ライフサイエンスコーパス: non-native

1 ndent of plant geographic origin (native vs. non-native).

2 ater than the effect of non-natives on other non-natives.

3 ystems that reported performance measures of non-native (157 species) and co-occurring native species

4 A limited set of non-native AIP analogs have been shown to inhibit AgrC r

5 analgesic (mean, 7.4; 95% CI, 4.0-10.8) than non-Native American patients (mean, 11.2; 95% CI, 7.2-15

6 pain score (mean, 6.5; 95% CI, 3.6-9.4) than non-Native American patients (mean, 8.1; 95% CI, 6.3-9.9

7 MP-2 and MMP-9 was redesigned to incorporate non-native amino acids (Flp and mep), resulting in an in

8 Libraries of peptides possessing non-native amino acids were screened for time to 50% pho

9 ding aliphatic, nonpolar, basic, acidic, and non-native amino acids.

10 -aminobutyric acid when SyrB1 presents these non-native amino acids.

11 structural features of both native AIPs and non-native analogues that are essential for activity.

12 ing tile-based F-ratio analysis whereby four non-native analytes were spiked into diesel fuel at seve

13 nction of C&A participants to individuals of non-native ancestry in Oklahoma (NNIs).

14 that md is independent of initial amounts of non-native ancestry.

15 hich all individuals have the same amount of non-native ancestry.

16 as used for the focus groups, of whom 4 were non-native and 7 native speakers of English.

17 er thermal treatments needed to give rise to non-native and aggregated species.

18 s are asymmetrical with interactions between non-native and native plants.

19 When native predators had access to non-native and native prey simultaneously, predator abun

20 Macrocyclic products bearing non-native and rigidifying structural motifs, isotopic l

21 Using an RBC model displaying a single, non-native antigen and live malaria parasite-infected RB

22 ptor (EpoR), to dimerize EpoR ectodomains in non-native architectures.

23 st to previous studies, we observed that the non-native assemblage was surprisingly unresponsive to e

24 tic pathways leading to either maturation or non-native association and provide a starting point for

25 Wolbachia to induce parthenogenesis in these non-native backgrounds.

26 ing that hydrolysis yielded an intermediate (non-native) beta-Lg state.

27 he degree of discrimination of native versus non-native binding and the optimization of which becomes

28 s, NBs lose niche position and relocate to a non-native brain region that is rich in neurosecretory n

29 tic diversity in the invasion success of the non-native bumblebee, Bombus hypnorum, in the United Kin

30 ignal type 1 (PTS1) for rapidly sequestering non-native cargo proteins.

31 nanocages can be used to capture and release non-native cargos.

32 Finally, we describe the discovery of non-native catalytic functions that may provide future o

33 Using this approach, we incorporated various non-native chemical modifications into chromatin in vivo

34 In this study, a non-native chemical species, bromodeoxyuridine (BrdU), w

35 nt to measure the population dynamics of the non-native cladoceran zooplankter Daphnia lumholtzi and

36 Understanding how the non-native client proteins bound to HtpG refold is of ce

37 Non-native competitive species could, however, have nega

38 ze a three-dimensional structure obtained in non-native conditions.

39 ses Luciferase to get trapped in very stable non-native configurations involving interactions between

40 : high affinity is maintained upon binding a non-native conformation by offsetting enthalpic penaltie

41 9 targets the SUMOylation of a transitional, non-native conformation of F508del NBD1: (a) its modific

42 ate that the Hsp27-Ubc9 pathway recognizes a non-native conformation of mutant NBD1, which leads to i

43 evealed the unfolded GQ exhibits a compacted non-native conformation reminiscent of the protein molte

44 dly in solution, proceeds through a compact, non-native conformation that forms within the peptide tu

45 red and folds to a thermodynamically stable, non-native conformation, termed refolded pepsin, which i

46 of a peroxidase active state, which is a key non-native conformational state in apoptosis.

47 The native conformation is stabilized while non-native conformations are destabilized by our optimiz

48 atically create such diverse and well-packed non-native conformations from any protein structure shou

49 A key problem is that non-native conformers generate high ESI charge states, r

50 IM-MS data on non-native conformers should therefore be interpreted wi

51 reams, and lowest of all in streams draining non-native conifers.

52 Non-native contacts can, however, influence folding kine

53 able predictions, including the formation of non-native contacts during the transition which we were

54 was an unstructured N-terminus stabilized by non-native contacts in a conformation that is topologica

55 y to native language phonemic contrasts than non-native contrasts.

56 riseusin C, 4'-deacetyl-griseusin A, and two non-native counterparts in 11-14 steps is reported.

