ライフサイエンスコーパス: antimicrobial peptide

1 isms that induce intestinal expression of an antimicrobial peptide.

2 aS1-casein (1-23) is an immunomodulatory and antimicrobial peptide.

3 istin has led to resistance to this cationic antimicrobial peptide.

4 ys-Tyr-Arg), a small (653Da) and hydrophilic antimicrobial peptide.

5 utionary relationship between chemokines and antimicrobial peptides.

6 releasate, and synthetic platelet-associated antimicrobial peptides.

7 PG can inhibit TLR activation in response to antimicrobial peptides.

8 riaxone resulted in greater reduction of key antimicrobial peptides.

9 hogenic bacteria: a new strategy to generate antimicrobial peptides.

10 ut microbiota and on the expression of ileal antimicrobial peptides.

11 tation, low pH, and the presence of cationic antimicrobial peptides.

12 de destruxin A by increasing the activity of antimicrobial peptides.

13 with enhanced expression of IL-22-inducible antimicrobial peptides.

14 e increased bacterial load and expression of antimicrobial peptides.

15 gh alterations in the urinary microbiome and antimicrobial peptides.

16 uires PhoP to resist killing by host derived antimicrobial peptides.

17 information for the design of new synthetic antimicrobial peptides.

18 tion and abscess formation; and host-derived antimicrobial peptides.

19 ability to hydrolyze milk casein to generate antimicrobial peptides.

20 acillus subtilis controlling the response to antimicrobial peptides.

21 ng changes in Mg(2+) concentrations, pH, and antimicrobial peptides.

22 ycles designed to mimic facially amphiphilic antimicrobial peptides.

23 nds to low extracellular Mg(++) and cationic antimicrobial peptides.

24 egates by other amyloid-forming proteins and antimicrobial peptides.

25 macrophage granules as also observed in most antimicrobial peptides.

26 ations with natural moisturizing factors and antimicrobial peptides.

27 to an upregulation in the expression of key antimicrobial peptides.

28 tasis and reduction in the production of gut antimicrobial peptides.

29 Liver-expressed antimicrobial peptide 2 (LEAP2) was recently described a

30 Here, we hypothesized that liver-enriched antimicrobial peptide-2 (LEAP2), a recently characterize

31 that plasma levels of plasma liver-enriched antimicrobial peptide-2 (LEAP2), a recently identified h

32 priming/coating dentin with amphipathic and antimicrobial peptides (AAMPs) to obtain hydrophobic/wat

33 ides (LDAQSAPLR, LKGYGGVSLPEW, and LKALPMH), antimicrobial peptides (AASDISLLDAQSAPLR, IIAEKTKIPAVF,

34 We propose a topological model for linear antimicrobial peptide activity based on the increase in

35 -positive burn patients with altered urinary antimicrobial peptide activity developed either an E. fa

36 Furthermore, the antimicrobial peptide activity in burn patients was more

37 udy developed novel highly active food-grade antimicrobial peptides affecting a wide range of bacteri

38 rization of urinary bacterial microbiome and antimicrobial peptides after burn injury to identify pot

39 Here we report discovery of a new antimicrobial peptide, albopeptide, through NMR analysis

40 ed a peptidase to specifically degrade these antimicrobial peptides, allowing the bacteria to escape

41 ikrein, promoting neutrophils to release the antimicrobial peptide alpha-defensin-1, which enhances f

42 ohol and zinc deficiency on Paneth cell (PC) antimicrobial peptides, alpha-defensins, and to define t

43 of parallel heterodimer formation of the two antimicrobial peptides already at low concentrations and

44 Recently, the frog skin-derived antimicrobial peptide (AMP) Esc(1-21) and its diastereom

45 ccharide-binding protein (LBP), and duodenal antimicrobial peptide (AMP) expression at baseline were

46 typhi infects Drosophila cells and increases antimicrobial peptide (AMP) gene expression, indicating

47 and Relish, have been identified to activate antimicrobial peptide (AMP) gene expression.

48 VINR is required for the induction of antimicrobial peptide (AMP) genes but dispensable for an

49 treatment also suppressed the expression of antimicrobial peptide (AMP) genes.

