ライフサイエンスコーパス: mimicry

1 nformational changes via receptor functional mimicry.

2 etal color patterns as a result of Mullerian mimicry.

3 Broad categorization favors the evolution of mimicry.

4 ccasional strong selection for interspecific mimicry.

5 on of ancestral elements facilitated pattern mimicry.

6 dator psychology is crucial to understanding mimicry.

7 pressed or its activity suppressed by target mimicry.

8 dsx haplotype that occurred at the origin of mimicry.

9 in of TAF1 previously implicated in TATA-box mimicry.

10 pot of shape-tuning alleles involved in wing mimicry.

11 itopes, consistent with neoantigen molecular mimicry.

12 otein-protein interactions by intramolecular mimicry.

13 s natural products in terms of stability and mimicry.

14 lternative angiogenic pathways, and vascular mimicry.

15 ed on flawed reasoning and obscured by model mimicry.

16 specific inhibition through transition-state mimicry.

17 ascular co-option and angiotropism/pericytic mimicry.

18 he viruses infecting related hosts, and host-mimicry.

19 providing overwhelming support for Batesian mimicry.

20 delivery, bioimaging, biocatalysis, and cell mimicry.

21 rolling placental morphogenesis and vascular mimicry.

22 g among ants or defending themselves through mimicry.

23 ribe a remarkable case of plastic aggressive mimicry.

24 , endocrine disruption, and primer pheromone mimicry.

25 ewly emerged host morph to escape parasites' mimicry.

26 , providing further evidence for mechanistic mimicry.

27 glycan-mediated immune evasion via molecular mimicry.

28 reat possibility in accomplishing rare earth mimicry.

29 y those regarding the evolution of imperfect mimicry.

30 individuals display signatures of behavioral mimicry.

31 lex is tested during assembly via structural mimicry.

32 lar architecture of Heliconius color pattern mimicry.

33 nels without EC, referred to as vasculogenic mimicry.

34 the action of human selection on Vavilovian mimicry.

35 th special focus on testing for exact facial mimicry.

36 a, further emphasizing the relevance of this mimicry.

37 gh protein sequestration or protein-scaffold mimicry.

38 en imperfect: why does selection not improve mimicry?

39 ing of noxious models is disrupted (Batesian mimicry [3]), or receivers become more vigilant and lear

40 o match the host (Batesian and/or Wasmannian mimicry [3]).

41 d learn to avoid perilous mimics (aggressive mimicry [4]).

42 at, in butterfly species exhibiting Batesian mimicry, a multi-gene complex or 'supergene' controls th

43 hat a single gene, doublesex (dsx), controls mimicry across multiple taxa, but with species-specific

44 ction, and reveal divergent capsid-based EB1 mimicry across retroviral species.

45 It is widely believed this mimicry acts as a social glue, leading to increased rapp

46 precise identification of a locus underlying mimicry, adding to unprecedented recent discoveries in m

47 introgression, our analyses reveal distinct mimicry alleles.

48 ions in these pathways function as oncogenic mimicries and allow transformed pre-B cells to bypass ch

49 e also find cooperativity between structural mimicry and a crucial peptide "hot spot" and demonstrate

50 rgone an adaptive radiation for wing-pattern mimicry and are influenced by distinct selection regimes

51 eal the molecular basis for the I942 vs cAMP mimicry and competition, but also suggest that the parti

52 whether sleep deprivation affects emotional mimicry and contagion.

53 ular mechanisms will extend our knowledge of mimicry and contribute to our understanding of the origi

54 e doublesex, we show that sexually dimorphic mimicry and female-limited polymorphism are evolutionari

55 9 inhibits NF-kappaB activation by molecular mimicry and has a motif near the N terminus that is cons

56 Mimicry and melanism in Lepidoptera provided the first c

57 y from perceptual exploitation and integrate mimicry and multicomponent signalling theory for the fir

58 d in glioma, glioma stem cells, vasculogenic mimicry and neovasculature.

