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dc.contributor.authorBjånesøy, Trine Elholmen_US
dc.contributor.authorAndreassen, Bettina Kulleen_US
dc.contributor.authorBratland, Eiriken_US
dc.contributor.authorReiner, Andrew Henryen_US
dc.contributor.authorIslam, Shahinulen_US
dc.contributor.authorHusebye, Eystein Sverreen_US
dc.contributor.authorBakke, Mariten_US
dc.date.accessioned2014-12-02T13:12:21Z
dc.date.available2014-12-02T13:12:21Z
dc.date.issued2014-03-22eng
dc.identifier.issn0161-5890
dc.identifier.urihttps://hdl.handle.net/1956/8803
dc.description.abstractAutoimmune Addison's Disease (AAD) is an endocrine and immunological disease of uncertain pathogenesis resulting from the immune system's destruction of the hormone producing cells of the adrenal cortex. The underlying molecular mechanisms are largely unknown, but it is commonly accepted that a combination of genetic susceptibility and environmental impact is critical. In the present study, we identified multiple hypomethylated gene promoter regions in patients with isolated AAD using DNA isolated from CD4+ T cells. The identified differentially methylated regions were distributed evenly across the 10.5-kb-promoter regions covered by the array, and a substantial number localized to promoters of genes involved in immune regulation and autoimmunity. This study reveals a hypomethylated status in CD4+ T cells from AAD patients and indicates differential methylation of promoters of key genes involved in immune responses.en_US
dc.language.isoengeng
dc.publisherElseviereng
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/eng
dc.subjectDNA methylationeng
dc.subjectEpigeneticseng
dc.subjectAutoimmunityeng
dc.subjectAutoimmune Addison's Diseaseeng
dc.subjectAdrenal glandeng
dc.titleAltered DNA methylation profile in Norwegian patients with Autoimmune Addison’s Diseaseen_US
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2014 The Authors. Published by Elsevier Ltd
dc.identifier.doihttps://doi.org/10.1016/j.molimm.2014.02.018
dc.identifier.cristin1150327
dc.source.journalMolecular Immunology
dc.source.4059
dc.source.pagenumber208-216


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