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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

25 overs the contribution of the chloroplast to pathogen associated molecular pattern and effector trigg

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

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

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

29 These results implicate Z-RNA as a new pathogen-associated molecular pattern and describe a ZBP

30 s minimal peptide epitope Crip21, serve as a pathogen-associated molecular pattern and specifically b

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

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

33 Pathogen-associated molecular patterns and damage-associ

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

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

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

37 e and adaptive immune systems by recognizing pathogen-associated molecular patterns and inducing the

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

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

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

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

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

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

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

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

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

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

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

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

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

51 receptors or Toll-like receptors that sense pathogen-associated molecular patterns, and signal downs

52 er sites such as the intestinal tract, where pathogen-associated molecular patterns are abundant, cyt

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

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

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

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

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

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

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

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

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

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

63 lso demonstrate that one of the major fungal pathogen-associated molecular patterns, beta-glucan, dir

64 onize the stimulatory effect of a variety of pathogen associated molecular patterns by inhibiting IRF

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

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

67 Recognition of pathogen-associated molecular patterns by innate immune

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

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

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

71 Recognition of pathogen-associated molecular patterns by pattern recogn

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

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

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

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

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

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

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

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

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

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

82 ese responses to environmental cues, such as pathogen-associated molecular patterns, damage-associate

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

84 ysaccharides (LPS), cytokines and damage- or pathogen-associated molecular patterns (DAMPs/PAMPs) fro

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

86 Pathogen-associated molecular patterns (e.g., dsRNA) act

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

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

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

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

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

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

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

94 Pathogen-associated molecular patterns in gram-positive

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

96 Here, we show that CCN1 binds bacterial pathogen-associated molecular patterns including peptido

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

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

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

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

101 In the setting of infection, pathogen-associated molecular patterns induce emergency

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

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

104 Multiple pathogen-associated molecular pattern-induced TLR pathwa

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

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

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

108 4 (NLRC4)/Ipaf is involved in recognition of pathogen-associated molecular patterns leading to caspas

109 wo signals: first, priming by recognition of pathogen-associated molecular patterns leads to the prod

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

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

112 Upon activation with pathogen-associated molecular patterns, metabolism of ma

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

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

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

116 Bacterial pathogen-associated molecular pattern molecules (PAMPs)

117 Pathogen-associated molecular pattern molecules (PAMPs)

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

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

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

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

122 Among mice deficient in receptors for pathogen-associated molecular patterns, MyD88(-/-) and S

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

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

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

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

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

128 indicating a conserved but insufficient PTI [pathogen associated molecular pattern (PAMP) triggered i

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

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

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

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

133 It represents a key pathogen-associated molecular pattern (PAMP) during infe

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

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

136 5' triphosphate (5'ppp) of the HCV RNA and a pathogen-associated molecular pattern (PAMP) motif locat

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

138 ctivation of S. aureus lipoproteins, a major pathogen-associated molecular pattern (PAMP) of extracel

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

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

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

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

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

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

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

146 promote immune evasion by masking of a major pathogen-associated molecular pattern (PAMP), beta-gluca

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

148 thodes of seedlings treated with a bacterial pathogen-associated molecular pattern (PAMP), flagellin

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

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

151 t from effector-triggered immunity (ETI) and pathogen-associated molecular pattern (PAMP)-triggered i

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

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

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

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

156 1 combines with the LRR-RLKs FLS2 and EFR in pathogen-associated molecular pattern (PAMP)-triggered i

157 1-associated kinase 1 (BAK1) is required for pathogen-associated molecular pattern (PAMP)-triggered i

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

159 Plant immunity consists of two arms: pathogen-associated molecular pattern (PAMP)-triggered i

160 eveal the PUN RNA to be a CoV MDA5-dependent pathogen-associated molecular pattern (PAMP).

161 eriod, these APCs are profoundly modified by pathogen-associated molecular pattern (PAMP)/damage-asso

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

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

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

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

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

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

168 tected by fixed, germline encoded receptors, pathogen-associated molecular pattern (PAMPs) subsequent

169 Microbial pathogen-associated molecular patterns (PAMPs) activate

170 Pathogen-associated molecular patterns (PAMPs) activate

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

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

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

174 As produced during viral infections serve as pathogen-associated molecular patterns (PAMPs) and bind

175 TLRs) are a class of proteins that recognize pathogen-associated molecular patterns (PAMPs) and damag

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

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

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

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

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

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

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

183 Pathogen-associated molecular patterns (PAMPs) are detec

184 Pathogen-associated molecular patterns (PAMPs) are known

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

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

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

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

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

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

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

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

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

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

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

196 the current concept of bacterial infections, pathogen-associated molecular patterns (PAMPs) derived f

197 When pathogen-associated molecular patterns (PAMPs) displayed

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

199 Pathogen-associated molecular patterns (PAMPs) have the

200 recognition receptors (PRRs) that recognize pathogen-associated molecular patterns (PAMPs) in microb

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

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

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

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

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

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

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

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

209 Although pathogen-associated molecular patterns (PAMPs) produced

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

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

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

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

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

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

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

217 Pathogen-associated molecular patterns (PAMPs) that sign

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 Translocation of pathogen-associated molecular patterns (PAMPs) was deter

222 ed in response to diverse stimuli, including pathogen-associated molecular patterns (PAMPs)(1).

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

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

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

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

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

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

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

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

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

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

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

238 ction with rice pathogens and treatment with pathogen-associated molecular patterns (PAMPs).

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

240 is rapidly phosphorylated upon perception of pathogen-associated molecular patterns (PAMPs).

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

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

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

244 ic organisms that are collectively known as "pathogen-associated molecular patterns" (PAMPs) or host-

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

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

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

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

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

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

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

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

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

254 r imposed by the outer membrane and offers a pathogen-associated molecular pattern recognized by inna

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

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

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

258 pose an evolutionary scenario beginning with pathogen-associated molecular pattern(s) (PAMPs) being p

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

260 As pathogen-associated molecular pattern sensors, the TLRs

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

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

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

264 SOL, like EDR4, is induced in response to pathogen-associated molecular patterns such as flg22.

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

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

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

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

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

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

271 nnate immune response by recognition of both pathogen-associated molecular patterns that are engulfed

272 cans from microbial pathogens are well known pathogen-associated molecular patterns that are recogniz

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

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

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

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

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

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

279 Microbiota-shed pathogen-associated molecular patterns translocate from

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

281 f PM depolarization and negatively regulates pathogen-associated molecular pattern-triggered immunity

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

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

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

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

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

287 r-triggered immunity (ETI) responses but not 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 ike effectors and involved in suppression of pathogen-associated molecular pattern-triggered immunity

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

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

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

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

295 gesting that processes beyond recognition of pathogen-associated molecular patterns were required for

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