50 so is reported to prevent interaction of the antimicrobial peptide (AMP) LL-37 with the meningococcal

51 interleukin (IL)-23 and IL-22, which promote antimicrobial peptide (AMP) production and bacterial cle

52 The antimicrobial peptide (AMP) RNase 7 is constitutively ex

53 human granulysin, is a cationic amphiphilic antimicrobial peptide (AMP) that is produced by cytotoxi

54 We have previously described an antimicrobial peptide (AMP) Ubiquicidin (fragment UBI(29

55 idin was originally identified as a cationic antimicrobial peptide (AMP), but its putative expression

56 Protegrin-1 (PG-1) is a potent antimicrobial peptide (AMP).

57 s designing and testing new potent selective antimicrobial peptides (AMP) are increasingly attractive

58 Antimicrobial peptides (AMP) are molecules consisting of

59 Antimicrobial peptides (AMP) were upregulated in vaginal

60 e cationic and amphiphilic character of many antimicrobial peptides (AMP).

61 nnate interleukin 1 receptor, type 1 and the antimicrobial peptide(AMP) adrenomedullin.

62 n of membrane-disrupting antibiotics such as antimicrobial peptides (AMPs) and AMP mimetics is necess

63 Understanding how antimicrobial peptides (AMPs) and other membrane-active

64 Antimicrobial peptides (AMPs) are a potential source of

65 Here, we demonstrate that antimicrobial peptides (AMPs) are an effective antibiofi

66 Antimicrobial peptides (AMPs) are an important component

67 Antimicrobial peptides (AMPs) are central components of

68 Antimicrobial peptides (AMPs) are components of immune d

69 Antimicrobial peptides (AMPs) are essential components o

70 Antimicrobial peptides (AMPs) are generally cationic and

71 Antimicrobial peptides (AMPs) are innate immune molecule

72 Antimicrobial peptides (AMPs) are key effectors of the i

73 Antimicrobial peptides (AMPs) are naturally occurring pe

74 Antimicrobial peptides (AMPs) are promising antimicrobia

75 Many organisms rely on antimicrobial peptides (AMPs) as a first line of defense

76 toria aurea secrete numerous closely related antimicrobial peptides (AMPs) as an effective chemical d

77 In this regard, antimicrobial peptides (AMPs) can be used as effective b

78 We hypothesized that permeability-increasing antimicrobial peptides (AMPs) could lower the amount of

79 inical translation of cationic alpha-helical antimicrobial peptides (AMPs) has been hindered by struc

80 The activity of antimicrobial peptides (AMPs) has been investigated exte

81 As an alternative choice, antimicrobial peptides (AMPs) have attracted lots of att

82 ng a serious threat to global public health, antimicrobial peptides (AMPs) have become a promising ar

83 Membrane permeabilizing antimicrobial peptides (AMPs) have long been considered

84 Antimicrobial peptides (AMPs) have shown rapid and poten

85 The co-localization of histones with antimicrobial peptides (AMPs) in immune cells suggests t

86 Further, we show that genes for antimicrobial peptides (AMPs) including human beta-defen

87 Resistance to antimicrobial peptides (AMPs) is a key feature of urogen

88 The application of antimicrobial peptides (AMPs) is largely hindered by the

89 tion of matrix metalloproteinases (MMPs) and antimicrobial peptides (AMPs) is observed.

90 Amphiphilicity in a-helical antimicrobial peptides (AMPs) is recognized as a signatu

91 Protection against antimicrobial peptides (AMPs) often involves the paralle

92 Antimicrobial peptides (AMPs) play an important role in

93 nes (CMs) from the attack of antibiotics and antimicrobial peptides (AMPs) produced by the innate imm

94 Antimicrobial peptides (AMPs) represent a promising ther

95 Antimicrobial peptides (AMPs) represent promising altern

96 Antimicrobial peptides (AMPs) serve critical roles in mu

97 Antimicrobial peptides (AMPs) that disrupt bacterial mem

98 rvival is enabled by an immense diversity of antimicrobial peptides (AMPs) that maintain homeostasis

99 Skin and mucosal epithelia deploy antimicrobial peptides (AMPs) to eliminate harmful micro

100 tides with the right properties, for example Antimicrobial peptides (AMPs), can disrupt this protecti

101 the use of exogenous surfactants to deliver antimicrobial peptides (AMPs), like CATH-2, to infected

102 formation amphipathic alpha-helical cationic antimicrobial peptides (AMPs), seven with "specificity d

103 h the web-like strands of DNA is an array of antimicrobial peptides (AMPs), which facilitate the extr

104 There are some approximately 1,100 known antimicrobial peptides (AMPs), which permeabilize microb

105 l diversity and stimulated to release stored antimicrobial peptides (AMPs).

106 ides (CPPs) and the bactericidal activity of antimicrobial peptides (AMPs).

