نتایج جستجو برای: rs1004819

تعداد نتایج: 15  

Journal: :Rheumatology 2013
Bruno Filipe Bettencourt Fabiana Leal Rocha Helena Alves Rosa Amorim Joana Caetano-Lopes Elsa Vieira-Sousa Fernando Pimentel-Santos Manuela Lima Graça Porto Jaime C Branco João Eurico Fonseca Jácome Bruges-Armas

OBJECTIVE The association of non-MHC genes with AS has been recently suggested. We aimed to investigate the association of the ERAP1, IL23R and TNFSF15 regions and the susceptibility to and protection from AS in HLA-B27-positive individuals. METHODS A total of 200 unrelated AS patients and 559 healthy unrelated subjects, all HLA-B27 positive, were tested. Twenty single nucleotide polymorphism...

2017
Sarah Fischer Erzsébet Kövesdi Lili Magyari Veronika Csöngei Kinga Hadzsiev Béla Melegh Péter Hegyi Patrícia Sarlós

AIM To investigate the association of seven single nucleotide polymorphisms (SNPs) of the IL23R gene with the clinical picture of ulcerative colitis (UC). METHODS Genomic DNA samples of 131 patients (66 males, 65 females, mean age 55.4 ± 15.8 years) with Caucasian origin, diagnosed with UC were investigated. The diagnosis of UC was based on the established clinical, endoscopic, radiological, ...

Journal: :Digestive surgery 2012
Ziad Kanaan Surriya Ahmad Natalia Bilchuk Crystal Vahrenhold Jianmin Pan Susan Galandiuk

AIM To investigate genotype-phenotype correlations in patients with perianal Crohn's disease (PCD) in order to determine which factors predispose to development of perianal disease in Crohn's patients. METHODS Seven-hundred and ninety-five Caucasian individuals (317 CD patients and 478 controls without inflammatory bowel disease, IBD) were prospectively enrolled into a clinical/genetic databa...

Journal: :Clinical and experimental rheumatology 2009
F M Pimentel-Santos D Ligeiro M Matos A F Mourão E Sousa P Pinto A Ribeiro M Sousa A Barcelos F Godinho M Cruz J E Fonseca H Guedes-Pinto H Trindade D M Evans M A Brown J C Branco

OBJECTIVE Association between ankylosing spondylitis (AS) and two genes, ERAP1 and IL23R, has recently been reported in North American and British populations. The population attributable risk fraction for ERAP1 in this study was 25%, and for IL23R, 9%. Confirmation of these findings to ERAP1 in other ethnic groups has not yet been demonstrated. We sought to test the association between single ...

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