ライフサイエンスコーパス: pathogen-associated molecular pattern

1 se transcription product comprises the HIV-1 pathogen-associated molecular pattern.

2 NA as the principal innate immune-activating pathogen-associated molecular pattern.

3 ased levels of double-stranded RNA, a potent pathogen-associated molecular pattern.

4 nents of the fungal cell wall and key fungal pathogen-associated molecular patterns.

5 es microbes from self by detecting conserved pathogen-associated molecular patterns.

6 strong affinity between rSp0032 and several pathogen-associated molecular patterns.

7 ich were originally identified as sensors of pathogen-associated molecular patterns.

8 walls and is one of the well-studied microbe/pathogen-associated molecular patterns.

9 ecific subcellular compartments and can bind pathogen-associated molecular patterns.

10 for many of the responses of macrophages to pathogen-associated molecular patterns.

11 immune system uses various proteins to sense pathogen-associated molecular patterns.

12 ceptors that recognize microbial products or pathogen-associated molecular patterns.

13 y in plants can be triggered by microbe- and pathogen-associated molecular patterns.

14 he inflammatory response elicited by its own pathogen-associated molecular patterns.

15 ent with methyl jasmonate, Pep peptides, and pathogen-associated molecular patterns.

16 by innate immune cells recognizing conserved pathogen-associated molecular patterns.

17 increased susceptibility to danger- but not pathogen-associated molecular patterns.

18 cell death and discriminates danger- versus pathogen-associated molecular patterns.

19 by pattern recognition molecules recognizing pathogen-associated molecular patterns.

20 oglia recognize and are activated by various pathogen-associated molecular patterns.

21 fense-expressing plants after treatment with pathogen-associated molecular patterns.

22 o tumour-necrosis factor (TNF), IL-1beta and pathogen-associated molecular patterns.

23 of immunity triggered by host recognition of pathogen-associated molecular patterns.

24 agonist properties with typical features of pathogen-associated molecular patterns.

25 ons, such as TLRs, which allow them to sense pathogen-associated molecular patterns.

26 ) family, detect stress, danger stimuli, and pathogen-associated molecular patterns.

27 rich repeat domain responsible for detecting pathogen-associated molecular patterns, a membrane spann

28 Toll-like receptors (TLRs) recognize pathogen-associated molecular patterns, act through adap

29 Danger- and pathogen-associated molecular patterns activate Nod-like

30 ng lectin (encoded by MBL2) bind to specific pathogen-associated molecular patterns, activate the com

31 ody, a tissue of neural crest origin, detect pathogen associated molecular patterns and danger associ

32 though the role of NLRP3 in host response to pathogen associated molecular patterns and danger associ

33 TLRs are immune receptors that recognize pathogen associated molecular patterns and then signal a

34 the role of post-translational responses to pathogen-associated molecular pattern and damage-associa

35 a nonstructural protein encoded by EBV is a pathogen-associated molecular pattern and that it has im

36 nthomonas species, confirming that Ax21 is a pathogen-associated molecular pattern and that XA21 is a

37 crophages is activated by the recognition of pathogen-associated molecular patterns and by many struc

38 n integrates environmental cues derived from pathogen-associated molecular patterns and cell-intrinsi

39 Pathogen-associated molecular patterns and damage-associ

40 proteins, NLRs, are intracellular sensors of pathogen-associated molecular patterns and damage-associ

41 Recognition of pathogen-associated molecular patterns and danger-associ

42 metabolic profiles rather similar to that of pathogen-associated molecular patterns and discuss how s

43 role as a recognition molecule of exogenous pathogen-associated molecular patterns and initiator of

44 gal cell wall is decorated with multifarious pathogen-associated molecular patterns and is the main t

45 chaffeensis PBP provides novel insights into pathogen-associated molecular patterns and pathogenesis

46 litatively modulates macrophage responses to pathogen-associated molecular patterns and pathogens by

47 ses to microbes are the interactions between pathogen-associated molecular patterns and pattern recog

