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1 ence of RNA, presumably for interaction with Toll-like receptor 7.
2 highly conserved cysteine residue (Cys98) on Toll-like receptor-7.
3 d RNA of HIV-1 encodes multiple uridine-rich Toll-like receptor 7/8 (TLR7/8) ligands that induce stro
4 cal intravital microscopy, we show that upon Toll-like receptor 7/8 (TLR7/8)-mediated inflammation of
5 -201 cells, can be activated by the specific Toll-like receptor 7/8 activator, R848, to release TNFal
6 application of Aldara cream, containing the Toll-like receptor 7/8 agonist Imiquimod, is a widely us
7 ammatory conditions, exposure of APCs to the Toll-like receptor 7/8 agonist R848 increases nanocluste
12 d produced significantly less IFN-alpha upon Toll-like receptor 7/9 (TLR7/9) engagement than controls
13 Nucleic acids from microbes are sensed by Toll-like receptors 7/9 (TLR7/9), which are selectively
16 polyomavirus (JCV) capsid protein VP1, and a Toll-like receptor 7 agonist used as adjuvant, was well
17 e isolated from whole blood, stimulated with Toll-like receptor 7 agonist, and analyzed by means of e
22 ing recombinant Sm-p80 protein formulated in Toll-like receptor 7 and Toll-like receptor 9 agonists,
23 ce interferon alpha following stimulation of Toll-like receptor 7 and upregulation of interferon-stim
24 y to produce type I IFN after challenge with Toll-like receptor-7 and -9 ligands, or murine cytomegal
26 re inhibited by ligation of Fc receptors and Toll-like receptors 7 and 8 in a PKCbeta-dependent manne
27 B cells and plasmacytoid dendritic cells via Toll-like receptors 7 and 9 suggested that agents that b
28 ferentiation and T cell activation, activate Toll-like receptor 7, and are linked to neurodegeneratio
29 ficiency in FcgammaRIIB or overexpression of Toll-like receptor 7 are protected from death caused by
32 us sensing occurred in endosomes via a MyD88-Toll-like receptor 7-dependent mechanism and stimulated
33 spectively, retaining the ability to trigger Toll-like receptor 7 exclusively, and expanded human all
35 ce was associated with an increase in B cell Toll-like receptor 7 expression, increased serum levels
36 cells both in vivo and in vitro, leading to Toll-like receptor 7 hyporesponsiveness and impaired IFN
37 Ankara (MVA) boost) and stimulation of TLR7 (Toll-like receptor 7) improves virologic control and del
39 tive orally active small molecule agonist of Toll-like receptor 7--in chimpanzees with chronic HBV in
40 macytoid dendritic cell (pDC) activation via Toll-like receptor 7, inducing type I IFN and inflammato
41 ABCs and demonstrated that signaling through Toll-like receptor 7 is crucial for development of this
42 et al. used mouse models to demonstrate that Toll-like receptor 7 is required for the generation of a
45 it, colony stimulating factor 3 receptor and toll-like receptor 7 mRNA expression increases in the th
47 l replication, direct cell-cell contact, and Toll-like receptor 7 signaling, and we show that the act
49 otypes and clinical phenotypes, and assessed Toll-like receptor 7 (TLR-7)-stimulated MIF production i
53 molecule immune response modifier that is a Toll-like receptor 7 (TLR7) agonist induces IL-12 and TN
54 od is a topical immune response modifier and Toll-like receptor 7 (TLR7) agonist that induces the imm
55 eport that intravenous administration of the Toll-like receptor 7 (TLR7) agonist, R848 in combination
58 use in plasmacytoid DC (pDC) stimulated with Toll-like receptor 7 (TLR7) agonists, Erk1/2 activation
60 ues report that platelets express functional TOLL-like receptor 7 (TLR7) and contribute to host survi
61 se include endosomal recognition through the Toll-like receptor 7 (TLR7) and cytosolic recognition th
62 e maturation of dendritic cells (DC) through Toll-like receptor 7 (TLR7) and its adaptor molecule MyD
63 e plasmacytoid dendritic cells (pDC) through Toll-like receptor 7 (TLR7) and its adaptor molecule, My
65 on pattern-recognition receptors, including Toll-like receptor 7 (TLR7) and retinoic acid inducible
66 acid-binding innate immune receptors such as Toll-like receptor 7 (TLR7) and TLR9 have been implicate
68 we present evidence showing that a ligand of Toll-like receptor 7 (TLR7) can induce anti-HCV immunity
73 shown that a moderate increase of the innate Toll-like receptor 7 (TLR7) is sufficient for the develo
74 pha (IFN-alpha) in response to HIV-1-encoded Toll-like receptor 7 (TLR7) ligands than pDCs derived fr
76 s to viruses that are recognized through the Toll-like receptor 7 (TLR7) or TLR9 signaling pathway.
77 ne innate inflammatory responses mediated by Toll-like receptor 7 (TLR7) remain to be fully elucidate
82 differentiation-associated gene 5 (MDA5) and Toll-like receptor 7 (TLR7) to induce transcription of t
86 endosomal uptake, and probably signaling via Toll-like receptor 7 (TLR7) were critical for sensing of
87 ic stimulation via B-cell antigen receptors, toll-like receptor 7 (TLR7), and IFNgamma receptors on B
88 ess pattern recognition receptors, including Toll-like receptor 7 (TLR7), which recognizes guanosine-
89 nity-purified anti-Ro60 antibody induces the Toll-like receptor 7 (TLR7)-dependent generation of supe
91 interferon (IFN-alpha/beta) production in a Toll-like receptor 7 (TLR7)-dependent, virus-independent
92 We investigated the hypothesis that reduced Toll-like receptor 7 (TLR7)-derived signaling drove the
98 a new systemic immunostimulatory agent, the Toll-like receptor-7 (TLR7) agonist R848, to augment rad
99 r rapid excitation of nociceptor neurons via toll-like receptor-7 (TLR7) and its coupling to TRPA1 io
100 Imiquimod is a small-molecule ligand of Toll-like receptor-7 (TLR7) that is licensed for the tre
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