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020 ▼a 9780438342866
035 ▼a (MiAaPQ)AAI10841672
035 ▼a (MiAaPQ)uab:12401
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0820 ▼a 616.079
1001 ▼a Shin, Boyoung.
24510 ▼a Regulation of Effector CD4 T Cell Pathogenicity during Chronic Inflammation.
260 ▼a [S.l.] : ▼b The University of Alabama at Birmingham., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 148 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 80-01(E), Section: B.
500 ▼a Adviser: Laurie E. Harrington.
5021 ▼a Thesis (Ph.D.)--The University of Alabama at Birmingham, 2018.
520 ▼a Effector CD4 T cells are essential for the balance between pro- and anti-inflammatory immune responses during homeostasis. Dysregulation of effector CD4 T cell responses results in chronic inflammatory disorders such as Inflammatory Bowel Diseas
520 ▼a Different subsets of effector CD4 T cells utilize distinct metabolic pathways. We find that Th17 differentiation occurs in conjunction with a robust increase of ATP-linked mitochondrial respiration, which fuels energy demand. Interestingly, mito
520 ▼a We also find that the differentiation state of CD4 T cells contributes to pathogenicity. A transcriptome analysis of effector CD4 T cells from chronic intestinal inflammation reveals that CD4 T cells exist as a spectrum of differentiation states
590 ▼a School code: 0005.
650 4 ▼a Immunology.
690 ▼a 0982
71020 ▼a The University of Alabama at Birmingham. ▼b Joint Health Sciences.
7730 ▼t Dissertation Abstracts International ▼g 80-01B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0005
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14999798 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자