48 ng growth factor-beta through recognition of pathogen-associated molecular patterns and phosphatidyls

49 tracellular receptors that recognize various pathogen-associated molecular patterns and play crucial

50 Microglia are activated by pathogen-associated molecular patterns and produce proin

51 inflammation through their ability to sense pathogen-associated molecular patterns and products of t

52 pattern recognition receptors that recognize pathogen-associated molecular patterns and signal throug

53 F1 inhibits ethylene biosynthesis induced by pathogen-associated molecular patterns and that Arabidop

54 le for this protein in cytokine induction by pathogen-associated molecular patterns and viruses.

55 LPS is a pathogen-associated molecular pattern, and several patho

56 ocessing in response to bacterial infection, pathogen-associated molecular patterns, and damage-assoc

57 xpress Toll-like receptors (TLRs), recognize pathogen-associated molecular patterns, and mediate the

58 through which signals from helper T cells or pathogen-associated molecular patterns are delivered.

59 NF-kappaB is activated after pathogen-associated molecular patterns are detected, lea

60 tem detects HCV infection, including how HCV pathogen-associated molecular patterns are generated dur

61 During acute HIV-1 infection, viral pathogen-associated molecular patterns are recognized by

62 TLRs are stimulated both by pathogen-associated molecular patterns as well as by dam

63 h multiple signals, including recognition of pathogen-associated molecular patterns, as well as signa

64 XA21 is degraded in the presence of the pathogen-associated molecular pattern Ax21 when XB24 is

65 The rice PRR XA21 recognizes the pathogen-associated molecular pattern, Ax21 (activator o

66 is study demonstrates that in the absence of pathogen-associated molecular patterns, Batf3-dependent

67 g a lectin-like domain that binds the fungal pathogen-associated molecular pattern beta-glucan and se

68 e report that recognition of purified fungal pathogen-associated molecular pattern beta-glucan by hum

69 tent with the concept that bacteria modulate pathogen-associated molecular patterns by expression of

70 rly in the course of infection, detection of pathogen-associated molecular patterns by innate immune

71 Recognition of pathogen-associated molecular patterns by innate immune

72 y against microbes depends on recognition of pathogen-associated molecular patterns by innate recepto

73 Likewise, recognition of pathogen-associated molecular patterns by monocytes and

74 vated upon cytosolic sensing of a variety of pathogen-associated molecular patterns by Nod-like recep

75 Recognition of pathogen-associated molecular patterns by pattern recogn

76 of signaling evoked by direct perception of pathogen-associated molecular patterns by plant cells un

77 n, innate immune cells are able to recognize pathogen-associated molecular patterns by receptors such

78 In innate immune sensing, the detection of pathogen-associated molecular patterns by recognition re

79 rgency myelopoiesis, involves recognition of pathogen-associated molecular patterns by the common mye

80 of danger-associated molecular patterns and pathogen-associated molecular patterns by the nervous sy

81 Recognition of pathogen-associated molecular patterns by Toll-like rece

82 l capsids were sensed at the cell surface as pathogen-associated molecular patterns by Toll-like rece

83 Recognition of pathogen-associated molecular patterns by Toll-like rece

84 The identification of pathogen-associated molecular patterns, conserved microb

85 ition receptors contain a binding domain for pathogen-associated molecular patterns coupled to a sign

86 loaded with Ag and surface modified with the pathogen-associated molecular pattern CpG oligodeoxynucl

87 stem recognizes both damage (or danger)- and pathogen-associated molecular patterns (DAMP and PAMP, r

88 flammation mediated by damage-associated and pathogen-associated molecular patterns (DAMPs and PAMPs)

89 late monophosphate (c-di-AMP) is an emerging pathogen-associated molecular pattern during intracellul

90 nd FLS2 mediate recognition of the bacterial pathogen-associated molecular patterns EF-Tu and flagell

91 The bacterial pathogen-associated molecular pattern elicitor lipopolys

92 generation of reactive oxygen species after pathogen-associated molecular pattern elicitor treatment

93 otein signaling is directly activated by the pathogen-associated molecular pattern flagellin peptide

94 require potent adjuvants, as they lack known pathogen-associated molecular patterns found in attenuat

95 Chitin acts as a pathogen-associated molecular pattern from fungal pathog

96 immunity that specifically recognize diverse pathogen-associated molecular patterns from pathogens.

