コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 fumigatus serving as a key vitality-sensing pattern recognition receptor.
2 al transduction downstream of this important pattern recognition receptor.
3 ulate that NKp46/NCR1 may be a novel type of pattern recognition receptor.
4 y shows that a metabolic enzyme can act as a pattern recognition receptor.
5 ive bacterial protein can activate CD36 as a pattern recognition receptor.
6 ered by surface IgE cross-linking or through pattern recognition receptors.
7 r alarmins that can trigger inflammation via pattern recognition receptors.
8 ne system recognizes microbial pathogens via pattern recognition receptors.
9 eractions between TLR and Siglec families of pattern recognition receptors.
10 responses after engagement and signaling by pattern recognition receptors.
11 protection from detection by host cytosolic pattern recognition receptors.
12 (TLRs), an evolutionarily ancient family of pattern recognition receptors.
13 s undergoing ER stress or stimulated through pattern recognition receptors.
14 but are strongly induced upon activation of pattern recognition receptors.
15 suggest an evasion of detection by host cell pattern recognition receptors.
16 ription factor that is activated by multiple pattern-recognition receptors.
17 iggered immunity, including glycosylation of pattern-recognition receptors.
21 recognize a wide array of self-antigens via pattern recognition receptors, adaptive immunity activat
26 stream of a calcium influx, and required the pattern recognition receptor and adaptor STING but not c
29 be-associated molecular patterns (MAMPs) via pattern recognition receptors and activate innate immune
32 effects not only toward C5aR1 but also other pattern recognition receptors and innate immune systems,
33 analyzed with cytofluorimetric analysis for pattern recognition receptors and intracellular signals,
35 OMV, and LPS groups consisting of bacterial pattern recognition receptors and neutrophil activation
37 defense that up-regulates the expression of pattern recognition receptors and sustains inflammatory
38 ia survive in macrophages despite triggering pattern recognition receptors and T cell-derived IFN-gam
39 onse to bacteria, including acting as hybrid pattern recognition receptors and TCR coreceptors, and t
40 hat the Brassicaceae may have evolved unique pattern-recognition receptors and antimicrobial root met
42 by innate immune activation mediated through pattern-recognition receptors and endothelial-to-mesench
43 l established; this is mediated primarily by pattern-recognition receptors and is central to the acti
45 infection is sensed by a variety of cellular pattern-recognition receptors and triggers the synthesis
46 med gene expression of LC-related molecules, pattern recognition receptors, and enhanced expression o
47 C. elegans lacks homologs of most mammalian pattern recognition receptors, and how nematodes detect
49 ation of several pathogenesis-related genes, pattern recognition receptors, and resistance genes, whi
50 ncRNAs expressed in cancer cells with innate pattern recognition receptors, and thereby assign a prev
55 l-like receptors (TLRs), first identified as pattern recognition receptors, are now recognized to ser
56 tion, which established danger signaling via pattern recognition receptors as a new concept of kidney
58 strate that langerin not only functions as a pattern recognition receptor but also as an adhesion rec
59 studies have demonstrated that signaling by pattern recognition receptors can regulate metabolic pro
61 advanced glycation end products (RAGE) is a pattern recognition receptor capable of recognizing mult
62 of the ER, acting as a guard receptor and a pattern recognition receptor, capable both of sensing ce
64 pensable for cytokine-dependent induction of pattern recognition receptor, cell adhesion, or chemotax
66 3 inflammasome, a multiprotein intracellular pattern recognition receptor complex that facilitates th
67 ulating the composition of a serine protease-pattern recognition receptor complex, MBL-associated ser
68 ry thus provides a critical link between the pattern-recognition receptor complex and calcium-depende
69 inase BOTRYTIS-INDUCED KINASE1 (BIK1) of the pattern-recognition receptor complex, and this triggers
71 tory signalling and are a repository for the pattern-recognition receptor cyclic GMP-AMP synthase (cG
74 e endocytic C-type lectin receptors serve as pattern recognition receptors, detecting pathogens by th
75 hus, NLRP3 mediated by ASC appears to be the pattern recognition receptor driving HBoV1 infection-ind
76 zed by distinct families of germline-encoded pattern recognition receptors, endogenous and pathogen-d
79 lso activate microglia via interactions with pattern recognition receptors expressed on microglia.
