نتایج جستجو برای: hla drb1

تعداد نتایج: 40277  

2010
Misa Suzuki Akira Meguro Masao Ota Eiichi Nomura Tetsuo Kato Naoko Nomura Kenji Kashiwagi Fumihiko Mabuchi Hiroyuki Iijima Kazuhide Kawase Tetsuya Yamamoto Makoto Nakamura Akira Negi Takeshi Sagara Teruo Nishida Masaru Inatani Hidenobu Tanihara Makoto Aihara Makoto Araie Takeo Fukuchi Haruki Abe Tomomi Higashide Kazuhisa Sugiyama Takashi Kanamoto Yoshiaki Kiuchi Aiko Iwase Shigeaki Ohno Hidetoshi Inoko Nobuhisa Mizuki

PURPOSE Normal tension glaucoma (NTG) is a subtype of glaucoma in which intraocular pressure is within the statistically normal range. NTG may be associated with an immune disorder. The aim of this study was to determine whether specific alleles in the human leukocyte antigen (HLA)-DRB1 and HLA-DQB1 genes correlated with NTG in Japanese patients. METHODS We genotyped the HLA-DRB1 and HLA-DQB1...

Batool Mutar Mahdi Haider Hashim Zalzala Hyam Raouf Laheeb Ali Abid Tawfik Jasim Mohammad Al-Marzook Zena Nehad

Background: Cholecystitis is one of the major digestive diseases. Its prevalence is particularly high in some populations. Significant risk factors associated with cholecystitis include age, sex, obesity, diet, parity and type 2 diabetes. Objective: To determine the association between HLA-DRB1 and cholecystitis. Methods: This casecontrol study included forty Iraqi Arab patients who had cholecy...

Journal: :Clinical and vaccine immunology : CVI 2008
Najat Mahdi Khadija Al-Ola Abeer M Al-Subaie Muhallab E Ali Zaid Al-Irhayim A Qader Al-Irhayim Wassim Y Almawi

We investigated the association of HLA class II alleles and haplotypes with sickle cell anemia vaso-occlusive crisis (VOC). DRB1*100101 was positively associated, while DRB1*140101, DRB1*150101, and DQB1*060101 were negatively associated, with VOC. Both susceptible (DRB1*100101-DQB1*050101) and protective (DRB1*110101-DQB1*030101 and DRB1*150101-DQB1*060101) haplotypes were identified, indicati...

Journal: :The European respiratory journal 2016
Johan Grunewald Ylva Kaiser Mahyar Ostadkarampour Natalia V Rivera Francesco Vezzi Britta Lötstedt Remi-André Olsen Lina Sylwan Sverker Lundin Max Käller Tatiana Sandalova Kerstin M Ahlgren Jan Wahlström Adnane Achour Marcus Ronninger Anders Eklund

In pulmonary sarcoidosis, CD4(+) T-cells expressing T-cell receptor Vα2.3 accumulate in the lungs of HLA-DRB1*03(+) patients. To investigate T-cell receptor-HLA-DRB1*03 interactions underlying recognition of hitherto unknown antigens, we performed detailed analyses of T-cell receptor expression on bronchoalveolar lavage fluid CD4(+) T-cells from sarcoidosis patients.Pulmonary sarcoidosis patien...

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2009
H M Farouk H E Mansour S A Rahman A A Mostafa H A Shamy W A Zarouk

Our objective was to determine whether the presence of the human leukocyte antigen HLA-DRB1 locus is associated with production of anti-cyclic citrullinated peptide antibodies (anti-CCP Abs) and to what extent they are associated with increased susceptibility to and severity of rheumatoid arthritis (RA) in Egyptian patients. Twenty-nine RA patients gave informed consent to participate in a case...

Journal: :Annals of the rheumatic diseases 2008
A L Feitsma A H M van der Helm-van Mil T W J Huizinga R R P de Vries R E M Toes

Rheumatoid arthritis (RA) is a complex genetic disorder in which the HLA region contributes most to the genetic risk. HLA-DRB1 molecules containing the amino acid sequence QKRAA/QRRAA/RRRAA (ie, HLA-DRB1*0101, *0102, *0401, *0404, *0405, *0408, *0410, *1001 and *1402) at position 70-74 in the third hypervariable region of the DRB1 chain are associated with susceptibility to RA. HLA-DRB1 molecul...

2018
Douglas S Goodin Pouya Khankhanian Pierre-Antoine Gourraud Nicolas Vince

OBJECTIVE To determine the relationship between highly-conserved extended-haplotypes (CEHs) in the major histocompatibility complex (MHC) and MS-susceptibility. BACKGROUND Among the ~200 MS-susceptibility regions, which are known from genome-wide analyses of single nucleotide polymorphisms (SNPs), the MHC accounts for roughly a third of the currently explained variance and the strongest MS-as...

2015
Ettie M. Lipner Yaron Tomer Janelle A. Noble Maria C. Monti John T. Lonsdale Barbara Corso David A. Greenberg

We conducted linkage analysis to follow up earlier work on microvascular complications of type 1 diabetes (T1D). We analyzed 415 families (2,008 individuals) previously genotyped for 402 SNP markers spanning chromosome 6. We did linkage analysis for the phenotypes of retinopathy and nephropathy. For retinopathy, two linkage peaks were mapped: one located at the HLA region and another novel locu...

Journal: :PLoS Genetics 2009
Sreeram V. Ramagopalan Narelle J. Maugeri Lahiru Handunnetthi Matthew R. Lincoln Sarah-Michelle Orton David A. Dyment Gabriele C. DeLuca Blanca M. Herrera Michael J. Chao A. Dessa Sadovnick George C. Ebers Julian C. Knight

Multiple sclerosis (MS) is a complex trait in which allelic variation in the MHC class II region exerts the single strongest effect on genetic risk. Epidemiological data in MS provide strong evidence that environmental factors act at a population level to influence the unusual geographical distribution of this disease. Growing evidence implicates sunlight or vitamin D as a key environmental fac...

Journal: :Tissue antigens 2011
L Matevosyan S Chattopadhyay V Madelian S Avagyan M Nazaretyan A Hyussian E Vardapetyan R Arutunyan F Jordan

Human leukocyte antigen (HLA)-A, HLA-B, and HLA-DRB1 gene frequencies were investigated in 4279 unrelated Armenian bone marrow donors. HLA alleles were defined by using PCR amplification with sequence specific primers (PCR-SSP) high- and low-resolution kits. The aim of this study was to examine the HLA diversity at the high-resolution level in a large Armenian population sample, and to compare ...

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