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020 ▼a 9780355663044
035 ▼a (MiAaPQ)AAI10745010
035 ▼a (MiAaPQ)wustl:12421
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0491 ▼f DP
0820 ▼a 616.99
1001 ▼a Meyer, Melissa A. ▼0 (orcid)0000-0003-3050-4819
24510 ▼a Tumors Interrupt IRF8-Mediated Dendritic Cell Development to Overcome Immune Surveillance.
260 ▼a [S.l.] : ▼b Washington University in St. Louis., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 119 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-07(E), Section: B.
500 ▼a Adviser: David G. DeNardo.
5021 ▼a Thesis (Ph.D.)--Washington University in St. Louis, 2018.
506 ▼a This item is not available from ProQuest Dissertations & Theses.
520 ▼a Tumors employ multiple mechanisms to evade immune surveillance. One mechanism is tumor-induced myelopoiesis, which expands immune suppressive granulocytes and monocytes to create a protective tumor niche shielding even antigenic tumors. As myelo
590 ▼a School code: 0252.
650 4 ▼a Oncology.
650 4 ▼a Cellular biology.
650 4 ▼a Immunology.
690 ▼a 0992
690 ▼a 0379
690 ▼a 0982
71020 ▼a Washington University in St. Louis. ▼b Biology & Biomedical Sciences (Molecular Cell Biology).
7730 ▼t Dissertation Abstracts International ▼g 79-07B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0252
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14996844 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자 ▼b 관리자