LDR | | 01891nmm uu200397 4500 |
001 | | 000000332943 |
005 | | 20240805171901 |
008 | | 181129s2018 |||||||||||||||||c||eng d |
020 | |
▼a 9780355867145 |
035 | |
▼a (MiAaPQ)AAI10793699 |
035 | |
▼a (MiAaPQ)wustl:12518 |
040 | |
▼a MiAaPQ
▼c MiAaPQ
▼d 248032 |
082 | 0 |
▼a 616.079 |
100 | 1 |
▼a Briseno, Carlos Gustavo.
▼0 (orcid)0000-0002-4159-3864 |
245 | 10 |
▼a Transcriptional Regulation of Dendritic Cell Function. |
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 254 p. |
500 | |
▼a Source: Dissertation Abstracts International, Volume: 79-09(E), Section: B. |
500 | |
▼a Adviser: Kenneth M. Murphy. |
502 | 1 |
▼a Thesis (Ph.D.)--Washington University in St. Louis, 2018. |
506 | |
▼a This item is not available from ProQuest Dissertations & Theses. |
520 | |
▼a Dendritic cells (DCs) are professional antigen presenting cells conventionally thought to mediate cellular adaptive immune responses. DC diversification into functional subsets provides for modules of pathogen sensing and cytokine production tha |
520 | |
▼a A single master regulator of DC2 development has yet to be identified. The transcription factor RelB has been thought to be required for DC2 development. We found that DC development was independent of a cell-intrinsic action of RelB in most tis |
590 | |
▼a School code: 0252. |
650 | 4 |
▼a Immunology. |
690 | |
▼a 0982 |
710 | 20 |
▼a Washington University in St. Louis.
▼b Biology & Biomedical Sciences (Immunology). |
773 | 0 |
▼t Dissertation Abstracts International
▼g 79-09B(E). |
773 | |
▼t Dissertation Abstract International |
790 | |
▼a 0252 |
791 | |
▼a Ph.D. |
792 | |
▼a 2018 |
793 | |
▼a English |
856 | 40 |
▼u http://www.riss.kr/pdu/ddodLink.do?id=T14997765
▼n KERIS |
980 | |
▼a 201812
▼f 2019 |
990 | |
▼a 관리자 |