97 ugh the generation and accumulation of viral pathogen-associated molecular patterns has been well cha

98 chanisms governing the innate recognition of pathogen-associated molecular patterns have been well de

99 belonging to the classes of the damage- and pathogen-associated molecular patterns, i.e. oligogalact

100 e considered the primary cells to respond to pathogen associated molecular patterns in the liver, rec

101 Pathogen-associated molecular patterns in gram-positive

102 sterile conditions to avoid the influence of pathogen-associated molecular patterns in subsequent exp

103 deficiency during activation with bacterial pathogen associated molecular patterns, including heat-k

104 mmunity are initiated upon the perception of pathogen-associated molecular patterns, including peptid

105 rates the role of ferrous iron (Fe(2+)) as a pathogen-associated molecular pattern-independent agonis

106 the host cell inflammasome response to other pathogen-associated molecular patterns, indicated by red

107 te immunity, we defined the effects of CS on pathogen-associated molecular pattern-induced (PAMP-indu

108 Pathogen- and pathogen-associated molecular pattern-induced focal accu

109 K4 activity was found to negatively regulate pathogen-associated molecular pattern-induced reactive o

110 Multiple pathogen-associated molecular pattern-induced TLR pathwa

111 Wnts also alter DC responses to microbe- or pathogen-associated molecular patterns, inhibiting proin

112 Upon detection of pathogen-associated molecular patterns, innate immune re

113 arising from the organismal distribution of pathogen-associated molecular patterns is a major cause

114 Innate immune cell activation triggered by pathogen-associated molecular patterns is mediated by va

115 ity is broad and based on the recognition of pathogen-associated molecular patterns, it is uniquely r

116 4 (NLRC4)/Ipaf is involved in recognition of pathogen-associated molecular patterns leading to caspas

117 or; PRR, pattern recognition receptor; PAMP, pathogen-associated molecular pattern; LPS, lipopolysacc

118 Inflammation induced by recognition of pathogen-associated molecular patterns markedly affects

119 Pathogen-associated molecular pattern-mediated NO genera

120 ouble-stranded (ds) RNA substrate, a typical pathogen-associated molecular pattern molecule, to induc

121 the same signaling pathways evoked by danger/pathogen associated molecular pattern molecules.

122 he patient's myeloid cells with a variety of pathogen-associated molecular pattern molecules (PAMPs)

123 Bacterial pathogen-associated molecular pattern molecules (PAMPs)

124 Pathogen-associated molecular pattern molecules (PAMPs)

125 act as an innate immune sensor of microbial pathogen-associated molecular pattern molecules (PAMPs)

126 er of pathogens, including helminths, act as pathogen-associated molecular pattern molecules (PAMPs),

127 primary HLSECs transfected with HCV-specific pathogen-associated molecular pattern molecules increase

128 a luciferase reporter, and the HCV-specific pathogen-associated molecular pattern molecules.

129 I elicits NET formation by means of multiple pathogen-associated molecular patterns (most notably end

130 In response to proinflammatory cytokines and pathogen-associated molecular patterns, NF-kappaB activa

131 pattern recognition receptors in recognizing pathogen-associated molecular patterns of Mycobacterium

132 ost pattern recognition molecules that sense pathogen-associated molecular patterns of the invading p

133 ieu due to the robust production elicited by pathogen-associated molecular patterns on cells of the i

134 ine development, multivalent presentation of pathogen-associated molecular patterns on the particle s

135 elf-motifs within viral products (known as a pathogen-associated molecular pattern or PAMP) to trigge

