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1 -like receptors, C-type lectin receptors and NOD-like receptors.
2 of pathogen-associated molecular patterns by Nod-like receptors.
3 ammasome components, including caspase 1 and Nod-like receptors.
4 responses mediated by both the TLRs and the NOD-like receptors.
5 TLRs, and nucleotide oligomerization domain (NOD)-like receptors.
6 r Toll-like receptors (TLRs) 1, 2, 4, and 6; NOD-like receptor 2; and the signaling adaptor molecule
7 e nucleotide-binding oligomerization domain (NOD)-like receptor 3 (NLRP3) inflammasome has been impli
9 hogen-associated molecular patterns activate Nod-like receptor 3, which activates caspase-1 through t
11 or and regulatory interactions with TLRs and Nod-like receptors, Ag presentation, naive T cell repert
14 hat have common structural features with the Nod-like receptors and are essential for protection agai
15 cells as microbial sensors through TLRs and Nod-like receptors and identify Nod1 and RICK as importa
17 complex, plant R proteins and related animal Nod-like receptors, and with the Hsp90 molecular chapero
18 d nucleotide binding oligomerization domain (NOD)-like receptors are critical for IL-1-dependent host
20 in leucine-rich-repeat-containing receptors; NOD-like receptors) are a class of pattern recognition r
21 e cluster also encoding a lipase (SBP) and a Nod-like receptor, both of which display the PP motif.
22 d nucleotide-binding oligomerization domain (NOD)-like receptor C4 (NLRC4) were associated with neutr
24 em (T3SS) needle complex that induces NLRC4 (NOD-like receptor C4) activation, interleukin-1beta (IL-
27 beta by sterile particles is mediated by the NOD-like receptor containing a pyrin domain 3 (NLRP3) in
28 B. abortus was diminished in the absence of Nod-like receptor containing a pyrin domain 3 and absent
30 ors encoding a PYD belong to the families of NOD-like receptors containing a PYD (NLRPs) or AIM2-like
32 r nucleotide-binding oligomerization domain (NOD)-like receptors, detect tissue damage or microbial i
33 re, we demonstrate that double deficiency of Nod like receptor family, pyrin domain containing 3 (NLR
34 e nucleotide-binding oligomerization domain (NOD)-like receptor family pyrin domain containing 12 (NL
35 d nucleotide-binding oligomerization domain (NOD)-like receptor family, pyrin domain containing 3 act
36 Nucleotide-binding oligomerization domain (NOD)-like receptor family, pyrin domain-containing prote
37 e nucleotide-binding oligomerization domain (NOD)-like receptors family members are key for innate im
41 e recently found that asbestos activates the nod-like receptor family member containing a pyrin domai
42 learance during IAV infection.IMPORTANCE The NOD-like receptor family member NLRC5 is known to regula
43 f caspase-1, through a process requiring the NOD-like receptor family member NLRP3 and the inflammaso
46 show that NOD1 and NOD2, two members of the NOD-like receptor family of PRRs, are important mediator
47 ion-induced caspase-1 activation occurs by a Nod-like receptor family protein 3-independent mechanism
48 flow, and local tissue hypoxia activate the NOD-like receptor family pyrin domain containing 3 infla
49 tely on inhibition of the IL-1beta-producing NOD-like receptor family pyrin domain containing 3 infla
50 nt Domain (CARD)), pro-caspase-1, and NLRP3 (NOD-Like Receptor family Pyrin domain containing 3).
