ライフサイエンスコーパス: collective

1 vidual cell motion can actually increase the collective accuracy of a cluster by improving fluidity.

2 ronmental degradation indicates the need for collective action among nations and states to avoid cumu

3 heory that explains how emergent projects of collective action are progressed in complex organisation

4 e from group-defended critical resources and collective action benefits that result from social coope

5 ndividual contractile responses of MUs whose collective action determines the trajectory of changes i

6 Cooperation in collective action dilemmas usually breaks down in the ab

7 How can collective action evolve when individuals benefit from c

8 he Global Action Plan on HIVDR is a call for collective action grounded on normative guidance providi

9 tudy of one of the most striking examples of collective action in nonhuman animals, territorial bound

10 Cell-free studies have demonstrated how collective action of actin-associated proteins can organ

11 Thus, the collective action of antigen dispersal and DC positionin

12 According to one influential perspective, collective action problems are common, especially when g

13 benefits realised from resource defence and collective action profoundly affect insider-outsider con

14 interested in the provision of public goods, collective action, and prosocial behavior, and we give s

15 y deserves more consideration in research on collective action.

16 ial reality, by virtue of their influence on collective action.

17 , embrace ecological principles, and inspire collective action.

18 ls, individuals can choose to participate in collective actions as well as punish free riders.

19 Promoting only participation in collective actions is not effective.

20 el where clustering receptors leads to their collective activation by stabilizing an extended ordered

21 Here we describe the collective activity in such mixed populations, treating

22 lf-perpetuating changes in the individual or collective activity of proteins.

23 Raman spectroscopy showed the collective alignment of MA(+) cations within the intrins

24 can exhibit, we show that the phenomenon of Collective Almost Synchronisation (CAS), which describes

25 and facilitating the role of individuals in collective and collaborative actions that will modify th

26 We find that group size critically affects collective and individual acoustic traits: cohesive acou

27 ells and their impact on the cell biology of collective and individual cell migratory behaviors.

28 ellular phenomena, motile cells group into a collective and migrate persistently in a directed manner

29 migration programs, including multicellular, collective, and single-cell mesenchymal or amoeboid migr

30 The striking patterns of collective animal behavior, including ant trails, bird f

31 atures of glass-forming (GF) liquids such as collective atomic motion in the form of string-like atom

32 ar to crystal grains so that the string-like collective atomic motion is concentrated in regions betw

33 The collective atomic-scale defect disorder improves the zT

34 an acronym and IUPAC-like name derived from collective author knowledge.

35 Here, we uncover, experimentally, a mode of collective bacterial motility in humid environment throu

36 (3) attempts to design intended patterns of collective behavior and dynamic assembly; (4) speculativ

37 an external periodic forcing exhibit complex collective behavior and self-assembled patterns.

38 Yet research in collective behavior has largely neglected habitat influe

39 putations and social interactions underlying collective behavior in groups of animals are of great et

40 of stereotyped behavioral modes, studies of collective behavior largely ignored these findings; inst

41 Fundamentally, collective behavior must arise from the actions of indiv

42 result constitutes a proof of principle for collective behavior of macroscopically delocalized atomi

43 exes are introduced, and then we examine the collective behavior of pigment-pigment and pigment-prote

44 martensitic in nature when one considers the collective behavior of the double-twist cylinders.

45 To capture the collective behavior on the long timescales of fusion, we

46 nhibition of locomotion can display coherent collective behavior when in groups, even in the absence

47 capable of spectacular achievements through collective behavior, but examples of such behavior in fr

48 tern formation in space, as manifestation of collective behavior.

49 insects use olfactory cues to organize their collective behavior.

50 stent inter-individual differences may drive collective behavior.

51 ol, and intermotor communications leading to collective behavior.

52 communication that bacteria use to regulate collective behaviors.

53 hese subcolonies' performance in a series of collective behaviour assays and finally exposed colonies

54 s offers a step towards rudimentary forms of collective behaviour in communities of artificial cell-l

55 However, the mechanisms responsible for collective behaviour in mosquitoes are not well understo

56 in living fluids and can strongly affect the collective behaviour in prominent biological processes,

57 unities, and provide a strategy for inducing collective behaviour in soft matter microcompartmentaliz

58 Also, the collective behaviour of genes in a subnetwork is a much

59 We study the collective behaviour of network aligners and observe tha

60 led artificial spin ice can lead to specific collective behaviour, including emergent magnetic monopo

61 zation may have strong consequences on their collective behaviours and their vulnerability to disease

62 ed, in part, by a group's ability to execute collective behaviours unachievable by solitary individua

63 anipulation molecules as a method to control collective behaviours.

