ライフサイエンスコーパス: antimicrobial peptide

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

2 isms that induce intestinal expression of an antimicrobial peptide.

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

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

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

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

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

8 ycles designed to mimic facially amphiphilic antimicrobial peptides.

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

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

11 and PGLa are among the best-studied cationic antimicrobial peptides.

12 nctional mechanism akin to that for cationic antimicrobial peptides.

13 NF-kappaB/PARP-1-dependent transcription of antimicrobial peptides.

14 ovel mechanism to prevent over-activation of antimicrobial peptides.

15 e structure and function of these beta-sheet antimicrobial peptides.

16 EPI-/- skin exhibited enhanced expression of antimicrobial peptides.

17 lobin, broadly described as a rich source of antimicrobial peptides.

18 re an important class of naturally-occurring antimicrobial peptides.

19 rophobic peptides, known characteristics for antimicrobial peptides.

20 lective membrane-permeabilizing abilities of antimicrobial peptides.

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

22 EPI-/- skin exhibited enhanced expression of antimicrobial peptides.

23 ke, and immune-related transcripts including antimicrobial peptides.

24 s that are part of the bacteriocin family of antimicrobial peptides.

25 re, we can conclude that both ARACINs act as antimicrobial peptides.

26 mmatory responses and mediates resistance to antimicrobial peptides.

27 ially, increase susceptibility to endogenous antimicrobial peptides.

28 for increased expression of lung epithelial antimicrobial peptides.

29 ignificant similarity to currently available antimicrobial peptides.

30 e increased bacterial load and expression of antimicrobial peptides.

31 gh alterations in the urinary microbiome and antimicrobial peptides.

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

33 information for the design of new synthetic antimicrobial peptides.

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

35 ability to hydrolyze milk casein to generate antimicrobial peptides.

36 acillus subtilis controlling the response to antimicrobial peptides.

37 We analyze three amphipathic antimicrobial peptides, a class of membrane-associated m

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

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

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

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

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

43 ity to cell lysis (1.78-fold; P = 0.032) and antimicrobial peptide (AMP) (LL-37) killing (MIC, 8 muM

44 The large variety of antimicrobial peptide (AMP) databases developed to date

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

46 nt gut flora to promote chronic increases in antimicrobial peptide (AMP) gene expression that comprom

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

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

49 t the IMD pathway may regulate expression of antimicrobial peptide (AMP) genes in the midgut, and be

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

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

52 Antimicrobial peptides (AMP) are defense effectors of th

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

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

55 A large number of antimicrobial peptides (AMPs) acts with high selectivity

56 mmune responses by the epithelium, including antimicrobial peptides (AMPs) and cytokines, are critica

57 nt to high levels of inflammation-associated antimicrobial peptides (AMPs) and have identified a mech

58 ers were enriched in transcripts that encode antimicrobial peptides (AMPs) and immune response.

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

60 Antimicrobial peptides (AMPs) are a class of host-defens

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

62 Antimicrobial peptides (AMPs) are an important component

63 Antimicrobial peptides (AMPs) are anti-infectives that m

64 Antimicrobial peptides (AMPs) are innate immune molecule

65 Antimicrobial peptides (AMPs) are naturally occurring pe

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

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

68 We investigated the phenomena of antimicrobial peptides (AMPs) directly attacking the cyt

69 sign of structural mimics of membrane active antimicrobial peptides (AMPs) for which activities in vi

70 alpha-Helical antimicrobial peptides (AMPs) generally have facially am

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

72 In recent years, antimicrobial peptides (AMPs) have been utilized as pote

73 Synthetic antimicrobial peptides (AMPs) have recently received sub

74 In contrast, antimicrobial peptides (AMPs) have retained broad spectr

75 Antimicrobial peptides (AMPs) have shown rapid and poten

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

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

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

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

80 Antimicrobial peptides (AMPs) play an important role in

81 Antimicrobial peptides (AMPs) represent a promising ther

82 Many antimicrobial peptides (AMPs) selectively target and for

83 acteriostatic and bactericidal mechanisms of antimicrobial peptides (AMPs) should help in the design