80 tly to infectious Ags through stimulation of pattern recognition receptors expressed on their surface
82 f the C-type lectin receptor family serve as pattern recognition receptors facilitating pathogen upta
84 mune receptor, a member of the peptidoglycan pattern recognition receptor family (PGRP-LC), is requir
85 report serves as the first description of a pattern recognition receptor for CCHFV and highlights a
86 y an unrecognized role for SAA1 as a soluble pattern recognition receptor for conserved FABPs found i
87 tors identified RIG-I as the major cytosolic pattern recognition receptor for detection of ZIKV.IMPOR
88 n receptors (CLRs) have emerged as important pattern recognition receptors for infectious danger.
89 athogenic Th cell types via the signaling of pattern recognition receptors for innate immune response
90 uitination of dectin-1 and dectin-2, two key pattern-recognition receptors for sensing Candida albica
92 ed gene 5 (MDA-5, IFIH1), a cytosolic innate pattern recognition receptor, functions as a first line
93 ng 10); however, the mechanism by which this pattern recognition receptor governs DC migration remain
94 d TLRs, the signals emanating from different pattern recognition receptors have to be integrated to a
95 timulatory effects through the activation of pattern recognition receptors; however, synthetic versio
96 ycation end-products (RAGE) is a multiligand pattern recognition receptor implicated in diverse chron
97 cent studies reveal that CRIg functions as a pattern recognition receptor in vivo for Kupffer cells (
98 e of transcriptional responses downstream of pattern recognition receptors in informing the adaptive
101 DAP12, a signaling adapter for multiple pattern recognition receptors in myeloid and natural kil
102 e due to downregulated expression of a viral pattern-recognition receptor in alveolar macrophages.
106 ely activate distinct subtypes of macrophage pattern recognition receptors, including bacterial toll-
107 their environment through the expression of pattern recognition receptors, including Toll-like recep
108 spond to the gut microbiota through multiple pattern-recognition receptors, including TLRs and NLRs.
110 be-associated molecular patterns (MAMPs) via pattern recognition receptors, internal cellular signali
112 ber of the Nod-like receptor (NLR) family of pattern recognition receptors, is a bacterial sensor tha
114 autophagy induced by nutrient deprivation or pattern recognition receptors, less is known about the e
115 canonical FoxP3(+ )T(REGS) is unaffected by pattern recognition receptor ligation and is modulated b
116 edicago truncatula possess very similar LysM pattern-recognition receptors, LjLYS6/MtLYK9 and MtLYR4,
117 nated EndoU that facilitates evasion of host pattern recognition receptor MDA5, but the target of End
118 inhibition of translation elongation blocked pattern recognition receptor-mediated XBP1 splicing, mim
119 ral infection triggers host defenses through pattern-recognition receptor-mediated cytokine productio
120 us mouse hepatitis virus (MHV) activates the pattern recognition receptors melanoma differentiation-a
121 bition of IFN-gamma-induced genes, including pattern recognition receptors, MHC class II genes, and I
122 ic microbes, but mounting data suggest these pattern recognition receptors might also play key roles
123 ibroblasts showed that RIG-I is the critical pattern recognition receptor needed for the influenza B
124 stream signaling following activation of the pattern recognition receptors NOD1 and NOD2, leading to
125 previously showed an important role for the pattern recognition receptor NOD2 in skin wound repair.
130 ball-induced musculoskeletal trauma activate pattern-recognition receptors of the innate immune syste
132 ival correlated with decreased expression of pattern recognition receptors on host phagocytes known t
133 Misfolded and aggregated proteins bind to pattern recognition receptors on microglia and astroglia
134 scuss how lipid ligands on OMVs engage these pattern recognition receptors on the membranes and in th
135 am regulatory proteins, classically known as pattern-recognition receptors, operate to assess infecti
136 in individuals carrying genetic variants in pattern recognition receptors or adaptors would result i
137 esignated biological binding partners, be it pattern recognition receptors or carbohydrate binding le
138 inflammasomes represent a central cytosolic pattern recognition receptor pathway leading to the gene
139 t that the Toll-like receptor 9 (TLR9)-MyD88 pattern-recognition receptor pathway is uniquely capable
142 sense microbial signatures via activation of pattern recognition receptors (PPRs), which trigger a ra
143 variety of gut commensals and pathogens, and pattern recognition receptor (PRR) ligands, and investig
145 rization domain 1 (NOD1) is an intracellular pattern recognition receptor (PRR) responsible for sensi
146 tion in macrophages decreases cytokines upon pattern recognition receptor (PRR) restimulation; cytoki
