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020 ▼a 9780438190627
035 ▼a (MiAaPQ)AAI10829391
035 ▼a (MiAaPQ)mayo:10497
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0491 ▼f DP
0820 ▼a 576.6
1001 ▼a Kumar, Swati.
24510 ▼a Sensing of HIV-1 by the Innate Immune System.
260 ▼a [S.l.] : ▼b College of Medicine - Mayo Clinic., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 160 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.
500 ▼a Advisers: David Dingli
5021 ▼a Thesis (Ph.D.)--College of Medicine - Mayo Clinic, 2018.
520 ▼a TREX1, a major mammalian exonuclease, has been reported to degrade cytosolic immune-stimulatory DNA, including viral DNA generated during HIV-1 infection, but the dynamic range of its capacity to suppress innate immune stimulation is unknown, wh
520 ▼a The nearly complete lack of innate immune induction despite equal to increased viral integration observed when the TREX1 protein level is experimentally elevated indicates that integration-competent genomes are shielded from cytosolic sensor-eff
520 ▼a In the second part of this thesis, we investigate how perturbations of the intricately linked early post entry events of reverse transcription and uncoating and remodeling of viral cores affect sensing of viral nucleic acids. Reverse transcripti
520 ▼a Taken together, our studies showed that the PAMPs sensed after viral entry contain DNA, are TREX1 and cGAS substrates, and are derived from incomplete reverse transcription products. In contrast, the experiments demonstrated that full-length int
590 ▼a School code: 1542.
650 4 ▼a Virology.
690 ▼a 0720
71020 ▼a College of Medicine - Mayo Clinic. ▼b Virology and Gene Therapy.
7730 ▼t Dissertation Abstracts International ▼g 79-12B(E).
773 ▼t Dissertation Abstract International
790 ▼a 1542
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14999300 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자 ▼b 관리자