Utilize este identificador para referenciar este registo:
|Título:||Autoimmune diseases association study with the KIAA1109–IL2–IL21 region in a Tunisian population|
|Palavras-chave:||Systemic lupus erythematosus|
|Citação:||Bouzid, D., Fourati, H., Amouri, A. et al. Mol Biol Rep (2014) 41: 7133. https://doi.org/10.1007/s11033-014-3596-5|
|Resumo:||Autoimmune diseases (ADs) share several genetic factors resulting in similarity of disease mechanisms. For instance polymorphisms from the KIAA1109-interleukin 2 (IL2)-IL21 block in the 4q27 chromosome, has been associated with a number of autoimmune phenotypes. Here we performed a haplotype-based analysis of this AD related region in Tunisian patients. Ten single nucleotide polymorphisms (rs6534347, rs11575812, rs2069778, rs2069763, rs2069762, rs6852535, rs12642902, rs6822844, rs2221903, rs17005931) of the block were investigated in a cohort of 93 systemic lupus erythematosus (SLE), 68 ulcerative colitis (UC), 39 Crohn's disease (CD) patients and 162 healthy control subjects of Tunisian origin. In SLE population, haplotypes AGCAGGGTC, AGAAGAGTC, AGAAGGGTC and AGCCGAGTC provided significant evidence of association with SLE risk (p = 0.013, 0.028, 0.018 and 0.048, respectively). In the UC population, haplotype AGCCGGGTC provided a susceptibility effect for UC (p = 0.025). In the CD population, haplotype CAGGCC showed a protective effect against the development of CD (p = 0.038). Haplotype AAGGTT provided significant evidence to be associated with CD risk (p = 0.007). Our results support the existence of the associations found in the KIAA1109/IL2/IL21 gene region with ADs, thus confirms that the 4q27 locus may contribute to the genetic susceptibility of ADs in the Tunisian population.|
|Descrição:||This deposit is composed by a publication in which the IGC's authors have had the role of collaboration (it's a collaboration publication). This type of deposit in ARCA is in restrictedAccess (it can't be in open access to the public), and can only be accessed by two ways: either by requesting a legal copy from the author (the email contact present in this deposit) or by visiting the following link: https://link.springer.com/article/10.1007%2Fs11033-014-3596-5|
This deposit is composed by the main article plus the supplementary materials of the publication.
This publication hasn't any creative commons license associated.
Further funders are not indicated in the document.
|Versão do Editor:||https://link.springer.com/article/10.1007%2Fs11033-014-3596-5|
|Aparece nas colecções:||DG - Artigos em revistas científicas|
Ficheiros deste registo:
|Bouzid,D._Mol.Biol.Rep._(2014).pdf||main article||454,84 kB||Adobe PDF||Ver/Abrir Acesso Restrito. Solicitar cópia ao autor!|
|Bouzid,D._Mol.Biol.Rep._(2014)_SM.pdf||supplementary materials||196,66 kB||Adobe PDF||Ver/Abrir Acesso Restrito. Solicitar cópia ao autor!|
Todos os registos no repositório estão protegidos por leis de copyright, com todos os direitos reservados.