57 e type (ST) distributions between native and non-native countries and that ERIC I and II STs mainly h

58 on in transversal tubules (T-tubules) to the non-native crest of the sarcolemma, where their open pro

59 n rivers, populations of multiple species of non-native cyprinid fishes are present, including black

60 dance, we applied eDNA technology to the six non-native cyprinid species putatively present in a 2.6

61 on spread from known introduction points or non-native distributions and ignore the transport proces

62 Remarkably, the introduction of a non-native disulfide bond was critical for formation of

63 ce, codon optimization and the addition of a non-native disulfide bond.

64 hain all-atom simulations predicted that one non-native disulfide in particular, between Cys(32) and

65 characterized, but our understanding of how non-native disulfides are reduced so that the correct or

66 secretion of proteins that are known to form non-native disulfides during their folding.

67 that the crucial role of ERdj5 is to reduce non-native disulfides formed during productive folding a

68 l assay to demonstrate that the reduction in non-native disulfides requires NADPH as the ultimate ele

69 malous thiol/disulfide exchange resulting in non-native disulfides, a hallmark of ALS that is related

70 the folding of proteins that form obligatory non-native disulfides.

71 ure as well as those that are not, so-called non-native disulfides.

72 of FPs misfold and fail to fluoresce due to non-native disulphide bond formation.

73 strate potential consequences of introducing non-native ecosystem engineers to lakes worldwide.

74 died how electron transfer from substrate to non-native electron acceptors can differentially modify

75 lectrostatic interactions, and in particular non-native electrostatic interactions, are involved in f

76 er, and in particular we uncover the role of non-native electrostatic interactions.

77 es using a chemical cross-linker and removed non-native Env by immunodepletion with non-neutralizing

78 structures of membrane proteins obtained in non-native environments.

79 involve the use of, or otherwise stabilize, non-native environments.

80 We then examine non-native enzyme activities that have been exploited fo

81 rete tissue-types in the seed in which these non-native fatty acids preferentially accumulated.

82 We also describe the distribution of these non-native fatty acids within C. sativa seed lipids, and

83 only underlie covariation between native and non-native faunas, especially in highly variable environ

84 rmine covariation in abundance of native and non-native fish species in a highly variable desert rive

85 errae, is known to be negatively impacted by non-native fish, while the threatened toad, Anaxyrus can

86 onal uniqueness was higher in native than in non-native fishes.

87 e free-energy landscape discriminate against non-native folds.

88 ndustrial processing, betalg is often in its non-native form in food products, which can modify the F

89 rm the predicted benefits of introduction of non-native forms of Rubisco with higher carboxylation ra

90 events shows that bS16 binds both native and non-native forms of the rRNA.

91 Plant nanobionics aims to embed non-native functions to plants by interfacing them with

92 Locally in that comparison, non-native gardens had lower host specificity; while amo

93 meter, md, that measures the degree to which non-native genes are evenly distributed among individual

94 pulations is quantifying the degree to which non-native genes have become evenly mixed among individu

95 spectral coverage for harvesting light using non-native genetically-encoded light-absorbers, thereby

96 mum extent to which orang-utans representing non-native, geographically and reproductively isolated t

97 ordered, and even well-folded proteins adopt non-native geometries during synthesis, folding, transpo

98 are narrow, and thus the ability to colonize non-native habitats requires that a number of conditions

99 as disrupted whereas replacing the AH with a non-native helical sequence restored CPX function.

100 ms "slow" phase of refolding, attributed to non-native helical structure frustrating microsecond ref

101 Mutagenesis demonstrated that D46 suppresses non-native Hh precursor autoprocessing and is indispensa

102 nd the reconstitution of desired traits in a non-native host is considered.

103 plasmid partitioning proteins in native and non-native hosts reveal chromosome-hitchhiking as the li

104 plants were equally important in determining non-native hosts.

105 ins and indicate that model systems based on non-native Httex1 sequences may not accurately reproduce

106 king, interactions are mediated by transient non-native hydrogen bonds, which efficiently catch the i

107 y trapped conformations caused by long-lived non-native hydrogen bonds.

108 alysis reveals that kanamycin B stabilizes a non-native, idiosyncratic conformation of the riboswitch

109 t native phonemic contrasts differently from non-native, implying that perceptual specialization and

110 ersity among tree species and among sites on non-natives in all comparisons.

111 ce mate-finding Allee effects in an invading non-native insect population.

112 ids induces formation of some weak transient non-native interactions in the folding transition state,

113 itial S4-RNA complexes pass through a stable non-native intermediate before converting to the native

114 W42Q aggregation required formation of a non-native intramolecular disulfide bond but not intermo

115 tigated the ecological effects of native and non-native invaders across levels of biological organisa

116 cies introductions exceeded those induced by non-native invaders.

