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1 rolling placental morphogenesis and vascular mimicry.
2 g among ants or defending themselves through mimicry.
3 pot of shape-tuning alleles involved in wing mimicry.
4 ribe a remarkable case of plastic aggressive mimicry.
5 , endocrine disruption, and primer pheromone mimicry.
6 ewly emerged host morph to escape parasites' mimicry.
7 , providing further evidence for mechanistic mimicry.
8 reat possibility in accomplishing rare earth mimicry.
9 y those regarding the evolution of imperfect mimicry.
10 er-initiating cells (CICs) by inducing viral mimicry.
11 pressed or its activity suppressed by target mimicry.
12 fficient to program these cells for vascular mimicry.
13 ens subvert this mechanism through molecular mimicry.
14 GPI) and thus can induce antiCl by molecular mimicry.
15 ir initial priming could occur via molecular mimicry.
16 laminin, a phenomenon known as vasculogenic mimicry.
17 binding site that involves striking receptor mimicry.
18 e receptor (TLR) signaling through molecular mimicry.
19 innate immune system, and (3) host function mimicry.
20 ement of a flexible paratope in the observed mimicry.
21 red when studying the evolution of imperfect mimicry.
22 small-bodied individuals leads to imperfect mimicry.
23 ed to be normally distributed using spectral mimicry.
24 and may be an important driver of imperfect mimicry.
25 dependent uptake of EBOV occurs by apoptotic mimicry.
26 itopes, consistent with neoantigen molecular mimicry.
27 otein-protein interactions by intramolecular mimicry.
28 dsx haplotype that occurred at the origin of mimicry.
29 s natural products in terms of stability and mimicry.
30 lternative angiogenic pathways, and vascular mimicry.
31 ed on flawed reasoning and obscured by model mimicry.
32 specific inhibition through transition-state mimicry.
33 ascular co-option and angiotropism/pericytic mimicry.
34 in of TAF1 previously implicated in TATA-box mimicry.
35 providing overwhelming support for Batesian mimicry.
36 delivery, bioimaging, biocatalysis, and cell mimicry.
37 ing of noxious models is disrupted (Batesian mimicry [3]), or receivers become more vigilant and lear
40 at, in butterfly species exhibiting Batesian mimicry, a multi-gene complex or 'supergene' controls th
42 precise identification of a locus underlying mimicry, adding to unprecedented recent discoveries in m
43 te to the functional differences between dsx mimicry alleles, and protein sequence evolution may also
44 ions in these pathways function as oncogenic mimicries and allow transformed pre-B cells to bypass ch
45 e also find cooperativity between structural mimicry and a crucial peptide "hot spot" and demonstrate
46 rgone an adaptive radiation for wing-pattern mimicry and are influenced by distinct selection regimes
47 fuse the principles of enacted and expected mimicry and condition their application on two similarit
49 e doublesex, we show that sexually dimorphic mimicry and female-limited polymorphism are evolutionari
50 on to the problem resides in the practice of mimicry and imitation, the expectation of opponent's mim
52 y from perceptual exploitation and integrate mimicry and multicomponent signalling theory for the fir
53 trategies and learning algorithms, shows how mimicry and relative similarity outperforms all the oppo
55 a major driver of the evolution of imperfect mimicry and that other factors, such as ecological commu
56 ribosome customization through trans-kingdom mimicry and the mechanics of species-specific leader act
59 nsistent with strong selection for Mullerian mimicry and with known Z-linked hybrid incompatibility.
60 ationships that provide protective (Batesian mimicry) and predatory (aggressive mimicry) benefits to
61 coloration and behavior, chemical defenses, mimicry, and advertisement of unprofitability (conspicuo
62 ty does not necessarily result in structural mimicry, and despite the need for cross-reactivity, anti
63 cell lines also programmed them for vascular mimicry, and SERPINE2 and SLPI were overexpressed prefer
64 fits surpass those generated by natural flow mimicry, and were retained across periods of heightened
65 s found to mediate VEGF-induced vasculogenic mimicry, angiogenesis and migration/invasion, with invol
66 ad or drift, the bystander effect, molecular mimicry, anti-idiotype theory, antigenic complementarity
67 ascular co-option and angiotropism/pericytic mimicry are closely related if not identical processes.
70 otective CD8+ T cells, identifying molecular mimicry as a mechanism to enforce tolerance in the gut.
71 ime scales, challenging traditional views of mimicry as a stable evolutionary 'end point' and suggest
74 ctive T-cell recognition, known as molecular mimicry, as well as bystander T-cell activation, culmina
75 t control the laryngeal muscles and subserve mimicry, as well as the cardiovascular and respiratory s
78 ior to intentional imitation, the dyad shows mimicry behaviors, which are automatic, but do not fade
80 n of the immune system, or due to structural mimicry between domains of the toxoid molecule and a sub
85 Most models focus on issues of molecular mimicry between the E2 subunit of the pyruvate dehydroge
86 sting adaptive introgression of wing pattern mimicry between these two distantly related species.
