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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
13 Nucleotide-binding oligomerization domain (NOD)-like receptors, also known as nucleotide-binding le
14 f nucleotide-binding oligomerization domain (NOD)-like receptors and DEAD-box or DEAH-box RNA helicas
16 hat have common structural features with the Nod-like receptors and are essential for protection agai
17 all RNAs, including microRNAs, that regulate NOD-like receptors and defence signalling pathways in th
18 cells as microbial sensors through TLRs and Nod-like receptors and identify Nod1 and RICK as importa
19 IRF5 signaling axis functions independent of NOD-like receptors and is critically required for the re
21 complex, plant R proteins and related animal Nod-like receptors, and with the Hsp90 molecular chapero
22 d nucleotide binding oligomerization domain (NOD)-like receptors are critical for IL-1-dependent host
25 ding oligomerization domain-like receptor or NOD-like receptors are pattern recognition receptors cap
26 in leucine-rich-repeat-containing receptors; NOD-like receptors) are a class of pattern recognition r
27 e nucleotide-binding oligomerization domain (NOD)-like receptors belong to the family of pattern reco
28 e cluster also encoding a lipase (SBP) and a Nod-like receptor, both of which display the PP motif.
29 d nucleotide-binding oligomerization domain (NOD)-like receptor C4 (NLRC4) were associated with neutr
31 em (T3SS) needle complex that induces NLRC4 (NOD-like receptor C4) activation, interleukin-1beta (IL-
35 e nucleotide-binding oligomerization domain (NOD)-like receptor containing pyrin domain 3 (NLRP3) inf
36 beta by sterile particles is mediated by the NOD-like receptor containing a pyrin domain 3 (NLRP3) in
37 B. abortus was diminished in the absence of Nod-like receptor containing a pyrin domain 3 and absent
39 ors encoding a PYD belong to the families of NOD-like receptors containing a PYD (NLRPs) or AIM2-like
41 r nucleotide-binding oligomerization domain (NOD)-like receptors, detect tissue damage or microbial i
42 e transcriptional upregulation of the NLRP3 (Nod Like Receptor Family Pyrin Domain-Containing 3) infl
43 e transcriptional upregulation of the NLRP3 (Nod Like Receptor Family Pyrin Domain-Containing 3) infl
44 re, we demonstrate that double deficiency of Nod like receptor family, pyrin domain containing 3 (NLR
45 e nucleotide-binding oligomerization domain (NOD)-like receptor family pyrin domain containing 12 (NL
46 d nucleotide-binding oligomerization domain (NOD)-like receptor family, pyrin domain containing 3 act
47 Nucleotide-binding oligomerization domain (NOD)-like receptor family, pyrin domain-containing prote
48 e nucleotide-binding oligomerization domain (NOD)-like receptors family members are key for innate im
52 n facilitated by breastmilk feeding promotes NOD-like receptor family CARD domain containing 5 (Nlrc5
54 in-interaction network, missense variants in NOD-like receptor family genes (NOD2, NLRC4, NLRP3, and
56 e recently found that asbestos activates the nod-like receptor family member containing a pyrin domai
57 learance during IAV infection.IMPORTANCE The NOD-like receptor family member NLRC5 is known to regula
59 f caspase-1, through a process requiring the NOD-like receptor family member NLRP3 and the inflammaso
63 show that NOD1 and NOD2, two members of the NOD-like receptor family of PRRs, are important mediator
64 ion-induced caspase-1 activation occurs by a Nod-like receptor family protein 3-independent mechanism
65 reated group via engagement of the canonical NOD-like receptor family pyrin domain containing 3 (NLRP
66 mplications, in particular activation of the Nod-like receptor family pyrin domain containing 3 (NLRP
67 tau pathology, with evidence suggesting the nod-like receptor family pyrin domain containing 3 (NLRP
68 mplications, in particular activation of the Nod-like receptor family pyrin domain containing 3 (NLRP
69 flow, and local tissue hypoxia activate the NOD-like receptor family pyrin domain containing 3 infla
70 tely on inhibition of the IL-1beta-producing NOD-like receptor family pyrin domain containing 3 infla
71 ultures, internalized MAC also causes NLRP3 (NOD-like receptor family pyrin domain containing 3) tran
72 nt Domain (CARD)), pro-caspase-1, and NLRP3 (NOD-Like Receptor family Pyrin domain containing 3).