117 in structuring biotic interactions, using a non-native invasive grass, Microstegium vimineum, in its

118 N ratio, were invaded to a greater extent by non-native invasive species than ectomycorrhizal (ECM) d

119 Non-native, invasive grasses have been linked to altered

120 rogressively favoring mapping of native over non-native language across the first year of life.

121 e able to demonstrate that (3) speaking in a non-native language involves more auditory feedback and

122 Non-native ligands capable of intercepting AIP:AgrC bind

123 nd gp41 was an effective method for removing non-native-like Env.

124 sed validation allowed the identification of non-native-like features in several membrane proteins an

125 nt long-range contacts, both native-like and non-native-like, have previously been shown to be presen

126 o- and regioselectivity as well as result in non-native linkages that may suffer from instability in

127 t experiment above the invasive range of two non-native lowland shrubs, Scotch broom (Cytisus scopari

128 e introduction and range size indicates that non-native marine invertebrate species are not at equili

129 identity native to the cells in situ even in non-native media, and significantly greater cellular acc

130 truncated proteins) as well as the use of a non-native membrane mimetic environment (e.g., micelles)

131 Here we use four non-native metabolic reactions to rewire central carbon

132 ineering these enzymes for the production of non-native metabolites has been a long-standing goal.

133 odulin kinase II-mediated phosphorylation in non-native microdomains and resulted in an elevated ICa,

134 ration at pH 6.8 and 8.0 led to formation of non-native monomers and reduced the DH to 75%, but showe

135 in vitro, and use them to infect native and non-native mosquito vectors.

136 Most strikingly, in non-native musicians, neural responses to the formant fr

137 ative speakers, non-native nonmusicians, and non-native musicians.

138 We screened a focused library of synthetic, non-native N-acyl l-homoserine lactones and identified c

139 to be hijacked to induce the degradation of non-native neo-substrates using bivalent compounds known

140 syllable in three groups of native speakers, non-native nonmusicians, and non-native musicians.

141 e formant frequencies of speech, compared to non-native nonmusicians, suggesting that automatic encod

142 In contrast, the other two are non-native oligomers in which the native dimer interface

143 s bad neighbours, but the negative effect of non-natives on natives was around two times greater than

144 around two times greater than the effect of non-natives on other non-natives.

145 A) pathway genes in Synechocystis endowing a non-native pathway for carbon flux amplification to isop

146 MRSA strains have acquired a non-native penicillin-binding protein called PBP2a that

147 CRP, in its non-native pentameric structural conformation, binds to

148 tructural elements that control AIP-III (and non-native peptide) activity: (1) a tri-residue hydropho

149 A set of non-native peptides was identified that can inhibit all

150 lopment of infant preference for native over non-native phonemes remain unclear.

151 urs at the expense of the ability to process non-native phonemes.

152 chanisms underlying processing of native and non-native phonemic contrasts were recently delineated i

153 e break also disrupted durable learning on a non-native phonetic classification task.

154 ggesting that high diversities of native and non-native plant species are compatible with one another

155 ions have not been observed and suggest that non-native plant species are not a threat to floral dive

156 ely forecasted the observed novel use of 459 non-native plant species by native herbivores.

157 mmunity composition: cover of graminoids and non-native plant species significantly increased, and co

158 itish sites do not differ between native and non-native plant species.

159 ecies than in the presence of a neighbouring non-native plant species.

160 ge of a situation in which a highly invasive non-native plant, Centaurea solstitialis L. (yellow star

161 ajor habitat types that interactions between non-native plants are asymmetrical with interactions bet

162 Non-native plants are now a pervasive feature of ecosyst

163 n a mesocosm experiment comparing native and non-native plants from California grasslands.

164 A negative effect of non-native plants on aggregate stability was also observ

165 ng our ability to predict the full impact of non-native plants on herbivores.

166 If true, then non-native plants should often benefit from low competit

167 In contrast, the performance of non-native plants was five times higher in the presence

168 Non-native plants were always bad neighbours, but the ne

169 in herbivore communities between native and non-native plants, focusing on how plant relatedness and

170 Native herbivores often colonise non-native plants, potentially reducing invasion success

171 t functional groups, and cover of native and non-native plants.

172 king W42Q mutant of gammad-crystallin formed non-native polymers starting from a native-like state un

173 Both the release of non-native populations from natural enemies, such as par

174 ound that China is the likely source of most non-native populations, with at least four separate intr

175 However, if non-native prey displace native prey, then an invader's

176 Although non-native prey may have a lower per capita value than n

177 ed a meta-analysis to quantify the effect of non-native prey on native predator populations.