107 GCTLs) to evade the bactericidal capacity of antimicrobial peptides (AMPs).

108 f vitamin C lipid nanoparticles that deliver antimicrobial peptide and cathepsin B (AMP-CatB) mRNA.

109 Mg(2+) , Ca(2+) , pH and to the presence of antimicrobial peptides and activating the expression of

110 activate gSCCs upregulates the expression of antimicrobial peptides and ameliorates ligature-induced

111 pT, which confers resistance to host-derived antimicrobial peptides and bile, respectively.

112 f PCs and ISCs, which enhanced production of antimicrobial peptides and caused microbiome changes.

113 y in the intestine, through the induction of antimicrobial peptides and chemotactic genes.

114 eptide pores for understanding the action of antimicrobial peptides and for the design of pores with

115 rcapnia-induced reductions in Dipt and other antimicrobial peptides and improves resistance of CO2-ex

116 zed by altered mucus-associated proteins and antimicrobial peptides and increased susceptibility to c

117 so protects Acinetobacter from G. mellonella antimicrobial peptides and limits their expression.

118 odiscs have also allowed characterization of antimicrobial peptides and membrane proteins embedded in

119 t be considered a possible mode of action of antimicrobial peptides and other membrane-active drugs o

120 More than 40 antimicrobial peptides and proteins (AMPs) are expressed

121 Bacteria exploit an arsenal of antimicrobial peptides and proteins to compete with each

122 ifferentiation of keratinocytes and inducing antimicrobial peptides and selected chemokines.

123 Furthermore, host defense antimicrobial peptides and small-molecule peptide mimeti

124 clease chimeras; enzymes for detoxification; antimicrobial peptides and toxin-antitoxin systems assoc

125 promoted marked changes in the expression of antimicrobial peptides, and antibiotic treatment of V33

126 ading pathogens via reactive oxygen species, antimicrobial peptides, and neutrophil serine proteases

127 amphipathic, both classic characteristics of antimicrobial peptides, and we observed that IFN-beta ca

128 Biochemical studies suggested that the antimicrobial peptide apidaecin (Api) inhibits protein s

129 Linear cationic antimicrobial peptides are a diverse class of molecules

130 To counteract, antimicrobial peptides are being explored as possible al

131 Antimicrobial peptides are components of innate immune r

132 Antimicrobial peptides are components of the innate immu

133 New antimicrobial peptides are emerging as promising alterna

134 Antimicrobial peptides are important candidates for deve

135 Host antimicrobial peptides are inactivated by the capsule as

136 Due to their unique mode of action, antimicrobial peptides are novel alternatives to traditi

137 Antimicrobial peptides are short peptides secreted by th

138 ed Toll activation, and induced synthesis of antimicrobial peptides are stimulated via hemolymph (ser

139 eptide), MppA (murein tripeptide), and SapA (antimicrobial peptides) are Cluster C proteins known to

140 strategies, such as probiotics, lysins, and antimicrobial peptides, are in various stages of develop

141 Host defense peptides, also known as antimicrobial peptides, are key elements of innate host

142 host defence peptides (CHDP), also known as antimicrobial peptides, are naturally occurring peptides

143 ich refer to a series of small, proline-rich antimicrobial peptides, are predominantly active against

144 local expression of the cathelicidin-related antimicrobial peptide as well as evidence of defective m

145 nomenon that is important to the function of antimicrobial peptides as well as the pathological effec

146 flies resulted in diminished upregulation of antimicrobial peptides associated with both the Toll and

147 efensins are among the most highly expressed antimicrobial peptides at this mucosal surface in many m

148 er, bacterial thymidine kinase, antibiotics, antimicrobial peptides, bacterial antibodies, bacterioph

149 )-OH (3-4 d), the preparation of the labeled antimicrobial peptide BODIPY-cPAF26 by solid-phase synth

150 A group of short cationic antimicrobial peptides, called cathelicidins, have previ

151 ertain legumes, the host deploys a number of antimicrobial peptides, called nodule cysteine-rich (NCR

152 ding enzymes involved in the biosynthesis of antimicrobial peptides, camalexin, and 4-OH-ICN, as well

153 Colistin is a cationic antimicrobial peptide (CAMP) antibiotic that permeabiliz

154 The innate immune element, cathelicidin antimicrobial peptide (CAMP), is vital in the formation

155 Cationic antimicrobial peptides (CAMPs) have served as therapeuti

156 Cationic antimicrobial peptides (CAMPs), such as polymyxins, are

157 r resistance to membrane disrupting cationic antimicrobial peptides (CAMPs), such as polymyxins.