136 masome complex requires cytosolic sensing of pathogen-associated molecular patterns or danger-associa

137 Intratumoral therapy with pathogen-associated molecular patterns or recombinant vi

138 tput of Toll-like receptor (TLR) response to pathogen associated molecular patterns (PAMP), and (iii)

139 Foreign RNA serves as pathogen-associated molecular pattern (PAMP) and is a po

140 Plasmodium RNA as a previously unrecognized pathogen-associated molecular pattern (PAMP) capable of

141 eties of its natural Gram negative bacterial pathogen-associated molecular pattern (PAMP) counterpart

142 ts reveal c-di-AMP to be a key mycobacterial pathogen-associated molecular pattern (PAMP) driving hos

143 tional CTLs is specific to the nature of the pathogen-associated molecular pattern (PAMP) encountered

144 port that the exposure of beta-glucan, a key pathogen-associated molecular pattern (PAMP) located at

145 5' triphosphate (5'ppp) of the HCV RNA and a pathogen-associated molecular pattern (PAMP) motif locat

146 athogen recognition receptor that recognizes pathogen-associated molecular pattern (PAMP) motifs to d

147 The nucleus is unlikely to have pathogen-associated molecular pattern (PAMP) receptors f

148 RNA to deplete proteins involved in specific pathogen-associated molecular pattern (PAMP) recognition

149 sting that malaria parasites harbor a common pathogen-associated molecular pattern (PAMP) recognized

150 a subset of genes involved in immunity, and pathogen-associated molecular pattern (PAMP) signals rep

151 pidly biochemically activated in response to pathogen-associated molecular pattern (PAMP) stimulation

152 sence of a single Sh3bp2 cherubic allele and pathogen-associated molecular pattern (PAMP) stimulation

153 (LPS) of Gram-negative bacteria is a common pathogen-associated molecular pattern (PAMP) that induce

154 surface glycoprotein, VSV-G, was likely the pathogen-associated molecular pattern (PAMP) that initia

155 These methods revealed that dsRNA, a pathogen-associated molecular pattern (PAMP), comprised

156 We show that XopN action in planta reduced pathogen-associated molecular pattern (PAMP)-induced gen

157 ouse bone marrow-derived dendritic cell (DC) pathogen-associated molecular pattern (PAMP)-induced pro

158 A tradeoff between pathogen-associated molecular pattern (PAMP)-triggered i

159 initial defense responses from the plant is pathogen-associated molecular pattern (PAMP)-triggered i

160 dicating that AvrPiz-t functions to suppress pathogen-associated molecular pattern (PAMP)-triggered i

161 osest homologue, CRH1, are also required for pathogen-associated molecular pattern (PAMP)-triggered i

162 1 combines with the LRR-RLKs FLS2 and EFR in pathogen-associated molecular pattern (PAMP)-triggered i

163 1-associated kinase 1 (BAK1) is required for pathogen-associated molecular pattern (PAMP)-triggered i

164 erium Pseudomonas syringae can suppress both pathogen-associated molecular pattern (PAMP)-triggered i

165 ntegral part of the signaling cascade during pathogen-associated molecular pattern (PAMP)-triggered i

166 prises membrane glycoproteins that recognize pathogen-associated molecular patterns (PAMP) and mediat

167 ed processes, such as hyperresponsiveness to pathogen-associated molecular patterns (PAMP), enhanced

168 The inflammasome NLRP3 is activated by pathogen associated molecular patterns (PAMPs) during in

169 an be elicited by infection (sepsis) through pathogen associated molecular patterns (PAMPs) or throug

170 Chronic stimulation by bacterial pathogen associated molecular patterns (PAMPs), such as

171 ease resistance through their recognition of pathogen associated molecular patterns (PAMPs).

