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Article: GITRL modulates the activities of p38 MAPK and STAT3 to promote Th17 cell differentiation in autoimmune arthritis

TitleGITRL modulates the activities of p38 MAPK and STAT3 to promote Th17 cell differentiation in autoimmune arthritis
Authors
KeywordsAutoimmune arthritis
GITRL
Immune response
Immunity
Immunology and Microbiology Section
P38 MAPK
STAT3
Th17 cells
Issue Date2016
PublisherImpact Journals LLC. The Journal's web site is located at http://www.impactjournals.com/oncotarget/index.html
Citation
Oncotarget, 2016, v. 7 n. 8, p. 8590-8600 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/232150
ISSN
2016 Impact Factor: 5.168
2020 SCImago Journal Rankings: 1.373
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorTang, X-
dc.contributor.authorTian, J-
dc.contributor.authorMa, J-
dc.contributor.authorWang, J-
dc.contributor.authorQi, C-
dc.contributor.authorRui, K-
dc.contributor.authorWang, Y-
dc.contributor.authorXu, H-
dc.contributor.authorLu, L-
dc.contributor.authorWang, S-
dc.date.accessioned2016-09-20T05:28:04Z-
dc.date.available2016-09-20T05:28:04Z-
dc.date.issued2016-
dc.identifier.citationOncotarget, 2016, v. 7 n. 8, p. 8590-8600-
dc.identifier.issn1949-2553-
dc.identifier.urihttp://hdl.handle.net/10722/232150-
dc.languageeng-
dc.publisherImpact Journals LLC. The Journal's web site is located at http://www.impactjournals.com/oncotarget/index.html-
dc.relation.ispartofOncotarget-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAutoimmune arthritis-
dc.subjectGITRL-
dc.subjectImmune response-
dc.subjectImmunity-
dc.subjectImmunology and Microbiology Section-
dc.subjectP38 MAPK-
dc.subjectSTAT3-
dc.subjectTh17 cells-
dc.titleGITRL modulates the activities of p38 MAPK and STAT3 to promote Th17 cell differentiation in autoimmune arthritis-
dc.typeArticle-
dc.identifier.emailLu, L: liweilu@hkucc.hku.hk-
dc.identifier.authorityLu, L=rp00477-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.18632/oncotarget.6535-
dc.identifier.scopuseid_2-s2.0-84961665290-
dc.identifier.hkuros264626-
dc.identifier.volume7-
dc.identifier.issue8-
dc.identifier.spage8590-
dc.identifier.epage8600-
dc.identifier.isiWOS:000375618100012-
dc.publisher.placeUnited States-
dc.identifier.issnl1949-2553-

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