64 Cooperative behaviors provide a collective benefit, but are considered costly for the in

65 ative behaviour among individuals provides a collective benefit, but is considered costly.

66 the structure of the individual peptides and collective biointerface at the material surface.

67 show that marine picocyanobacteria have the collective capacity to encode thousands of different cyc

68 Here we focus on collective cell behavior in the female germline cyst in

69 Mechanical forces play critical roles in collective cell behaviors such as cell migration, prolif

70 did not promote a 'leader-follower' mode of collective cell invasion, demonstrating that matrix remo

71 At the collective cell level, the model simulations show that a

72 ersatile, and cost-effective method to study collective cell migration and wound healing.

73 etween substrate viscosity and elasticity on collective cell migration by adherent cells is highly ph

74 lular matrix (ECM) is a crucial precursor to collective cell migration in wound closure and cancer me

75 Collective cell migration is a highly regulated process

76 Collective cell migration plays a pivotal role in the fo

77 Collective cell migration plays an important role in dev

78 Collective cell migration underlies many biological proc

79 s cell-cell contact dynamics and coordinated collective cell migration.

80 cell mechanical responses during single and collective cell migration.

81 DCK) cells as a model system to quantify the collective cell migration.

82 Collective cell movement is critical to the emergent pro

83 ns can be applied to more complex systems of collective cell movement without prior knowledge of the

84 etic tweezers, and cell-cell cohesion during collective cell movements, further highlight that tensio

85 lance stresses within the tissue to regulate collective cell movements.

86 First, collective cell protection results from inhibition of ph

87 Here we derive a physical description of collective cellular movements from first principles, whi

88 The multidimensional and collective character of challenges facing refugee childr

89 ions to the binding energy from delocalized, collective charge fluctuations-in contrast to complexes

90 With theory and simulation, we show collective chemotaxis is limited by cell-to-cell variati

91 ferential thresholds to a model for making a collective choice among multiple options.

92 The application of neural models to collective choice shows fundamental similarities between

93 erent attacks that are more general than the collective class of attacks usually considered.

94 n exposure studies as urban water represents collective community-wide exposure.

95 urally extended to study social dynamics and collective computation in general settings.

96 The collective contigs for each strain were annotated using

97 The collective coordinate approach generalized for ferrimagn

98 e realize a detailed characterization of the collective Coulomb blockade transition, which is the fin

99 The collective data corroborate a mechanism involving nickel

100 These collective data indicate that VHR is a FAK phosphatase a

101 The collective data presented herein provide insight into th

102 The collective data suggest that the GPA and GPB receptors a

103 of relative option quality, which enables a collective decision maker to efficiently choose the best

104 The general features of this collective decision-making by a group of simple yes/no u

105 While collective decision-making is recognised as a significan

106 ing of animal groups [3, 4], including their collective decision-making, foraging performance, and pr

107 Surprisingly, cell collectives, despite their finite size, show features of

108 ry calculations, and theoretical modeling of collective dipole interactions in tubulin to investigate

109 growing interest in the unusual intermittent collective displacements of a large number of particles

110 Collective domain motions are identified by the principa

111 ents expose single-grain and multiple-grain, collective dynamic features that mimic those either obse

112 orrelations are not universally true, nor do collective dynamics follow the trends suggested by model

113 tween the pressure and density dependence of collective dynamics in bulk water and in concentrated pr

114 erimental models that can be used to explore collective dynamics in well-defined cell networks is sti

115 s to efficiently generate information on the collective dynamics of any structure in PDB format, user

116 Here we report on the collective dynamics of cultured murine neural progenitor

117 Here, we report the emergence of the collective dynamics of endocytic proteins as periodic tr

118 In many social and biological networks, the collective dynamics of the entire system can be shaped b

119 Further visualization of collective effect of 1181 microRNAs-mRNAs pairs and prot

120 f genuinely entangled particles based on the collective effect of directed emission combined with the

121 gle area, making it difficult to infer their collective effect on behavioral responses mediated by ac

122 uch as air traffic and social organisations, collective effects emerge from their many components' dy

123 We also present the collective effects observed in assemblies of interacting

124 peractivation of the pathway, or through the collective effects of common alleles.