172 P. patens required for immunity triggered by pathogen associated molecular patterns (PAMPs).

173 Microbial pathogen-associated molecular patterns (PAMPs) activate

174 These receptors recognize pathogen-associated molecular patterns (PAMPs) and activ

175 Transmembrane receptors recognize conserved pathogen-associated molecular patterns (PAMPs) and activ

176 ein that regulates plant immune responses to pathogen-associated molecular patterns (PAMPs) and bacte

177 e stimulation by environmental or endogenous pathogen-associated molecular patterns (PAMPs) and dange

178 Intestinal mast cells express numerous pathogen-associated molecular patterns (PAMPs) and have

179 -I, MDA-5, and LGP2) recognize viral RNAs as pathogen-associated molecular patterns (PAMPs) and initi

180 Plant perception of pathogen-associated molecular patterns (PAMPs) and other

181 udomonas syringae involves both detection of pathogen-associated molecular patterns (PAMPs) and recog

182 on of innate immunity through the release of pathogen-associated molecular patterns (PAMPs) and their

183 dritic cells (DCs) are directly activated by pathogen-associated molecular patterns (PAMPs) and under

184 Pathogen-associated molecular patterns (PAMPs) are detec

185 Pathogen-associated molecular patterns (PAMPs) are known

186 In Arabidopsis thaliana, responses to pathogen-associated molecular patterns (PAMPs) are media

187 n shown to close in response to bacteria and pathogen-associated molecular patterns (PAMPs) as part o

188 ptors (TLRs) exert a key role in recognizing pathogen-associated molecular patterns (PAMPs) but have

189 Recognition of conserved pathogen-associated molecular patterns (PAMPs) by host p

190 the generation of interferon (IFN)-inducing pathogen-associated molecular patterns (PAMPs) by influe

191 Innate immunity relies on the perception of pathogen-associated molecular patterns (PAMPs) by patter

192 s can detect invaders via the recognition of pathogen-associated molecular patterns (PAMPs) by patter

193 mponent of plant defense is the detection of pathogen-associated molecular patterns (PAMPs) by plasma

194 e potential pathogens via the recognition of pathogen-associated molecular patterns (PAMPs) by surfac

195 In plants, perception of pathogen-associated molecular patterns (PAMPs) by surfac

196 Recognition of pathogen-associated molecular patterns (PAMPs) by surfac

197 Perception of pathogen-associated molecular patterns (PAMPs) constitut

198 ing virion RNA display at least two distinct pathogen-associated molecular patterns (PAMPs) containin

199 A variety of RNA-related pathogen-associated molecular patterns (PAMPS) have been

200 (GH12) proteins act as virulence factors and pathogen-associated molecular patterns (PAMPs) in oomyce

201 yndrome (TRAPS), whilst both spontaneous and pathogen-associated molecular patterns (PAMPs) induced I

202 by recognizing microbial molecules known as pathogen-associated molecular patterns (PAMPs) inducing

203 Concealing pathogen-associated molecular patterns (PAMPs) is a prin

204 n of pattern-recognition receptors (PRRs) by pathogen-associated molecular patterns (PAMPs) is in ess

205 Activation of PRRs by their respective pathogen-associated molecular patterns (PAMPs) leads to

206 ous ligand-binding ectodomains that perceive pathogen-associated molecular patterns (PAMPs) or damage

207 n-recognition receptors (PRRs) and cell wall pathogen-associated molecular patterns (PAMPs) orientate

208 Although pathogen-associated molecular patterns (PAMPs) produced

209 gh Toll-like receptor 2 (TLR2); however, the pathogen-associated molecular patterns (PAMPs) responsib

210 Plant recognition of pathogen-associated molecular patterns (PAMPs) such as b

211 mmunostimulatory factors and presentation of pathogen-associated molecular patterns (PAMPs) that are

212 stem of humans and other mammals responds to pathogen-associated molecular patterns (PAMPs) that are

213 icrobes relies on the detection of conserved pathogen-associated molecular patterns (PAMPs) that are

214 attern recognition receptors (PRRs) to sense pathogen-associated molecular patterns (PAMPs) that are

