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LDR02019nmm uu200421 4500
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00520240805163347
008181129s2018 |||||||||||||||||c||eng d
020 ▼a 9780438146495
035 ▼a (MiAaPQ)AAI10837209
035 ▼a (MiAaPQ)ucla:17129
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0820 ▼a 612
1001 ▼a Jacob, Noam.
24510 ▼a Contributors to Intestinal Fibrosis in the TNFSF15/TL1A Pathway.
260 ▼a [S.l.] : ▼b University of California, Los Angeles., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 111 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.
500 ▼a Adviser: Joseph R. Pisegna.
5021 ▼a Thesis (Ph.D.)--University of California, Los Angeles, 2018.
520 ▼a Tumor necrosis factor-like cytokine 1A (TL1A, TNFSF15) is implicated in inflammatory bowel disease (IBD), modulating the location and severity of intestinal inflammation and fibrosis. TL1A expression is increased in inflamed gut mucosa and assoc
520 ▼a We show that the gut microbiome is required for TL1A-mediated intestinal fibrosis and optimal fibroblast activation into myofibroblasts. Moreover, we provide evidence that the TL1A-mediated intestinal fibrotic phenotype requires cues provided by
520 ▼a To evaluate for a selective role of direct TL1A-DR3 signaling on fibroblasts in fibrostenosing IBD, TL1A over-expressing naive T cells (Tl1a-Tg) were transferred into Rag-/- mice
590 ▼a School code: 0031.
650 4 ▼a Physiology.
650 4 ▼a Biology.
690 ▼a 0719
690 ▼a 0306
71020 ▼a University of California, Los Angeles. ▼b Molec, Cell, & Integ Physiology 0568.
7730 ▼t Dissertation Abstracts International ▼g 79-12B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0031
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14999547 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자