59 ribosome customization through trans-kingdom mimicry and the mechanics of species-specific leader act

60 vation patterns across muscles during facial mimicry and to provide evidence for distinct patterns of

61 Angiotropism/pericytic mimicry and vascular co-option involve tumor cell intera

62 this control, diverse strategies of cellular mimicry and/or ribosome hijacking have evolved.

63 ationships that provide protective (Batesian mimicry) and predatory (aggressive mimicry) benefits to

64 coloration and behavior, chemical defenses, mimicry, and advertisement of unprofitability (conspicuo

65 ty does not necessarily result in structural mimicry, and despite the need for cross-reactivity, anti

66 abnormal microbial translocation, molecular mimicry, and dysregulation of both local and systemic im

67 in immunogenicity, pathogenicity, molecular mimicry, and immune evasion, expanding our understanding

68 cell lines also programmed them for vascular mimicry, and SERPINE2 and SLPI were overexpressed prefer

69 e due to their shared environment, emotional mimicry, and synchronized activities.

70 fits surpass those generated by natural flow mimicry, and were retained across periods of heightened

71 ascular co-option and angiotropism/pericytic mimicry are closely related if not identical processes.

72 ive metabolic manifestations of this fasting mimicry are enhanced gluconeogenesis and ketogenesis, wh

73 he mechanistic details of this cross-kingdom mimicry are poorly understood.

74 Discrete examples of microbial metabolite mimicry are shown to yield more potent and non-toxic the

75 t study by Dvorak et al. supports metabolite mimicry as a drug development strategy.

76 otective CD8+ T cells, identifying molecular mimicry as a mechanism to enforce tolerance in the gut.

77 ime scales, challenging traditional views of mimicry as a stable evolutionary 'end point' and suggest

78 pathway, suggests the co-option of molecular mimicry as a strategy for achieving its function.

79 med by risk haplotypes, supporting molecular mimicry as the key mechanism of RHD pathogenesis.

80 t control the laryngeal muscles and subserve mimicry, as well as the cardiovascular and respiratory s

81 nded butterflies forming multiple coexisting mimicry assemblages in the Amazon.

82 electively with protein targets through good mimicry at the other).

83 This reagent (i) exerts solvent mimicry because its size is comparable to water and (ii)

84 ior to intentional imitation, the dyad shows mimicry behaviors, which are automatic, but do not fade

85 (Batesian mimicry) and predatory (aggressive mimicry) benefits to other fishes [2, 6].

86 Examples of Mullerian mimicry between distantly related butterfly species prov

87 Molecular mimicry between HCMVpp65 peptide and host protein has th

88 Molecular mimicry between human and GAS proteins triggers proinfla

89 Most models focus on issues of molecular mimicry between the E2 subunit of the pyruvate dehydroge

90 sting adaptive introgression of wing pattern mimicry between these two distantly related species.

91 rocognitive mechanisms which lead to partial mimicry but are also likely to be influenced by evaluati

92 Thus, molecular mimicry by HIV-1 Env that promotes the evasion of host a

93 or heteroligation or the consequence of host mimicry by HIV-1.

94 SH2-binding phosphotyrosine motifs and motif mimicry by pathogenic bacterial effector proteins.

95 we identified a novel instance of lymphatic mimicry by which maternal endothelial cells promote SA r

96 and suggest routes for the improvement of E "mimicry" by E1 by increasing its recognition of the Fab

97 iduals, suggesting instead that near-perfect mimicry can be produced by a set of changes within a sin

98 ption are no longer formal requirements, and mimicry can evolve irrespective of the underlying proxim

99 Thus, increasing accuracy of parasites' mimicry can favour a newly emerged host morph to escape

100 Interface mimicry can identify more HPIs than sequence or complete

101 sion of TEs in cancer cells, inducing 'viral mimicry', causing interferon signalling and cancer cell

102 Together, these results demonstrate that mimicry changes the reward value of social stimuli, and

103 In this study we formally test if mimicry changes the reward value of the mimicker, using

104 stem cells have been shown to form vascular mimicry channels.

