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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
8                                Activation of Toll-like receptor 7/8 by means of topical application o
9      We show that activation of pDCs through Toll-like receptor 7/8 suppresses ILC2-mediated AHR and
10              Administration of an agonist to toll-like receptor-7/8, a receptor expressed primarily o
11  patients, following in vitro stimulation of Toll-like receptors 7/8.
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
14                        On treatment with the toll-like receptor 7 agonist imquimod (IMQ), Trim32 knoc
15         Toll-like receptor agonists like the Toll-like receptor 7 agonist R848 induce DC maturation a
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
18 nal screening effort identified a pyrimidine Toll-like receptor 7 and 8 dual agonist.
19 rge amounts of type 1 interferon (IFN) after Toll-like receptor 7 and 9 engagements.
20 nterferon-alpha in response to SIV and other Toll-like receptor 7 and 9 ligands ex vivo.
21       Through pattern recognition receptors (Toll-like receptor 7 and retinoic acid-inducible gene 1)
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
25                                              Toll-like receptors 7 and 8 (TLRs) have emerged as key t
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
30                              We investigated Toll-like receptor 7-deficient (Tlr7(-/-)) and myeloid d
31          Furthermore, when formulated with a toll-like receptor 7-dependent (TLR7) agonist recently d
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
34                                              Toll-like receptor 7 expression in cortical neurons was
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
38 nt with the known neurodegenerative role for toll-like receptor 7 in neurons.
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
43                  Because a major function of Toll-like receptor 7 is to induce type I interferons (IF
44            However, despite large amounts of Toll-like receptor 7-mediated IFN-alpha, produced by pDC
45 it, colony stimulating factor 3 receptor and toll-like receptor 7 mRNA expression increases in the th
46         The small molecule GS-9620 activates Toll-like receptor 7 signaling in immune cells of chimpa
47 l replication, direct cell-cell contact, and Toll-like receptor 7 signaling, and we show that the act
48 , where the nucleic acid components activate Toll-like receptor 7 (TLR-7) or TLR-9.
49 otypes and clinical phenotypes, and assessed Toll-like receptor 7 (TLR-7)-stimulated MIF production i
50 so show that HIV-1-induced IKpDC depended on Toll-like receptor 7 (TLR7) activation.
51         Provision of CD40-specific antibody, Toll-like receptor 7 (TLR7) agonist and interleukin-2 (I
52                     Imiquimod is a synthetic Toll-like receptor 7 (TLR7) agonist approved for the top
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
56                               Small molecule Toll-like receptor 7 (TLR7) agonists have been used as v
57                            Pteridinone-based Toll-like receptor 7 (TLR7) agonists were identified as
58 use in plasmacytoid DC (pDC) stimulated with Toll-like receptor 7 (TLR7) agonists, Erk1/2 activation
59          This research examined the roles of Toll-like receptor 7 (TLR7) and autophagy in IFN-alpha p
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
64 luenza genomic RNA and signaling by means of Toll-like receptor 7 (TLR7) and MyD88.
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
67                        IRF-5 is activated by Toll-like receptor 7 (TLR7) and TLR9 via the MyD88 pathw
68 we present evidence showing that a ligand of Toll-like receptor 7 (TLR7) can induce anti-HCV immunity
69                                              Toll-like receptor 7 (TLR7) detects viral RNA, but can b
70                                              Toll-like receptor 7 (Tlr7) has been linked to systemic
71                                              Toll-like receptor 7 (TLR7) is expressed on multiple typ
72                                              Toll-like receptor 7 (TLR7) is required for promoting ge
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
75                                              Toll-like receptor 7 (TLR7) mediates autoantigen and vir
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
78                                              Toll-like receptor 7 (TLR7) signaling predominantly regu
79 e the immune response in dendritic cells via Toll-like receptor 7 (TLR7) signaling.
80                                              Toll-like receptor 7 (TLR7) signals to B cells are criti
81                                              Toll-like receptor 7 (TLR7) stimulation in the airways m
82 differentiation-associated gene 5 (MDA5) and Toll-like receptor 7 (TLR7) to induce transcription of t
83                                              Toll-like receptor 7 (TLR7) triggers antiviral immune re
84              Imiquimod (IQ) is an agonist of Toll-like receptor 7 (TLR7) used to treat various infect
85                     We found that functional Toll-like receptor 7 (TLR7) was expressed in C-fiber pri
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
90                             The induction of toll-like receptor 7 (TLR7)-dependent type I interferons
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
93 cognition of intracellular Y. pestis by host Toll-like receptor 7 (TLR7).
94  and this response is attributed to platelet Toll-like receptor 7 (TLR7).
95 tion induced by compound CL097, a ligand for Toll-like receptor 7 (TLR7).
96 antibody production was largely dependent on Toll-like receptor 7 (TLR7).
97 port that several guanosine analogs activate Toll-like receptor 7 (TLR7).
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
101        A candidate gene on the X chromosome, toll-like receptor 7, was then examined.

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