51 CRC development, where mice deficient in the NOD-like receptor family pyrin domain containing 6 (NLRP
52 his study aims to compare salivary levels of nod-like receptor family pyrin domain containing protein
53 to IL-1 and IL-18, suggesting a role for the NOD-like receptor family pyrin domain containing-3 infla
54 ins induced release of IL-1beta dependent on NOD-like receptor family pyrin domain-containing 3 (NLRP
56 manner, which leads to the activation of the NOD-like receptor family pyrin domain-containing protein
60 ain (Nod)1, a member of the intracytoplasmic Nod-like receptor family, induced potent secretion of th
62 ns of chitosan, but not chitin, activate the NOD-like receptor family, pyrin domain containing 3 (NLR
64 of the mature IL-1beta form depended on the NOD-like receptor family, pyrin domain containing 3 (NLR
65 We hypothesized that Gal3 is a key to induce NOD-like receptor family, pyrin domain containing 3 (NLR
67 an neutrophils express key components of the NOD-like receptor family, pyrin domain containing 3 (NLR
69 eroxide in the mechanisms tightly regulating NOD-like receptor family, pyrin domain containing 3 acti
71 nt thinking, an early intervention targeting NOD-like receptor family, pyrin domain containing 3 infl
72 t transient, increase in the activity of the NOD-like receptor family, pyrin domain containing 3 infl
74 recent evidence that the NOD2 target, NLRP3 (NOD-like receptor family, pyrin domain containing 3) is
75 leading to enhanced Caspase-1/Caspase-4- and NOD-like receptor family, pyrin domain containing 3-depe
77 re we show that bee venom is detected by the NOD-like receptor family, pyrin domain-containing 3 infl
78 tidylarginine deiminase 4, and activates the NOD-like receptor family, pyrin domain-containing 3 infl
79 1 and NOD2, two members of the intracellular NOD-like receptor family, sense bacterial peptidoglycan-
80 2, the founding members of the intracellular NOD-like receptor family, sense conserved motifs in bact
81 lular stress is activation of members of the NOD-like receptor family, such as NLRP3, to assemble cas
85 omoting colon tumorigenesis, but the role of Nod-like receptors in regulating tumorigenesis remains u
86 as HMGB1 and IL-1beta, Toll-like receptors, Nod-like receptors including NLRC4, NLRP3 and NLRP4, and
89 ror rate, FWER p-value <0.05), including the NOD-like receptor inflammasome (NLR; p < 0.001), toll-li
90 roducts in the cytosol of mammalian cells by NOD-like receptors leads to the activation of caspase-1
91 the detection of bacterial products through Nod-like receptors leads to the secretion of mature inte
93 MAPK, mitogen-activated protein kinase; NLR, NOD-like receptors; LRR, leucine-rich repeats; DC, dendr
94 mmune receptors, the Toll-like receptors and Nod-like receptors, many of which are upstream of nuclea
95 ment in vivo results in up-regulation of the Nod-like receptor member Nod1, which recognizes the prod
99 e nucleotide-binding oligomerization domain (NOD)-like receptor (NLR) (nucleotide-binding domain leuc
100 cleotide-binding and oligomerization domain (NOD)-like receptor (NLR) family contribute to immune res
101 pathways and Nuclear Oligomerization Domain (NOD)-Like Receptor (NLR) pathways and Caspase networks.
102 Nucleotide-binding, oligomerization domain (NOD)-like receptor (NLR) proteins are a family of innate
105 agellin secreted by Salmonella activates the Nod-like receptor (NLR) family CARD domain containing pr
106 cular mechanisms promoting activation of the Nod-like Receptor (NLR) family member NLRP3 inflammasome
108 flammasome, a multiprotein complex formed by NOD-like receptor (NLR) family members, has recently bee
115 h several inflammasome components, including NOD-like receptor (NLR) family pyrin domain-containing 3
120 sensed and restricted in vivo, especially by NOD-like receptor (NLR) inflammasomes, is largely unknow
121 ld be rescued by administration of bacterial Nod-like receptor (NLR) ligands (the NOD1 ligand MurNAcT
122 C)/PYCARD, a central adaptor molecule in the Nod-like receptor (NLR) pathway, regulates the IL-18/IFN
125 previously reported inhibitory effect of the Nod-like receptor (NLR) protein NLRX1 on NF-kappaB- and
130 ing evidence highlights additional roles for Nod-like receptors (NLR) in nonhematopoietic cells.