87 rocognitive mechanisms which lead to partial mimicry but are also likely to be influenced by evaluati
94 and suggest routes for the improvement of E "mimicry" by E1 by increasing its recognition of the Fab
95 iduals, suggesting instead that near-perfect mimicry can be produced by a set of changes within a sin
96 evolves to resemble different model species--mimicry can drive within-species morphological diversifi
97 ption are no longer formal requirements, and mimicry can evolve irrespective of the underlying proxim
100 sion of TEs in cancer cells, inducing 'viral mimicry', causing interferon signalling and cancer cell
101 Together, these results demonstrate that mimicry changes the reward value of social stimuli, and
104 m of floral mimicry could represent a common mimicry class with specialization possible along multipl
106 we investigate the extent of the velvet ant mimicry complex beyond Dasymutilla by examining distribu
110 ule, either by expression of a miR390 target mimicry construct or mutations in ARGONAUTE7, enhances n
111 during inflammatory responses, and molecular mimicry contribute to the initiation of autoantibody pro
112 (e.g. tropical forests), this form of floral mimicry could represent a common mimicry class with spec
113 oP and subvert PAF function, suggesting that mimicry-driven immune evasion is a common paradigm among
115 ubtedly affects the development of imperfect mimicry, ecological community context has largely been i
117 tem to test hypotheses about aposematism and mimicry, especially those regarding the evolution of imp
118 our understanding of the role of learning in mimicry evolution, and shows that imperfect mimicry is e
119 propose a novel conceptual framework whereby mimicry evolves if a receiver perceives the similarity b
122 widely recognized to exhibit nanoscale atom mimicry features reminiscent of traditional picoscale at
123 framework enables us to formally distinguish mimicry from perceptual exploitation and integrate mimic
127 s from a recent radiation in which supergene mimicry has been isolated to the gene doublesex, we show
129 show that hosts subjected to the best cuckoo mimicry have evolved the most recognizable egg pattern s
130 ell cross-reactivity underpins the molecular mimicry hypothesis in which microbial peptides sharing s
131 ng the perceptual biases exploited by floral mimicry illuminates the evolution of these signals.
134 examples of sexual dimorphism is sex-limited mimicry in butterflies, a phenomenon in which one sex--u
135 We investigate a potential case of sexual mimicry in Drosophila erecta, in which females show cont
136 rovide a mechanistic framework for molecular mimicry in Graves' disease, where early precursor B cell
137 c analysis has now shown that, surprisingly, mimicry in Heliconius butterflies and melanism in pepper
139 c inflammation in angiotropism and pericytic mimicry in melanoma progression, metastasis, tumor cell
144 emical evidence of this carbohydrate-peptide mimicry in the case of mAb 2D10 had been established ear
145 ere not documented in earlier assessments of mimicry in velvet ants, and are newly described here.
147 We have proposed a mechanism of molecular mimicry in which Abs against DENV nonstructural protein
148 Presented herein is a foldamer for strand mimicry in which dipolar repulsion is a central determin
151 domain, including all PVL signature and CD4 mimicry interactions, but not critical CDRH3 contacts wi
156 e evidence that this tolerance for imperfect mimicry is attributable to collaboration between the cha
163 00 years, it has been known that polymorphic mimicry is often switched by simple mendelian factors, y
168 notype among harmful species, while Batesian mimicry is similarity in which not all species are harmf
170 oration (often used as warning signals or in mimicry) is associated with heightened speciation rates
171 esents the first example of direct molecular mimicry leading to clinically relevant fatal toxicity, m
176 eciphering the structural basis of molecular mimicry, mAb 2D10 was isolated from a maturing immune re
182 dentification of this novel type of vascular mimicry may help in the development of targeted cancer t
185 proliferation, and VEGF-induced vasculogenic mimicry, migration/invasion as well as angiogenesis.
186 e place this review in the context of floral mimicry of a broader spectrum of nonfloral resources, an
189 ersonality factors that lead to more or less mimicry of an interaction partner in a given situation.
191 lizing antibodies, trimers of high antigenic mimicry of BG505.SOSIP could be obtained; negative-stain
193 ervation validates past indications that ion-mimicry of calcium and lead should play an important rol
195 n of cytoplasmic poxviruses.IMPORTANCE Viral mimicry of cellular signaling modulators provides clear
196 nean orchid Ophrys exaltata employs chemical mimicry of cuticular hydrocarbons, particularly the 7-al
197 actin-polymerizing pathways, suggesting that mimicry of different polymerization mechanisms influence
204 n for HIV-1 neutralization and/or structural mimicry of host Ags by conserved HIV-1 neutralization si
208 ains, which suggests mechanisms of bacterial mimicry of host signaling adaptor proteins, such as TIRA
213 nhibitors of protein complexes, often direct mimicry of natural amino acid residues does not lead to
217 The stepwise infection of flower organs and mimicry of ovary fertilization unveiled in this study gu
218 gh its partially positive gamma-methylene in mimicry of phenylalanine's quadrupolar interaction.