147 ion occurs in response to both virus-induced pattern recognition receptor (PRR) signaling and cellula
148 ntestinal microbes, and proper regulation of pattern recognition receptor (PRR) signaling is critical
151 also identified G-protein coupled and novel pattern recognition receptor (PRR), P2RY10, as a central
152 oorly understand how vitamin D affects viral pattern recognition receptor (PRR)-driven cytokine produ
153 eterminant of interindividual variability in pattern recognition receptor (PRR)-induced cytokines in
154 dehydrogenase (SDH) subunit A, and amplifies pattern recognition receptor (PRR)-induced SDH activity,
155 it the negative regulatory mechanisms of the pattern recognition receptor (PRR)-mediated inflammatory
156 ed kinase 1 (SlWak1), has been implicated in pattern recognition receptor (PRR)-triggered immunity (P
158 GN are proinflammatory through engagement of pattern recognition receptors (PRR) on resident tissue c
159 s, such as cytomegaloviruses (CMVs), through pattern-recognition receptor (PRR) pathways involving My
162 somes, HIV-1 somehow evades detection by the pattern-recognition receptor (PRR) Toll-like receptor 8
163 eterminant of interindividual variability in pattern-recognition receptor (PRR)-induced cytokines in
164 of JAK2 expression and signaling determined pattern-recognition receptor (PRR)-induced outcomes; whe
166 PAMPs/MAMPs) are detected as nonself by host pattern recognition receptors (PRRs) and activate patter
173 obe-associated molecular patterns (MAMPs) by pattern recognition receptors (PRRs) induces currents me
174 ar patterns (MAMPs) by cell-surface-resident pattern recognition receptors (PRRs) induces rapid, robu
175 sociated molecular patterns (PAMPs/MAMPs) by pattern recognition receptors (PRRs) is a key component
177 ge-associated molecular patterns (DAMPs) for pattern recognition receptors (PRRs) may represent one s
178 ining analogs of microbial products activate pattern recognition receptors (PRRs) on antigen-presenti
181 rtance of DAMPs, which signal through innate pattern recognition receptors (PRRs) or DAMP-specific re
187 have been made to therapeutically target the pattern recognition receptors (PRRs) such as the Toll-li
189 ted molecular patterns (PAMPs/DAMPs) through pattern recognition receptors (PRRs) such as Toll-like r
190 consist of two distinct groups of proteins: pattern recognition receptors (PRRs) that detect viral i
191 obe-associated molecular patterns (MAMPs) by pattern recognition receptors (PRRs) that initiate quant
193 ular patterns (PAMPs) that are recognized by pattern recognition receptors (PRRs) to activate pattern
195 s (RKs) and receptor-like proteins (RLPs) as pattern recognition receptors (PRRs) to monitor their ap
196 s (RKs) and receptor-like proteins (RLPs) as pattern recognition receptors (PRRs) to sense pathogen-a
198 obe-associated molecular patterns (MAMPs) by pattern recognition receptors (PRRs) triggers the first
200 immune system senses viral infection through pattern recognition receptors (PRRs), leading to type I
201 viral RNA cleavage products of RNase L bind pattern recognition receptors (PRRs), like retinoic acid
202 how that low basal expression of RNA-sensing pattern recognition receptors (PRRs), or their co-recept
203 ammatory disorders is understanding how host pattern recognition receptors (PRRs), specifically toll-
205 cular patterns (PAMPs) are detected by plant pattern recognition receptors (PRRs), which gives rise t
206 cargos of plant trafficking pathways are the pattern recognition receptors (PRRs), which must be pres
211 ose-binding lectin (MBL)/ficolins, important pattern- recognition receptors (PRRs) of the complement
216 ude cell-intrinsic innate responses that use pattern-recognition receptors (PRRs) to detect viral pat
217 roduction of type I interferons triggered by pattern-recognition receptors (PRRs), but not that of th
220 nia, lung neutrophils increase expression of pattern recognition receptors, receptors for inflammator
222 genetic deletion of Toll-like receptor 4, a pattern recognition receptor responsive to LPS, prevente
223 te that differences in the activation of key pattern recognition receptors resulted in the induction
224 6)A-modified circRNA, directly activates RNA pattern recognition receptor RIG-I in the presence of ly
226 he detection of viral double-stranded RNA by pattern-recognition receptors (RIG-I/MDA-5) and that NKG
228 ide receptor 2 (FPR2) is a G protein-coupled pattern recognition receptor sensing both mitochondrial-
229 tified 129 immunity-related genes, including pattern recognition receptors, signal modulators, few me
230 racterized post-translational consequence of pattern recognition receptor signaling is the assembly o
231 be observed downstream of death receptor or pattern recognition receptor signaling under certain cel
232 analysis of the influence of human aging on pattern recognition receptors signaling and monocyte fun