105 m of floral mimicry could represent a common mimicry class with specialization possible along multipl

106 All members of this mimicry complex are characterised by a conspicuous golde

107 Here, we report a new multi-order mimicry complex that includes at least 140 different put

108 ss outcomes for the actors within a Batesian mimicry complex, where predators learn to differentiate

109 Mimicry complexes typically consist of multiple species

110 ule, either by expression of a miR390 target mimicry construct or mutations in ARGONAUTE7, enhances n

111 s demonstrated by overexpression of a target mimicry construct, which led to an increased SP6A expres

112 (e.g. tropical forests), this form of floral mimicry could represent a common mimicry class with spec

113 r due to common ancestry, making any kind of mimicry difficult to detect [9].

114 oP and subvert PAF function, suggesting that mimicry-driven immune evasion is a common paradigm among

115 e of their ability to implement vasculogenic mimicry during hypoxia.

116 s, but are thought also to act as protective mimicry during movement.

117 The mimicry efficiency of the previously designed scaffold 1

118 Peptide mimicry employing a combination of aza-amino acyl prolin

119 tem to test hypotheses about aposematism and mimicry, especially those regarding the evolution of imp

120 aptive introgression, an important aspect of mimicry evolution in Heliconius butterflies.

121 We conclude that mimicry evolution in this group was likely facilitated b

122 our understanding of the role of learning in mimicry evolution, and shows that imperfect mimicry is e

123 propose a novel conceptual framework whereby mimicry evolves if a receiver perceives the similarity b

124 Experiments relying on the chemical mimicry existing between VER and heme group suggest that

125 osome complexes for global pre-translocation mimicry explains the high efficiency observed for this I

126 widely recognized to exhibit nanoscale atom mimicry features reminiscent of traditional picoscale at

127 framework enables us to formally distinguish mimicry from perceptual exploitation and integrate mimic

128 dding to unprecedented recent discoveries in mimicry genetics.

129 In an example of molecular mimicry, globomycin appears to inhibit by acting as a no

130 s from a recent radiation in which supergene mimicry has been isolated to the gene doublesex, we show

131 ly young, and numerous cases of wing pattern mimicry have evolved within the last 2.5-4.5 Ma.

132 ng the perceptual biases exploited by floral mimicry illuminates the evolution of these signals.

133 Mimicry illustrates the power of selection to produce ph

134 interaction along this continuum: aggressive mimicry in aphids.

135 ely induces DNA replication stress and viral mimicry in cancer cells.

136 report that gut microbial molecular mimicry in concert with gut microbes that enhance Th17 c

137 We investigate a potential case of sexual mimicry in Drosophila erecta, in which females show cont

138 c analysis has now shown that, surprisingly, mimicry in Heliconius butterflies and melanism in pepper

139 Color pattern mimicry in Heliconius butterflies is a classic case stud

140 vioral and evolutionary processes leading to mimicry in light of classical community ecology.

141 c inflammation in angiotropism and pericytic mimicry in melanoma progression, metastasis, tumor cell

142 whether the same genes underlie polymorphic mimicry in Papilio swallowtail butterflies.

143 Consistent with the idea of molecular mimicry in protein interactions, RidL outcompeted TBC1D5

144 ere not documented in earlier assessments of mimicry in velvet ants, and are newly described here.

145 Presented herein is a foldamer for strand mimicry in which dipolar repulsion is a central determin

146 This results in a state of viral mimicry in which treated cells mount an innate immune re

147 sleep deprivation on emotional contagion and mimicry in young and older humans.

148 s inadvertently included the term 'pericytic mimicry' in relation to ref.

149 Batesian mimicry, in which harmless species (mimics) deter predat

150 Thus, dual mimicry increases odds for mistranslation through evasio

151 rtly mimicked and also whether covert facial mimicry involves distinct facial muscle activation patte

152 Covert facial mimicry involves subtle facial muscle activation in obse

153 Mimicry is a canonical example of adaptive signal design

154 Facial mimicry is a central feature of human social interaction

155 Molecular mimicry is a common mechanism used by many bacteria to e

156 Antigenic mimicry is a fundamental tenet of structure-based vaccin

157 Microbial metabolite mimicry is a novel way to expand on the chemical reperto

158 Supergene mimicry is a striking phenomenon but we know little abou

159 Vavilovian mimicry is an evolutionary process by which weeds evolve

160 Molecular mimicry is an evolutionary strategy adopted by viruses t

161 e evidence that this tolerance for imperfect mimicry is attributable to collaboration between the cha

162 Mimicry is being used in the design of polymers for biom

163 l emotion categories, suggesting that facial mimicry is emotion-specific, rather than just valence-ba

164 To test whether covert facial mimicry is emotion-specific, we measured facial electrom

165 mimicry evolution, and shows that imperfect mimicry is expected to be the norm.

