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dc.contributor.authorDelaleu, Nicolas Hervéen_US
dc.contributor.authorNguyen, Cuong Q.en_US
dc.contributor.authorPeck, Ammon B.en_US
dc.contributor.authorJonsson, Rolanden_US
dc.date.accessioned2012-01-20T12:17:28Z
dc.date.available2012-01-20T12:17:28Z
dc.date.issued2011-06-13eng
dc.PublishedArthritis Research & Therapy 2011, 13:217en
dc.identifier.issn1478-6354
dc.identifier.urihttps://hdl.handle.net/1956/5476
dc.description.abstractSjögren’s syndrome (SS), a systemic autoimmune disease, is characterized by infl ammation of exocrine tissues accompanied by a signifi cant loss of their secretory function. Clinical symptoms develop late and there are no diagnostic tests enabling early diagnosis of SS. Thus, particularly to study these covert stages, researchers turn to studying animal models where mice provide great freedom for genetic manipulation and testing the eff ect of experimental intervention. The present review summarizes current literature pertaining to both spontaneous and extrinsic-factor induced SS-like diseases in mouse models, discussing advantages and disadvantages related to the use of murine models in SS research.en_US
dc.language.isoengeng
dc.publisherBioMed Centraleng
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/2.0/eng
dc.titleSjögren’s syndrome: studying the disease in miceen_US
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2011 BioMed Central Ltd.
dc.identifier.doihttps://doi.org/10.1186/ar3313
dc.subject.nsiVDP::Medical disciplines: 700eng


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