234 rtant role for collaboration between TNF and pattern recognition receptor signals in promoting maxima
235 re sensed either directly, through cytosolic pattern-recognition receptors specific for bacterial lig
236 nd Mer (TAM) receptors in regulating chronic pattern recognition receptor stimulation and NOD2-induce
237 okines are attenuated after chronic NOD2 and pattern recognition receptor stimulation of macrophages;
239 ngal immunity involves fungal recognition by pattern recognition receptors such as C-type lectin rece
240 ated molecular patterns (DAMPS) by cytosolic pattern recognition receptors such as NOD-like receptors
242 one of the first lines of host defense, with pattern recognition receptors such as the Toll-like rece
243 ochondrial DAMPs such as mtDNA bind specific pattern recognition receptors such as Toll-like receptor
246 , rhIFN-gamma increased expression levels of pattern recognition receptors, such as Toll-like recepto
247 llular necrosis is initiated by a battery of pattern-recognition receptors, such as Toll-like recepto
248 Pellino-mediated regulation of signaling by pattern recognition receptors, T-cell and B-cell recepto
249 e cationic protein more similar to a soluble pattern recognition receptor than to conventional cytoki
250 ether, these results suggest that DRH-1 is a pattern recognition receptor that detects viral replicat
251 advanced glycation end products (RAGE) is a pattern recognition receptor that interacts with advance
256 ular relevance to viral infections are those pattern recognition receptors that activate type I inter
257 epeat (NLR) proteins are a diverse family of pattern recognition receptors that are essential mediato
259 NLRP1 and CARD8 are related germline-encoded pattern recognition receptors that form inflammasomes, b
260 ivate toll-like receptors (TLRs), a class of pattern recognition receptors that initiate innate immun
261 l IgM antibodies represent a class of innate pattern recognition receptors that recognize danger-asso
262 Toll-like receptors (TLR) are transmembrane pattern recognition receptors that recognize microbial l
263 ormyl-peptide receptors (FPRs) are important pattern recognition receptors that sense specific bacter
264 e response" is mediated by germ line-encoded pattern recognition receptors that trigger activation of
266 d induction is a consequence of signaling by pattern-recognition receptors that have been selected ov
267 peptide receptors (FPRs) serve as phagocyte pattern-recognition receptors that play a crucial role i
268 signals released by dying cells, the role of pattern recognition receptors, the diverse subtypes of r
269 mes containing unshielded RNAs that activate pattern recognition receptors, thereby promoting tumor g
270 IBCD1 as a previously unrecognized microbial pattern recognition receptor through which intestinal ep
272 l pathways that contain cytokine QTLs map to pattern recognition receptors (TLR1-6-10 cluster), cytok
274 of the differentiated keratinocyte-specific pattern recognition receptor TLR7, the Langerhans cell c
275 the adhesion molecules ICAM and VCAM and the pattern-recognition receptors TLR7 and TLR9 in the vascu
276 s revealed that ALV infection is detected by pattern-recognition receptors (TLR9 and TLR3) leading to
279 converge with those activated downstream of pattern recognition receptors to determine the type and
280 or efficient interaction of RNA ligands with pattern recognition receptors to enhance IFN production
281 lipoteichoic acid (LTA), which interact with pattern recognition receptors to mobilize immune respons
282 molecular patterns (DAMPs) and interact with pattern recognition receptors to modulate inflammatory r
283 lectins, such as galectin-1, can function as pattern recognition receptors to reduce infection and in
284 , and antioxidants and express innate immune pattern recognition receptors to respond to inhaled fore
285 sociated molecular patterns (PAMPs) and bind pattern recognition receptors to stimulate IFN productio
288 tivity, and requires no interaction with the pattern recognition receptor, Toll-like receptor 2 (TLR2
289 expression in response to activators of the pattern recognition receptors, toll-like receptor-2 (TLR
290 cesses add or remove cargo proteins (such as pattern-recognition receptors, transporters, and other p
292 protein-mediated signaling through cytosolic pattern recognition receptors was required for polyinosi
293 at the expression of PTX3, a soluble form of pattern recognition receptor, was induced by infection w
295 signaling, granzyme B signaling and pathogen pattern recognition receptors, which are responsible for
296 ecular patterns (PAMPs) by surface-localized pattern recognition receptors, which initiates a series
297 n immune system utilizes several families of pattern recognition receptors, which survey the intracel
298 he innate immune system is activated through pattern recognition receptors-which include transmembran
299 Most NLR proteins function as cytosolic pattern recognition receptors with activation of downstr