73 CRC development, where mice deficient in the NOD-like receptor family pyrin domain containing 6 (NLRP
76 his study aims to compare salivary levels of nod-like receptor family pyrin domain containing protein
77 to IL-1 and IL-18, suggesting a role for the NOD-like receptor family pyrin domain containing-3 infla
78 ins induced release of IL-1beta dependent on NOD-like receptor family pyrin domain-containing 3 (NLRP
80 nd to the Toll-like receptor 4 and prime the nod-like receptor family pyrin domain-containing 3 infla
81 signaling or their downstream mediators (eg, nod-like receptor family pyrin domain-containing 3 infla
82 ssion of key inflammatory mediators, such as NOD-like receptor family pyrin domain-containing 3, inte
85 manner, which leads to the activation of the NOD-like receptor family pyrin domain-containing protein
88 s as well as expression of components of the NOD-like receptor family pyrin domain-containing protein
93 ain (Nod)1, a member of the intracytoplasmic Nod-like receptor family, induced potent secretion of th
96 an neutrophils express key components of the NOD-like receptor family, pyrin domain containing 3 (NLR
98 ata are pointing to an important role of the NOD-like receptor family, pyrin domain containing 3 (NLR
99 ns of chitosan, but not chitin, activate the NOD-like receptor family, pyrin domain containing 3 (NLR
100 er report that these effects are mediated by NOD-like receptor family, pyrin domain containing 3 (NLR
102 linked to gain-of-function mutations in the NOD-like receptor family, pyrin domain containing 3 (NLR
103 of the mature IL-1beta form depended on the NOD-like receptor family, pyrin domain containing 3 (NLR
104 We hypothesized that Gal3 is a key to induce NOD-like receptor family, pyrin domain containing 3 (NLR
105 eroxide in the mechanisms tightly regulating NOD-like receptor family, pyrin domain containing 3 acti
106 t transient, increase in the activity of the NOD-like receptor family, pyrin domain containing 3 infl
108 nt thinking, an early intervention targeting NOD-like receptor family, pyrin domain containing 3 infl
110 recent evidence that the NOD2 target, NLRP3 (NOD-like receptor family, pyrin domain containing 3) is
111 leading to enhanced Caspase-1/Caspase-4- and NOD-like receptor family, pyrin domain containing 3-depe
112 r interacting protein kinase 1), and NLRP12 (NOD-like receptor family, pyrin domain-containing 12)-PA
114 re we show that bee venom is detected by the NOD-like receptor family, pyrin domain-containing 3 infl
115 tidylarginine deiminase 4, and activates the NOD-like receptor family, pyrin domain-containing 3 infl
116 several studies have focused on the role of nod-like receptor family, pyrin domain-containing protei
117 1 and NOD2, two members of the intracellular NOD-like receptor family, sense bacterial peptidoglycan-
118 2, the founding members of the intracellular NOD-like receptor family, sense conserved motifs in bact
119 lular stress is activation of members of the NOD-like receptor family, such as NLRP3, to assemble cas
122 ide-binding domain leucine-rich repeat (NLR; NOD-like receptor) family of pattern recognition recepto
125 tosis, and signaling pathways including p53, NOD-like receptor, IL-17, NF-kappa B, and PI3K-Akt.
126 omoting colon tumorigenesis, but the role of Nod-like receptors in regulating tumorigenesis remains u
127 as HMGB1 and IL-1beta, Toll-like receptors, Nod-like receptors including NLRC4, NLRP3 and NLRP4, and
130 ror rate, FWER p-value <0.05), including the NOD-like receptor inflammasome (NLR; p < 0.001), toll-li
131 roducts in the cytosol of mammalian cells by NOD-like receptors leads to the activation of caspase-1
132 the detection of bacterial products through Nod-like receptors leads to the secretion of mature inte
134 MAPK, mitogen-activated protein kinase; NLR, NOD-like receptors; LRR, leucine-rich repeats; DC, dendr
135 mmune receptors, the Toll-like receptors and Nod-like receptors, many of which are upstream of nuclea
136 ment in vivo results in up-regulation of the Nod-like receptor member Nod1, which recognizes the prod
137 evidence for AS of LRR domain within several Nod-like receptors, most prominently the inflammasome se
141 e nucleotide-binding oligomerization domain (NOD)-like receptor (NLR) (nucleotide-binding domain leuc
142 cleotide-binding and oligomerization domain (NOD)-like receptor (NLR) family contribute to immune res
143 e nucleotide-binding oligomerization domain (NOD)-like receptor (NLR) family pyrin domain-containing
144 e nucleotide-binding oligomerization domain (NOD)-like receptor (NLR) family pyrin domain-containing
145 pathways and Nuclear Oligomerization Domain (NOD)-Like Receptor (NLR) pathways and Caspase networks.
