Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/49083
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dc.titleSTAT5 REGULATES HELPER T CELL LINEAGE COMMITMENT AND AUTOIMMUNITY
dc.contributor.authorSHENG WANQIANG
dc.date.accessioned2014-01-24T18:00:06Z
dc.date.available2014-01-24T18:00:06Z
dc.date.issued2013-08-07
dc.identifier.citationSHENG WANQIANG (2013-08-07). STAT5 REGULATES HELPER T CELL LINEAGE COMMITMENT AND AUTOIMMUNITY. ScholarBank@NUS Repository.
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/49083
dc.description.abstractCD4+ 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.isoen
dc.subjectHelper T cell, lineage commitment, STAT5, GM-CSF, EAE, colitis
dc.typeThesis
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.contributor.supervisorFU XIN-YUAN
dc.description.degreePh.D
dc.description.degreeconferredDOCTOR OF PHILOSOPHY
dc.identifier.isiutNOT_IN_WOS
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