LDR | | 00000nam u2200205 4500 |
001 | | 000000434076 |
005 | | 20200226140458 |
008 | | 200131s2019 ||||||||||||||||| ||eng d |
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▼a 9781085608848 |
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▼a (MiAaPQ)AAI13896339 |
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▼a MiAaPQ
▼c MiAaPQ
▼d 247004 |
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▼a 616 |
100 | 1 |
▼a Wang, Haiguang. |
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▼a How Lipid Specific T Cells become Effectors. |
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▼a [S.l.]:
▼b University of Minnesota.,
▼c 2019. |
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▼a Ann Arbor:
▼b ProQuest Dissertations & Theses,
▼c 2019. |
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▼a 177 p. |
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▼a Source: Dissertations Abstracts International, Volume: 81-02, Section: B. |
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▼a Advisor: Hogquist, Kristin A. |
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▼a Thesis (Ph.D.)--University of Minnesota, 2019. |
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▼a This item must not be sold to any third party vendors. |
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▼a This item must not be added to any third party search indexes. |
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▼a Invariant natural killer T (iNKT) cells are composed of at least three functionally distinct subsets, NKT1, NKT2 and NKT17. Through selective activation of these three iNKT effector subsets, iNKT cells can modulate immune responses and tissue homeostasis in different fashions. However, the developmental steps that drive iNKT cells into functional distinct subsets have not been elucidated, and thus their potential to be utilized in anti-cancer or autoimmune immunotherapies has not been realized, despite the fact that iNKT stimulatory lipids are well-tolerated in human trials. My dissertation research aims to fill this knowledge gap by investigating the following aspects of iNKT biology: 1) characterizing the multipotent progenitor for the iNKT effector subsets (in chapter 2) |
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▼a School code: 0130. |
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▼a Immunology. |
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▼a 0982 |
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▼a University of Minnesota.
▼b Comparative and Molecular Biosciences. |
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▼t Dissertations Abstracts International
▼g 81-02B. |
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▼t Dissertation Abstract International |
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▼a 0130 |
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▼a Ph.D. |
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▼a 2019 |
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▼a English |
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▼u http://www.riss.kr/pdu/ddodLink.do?id=T15491705
▼n KERIS
▼z 이 자료의 원문은 한국교육학술정보원에서 제공합니다. |
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▼a 202002
▼f 2020 |
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▼a ***1816162 |
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▼a E-BOOK |