166 However, in practice the study of mimicry is inconsistent across research fields, with the

167 In principle, what constitutes mimicry is independent of the taxonomic identity of the

168 Yet mimicry is often imperfect: why does selection not impro

169 In these systems, chemical mimicry is often used as an efficient way to exploit the

170 Mullerian mimicry is similarity in appearance or phenotype among h

171 notype among harmful species, while Batesian mimicry is similarity in which not all species are harmf

172 esents the first example of direct molecular mimicry leading to clinically relevant fatal toxicity, m

173 Mimicry leads to fluorescently labeled pyoS2(NTD) being

174 m resulting from early co-option of dsx as a mimicry locus, and that evolutionary turnover of dsx all

175 ntrogression as strong or stronger than this mimicry locus.

176 In a form of apoptotic mimicry, many enveloped viruses display phosphatidylseri

177 and has driven the evolution of intersexual mimicry, mating behaviours and reproductive polymorphism

178 point' and suggesting that insect and snake mimicry may have different evolutionary dynamics.

179 dentification of this novel type of vascular mimicry may help in the development of targeted cancer t

180 icates that viral infection via this exosome mimicry mechanism does not require an envelope glycoprot

181 contribute to the tracing of novel molecular mimicry mechanisms employed by pathogenic viruses.

182 Here, we are reporting a new "bio-mimicry" method by making use of the "in-vivo environmen

183 proliferation, and VEGF-induced vasculogenic mimicry, migration/invasion as well as angiogenesis.

184 s antibody bound the CD4 binding site by CD4 mimicry, mirroring human bNAbs 8ANC131, CH235, and VRC01

185 brafish, SerRSS101D/S241D, a phosphorylation-mimicry mutant, cannot suppress VEGFA expression to supp

186 e place this review in the context of floral mimicry of a broader spectrum of nonfloral resources, an

187 , we report a very specific type of chemical mimicry of a food source.

188 iable success, as for certain interfaces the mimicry of a single secondary structure element is insuf

189 Mimicry of activity patterns that predicted drinking phe

190 tations function through the same mechanism: mimicry of alpha-subunit binding.

191 navirus sequenced, resulting in the striking mimicry of an identical FURIN-cleavable peptide on the h

192 across lipid nanoparticles (liposomes) as a mimicry of biological membranes.

193 e therefore likely to involve some degree of mimicry of both the protein and glycan components of Env

194 ervation validates past indications that ion-mimicry of calcium and lead should play an important rol

195 rvation provides new insight into functional mimicry of carbohydrates by peptide ligands.

196 how poxviruses can be multifaceted in their mimicry of cellular proteins through the consolidation o

197 n of cytoplasmic poxviruses.IMPORTANCE Viral mimicry of cellular signaling modulators provides clear

198 nean orchid Ophrys exaltata employs chemical mimicry of cuticular hydrocarbons, particularly the 7-al

199 demands the development of a pharmaceutical mimicry of early-age pregnancy-mediated protection.

200 ndemic may be driven in part by its targeted mimicry of ENaC-alpha, a protein critical for the homeos

201 whose range of catalytic activities enables mimicry of endogenous, physiological PLD signaling.

202 Our results suggest that chemical mimicry of eukaryotic signalling molecules may be common

203 has many surprising features, especially its mimicry of fractalkine (CX3CL1).

204 Interestingly, floral mimicry of fruit is least documented in the literature,

205 iew, we summarize current research on floral mimicry of fruit.

206 Effector mimicry of gp130 suggests GSK-3 can regulate normal cyto

207 evolved as a response to pathogen molecular mimicry of host ligands for inhibitory receptors.