84 Antimicrobial peptides (AMPs) that disrupt bacterial mem

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

86 This database currently focuses on natural antimicrobial peptides (AMPs) with defined sequence and

87 The interaction of antimicrobial peptides (AMPs) with the inner membrane of

88 Those genes encoding secreted antimicrobial peptides (AMPs), however, have failed to e

89 ur goal was to identify transcripts encoding antimicrobial peptides (AMPs), one of the key components

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

91 to counter bacterial infections includes the antimicrobial peptides (AMPs), which have emerged as mod

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

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

94 f cytokines, chemokines, growth factors, and antimicrobial peptides (AMPs).

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

96 also identified EV cargo, which included an antimicrobial peptide and ASIC channel.

97 rly stages, with modulation of inflammatory, antimicrobial peptide and complement genes across all de

98 NK-lysin is an antimicrobial peptide and effector protein in the host i

99 ical applications, including the activity of antimicrobial peptides and a better understanding of mem

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

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

102 e for the importance of IL-17A regulation of antimicrobial peptides and IL-17F in the clearance of S.

103 ulosis is demonstrated by IL-36gamma-induced antimicrobial peptides and IL-36 receptor-dependent rest

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

105 uction, we demonstrate that a broad range of antimicrobial peptides and other cationic molecules caus

106 ble for their potential as bio-insecticides, antimicrobial peptides and peptide drug candidates.

107 Antimicrobial peptides and proteins (AMPs) are a diverse

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

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

110 by host nodule-specific cysteine rich (NCR) antimicrobial peptides and requires the participation of

111 intestinal homeostasis through induction of antimicrobial peptides and secretory IgA among others.

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

113 the manufacture and functional validation of antimicrobial peptides and vaccines and present combinat

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

115 helial Kazal-type-related inhibitor (LEKTI), antimicrobial peptides, and cytokines were evaluated by

116 d resistance to aminoglycosides and cationic antimicrobial peptides, and decreased resistance to cell

117 f the colonizing microbiota are resistant to antimicrobial peptides, and identify a common mechanism

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

119 ipid pores in amyloid disease, the action of antimicrobial peptides, and the assembly of the membrane

120 cactus mRNA levels, decreased expression of antimicrobial peptides, and vulnerability to infection b

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

122 Expression of the intestinal antimicrobial peptide, angiogenin-4, was suppressed in G

123 gulation of expression of genes encoding the antimicrobial peptides antigen-6/urokinase-type plasmino

124 Linear cationic antimicrobial peptides are a diverse class of molecules

125 Antimicrobial peptides are an important component of the

126 Antimicrobial peptides are components of the innate immu

127 o date acting as small signaling peptides or antimicrobial peptides are derived from nonfunctional pr

128 Antimicrobial peptides are important as the first line o

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

130 Fluorescent antimicrobial peptides are promising structures for in s

131 Since antimicrobial peptides are regulated by the IL-17 cytoki

132 Antimicrobial peptides are short peptides secreted by th

133 Antimicrobial peptides are small, cationic proteins that

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

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

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

137 Work by Guo et al. shows the potential of antimicrobial peptides as a tool to assess the role of i

138 vidence that copy number polymorphisms in an antimicrobial peptide associate with UTI risk.

139 to reduced expression of a gene encoding an antimicrobial peptide, B. tabaci c-type lysozyme.

140 ronmental challenges, with the production of antimicrobial peptides being one of their first lines of

141 aK13) mice correlated with expression of the antimicrobial peptide beta-defensin 3 (BD3, Defb3).

142 1 treatment resulted in the induction of the antimicrobial peptides beta-defensin 3, CRAMP, and chemo

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

144 hese findings show that the production of an antimicrobial peptide by adipocytes is an important elem

145 not abolish activation by low Mg(2+) or the antimicrobial peptide C18G.

146 PhoQ is activated by mildly acidic pH or the antimicrobial peptide C18G.

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

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

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

150 Cathelicidin antimicrobial peptide (CAMP) is a naturally occurring se

151 ed the function of ToxR and LeuO in cationic antimicrobial peptide (CAMP) resistance.