215 cleic acids constitute an important group of pathogen-associated molecular patterns (PAMPs) that effi

216 Pathogen-associated molecular patterns (PAMPs) that sign

217 responses may be initiated by recognition of pathogen-associated molecular patterns (PAMPs) that stim

218 es to vaccines require direct recognition of pathogen-associated molecular patterns (PAMPs) through p

219 Pretreatment of plants with pathogen-associated molecular patterns (PAMPs) to induce

220 Plant perception of pathogen-associated molecular patterns (PAMPs) triggers

221 t imposed through high conservation of viral Pathogen-Associated Molecular Patterns (PAMPs), and by t

222 Reactive oxygen species (ROS), pathogen-associated molecular patterns (PAMPs), and dama

223 cular patterns (DAMPs), but not to microbial pathogen-associated molecular patterns (PAMPs), are repr

224 obial-associated molecular patterns (MAMPs), pathogen-associated molecular patterns (PAMPs), danger-a

225 s suppress the cytokine response to multiple pathogen-associated molecular patterns (PAMPs), includin

226 eptors) are used by glial cells to recognize pathogen-associated molecular patterns (PAMPs), mediate

227 receptors (RLRs) that are activated by viral pathogen-associated molecular patterns (PAMPs), such as

228 Perception of pathogen-associated molecular patterns (PAMPs), such as

229 Signal one involves recognition of pathogen-associated molecular patterns (PAMPs), such as

230 Pathogen-associated molecular patterns (PAMPs), which ar

231 nexpected LPS glycosylation fuses two potent pathogen-associated molecular patterns (PAMPs).

232 oceroserate (PDIM) lipids to mask underlying pathogen-associated molecular patterns (PAMPs).

233 unity triggered upon perception of conserved pathogen-associated molecular patterns (PAMPs).

234 ense mechanism used to detect and respond to pathogen-associated molecular patterns (PAMPs).

235 ceptors, which are activated upon binding to pathogen-associated molecular patterns (PAMPs).

236 by recognizing a diverse array of conserved pathogen-associated molecular patterns (PAMPs).

237 set of signaling responses to some bacterial pathogen-associated molecular patterns (PAMPs).

238 tors (PRRs) that respond to ligands known as pathogen-associated molecular patterns (PAMPs).

239 tion of viral macromolecular motifs known as pathogen-associated molecular patterns (PAMPs).

240 phagy is controlled by recognizing conserved pathogen-associated molecular patterns (PAMPs).

241 all vesicles known as exosomes which contain pathogen-associated molecular patterns (PAMPs).

242 of well-characterized signaling pathways by pathogen-associated molecular patterns (PAMPs).

243 gen recognition receptors (PRR) engage viral pathogen-associated molecular patterns (PAMPs).

244 One important aspect is interaction with pathogen-associated molecular patterns (PAMPs)/danger-as

245 S in lungs from mice exposed to CS and viral pathogen-associated molecular patterns (PAMPs)/live viru

246 ibacters trigger plant immunity response via pathogen-associated molecular patterns (PAMPs, such as l

247 By analogy with microbial "pathogen-associated molecular patterns" (PAMPs), we post

248 gellin) associated with microbial pathogens (pathogen-associated molecular patterns, PAMPs), whereas

249 Upon perception of pathogen-associated molecular patterns, PEN3 becomes pho

250 ABC transporter, as a gene responsive to the pathogen-associated molecular pattern Pep-13.

251 beta-glucans are pathogen-associated molecular patterns present within fu

252 In the second pathway, damage-/pathogen-associated molecular pattern receptor genes cap

253 Toll-like receptors (TLRs), which are early pathogen associated molecular pattern receptors, in path

254 ligands to test whether triggering multiple pathogen-associated molecular pattern receptors could en

255 ual advance, in that NLRX1 is a modulator of pathogen-associated molecular pattern receptors rather t

256 tiple receptors including insulin receptors, pathogen-associated molecular pattern receptors, cytokin

257 resulting from the GI-2 deletion may affect pathogen-associated molecular pattern recognition by Tol

258 drawn attention to a strong relationship of pathogen-associated molecular pattern recognition with a

259 cytes caspase-1 activation is uncoupled from pathogen-associated molecular pattern recognition.