208 Molecular mimicry of host proteins by pathogens can lead to autoim

209 Molecular mimicry of human antigens related to RA was also detecta

210 omains in group II intron RNAs, and the tRNA mimicry of IRES RNAs.

211 deficiency virus type 1 (HIV-1) focus on the mimicry of its envelope spike (Env) due to its exposed l

212 would not require furin cleavage to achieve mimicry of mature Env spikes on virions.

213 with a design process that avoids atomistic mimicry of natural proteins.

214 Floral mimicry of nonfloral resources is found across many angi

215 We have delineated the mimicry of Ocr by focusing on the electrostatic contribu

216 The stepwise infection of flower organs and mimicry of ovary fertilization unveiled in this study gu

217 gh its partially positive gamma-methylene in mimicry of phenylalanine's quadrupolar interaction.

218 rs, poisonous spines, irritating sprays, and mimicry of plant parts, snakes and bird droppings, has b

219 n enabled the orchid to perfect its chemical mimicry of pollinator sex pheromones by escape from dele

220 rscore the opinion that microbial metabolite mimicry of promiscuous ligand-receptor interactions is w

221 different molecular strategies including the mimicry of prosurvival Bcl-2 proteins.

222 c protein functionalization strategies allow mimicry of PTMs(3,4), as well as formation of unnatural

223 It also shows that pharmacological mimicry of satiety with peptide YY3-36 can reverse this

224 Mimicry of such alpha-helical regions has met with consi

225 transcription in "nucleus" liposomes and the mimicry of the architecture of eukaryotic cells.

226 We demonstrate on-chip mimicry of the BBB structure and function by cellular in

227 Structural mimicry of the DENV E epitope by the E1 combining site i

228 surface is extensive and involves molecular mimicry of the DNA substrate.

229 A feature of these proteins is their mimicry of the envelope glycoprotein (Env) structure on

230 A feature of these proteins is their mimicry of the envelope glycoprotein structure on virus

231 ant can achieve pollination through chemical mimicry of the food sources of adult carnivorous animals

232 Hereby, the mimicry of the fundamental processes occurring in natura

233 eavage has been reported to be essential for mimicry of the mature viral spike by soluble versions of

234 The mimicry of the natural hierarchical assembly of biomolec

235 Artificial photosynthesis is the mimicry of the natural process of solar energy conversio

236 similarity does not translate to structural mimicry of the paired epitopes in complexes with HLA-A*0

237 different levels of structural and antigenic mimicry of the parent cleaved BG505.SOSIP.

238 ctive site communication and for beta-lactam mimicry of the peptidoglycan substrates, as foundational

239 tral inhibitors provide shape but not charge mimicry of the proposed intermediate and transition stat

240 fore, a molecular understanding and possible mimicry of the surface of insect cuticle has been a chal

241 e they have repeating structural motifs, but mimicry of these does not have to follow such well-defin

242 This is true despite the fact that mimicry of these gradients may be essential for the func

243 Mimicry of this homopolymer self-assembly using syntheti

244 This work reveals how shape and charge mimicry of transition state features can enable the rati

245 The microbiological features and clinical mimicry of tuberculosis infection pose diagnostic challe

246 found across many angiosperm families, with mimicry of varied models including carrion, dung, fungi,

247 However, mimicry of venomous coral snakes has remained controvers

248 This involves mimicry of visual, tactile, and chemical signals of fema

249 We found no effects of mimicry on rapport or trust ratings or implicit trust be

250 activation of miR827 activity through target mimicry or by overexpression a miR827-resistant cDNA of

251 America, multiple species converge on local mimicry patterns through parallel shifts of midabdominal

252 election acting on the same trait, maintains mimicry polymorphism in the toxic butterfly Heliconius n

253 stablish an engineered GPCR-ectodomain-based mimicry principle that differentiates between disease-ex

254 iller angle) were under selection during the mimicry process.

255 ext in the Discussion relating to 'pericytic mimicry', ref.

256 nius butterflies, a group with extraordinary mimicry-related wing pattern diversity.