152 oxicity and decreased resistance to cationic antimicrobial peptides (CAMP).

153 c pH, limited divalent cations, and cationic antimicrobial peptides (CAMP).

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

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

156 Defensins are small antimicrobial peptides capable of neutralizing human ade

157 Mice lacking the antimicrobial peptide cathelicidin experienced less seve

158 ionic nature and antimicrobial function with antimicrobial peptide cathelicidin.

159 ing E. coli with sublethal concentrations of antimicrobial peptides causes cells to filament, and tha

160 Cathelicidins constitute potent antimicrobial peptides characterized by a high cationic

161 It is also known that the formation of DNA-antimicrobial peptide complexes can lead to autoimmune d

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

163 s in susceptibility to these antibiotics and antimicrobial peptides correlated with in vivo attenuati

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

165 , wild type or deficient in cathelin-related antimicrobial peptide (CRAMP; an ortholog of the sole hu

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

167 The antimicrobial peptide database is an original database i

168 signalling system is a key regulator of this antimicrobial peptide defence.

169 Hence, and in contrast to the cationic antimicrobial peptide described in the following article

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

171 Our two most effective antimicrobial peptides displayed activity against multid

172 ation of our fluorogenic amino acid in short antimicrobial peptides does not impair their selectivity

173 ting chemokines (e.g., CXCL1 and CXCL5), and antimicrobial peptides (e.g., defensins), which act in c

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

175 Moreover, weaker expression of antimicrobial peptide-encoding genes and intervillous ba

176 ls reside in the small intestine and produce antimicrobial peptides essential for the host barrier, p

177 ne secretion in bronchoalveolar lavage, lung antimicrobial peptide expression by quantitative polymer

178 was concomitant with upregulation of either antimicrobial peptide expression or autophagy levels.

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

180 Guerin intracellular survival, downregulated antimicrobial peptide expression, and increased MCP-1/CC

181 h nodes, Th17 differentiation, and increased antimicrobial peptide expression.

182 found to repress IL-17 and IL-17-driven lung antimicrobial peptide expression.

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

184 inin 2 (MAG2) and PGLa are two alpha-helical antimicrobial peptides found in the skin of the African

185 mococcal capsule sensitizes the bacterium to antimicrobial peptides found on epithelial surfaces.

186 iated through the production of cathelicidin antimicrobial peptide from adipocytes because cathelicid

187 Maculatin 1.1 (Mac1) is an antimicrobial peptide from the skin of Australian tree f

188 response, including the robust induction of antimicrobial peptide gene expression.

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

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

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

192 ematophila induces expression of a subset of antimicrobial peptide genes and suppresses the melanizat

193 ed epithelial barrier, altered expression of antimicrobial peptide genes, and altered epithelial cell

194 t not rodent, cytotoxic granules contain the antimicrobial peptide granulysin (GNLY), which selective

195 Positively charged antimicrobial peptides have become promising agents for

196 Several cationic antimicrobial peptides have been investigated as potenti

197 yte transmigration, whereas the neutrophilic antimicrobial peptide HNP-1 is noted as a putative regul

198 the ability of the A549 cells to express the antimicrobial peptides human beta-defensin 2 (HBD-2) and

199 filaggrin and LEKTI was reduced, epithelial antimicrobial peptides (human beta-defensin-2, human bet

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

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

202 the role of IL-17 cytokines in production of antimicrobial peptides in a murine model of S. aureus na

203 o drive production of recombinant phytotoxic antimicrobial peptides in plant biofactories.