158 However, the alpha137-141 peptide, a natural antimicrobial peptide, can be obtained after hydrolysis

159 Natural alpha-helical cationic antimicrobial peptide (CAP) sequences are predominantly

160 Defensins are small antimicrobial peptides capable of neutralizing human ade

161 s included circulating concentrations of the antimicrobial peptide cathelicidin and recovery of lung

162 ionic nature and antimicrobial function with antimicrobial peptide cathelicidin.

163 filiis Similarly to mammalian chemokines and antimicrobial peptides, CK11 exerted its antimicrobial a

164 Evidence suggests that antimicrobial peptides, components of the innate immune

165 Defensins are cysteine-rich cationic antimicrobial peptides contributing to the innate immuni

166 gamma interferon (IFN-gamma) as well as the antimicrobial peptides CRAMP and mbetaD-3.

167 In contrast to most antimicrobial peptides, cWFW neither permeabilizes the m

168 asis, we selected S100A9 as a representative antimicrobial peptide DAMP.

169 f-the-art models on two AMP datasets and the Antimicrobial Peptide Database (APD)3 benchmark dataset.

170 As a consequence, levels of antimicrobial peptide derived from epithelial cells are

171 cies, it will help explain why resistance to antimicrobial peptides develops only slowly.

172 rcapnic suppression of the gene encoding the antimicrobial peptide Diptericin (Dipt), but did not inc

173 with the upregulation of genes encoding two antimicrobial peptides-diptericin and drosomycin-that ar

174 Our two most effective antimicrobial peptides displayed activity against multid

175 terial infection, inducing expression of the antimicrobial peptide Drosocin in respiratory epithelia

176 n the JNK-pathway by the immune effector and antimicrobial peptide Drosomycin.

177 s (e.g. involucrin, SERPINB7 and SERPINB13), antimicrobial peptides (e.g. B-defensins like DEFB4A, DE

178 Here we show that upon interaction with antimicrobial peptides, encapsulated pneumococci survive

179 Antimicrobial peptides exhibit various mechanisms of act

180 ion, and developmental stage) in analysis of antimicrobial peptide expression and their impact.

181 -7) and Candidatus arthromitus A decrease in antimicrobial peptide expression was predominantly obser

182 fected tongue but not to alterations in oral antimicrobial peptide expression.

183 owed that PHB affected the expression of the antimicrobial peptides ferritin (fer) and dicentracin (d

184 After quantifying tumor size and antimicrobial peptide gene expression, we found that Dro

185 kappaB precursor Relish, which drives robust antimicrobial peptide gene expression.

186 n of the NF-kappaB homolog Relish and robust antimicrobial peptide gene expression.

187 After adjusting for clinical predictors, an antimicrobial peptide gene signature (odds ratio [OR] 0.

188 ignificantly reduced the expression of seven antimicrobial peptide genes (AMPs) after bacterial chall

189 show that human dNK cells highly express the antimicrobial peptide granulysin (GNLY) and selectively

190 Here, we show that hepcidin antimicrobial peptide (Hamp), encoding the hormone hepci

191 Antimicrobial peptides have attracted considerable inter

192 Positively charged antimicrobial peptides have become promising agents for

193 the capsule sequesters most peptides, a few antimicrobial peptides have been identified that retain

194 We observed a shift in antimicrobial peptide hydrophobicity and activity betwee

195 1beta dependent pathway for secretion of the antimicrobial peptide IL-26 from human Th17 cells that i

196 g into adipocytes and producing cathelicidin antimicrobial peptide in response to Staphylococcus aure

197 wth of S. praecaptivus in the presence of an antimicrobial peptide in vitro, inactivation of both pho

198 LL-37 (human) and mouse cathelicidin-related antimicrobial peptide in vitro.

199 onse pathways can provide protection against antimicrobial peptides in E. faecalis at a significant c

200 of dendritic cells and reduced expression of antimicrobial peptides in intestinal epithelial cells.

201 act infection, suggesting a role for urinary antimicrobial peptides in susceptibility to select uropa

202 Virtual screening identified 21 potential antimicrobial peptides in the hydrolysates.

203 n the role of innate immune system proteins (antimicrobial peptides) in the inflammatory process asso

204 Antimicrobial peptides, in particular alpha-defensins ex

205 tion is lost upon pre-adaptation to bile and antimicrobial peptides, indicating the importance of the

206 eptation by PhoQ/PhoP may protect cells from antimicrobial peptide-induced stress or other conditions

207 rthermore, S. epidermidis isolates with high antimicrobial peptide-inducing and biofilm-forming capac

208 the expression of chemokines, cytokines, and antimicrobial peptides involved in pathogen clearance.