133 pathogen recognition receptors, known as PYD-Nod-like receptors (NLR), PAN, PYPAF, NALP, Nod, and Cat
135 -associated speck-like protein (ASC) and the NOD-like receptor NLRC4 are significantly down-regulated
136 in a mouse we recently described lacking the NOD-like receptor NLRP10 (NLR family, pyrin domain conta
139 aureus exoproteins through activation of the NOD-like receptors NLRP3 and NLRP4 and enhanced phagocyt
141 r nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs) and the adaptor ASC is believ
142 r nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs) and they initiate innate immu
143 e nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs) are a family of intracellular
144 cleotide oligomerization and binding domain (NOD)-like receptors (NLRs) are a major constituent of th
145 cleotide oligomerization and binding domain (NOD)-like receptors (NLRs) are important in the innate i
146 cleotide-binding and oligomerization domain (NOD)-like receptors (NLRs) have shaped our current under
147 f nucleotide binding oligomerization domain (NOD)-like receptors (NLRs) in innate detection of influe
148 cleotide oligomerization and binding domain (NOD)-like receptors (NLRs), caspase-1, and in some cases
149 n nucleotide binding oligomerization domain (NOD)-like receptors (NLRs), retinoic acid-inducible prot
156 influence of human polymorphisms in TLRs and Nod-like receptors (NLRs) on C. burnetii-induced cytokin
159 xamine the effects of glucocorticoids on the NOD-like receptors (NLRs), a central component of the in
160 ptors, including Toll-like receptors (TLRs), NOD-like receptors (NLRs), and RIG-1-like receptors (RLR
161 w the varied roles of one class of PRRs, the NOD-like receptors (NLRs), in immune responses and propo
162 The innate immune system encodes cytosolic Nod-like receptors (NLRs), several of which activate cas
163 Although they are among the best studied NOD-like receptors (NLRs), the therapeutic potential of
165 ogenous danger signals in the cytosol engage NOD-like receptors (NLRs), which assemble inflammasome c
169 like receptors and the more recently defined NOD-like receptors (NLRs): NODs, NALPs, NAIP and IPAF.
170 cleotide-binding and oligomerization domain (NOD)-like receptors NOD1 and NOD2 are cytosolic innate i
173 Nucleotide-binding oligomerization domain (NOD)-like receptors of which there are more than 20 rela
174 ins of plants (R-proteins) and the so-called NOD-like receptors of animals (NLRs) share a domain arch
175 mous substitutions in NOD-2, a member of the NOD-like receptor or NACHT-leucine-rich repeat (NLR) fam
178 reptococcus (GBS)-mediated activation of the Nod-like receptor-P3 (NLRP3) inflammasome in macrophages
179 cine-rich repeat-containing protein (NLR or (NOD-like)) receptors play a critical role in the innate
180 e nucleotide-binding oligomerization domain (NOD)-like receptor protein 3 (NLRP3) inflammasome to rec
181 his study was that sustained activity of the Nod-like receptor protein (NLRP)-3 inflammasome in wound
182 tosis, in T lymphocytes through induction of Nod-like receptor protein 3 (NLRP3) inflammasome complex
183 whether inhibition of a major product of the Nod-like receptor protein 3 (NLRP3) inflammasome with ca
184 strong activation of innate immunity induced Nod-like receptor protein 3 (NLRP3) inflammasome-indepen
185 a in bacterial clearance, and we showed that Nod-like receptor protein 3 (NLRP3), apoptosis-associate
188 cent studies revealed a crucial role for the NOD-like receptor protein Nlrp3 in regulating inflammati
189 review, we will summarize the centrality of Nod-like receptor proteins that assemble inflammasomes a
190 g domain, leucine-rich repeat containing, or NOD-like receptor) proteins is in inflammasome activatio
191 e nucleotide-binding oligomerization domain (NOD)-like receptor pyrin domain containing family of gen
193 ARD4 and NOD2/CARD15 proteins are members of NOD-like receptors recognizing specific motifs within pe
194 ind specific receptors [Toll-like receptors, NOD-like receptors, RIG-I-like receptors, AIM2-like rece
195 ike receptor (TLR), RIG-I-like receptor, and NOD-like receptor signaling pathways of the innate immun
196 arity of epithelial cells acts on intestinal NOD-like receptor signaling to mediate spatial specifici
198 d Proteobacteria phyla, we found that potent Nod-like receptor-stimulating bacteria in the upper airw
199 indings expand the potential ligands for the NOD-like receptors, suggesting that other xanthone compo
201 mprises an intracellular sensor (typically a Nod-like receptor), the precursor procaspase-1 and the a
203 cell surface (TLRs) and within the cytosol (Nod-like receptors) to promote inflammatory processes ai
204 dependent on caspase-1; however, the role of Nod-like receptors upstream of caspase-1 is unknown.
205 s of the large family of intracellular NLRs (NOD-like receptors), which also includes animal immune r
206 ncing of the newly discovered dsRNA receptor Nod-like receptor X-1 (NLRX-1), but not other previously
207 016) demonstrate in independent studies that Nod-like receptor X1 (NLRX1) may facilitate early system
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