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

205 Increased expression of antimicrobial peptides including human beta defensins (H

206 IGTPase expression induced antimicrobial peptides, including Dae2, previously shown

207 barrier defects, including downregulation of antimicrobial peptides, increased systemic distribution

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

209 Pore formation by membrane-active antimicrobial peptides is a classic strategy of pathogen

210 tivities demonstrated that CRAMP, a cationic antimicrobial peptide, is primarily responsible for S. a

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

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

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

214 t immune response through degradation of the antimicrobial peptide LL-37 and complement proteins C3,

215 he short-term effect on the abundance of the antimicrobial peptide LL-37 and the abundance and divers

216 The antimicrobial peptide LL-37 is generated upon proteolyti

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

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

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

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

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

222 o DNA through a mechanism antagonized by the antimicrobial peptide LL37, proposed to be involved in a

223 d role of LytA in removing capsule to combat antimicrobial peptides may explain why nearly all clinic

224 fensin-3 (hBD-3), an epithelial cell-derived antimicrobial peptide, mediates chemotaxis and activatio

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 The antimicrobial peptide nisin exerts its activity by a uni

229 ) were studied as potential carriers for the antimicrobial peptides nisin and pediocin.

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

231 ity to these antibiotics and to a variety of antimicrobial peptides of diverse origin and with differ

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

233 teration in morphologies after adsorption of antimicrobial peptides on bentonite and halloysite.

234 these interactions are disrupted by cationic antimicrobial peptides, or by the loss of negatively cha

235 whether the administration of the synthetic antimicrobial peptide Pep2.5 may attenuate the cardiac d

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

237 pcidin, a molecule first characterized as an antimicrobial peptide, plays a critical role in the regu

238 s simulation study of the interaction of the antimicrobial peptide, polymyxin B1 with complex models

239 Proline-rich antimicrobial peptides (PrAMPs) are instead actively tra

240 s of prokaryotic origin, including genes for antimicrobial peptides, presumably reflects an intimate

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

242 Antimicrobial peptides, produced by innate immune system

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

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

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 y regulating the expression of IL-22 and the antimicrobial peptides RegIIIbeta, RegIIIgamma, and calp

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

249 al that CarR regulates biofilm formation and antimicrobial peptide resistance in V. cholerae.

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 Short antimicrobial peptides rich in arginine (R) and tryptoph

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

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

257 ned and site-specifically oriented synthetic antimicrobial peptides (sAMPs) as novel recognition agen

258 activity of human cathelicidin LL-37, a host antimicrobial peptide secreted by both genital tract epi

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

260 Enteric alpha-defensins are antimicrobial peptides secreted by Paneth cells.

261 Bac7 is a proline-rich antimicrobial peptide, selective for Gram-negative bacte

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 The anionic antimicrobial peptide SP-B(N), derived from the N-termin

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 decreased resistance to killing by cationic antimicrobial peptides, such as polymyxin B and beta-def

270 The innate immune system, which includes antimicrobial peptides, such as the alpha-defensins, enc

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

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

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

274 ong those is hepcidin, a small cysteine-rich antimicrobial peptide that is also the key regulator of

275 demonstrated that CXCL14 is a broad-spectrum antimicrobial peptide that is expressed abundantly and c

276 The lantibiotic nisin is an antimicrobial peptide that is widely used as a food pres

277 studded with histones, granule enzymes, and antimicrobial peptides that are referred to as neutrophi

278 Thionins are plant-specific antimicrobial peptides that have been isolated from the

279 an evolutionary conserved family of cationic antimicrobial peptides that play a key role in host inna

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

281 Defensins are cationic antimicrobial peptides that serve as important component

282 barrier, IL-31 stimulated the expression of antimicrobial peptides, thereby inhibiting bacterial gro

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

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

285 anism by which human macrophages internalize antimicrobial peptides to improve their intracellular pa

286 Radiolabeled synthetic fragments of the antimicrobial peptide ubiquicidin are promising infectio

287 rt that keratinocytes integrate signals from antimicrobial peptides via MAVS signaling to amplify the

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

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

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

291 we show that C16G2, a specifically targeted antimicrobial peptide, was able to selectively kill cari

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

293 elevated levels of the human forms of these antimicrobial peptides were found in nasal secretions fr

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

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

296 ycin and a nonmembrane lytic, broad-spectrum antimicrobial peptide with efficient mammalian cell pene

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

298 Alpha defensins are antimicrobial peptides with expression in neutrophils an

299 ent of cellular responses to antibiotics and antimicrobial peptides within minutes.

300 vealed a novel oligomeric form of beta-sheet antimicrobial peptides within the unit cell: an antipara