209 olates stimulated nasal epithelia to produce antimicrobial peptides, killing pathogenic competitors,

210 The urinary bacterial microbiome and antimicrobial peptide levels and activity were compared

211 Urinary psoriasin and beta-defensin antimicrobial peptide levels were significantly reduced

212 ies revealed that dynorphin(1-13) induces an antimicrobial peptide-like response in Pseudomonas, with

213 adoptive transfer of macrophages containing antimicrobial peptides linked to cathepsin B in the lyso

214 cle tracking reveals effects of the cationic antimicrobial peptide LL-37 on the Escherichia coli cyto

215 stress signals Mg(2+) and a fragment of the antimicrobial peptide LL-37 result in modulated activity

216 showed less susceptibility to killing by the antimicrobial peptide LL-37 when compared with results o

217 ricidal interactions with human cathelicidin antimicrobial peptide LL-37, a frontline component of ho

218 ptibility to killing by lysosomal SF and the antimicrobial peptide LL-37, as well as attenuated survi

219 es the regulatory activity of Mg(2+) and the antimicrobial peptide LL-37, which positively and negati

220 inflammation, and enhanced expression of the antimicrobial peptide LL-37.

221 Antimicrobial peptides LL-37 and hBD1 demonstrated a pH-

222 al antiviral-signaling protein (MAVS) by the antimicrobial peptide LL37 and double stranded-RNA relea

223 il (PMN) infiltration and high levels of the antimicrobial peptide, LL37.

224 synergistic activity of the two well-studied antimicrobial peptides magainin 2 (MG2a) and PGLa using

225 coli Nissle 1917, to express and secrete the antimicrobial peptide, Microcin J25.

226 Unlike antimicrobial peptide mimics that eradicate biofilms thr

227 chemokines, cytokines, Toll-like receptors, antimicrobial peptides, monocytoid cell activation marke

228 lausibly be modified to produce a panoply of antimicrobial peptides now known.

229 Alamethicins (ALMs) are antimicrobial peptides of fungal origin.

230 Peptidase inhibitor 3 (PI3), a gene in the antimicrobial peptide pathway and known to be involved i

231 cell-penetrating and tumor-homing peptides, antimicrobial peptides, peptide hormones, growth factors

232 he resistance of V. fischeri to the cationic antimicrobial peptide polymixin B, which resembles antib

233 Proline-rich antimicrobial peptides (PrAMPs) are cationic antimicrobi

234 Proline-rich antimicrobial peptides (PrAMPs) are promising lead compo

235 d their numbers controlled by mucus-embedded antimicrobial peptides, preventing invasion of host tiss

236 ells induces a fibrotic cell fate that lacks antimicrobial peptides produced by mature adipocytes, hi

237 n favors bacterial persistence by inhibiting antimicrobial peptide production and, at the same time,

238 t cells upon amebic infection, regulation of antimicrobial peptide production by Paneth cells, the in

239 Surprisingly, adhesion molecule expression, antimicrobial peptide production, and reactive oxygen sp

240 oxia driven responses resulting in increased antimicrobial peptide production, maturation of the mucu

241 dysone positively regulates both molting and antimicrobial peptide production, so the inactivation of

242 early source of innate IL-17, which promotes antimicrobial peptide production, whereas pathogen-speci

243 Bacteriocins, which are bacterially produced antimicrobial peptide products, are candidates for broad

244 imed to validate the association between the antimicrobial peptides/proteins elafin and cathelicidin

245 il-like assembly not previously observed for antimicrobial peptides, providing structural evidence li

246 ent that is characterized by the presence of antimicrobial peptides, reactive oxygen species and pro-

247 alpha-, IL-17A-, and IL-22-induced CCL20 and antimicrobial peptide release from epidermal keratinocyt

248 hesis, superoxide production, migration, and antimicrobial peptide release.

249 ense peptides (HDPs), also known as cationic antimicrobial peptides, represent a diverse group of sma

250 scriptional regulator (Sant_4061) to control antimicrobial peptide resistance in vitro.

251 culture on solid medium and determination of antimicrobial peptide resistance.