146 Nucleotide-binding, oligomerization domain (NOD)-like receptor (NLR) proteins are a family of innate
148 d nucleotide binding oligomerization domain (Nod)-like receptors (NLR), Nod1 and Nod2, as novel regul
151 agellin secreted by Salmonella activates the Nod-like receptor (NLR) family CARD domain containing pr
152 timulation of innate immune receptors of the NOD-like receptor (NLR) family causes significant damage
153 cular mechanisms promoting activation of the Nod-like Receptor (NLR) family member NLRP3 inflammasome
155 flammasome, a multiprotein complex formed by NOD-like receptor (NLR) family members, has recently bee
162 scriptomic changes, including alterations in NOD-like receptor (NLR) family pyrin domain-containing 1
163 h several inflammasome components, including NOD-like receptor (NLR) family pyrin domain-containing 3
169 of nucleotide-binding leucine rich repeat or Nod-Like Receptor (NLR) genes as an important mechanism
170 r histocompatibility complex (MHC) genes and NOD-like receptor (NLR) genes, mediators of direct and i
171 bind to the enhancer region of two adjacent NOD-like receptor (NLR) genes, NLR family pyrin domain-c
172 sensed and restricted in vivo, especially by NOD-like receptor (NLR) inflammasomes, is largely unknow
173 ld be rescued by administration of bacterial Nod-like receptor (NLR) ligands (the NOD1 ligand MurNAcT
174 C)/PYCARD, a central adaptor molecule in the Nod-like receptor (NLR) pathway, regulates the IL-18/IFN
177 previously reported inhibitory effect of the Nod-like receptor (NLR) protein NLRX1 on NF-kappaB- and
180 n response to canonical stimuli initiated by NOD-like receptor (NLR), and apoptosis-associated speck-
183 riggered immunity but triggers intracellular NOD-like receptor (NLR)-mediated autoimmunity with an el
185 orphisms (SNP) of toll-like receptors (TLR), NOD-like receptors (NLR) and RIG-I-like receptors (RLR)
187 ing evidence highlights additional roles for Nod-like receptors (NLR) in nonhematopoietic cells.
190 pathogen recognition receptors, known as PYD-Nod-like receptors (NLR), PAN, PYPAF, NALP, Nod, and Cat
192 -associated speck-like protein (ASC) and the NOD-like receptor NLRC4 are significantly down-regulated
193 in a mouse we recently described lacking the NOD-like receptor NLRP10 (NLR family, pyrin domain conta
196 aureus exoproteins through activation of the NOD-like receptors NLRP3 and NLRP4 and enhanced phagocyt
198 r nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs) and the adaptor ASC is believ
199 r nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs) and they initiate innate immu
200 e nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs) are a family of intracellular
201 cleotide oligomerization and binding domain (NOD)-like receptors (NLRs) are a major constituent of th
202 cleotide oligomerization and binding domain (NOD)-like receptors (NLRs) are important in the innate i
203 cleotide-binding and oligomerization domain (NOD)-like receptors (NLRs) have shaped our current under
204 f nucleotide binding oligomerization domain (NOD)-like receptors (NLRs) in innate detection of influe
205 cleotide oligomerization and binding domain (NOD)-like receptors (NLRs), caspase-1, and in some cases
206 n nucleotide binding oligomerization domain (NOD)-like receptors (NLRs), retinoic acid-inducible prot
215 influence of human polymorphisms in TLRs and Nod-like receptors (NLRs) on C. burnetii-induced cytokin
218 yroptosis induction, we knocked down several NOD-like receptors (NLRs) with respective shRNAs in PBMC
219 xamine the effects of glucocorticoids on the NOD-like receptors (NLRs), a central component of the in
220 ptors, including Toll-like receptors (TLRs), NOD-like receptors (NLRs), and RIG-1-like receptors (RLR
221 leucine-rich repeat receptors, also known as NOD-like receptors (NLRs), are highly diversified, both
222 w the varied roles of one class of PRRs, the NOD-like receptors (NLRs), in immune responses and propo
223 The innate immune system encodes cytosolic Nod-like receptors (NLRs), several of which activate cas
224 Although they are among the best studied NOD-like receptors (NLRs), the therapeutic potential of
226 ogenous danger signals in the cytosol engage NOD-like receptors (NLRs), which assemble inflammasome c
232 like receptors and the more recently defined NOD-like receptors (NLRs): NODs, NALPs, NAIP and IPAF.
