DQBl alleles, respectively, by a low resolution SSP technique. Frequencies of DRB1 alleles varied from 0.5 % to 16.1 %. The most frequent was HLA-DRB1*11 (16.1 %), the least frequent HLA-DRB1*09 (0.4 %). Occurrence rates of HLA-DQB1 alleles ranged from 2.3 % to ...

Journal: :Molecular medicine reports 2009
Damacio R Kaimen-Maciel Edna Maria V Reiche Sueli D Borelli Helena K Morimoto Fabiano C Melo Josiane Lopes Raffael F Dorigon Christiane Cavalet Elton M Yamaguchi Thiago L Silveira Waldir V Da Silva Elizabeth R Comini-Frota Doralina G Brum Souza Eduardo A Donadi

Multiple sclerosis (MS) is a chronic autoimmune demyelinating disease of the central nervous system that causes neurological disorders in young adults. Previous studies in various populations highlighted an association between the HLA-DRB1*15 allele and MS. This study investigated the association between HLA-DRB1*15 and other HLA-DRB1 alleles and MS in a Brazilian Caucasian population sample fr...

Journal: : 2023

Aim.To study the immunogenetic prerequisites of idiopathic recurrent spontaneous pregnancy losses in humans allo- and autoimmune genesis. Methods. PCR-SSP (polymerase chain reaction with sequence-specific primers). Results. A comprehensive analysis distribution frequency allelic variants HLA-DRB1, HLA-DQA1, HLA-DQB1 genes testifies to an increased risk a total homology 50 % or more couples pres...

Journal: :Memorias do Instituto Oswaldo Cruz 2012
Rita da Graça Carvalhal Frazão Corrêa Dorlene Maria Cardoso de Aquino Arlene de Jesus Mendes Caldas Humberto de Oliveira Serra Fábio França Silva Maxwellem de Jesus Costa Ferreira Elton Jonh Freitas Santos Emygdia Rosa Rêgo Barros Pires Leal Mesquita

Epidemiological studies have demonstrated that the variability of the clinical response to infection caused by Mycobacterium leprae is associated with host genetic factors. The present study investigated the frequency of human leukocyte antigen (HLA) class II (DRB1) alleles in patients with leprosy from São Luís, Maranhão, Brazil. A case-control study was performed in 85 individuals with lepros...

2015
Makoto Hirasawa Katsunobu Hagihara Noriko Okudaira Takashi Izumi Anne de Groot

Idiosyncratic lapatinib-induced liver injury has been reported to be associated with human leukocyte antigen (HLA)-DRB1*07:01. In order to investigate its mechanism, interaction of lapatinib with HLA-DRB1*07:01 and its ligand peptide derived from tetanus toxoid, has been evaluated in vitro. Here we show that lapatinib enhances binding of the ligand peptide to HLA-DRB1*07:01. Furthermore in sili...

Journal: :international journal of pediatrics 0
shirin farivar genetic department, faculty of biological sciences, shahid beheshti university, general campus, tehran, iran. masoud dehghan tezerjani genetic department, faculty of biological sciences, shahid beheshti university, general campus, tehran, iran. reza shiari department of pediatrics, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, iran.

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 ...

ژورنال: :genetics in the 3rd millennium 0
شیرین فریور shirin farivar دکتری ژنتیک، استادیار دانشگاه شهید بهشتی، دانشکده علوم زیستی الهام هادی elham hadi رضا شیاری reza shiari

آرتریت آیدیوپاتیک اطفال شایع ترین بیماری روماتیسمی در اطفال می باشد و در مناطق مختلف براساس معیارهای مورد بررسی شیوع متفاوتی دارد. در این مطالعه همراهی آلل های hla-drb1 در33 کودک ایرانی مبتلا به آرتریت روماتوئید جوانان اولیگوارتیکولار ارزیابی شد. نمونه خون از 33 کودک مبتلا به آرتریت روماتوئید اولیگوارتیکولار جوانان و 45 فرد سالم (بعنوان گروه کنترل) تهیه و از نظر همراهی آلل های hla-drb1 با هم مق...

2009
Xia Huang Hua Ling Wei Mao Xianbin Ding Quanhua Zhou Mei Han Fang Wang Lei Cheng Hongyan Xiong

BACKGROUND The human immunodeficiency virus type 1(HIV-1) epidemic in Chongqing, China, is increasing rapidly with the dominant subtype of CRF07_BC over the past 3 years. Since human leukocyte antigen (HLA) polymorphisms have shown strong association with susceptibility/resistance to HIV-1 infection from individuals with different ethnic backgrounds, a recent investigation on frequencies of HLA...

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