178 Non-native prey should have a neutral to positive effect

179 Relative to native prey, non-native prey similarly or negatively affect native pr

180 te precursor peptide is engineered to have a non-native protease cleavage site that can be rapidly cl

181 landscape, which results in the formation of non-native protein aggregates that challenge the capacit

182 Non-native protein conformers generated by mutation or c

183 peptide strategy, we designed a peptide with non-native protein sequence, AP3, which exhibited potent

184 Computationally generated non-native protein structure conformations (or decoys) a

185 echanism involves extensive clearance of the non-native protein.

186 r chaperone-mediated kinetic partitioning of non-native proteins and may help explain the etiology of

187 sHsps complex with a variety of non-native proteins in an ATP-independent manner and, in

188 Molecular chaperones act on non-native proteins in the cell to prevent their aggrega

189 ATPase machine that rescues various forms of non-native proteins including the highly resistant amylo

190 biquitous chaperones that bind and sequester non-native proteins preventing their aggregation.

191 erones result in distinct binding modes with non-native proteins that ultimately define the activity

192 ar chaperone Hsc70 assists in the folding of non-native proteins together with its J domain- and BAG

193 cavities that open and close to encapsulate non-native proteins.

194 le hydrophobic segments across the length of non-native proteins.

195 largest fraction (20%) of the variability in non-native range size, while traits of the species and e

196 s had significant, but minimal, influence on non-native range size.

197 f species, especially of invasive species in non-native ranges, involves multiple challenges.

198 m new chemistry in vitro, the integration of non-native reactivity into metabolic pathways for small-

199 repertoire and fetal bovine serum (FBS) as a non-native reference.

200 Therefore, when phylogenetically distinct non-natives replace native plants, the community of imma

201 Forty-four non-native S/Se-alkylated Met analogues were synthesized

202 and our analysis of the simulations point to non-native salt bridges between helices as the source, w

203 d enabled the chemoenzymatic synthesis of 29 non-native SAM analogues.

204 of interconverting conformers that contain (non-)native secondary structure and lack the tightly pac

205 Efficient aerobic dehydrogenation of non-native secondary amine substrates, including pharmac

206 how that these truncated GFPs can bind other non-native sequences, and this promiscuity invites the p

207 ellulose degradation can be enhanced through non-native SLH domain GHs engineered into the genomes of

208 tentional switch mechanisms are activated in non-native speakers compared to native speakers.

209 Consequently, the networks of more fluent non-native speakers looked more like those of native spe

210 Non-native speakers of English who hold nursing qualific

211 e manifest at the neural level in native and non-native speakers of English who were overtly naming p

212 elated potential (ERP) and tested native and non-native speakers of English.

213 The difference between native and non-native speakers was further supported by finding tha

214 as further supported by finding that, within non-native speakers, there was less auditory feedback fo

215 ier for accessing biomedical information for non-native speakers.

216 ategies that reduce limiting factors such as non-native species and habitat degradation.

217 icting regions at risk from introductions of non-native species and the subsequent invasions is a fun

218 lytical approach to broadly evaluate whether non-native species are poised to respond more positively

219 Changing climate extremes and invasion by non-native species are two of the most prominent threats

220 e was almost no establishment success of the non-native species at moderate dispersal and reduced suc

221 ts at elevations above the invasive range of non-native species can clarify the relative contribution

222 plant communities may accumulate additional non-native species even if direct interactions between n

223 systems inhibit establishment of generalist non-native species from less diverse communities.

224 e hypothesis that climate change will favour non-native species has been examined exclusively through

225 perception of conservation managers to five non-native species in the UK, with these supplemented by

226 ation is likely to allow a greater influx of non-native species into both the Arctic and Antarctic pr

227 ships that can develop from introductions of non-native species into more complex ecosystems and at l

228 folded proteins, but only degradation of the non-native species is accelerated.

229 creasing in locations where the diversity of non-native species is increasing, suggesting that high d

230 e to climate change or the extent to which a non-native species may spread in novel environments.

231 would be of value both to bioassessment and non-native species monitoring.

232 However, during the invasion phase, non-native species must overcome many ecological and/or

233 on, establishment success and effects of the non-native species on native community structure and eco

234 e and non-native species richness and (2) do non-native species originate from higher diversity syste

235 At both spatial scales, however, nearly all non-native species originated from river basins with hig

236 the invasibility of native communities by a non-native species represented by core, midrange and per

237 strial (primarily plant) systems, native and non-native species responded similarly to environmental

238 gative relationship exist between native and non-native species richness and (2) do non-native specie

239 conflicting relationship between native and non-native species richness found at different spatial s

240 A negative relationship between native and non-native species richness in local assemblages was fou

241 r basin characteristics, species traits, and non-native species richness using binomial logistic regr

242 ctive of basin-wide differences in native or non-native species richness.