252 the concept that early assessment of urinary antimicrobial peptide responses and the bacterial microb

253 subject to the sub-lethal toxicity of these antimicrobial peptides, resulting in limited reproductiv

254 investigated immunoregulatory effects of the antimicrobial peptide RNase 7 on activated T cells.

255 DO1, SOCS3, and IL10), and a proinflammatory antimicrobial peptide (S100A7).

256 Significant upregulations of antimicrobial peptides (S100A8/fold change [FCH], 13.04;

257 Aurein 1.2 is a potent antimicrobial peptide secreted by frog Litoria aurea.

258 let-derived protein 3alpha (REG3alpha) is an antimicrobial peptide secreted by intestinal Paneth cell

259 Sublancin 168 is a highly potent and stable antimicrobial peptide secreted by the Gram-positive bact

260 Antimicrobial peptides secreted from S. capitis E12 were

261 for testosterone in Sertoli cell maturation, antimicrobial peptide secretion, and spermatogonial diff

262 rrectly deciphered the underlying grammar of antimicrobial peptide sequences, as demonstrated by the

263 frequencies of amino acid residues, in known antimicrobial peptide sequences.

264 The synthetic antimicrobial peptide SET-M33 has strong activity agains

265 les also contain two genes encoding specific antimicrobial peptides (SLPI and CAMP).

266 as a protein implicated in the transport of antimicrobial peptides such as bleomycin(7).

267 Cationic alpha-helical antimicrobial peptides such as BP100 are of increasing i

268 signaling induced the production of various antimicrobial peptides, such as angiogenin 4 and alpha-

269 However, those for many antimicrobial peptides, such as moricin, increased more

270 ance of membrane integrity and resistance to antimicrobial peptides, suggesting a role in gonococcal

271 findings challenge the preconceptions about 'antimicrobial' peptides, supporting the notion that thei

272 w the adsorption of the membrane-penetrating antimicrobial peptide Temporin L in different solutions.

273 The NEMURI protein is an antimicrobial peptide that can be secreted ectopically t

274 entified ribonuclease 7 (RNase 7) as a human antimicrobial peptide that has bactericidal activity aga

275 Polymyxins are a group of detergent-like antimicrobial peptides that are the ultimate line of def

276 a protective role through the production of antimicrobial peptides that increase tumor cell death.

277 Piscidins are histidine-enriched antimicrobial peptides that interact with lipid bilayers

278 n be used to evolve potentially advantageous antimicrobial peptides that lack these impediments from

279 our results revealed that the expression of antimicrobial peptides that play a vital role in insect

280 V. cholerae confers >100-fold resistance to antimicrobial peptides through aminoacylation of lipopol

281 and these released exosomes shuttle several antimicrobial peptides to carry out anti-C. parvum activ

282 Increased IL-1beta boosts local antimicrobial peptides to facilitate microbiota remodell

283 dels is a hurdle in the early development of antimicrobial peptides towards clinical applications.

284 enes within the epithelial compartment, with antimicrobial peptide transcripts evident in pelvic epit

285 t that the K. pneumoniae Sap (sensitivity to antimicrobial peptides) transporter contributes to bacte

286 We identify six antimicrobial peptides, two plant immune regulators and

287 antimicrobial peptides (PrAMPs) are cationic antimicrobial peptides unusual for their ability to pene

288 on by delivery mode and provides evidence of antimicrobial peptide upregulation in vaginal delivery c

289 a mutant S. aureus that is more sensitive to antimicrobial peptides was killed more efficiently by IF

290 onies over four weeks, and the expression of antimicrobial peptides was measured using multiplex quan

291 significantly enhanced and the induction of antimicrobial peptides was reduced in the absence of ear

292 a) defensin-1 (RTD-1), a natural macrocyclic antimicrobial peptide, was recently shown to be rapidly

293 a pivotal role in V. cholerae resistance to antimicrobial peptides, weapons of the innate immune sys

294 Cytokine and antimicrobial peptides were measured on a multiplex plat

295 the expression of the Toll pathway-mediated antimicrobial peptides when the flies were challenged wi

296 clavanin-MO, derived from a marine tunicate antimicrobial peptide, which exhibits potent antimicrobi

297 eficiencies in intestinal C-type lectins and antimicrobial peptides, which leads to dysbiosis of the

298 Nisin is an antimicrobial peptide with bacterial, fungicidal, viruci

299 Ubiquicidin is an antimicrobial peptide with great potential for nuclear i

300 Alpha defensins are antimicrobial peptides with expression in neutrophils an