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https://scholarbank.nus.edu.sg/handle/10635/49083
DC Field | Value | |
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dc.title | STAT5 REGULATES HELPER T CELL LINEAGE COMMITMENT AND AUTOIMMUNITY | |
dc.contributor.author | SHENG WANQIANG | |
dc.date.accessioned | 2014-01-24T18:00:06Z | |
dc.date.available | 2014-01-24T18:00:06Z | |
dc.date.issued | 2013-08-07 | |
dc.identifier.citation | SHENG WANQIANG (2013-08-07). STAT5 REGULATES HELPER T CELL LINEAGE COMMITMENT AND AUTOIMMUNITY. ScholarBank@NUS Repository. | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/49083 | |
dc.description.abstract | CD4+ T cells play crucial roles in host defense against various pathogens by orchestrating adaptive immune responses. Upon T-cell receptor activation by cognate antigen, naive CD4+ T cells are committed to differentiate into at least five major lineages: Th1, Th2, Th17, iTeg and Tfh cells, which are orchestrated by cytokine milieus signaling through Signal Transducer and Activa?tor of Transcription (STAT) family proteins. In my project, I have studied the regulatory roles of STAT5 in CD4+ T cell lineage commitment and two types of autoimmune diseases: experimental autoimmune encephalomyelitis and T cell-transfer colitis. | |
dc.language.iso | en | |
dc.subject | Helper T cell, lineage commitment, STAT5, GM-CSF, EAE, colitis | |
dc.type | Thesis | |
dc.contributor.department | BIOLOGICAL SCIENCES | |
dc.contributor.supervisor | FU XIN-YUAN | |
dc.description.degree | Ph.D | |
dc.description.degreeconferred | DOCTOR OF PHILOSOPHY | |
dc.identifier.isiut | NOT_IN_WOS | |
Appears in Collections: | Ph.D Theses (Open) |
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PhD thesis_NUS_Sheng Wanqiang_v3.pdf | 16.56 MB | Adobe PDF | OPEN | None | View/Download |
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