243 ignite policy changes and impact studies on non-native species than scientific evidence alone.

244 s is a prerequisite for the establishment of non-native species that become invasive, so knowledge of

245 most important vectors for the transport of non-native species to new aquatic environments.

246 naturalization and accumulation of multiple non-native species within ecosystems, which is frequentl

247 e more than nine times greater than those by non-native species).

248 s by altering competition between native and non-native species, but these effects may depend on biot

249 neral trend towards stronger responses among non-native species, including enhanced positive response

250 environments also preclude invasions by most non-native species, so identifying especially cold habit

251 ffects of corresponding growth of sympatric, non-native species, underscoring the importance of devel

252 ely ignored when forecasting the dynamics of non-native species.

253 xtirpations and preparing for the arrival of non-native species.

254 story-related intraspecific variation of the non-native species.

255 uence local biotic resistance to invasion by non-native species.

256 by the actual threats posed by the specific non-native species.

257 torical changes in land use and invasions of non-native species.

258 an temperature to favor the establishment of non-native species.

259 t and indirect interactions among native and non-native species.

260 species even if direct interactions between non-natives species are negative.

261 4 adults; 111 females) for associations with non-native speech category learning success.

262 sults suggest that individual differences in non-native speech-sound processing are to some extent de

263 ble regions of proteins and in proteins in a non-native state (i.e. misfolded or unfolded states).

264 In the non-native state (significantly explored at 380 K), the

265 This enhancement in the non-native state was due to glycine, as demonstrated by

266 eflecting the protein folding into a compact non-native state, as well as protein interactions with t

267 mental and computational methods to describe non-native states at atomic resolution.

268 between the native state and the average of non-native states versus the roughness measured by the v

269 Atlantic distribution, casting doubt on its non-native status in the NW Atlantic.

270 Pacific, several genetic traits support the non-native status of C. robusta.

271 ability to confidently ascertain native vs. non-native status of populations, particularly of those

272 81 and analogues containing cross-links with non-native stereochemical configurations.

273 structure, providing a rare example of such non-native structure formation in a folding pathway.

274 ly on-pathway and appears to have long-range non-native structure, providing a rare example of such n

275 nverting to the native complex, showing that non-native structures can offer a low free-energy path t

276 lution the transient formation of native and non-native structures in this acid-denatured state of AC

277 lizing conditions, wild-type myoc-OLF adopts non-native structures that readily fibrillize when incub

278 e found two reintroduced females were from a non-native subspecies, and have since produced at least

279 uorinase FlA1 for improved conversion of the non-native substrate 5'-chloro-5'-deoxyadenosine (5'-ClD

280 Interactions between the C terminus and the non-native substrate protein alter the binding position

281 ishing regulatory links between a MAPK and a non-native substrate.

282 lowing introduction of D-Ala into a range of non-native substrates.

283 of the native substrate or hydroxylation of non-native substrates.

284 evoked responses to discrimination of native/non-native syllable contrasts mostly in the left auditor

285 e demonstrate that PfACTI, when expressed in non-native systems, is capable of binding to and release

286 complex with free forms of either native or non-native T-synthase.

287 d functionally impoverished and dominated by non-native taxa.

288 d strongly discriminate against formation of non-native tertiary contacts, providing a sequence indep

289 causing variants investigated herein exhibit non-native tertiary structures under physiological condi

290 e single crystals and the {110} faces of the non-native tetragonal form.

291 m with low conformational free energy, while non-native tetraloop/tetraloop-receptor interactions are

292 cell differentiation, and local delivery of non-native therapeutic payloads, such as antibodies, in

293 prolyl bond led to enhanced population of a non-native [trans-MePro32]beta2m protein conformer, whic

294 n is restored by increased tRNA levels or by non-native tRNAs with exact-matching anticodons.

295 Pronounced differences in how native and non-native understory species use pre- and post-canopy e

296 ture herbivores on phylogenetically distinct non-natives vs. natives.

297 ifferences in communities on closely related non-natives were subtler, but displayed community shifts

298 sceptibility to mountain pine beetle and the non-native white pine blister rust (WPBR).

299 unity shifts and increased generalisation on non-natives within certain feeding guilds.

300 tive species richness prior to invasion by a non-native zooplankter, Daphnia lumholtzi.