234 cleotide-binding and oligomerization domain (NOD)-like receptors NOD1 and NOD2 are cytosolic innate i
238 Nucleotide-binding oligomerization domain (NOD)-like receptors of which there are more than 20 rela
239 ins of plants (R-proteins) and the so-called NOD-like receptors of animals (NLRs) share a domain arch
240 mous substitutions in NOD-2, a member of the NOD-like receptor or NACHT-leucine-rich repeat (NLR) fam
243 reptococcus (GBS)-mediated activation of the Nod-like receptor-P3 (NLRP3) inflammasome in macrophages
245 cine-rich repeat-containing protein (NLR or (NOD-like)) receptors play a critical role in the innate
246 e nucleotide-binding oligomerization domain (NOD)-like receptor protein 3 (NLRP3) inflammasome to rec
247 his study was that sustained activity of the Nod-like receptor protein (NLRP)-3 inflammasome in wound
248 as well as the inflammation mediated by the NOD-like receptor protein (NLRP)-3/caspase-1 signaling p
250 emodeling, cell osmolarity and regulation of NOD-like receptor protein 3 (NLRP3) inflammasome activit
251 ian leptin signalling, the activation of the NOD-like receptor protein 3 (NLRP3) inflammasome and mac
252 thies and highlight a potential role for the NOD-like receptor protein 3 (NLRP3) inflammasome as a ne
253 tosis, in T lymphocytes through induction of Nod-like receptor protein 3 (NLRP3) inflammasome complex
257 whether inhibition of a major product of the Nod-like receptor protein 3 (NLRP3) inflammasome with ca
258 eukin-1beta (IL-1beta), which is mediated by Nod-like receptor protein 3 (NLRP3) inflammasome, cathep
259 strong activation of innate immunity induced Nod-like receptor protein 3 (NLRP3) inflammasome-indepen
261 rating TXNIP to associate with mitochondrial nod-like receptor protein 3 (NLRP3) to activate inflamma
262 a in bacterial clearance, and we showed that Nod-like receptor protein 3 (NLRP3), apoptosis-associate
263 -2), inducible nitric oxide synthase (iNOS), nod-like receptor protein 3 (NLRP3), associated speck-li
264 this process leads to the activation of the Nod-like receptor protein 3 inflammasome and the subsequ
267 cent studies revealed a crucial role for the NOD-like receptor protein Nlrp3 in regulating inflammati
269 review, we will summarize the centrality of Nod-like receptor proteins that assemble inflammasomes a
270 g domain, leucine-rich repeat containing, or NOD-like receptor) proteins is in inflammasome activatio
271 e also increased measures of senescence, the nod like receptor pyrin domain containing 3 (NLRP3) infl
272 e nucleotide-binding oligomerization domain (NOD)-like receptor pyrin domain containing family of gen
273 by some immune receptors, they activate the NOD-like receptor pyrin 3-inflammasome and trigger IL-1b
274 n the regulatory region of the gene encoding NOD-like receptor pyrin domain containing 3 (NLRP3) have
277 n endothelial cells that assembles an NLRP3 (NOD-like receptor pyrin domain-containing protein 3) inf
280 ARD4 and NOD2/CARD15 proteins are members of NOD-like receptors recognizing specific motifs within pe
281 *Nucleotide binding oligomerization domain (Nod)-like receptors regulate cognition, anxiety and hypo
283 ind specific receptors [Toll-like receptors, NOD-like receptors, RIG-I-like receptors, AIM2-like rece
284 oteins with an architecture like that of the NOD-like receptors, SAMD9/9L molecular functions and dom
285 ike receptor (TLR), RIG-I-like receptor, and NOD-like receptor signaling pathways of the innate immun
286 arity of epithelial cells acts on intestinal NOD-like receptor signaling to mediate spatial specifici
287 in induced enrichment of pathways related to NOD-like receptor signaling, high metabolic demand, and
289 d Proteobacteria phyla, we found that potent Nod-like receptor-stimulating bacteria in the upper airw
290 indings expand the potential ligands for the NOD-like receptors, suggesting that other xanthone compo
292 cleotide binding and oligomerization domain (NOD)-like receptors that were found to control nonself r
293 mprises an intracellular sensor (typically a Nod-like receptor), the precursor procaspase-1 and the a
295 cell surface (TLRs) and within the cytosol (Nod-like receptors) to promote inflammatory processes ai
296 dependent on caspase-1; however, the role of Nod-like receptors upstream of caspase-1 is unknown.
297 s of the large family of intracellular NLRs (NOD-like receptors), which also includes animal immune r
298 udy, we explored how NAD(+) affects TLR4 and NOD-like receptor with a PYD-domain 3 (NLRP3) inflammaso
299 ncing of the newly discovered dsRNA receptor Nod-like receptor X-1 (NLRX-1), but not other previously
300 016) demonstrate in independent studies that Nod-like receptor X1 (NLRX1) may facilitate early system