260 In addition, the major pathogen associated molecular pattern recognizing recept

261 he host distinguishes between danger- versus pathogen-associated molecular patterns remains unresolve

262 y innate immune cells that upon encountering pathogen-associated molecular patterns respond by produc

263 Upon detection of intracellular pathogen-associated molecular patterns, RISC activity de

264 resent a class of previously uncharacterised pathogen-associated molecular patterns sensed by pattern

265 As pathogen-associated molecular pattern sensors, the TLRs

266 ies, particularly when CD4(+) T-cell help or pathogen-associated molecular pattern signals are limite

267 e receptor (NLR) proteins act as sensors for pathogen-associated molecular patterns, stress, or dange

268 monoubiquitylates Perforin-2 in response to pathogen associated molecular patterns such as LPS.

269 istance by diminishing surface expression of pathogen-associated molecular patterns, such as flagella

270 ogen detection is triggered by perception of pathogen-associated molecular patterns, such as flagelli

271 nnate immune system, mainly mediated through pathogen-associated molecular patterns, such as flagelli

272 LRs) recognize pathogens by interacting with pathogen-associated molecular patterns, such as the phos

273 dsRNA is a common pathogen-associated molecular pattern that is recognized

274 en Pseudomonas aeruginosa expresses not only pathogen-associated molecular patterns that activate NF-

275 ike receptor (TLR) signaling is triggered by pathogen-associated molecular patterns that mediate well

276 Chitin contains size-dependent pathogen-associated molecular patterns that stimulate TL

277 Despite the absence of exogenous microbial pathogen-associated molecular patterns, the Tfh cell res

278 Microbes are detected by the pathogen-associated molecular patterns through specific

279 ribute to cytokine production in response to pathogen associated molecular pattern-TLR-mediated stimu

280 While host immune receptors detect pathogen-associated molecular patterns to activate immun

281 rferon-driven events can lead to exposure of pathogen-associated molecular patterns to the host cytos

282 lated) electrolyte leakage and a compromised pathogen-associated molecular pattern-triggered immune r

283 duction elements that coordinate damage- and pathogen-associated molecular pattern-triggered immunity

284 r-triggered immunity (ETI) responses but not pathogen-associated molecular pattern-triggered immunity

285 s heterotrimeric G-protein complex modulates pathogen-associated molecular pattern-triggered immunity

286 r-triggered immunity (ETI) responses but not pathogen-associated molecular pattern-triggered immunity

287 Signaling components are shared between the pathogen-associated molecular pattern-triggered immunity

288 recognition receptor that is responsible for pathogen-associated molecular pattern-triggered immunity

289 The pathogen-associated molecular pattern-triggered immunity

290 cognition receptor complexes, which disrupts pathogen-associated molecular pattern-triggered immunity

291 Both proteasome subunits are required for pathogen-associated molecular pattern-triggered immunity

292 the proteasome is an essential component of pathogen-associated molecular pattern-triggered immunity

293 The importance of pathogen-associated molecular pattern-triggered immunity

294 tahrcC mutant, and decreased expression of a pathogen-associated molecular pattern-triggered marker g

295 infection, indicating that HCV dsRNA was the pathogen-associated molecular pattern triggering TLR3 si

296 innate inflammasome responses recognize the pathogen-associated molecular patterns which lead into t

297 ccharides that comprise the cell wall act as pathogen associated molecular patterns, which govern the

298 is required for recognition and detection of pathogen associated molecular patterns, which results in

299 ce, systemic inflammation was induced by the pathogen associated molecular pattern zymosan (intraperi

300 In response to the fungal-derived pathogen-associated molecular pattern zymosan, neutrophi