219 at position T + 2 likely reflect structural mimicry of phosphotransfer from the sensor kinase histid
220 rs, poisonous spines, irritating sprays, and mimicry of plant parts, snakes and bird droppings, has b
221 n enabled the orchid to perfect its chemical mimicry of pollinator sex pheromones by escape from dele
227 ium nanostructures open up opportunities for mimicry of the behavior of dynamic gels found in natural
232 ant can achieve pollination through chemical mimicry of the food sources of adult carnivorous animals
234 are modeled on species such as cuckoos where mimicry of the host phenotype confers high fitness to th
235 eavage has been reported to be essential for mimicry of the mature viral spike by soluble versions of
237 similarity does not translate to structural mimicry of the paired epitopes in complexes with HLA-A*0
239 ctive site communication and for beta-lactam mimicry of the peptidoglycan substrates, as foundational
240 tral inhibitors provide shape but not charge mimicry of the proposed intermediate and transition stat
243 The microbiological features and clinical mimicry of tuberculosis infection pose diagnostic challe
244 found across many angiosperm families, with mimicry of varied models including carrion, dung, fungi,
249 activation of miR827 activity through target mimicry or by overexpression a miR827-resistant cDNA of
250 pocretin producing neurons include molecular mimicry or bystander activation, and are likely a combin
251 ein E1B 19K, which we have termed "apoptotic mimicry." Our studies suggest the possibility that the p
252 ene can switch the entire wing pattern among mimicry phenotypes but may require multiple, tightly lin
255 election acting on the same trait, maintains mimicry polymorphism in the toxic butterfly Heliconius n
256 the forces behind the evolution of imperfect mimicry remain poorly studied, recent hypotheses suggest
259 we hypothesize that they form eight distinct mimicry rings (Figure 1A; Supplemental Information).
261 s show that, although the loci responding to mimicry selection are highly conserved between species,
262 to our knowledge, to demonstrate that MHC-I mimicry strategies used by MCMV to avoid NK cell control
264 m will provide insights toward viral protein mimicry, substrate recognition, and key interactive doma
265 ta that address the critical issue of what a mimicry supergene actually is at a functional level.
266 identify one of the largest known Mullerian mimicry systems worldwide and provide a novel system to
269 t has been shown to be a marker of pericytic mimicry, that is, the spreading of tumor cells in a peri
272 resolved conflict between the predictions of mimicry theory and empirical patterns in the distributio
273 lored the evolutionary dynamics of supergene mimicry, there are almost no empirical data that address
274 ra likely evolved the means to use olfactory mimicry to attract its nematode prey through the olfacto
275 disables neutrophils by exploiting molecular mimicry to degrade platelet-activating factor (PAF), a h
277 lts provide evidence for utilizing antigenic mimicry to elicit oligomannose-specific bnAbs to HIV-1.
278 Thus, repeated parasitism interacts with egg mimicry to exploit cognitive and sensory limitations in
282 small non-coding RNAs (sRNAs) use molecular mimicry to sequester multiple CsrA dimers away from mRNA
283 background of clonal deletion and molecular mimicry, two major pillars underlying our present unders
284 animals serve as models for a rich source of mimicry types, as non-venomous species benefit from redu
286 First, an analysis of the moderators of mimicry uncovers the various motivational, social, emoti
287 structures showed that induced-fit molecular mimicry underpins TRAV27/TRBV19(+)TCR specificity for th
288 tribute to vessel formation through vascular mimicry (VM) and/or endothelial transdifferentiation.
289 itive, NON-ENDOTHELIAL "vessels" or vascular mimicry (VM) channels in both tumor and angiogenesis in
291 nd cytokeratins consistent with vasculogenic mimicry (VM), a process whereby tumour cells form 'endot
292 ion and an increase in CD144(+) vasculogenic mimicry (VM), leading to formation of channels displayin
293 with known prognostic factors, vasculogenic mimicry (VM), the mature vasculature (von Willebrand Fac
295 ces, and we discuss conceptual frameworks of mimicry vs generalized food deception or pre-existing se
297 Higher proportions of BG505.SOSIP-trimer mimicry were observed in sc-gp140s with linkers of 6 or
298 uce Plg cross-reactive Abs through molecular mimicry, which can enhance Plg activation and may contri
299 These include loops that are well-suited to mimicry with macrocyclic compounds, and loops that are m
300 in a diversity of morphs displaying accurate mimicry with other local prey, although some of the form
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