257 Mimicry remains a key model for understanding signal evo

258 Two of these eight mimicry rings, red-headed Timulla and black-headed Timul

259 liconius erato some Mendelian loci affecting mimicry shifts are well known.

260 ducts, including macrocyclization or proline mimicry strategies.

261 our study unravels a sophisticated molecular mimicry strategy that is used by L. pneumophila to take

262 Using an apoptotic mimicry strategy, the C1-TcCalr association facilitates

263 identify one of the largest known Mullerian mimicry systems worldwide and provide a novel system to

264 In a dynamic mimicry task, experiment participants watched and repeat

265 as been amended to remove the term 'pericyte mimicry' that the authors had included inadvertently dur

266 t has been shown to be a marker of pericytic mimicry, that is, the spreading of tumor cells in a peri

267 resolved conflict between the predictions of mimicry theory and empirical patterns in the distributio

268 HMI-PRED relies on "interface mimicry" through which the microbial proteins hijack hos

269 ra likely evolved the means to use olfactory mimicry to attract its nematode prey through the olfacto

270 uggest that our construct may utilize ligand mimicry to avoid host attack and target the siRNA to HER

271 disables neutrophils by exploiting molecular mimicry to degrade platelet-activating factor (PAF), a h

272 We conclude that LegCs use SNARE mimicry to divert VAMP4-containing vesicles for fusion w

273 lts provide evidence for utilizing antigenic mimicry to elicit oligomannose-specific bnAbs to HIV-1.

274 ational approach exploiting solely interface mimicry to model potential HPIs.

275 nformational molecules that use exploitative mimicry to modulate sirtuin signalling through steroid r

276 The ability to design immunogens with high mimicry to viral proteins also makes possible the explor

277 We used "red blood cell mimicry" to achieve long sensor circulation times of up

278 animals serve as models for a rich source of mimicry types, as non-venomous species benefit from redu

279 since it appears more common than the other mimicry types.

280 acterial peptides demonstrate that molecular mimicry underpins cross-reactivity toward the gliadin ep

281 structures showed that induced-fit molecular mimicry underpins TRAV27/TRBV19(+)TCR specificity for th

282 tribute to vessel formation through vascular mimicry (VM) and/or endothelial transdifferentiation.

283 itive, NON-ENDOTHELIAL "vessels" or vascular mimicry (VM) channels in both tumor and angiogenesis in

284 ts linkage to alteration of the vasculogenic mimicry (VM) formation to influence the NSCLC cell invas

285 tient tumor slices displaying a vasculogenic mimicry (VM) phenotype.

286 nd cytokeratins consistent with vasculogenic mimicry (VM), a process whereby tumour cells form 'endot

287 ion and an increase in CD144(+) vasculogenic mimicry (VM), leading to formation of channels displayin

288 with known prognostic factors, vasculogenic mimicry (VM), the mature vasculature (von Willebrand Fac

289 ces, and we discuss conceptual frameworks of mimicry vs generalized food deception or pre-existing se

290 d that in a two-antibody cocktail, molecular mimicry was a major feature of mAb-GP interactions.

291 In conclusion, emotional contagion, but not mimicry, was affected by sleep deprivation.

292 prone to cause double-stranded RNA and viral mimicry, we observe low DNA methylation and high cryptic

293 Higher proportions of BG505.SOSIP-trimer mimicry were observed in sc-gp140s with linkers of 6 or

294 s article, we highlight microbial metabolite mimicry, whereby parent metabolites have weak interactio

295 uce Plg cross-reactive Abs through molecular mimicry, which can enhance Plg activation and may contri

296 by triggering a state of fasting and hypoxia mimicry, which includes activation of SIRT1, AMPK, and H

297 ne reactivity toward EBNA1 through molecular mimicry with ANO2 contributes to the etiopathogenesis of

298 These include loops that are well-suited to mimicry with macrocyclic compounds, and loops that are m

299 in a diversity of morphs displaying accurate mimicry with other local prey, although some of the form

300 Such antibodies are induced via molecular mimicry with the serum protein beta2-glycoprotein 1 (bet