125 provide precise context to help explore the collective effects of genes with biologically meaningful

126 ing mechanism that supports the emergence of collective effects of rotating ATP synthases in lipid me

127 Collective effects of the pair plasma may be also trigge

128 molecule-molecule interactions leading to a collective electromagnetic response.

129 lly modulated interaction strength cause the collective emission of matter-wave jets that resemble fi

130 independently on Twitter, contains distinct collective emotions associated with those cultural celeb

131 re being guided by study of the exposome (or collective environmental exposures beginning during the

132 fluence of central individuals dominates the collective estimation process, group estimates become mo

133 Collective evidence showed that adiponectin accumulates

134 We review here the collective evidence supporting this claim.

135 Strong coupling with some collective excitation mode has been indicated by a dispe

136 sed matter physics to describe an elementary collective excitation.

137 coronene, which again indicates the role of collective excitation.

138 ous symmetry-breaking properties, associated collective excitations and superfluid behaviour.

139 The description of quantized collective excitations stands as a landmark in the quant

140 These results are consistent with the collective experimental evidence that species richness i

141 thelial cells respond to minimal wounds in a collective fashion by increased contractility with subst

142 These collective findings point to a novel glycosylation-depen

143 These collective findings point toward a deformed B cell reper

144 The collective findings suggest chimpanzees exhibit cortical

145 t is not clear whether changes resulted from collective FODMAP restriction or removal of a single com

146 These networks may represent a collective foraging behavior of this parasite, which may

147 We showed that the collective frequency of unbinding events in WT-RBCs is n

148 These collective functions of SR-B1 ultimately affect programm

149 Then, we studied collective gene interaction patterns and uncovered highl

150 n individuals who have more to gain from the collective good or can produce it at low costs provide i

151 e demography accumulation curve in which the collective growth of the ensemble depends on the number

152 ver, the effect is typically small requiring collective heating of a large concentration or aggregate

153 e that there is valuable predictive power in collective human judgment, and we discuss the benefits a

154 e we consider a serious alternative based on collective human judgment.

155 onequilibrium, long-time-scale excitation of collective/hydrodynamic modes, and (iii) long-time-scale

156 d to the conformational change driven by the collective hydrogen bonding and the sequence-mandated to

157 better therapies that appropriately modulate collective immunotypes, rather than individual immune co

158 While the collective impact of marine viruses has become more appa

159 that the proposed method can achieve larger collective influence given the same number of seeds comp

160 Here we address this issue by exploring the collective influence in general threshold models of casc

161 fic, sequence-altered genes, with sufficient collective influence over dysregulated transcripts.

162 dividual's location, measured as the optimal collective influence to the structural integrity of the

163 r across observers suggests that the greater collective integration benefits for visual search arise

164 tection theory specifies the upper limit for collective integration benefits obtained by weighted ave

165 -making accuracy typically increases through collective integration of people's judgments into group

166 olution (CCE), the interplay between CCE and collective intelligence has remained unexplored.

167 overy of the "wisdom of crowds", theories of collective intelligence have suggested that the accuracy

168 Our findings thus show that collective intelligence in animal groups can accumulate

169 Collective intelligence is the ability of a group to per

170 bers is a key condition for the emergence of collective intelligence, but maintaining diversity is ch

171 fin Adf1, we examined how their pairwise and collective interactions with actin filaments regulate th

172 local concentration gradient, diffusion, and collective interactions.

173 These data support a symbiotic model of collective invasion where phenotypically distinct cell t

174 distributed individuals can form intelligent collective judgments.

175 Collective learning is a nascent field for the further a

176 Scaling to the collective level reveals a clear association between hab

177 ions in many aspects, such as individual and collective levels, temporal and spatial dimensions, cont

178 otion mechanisms both at the microscopic and collective levels.

179 embryo, but how cells move in a directed and collective manner has remained unclear.

180 ter simulations can aid in understanding how collective materials properties emerge from interactions

181 m a coevolved mutualism that maximizes their collective metabolic rate by recycling organic carbon th

182 duction is, thus, pertinent to understanding collective microbial behavior, such as virulence and bio

183 rnatives to biological systems for examining collective microscopic dynamics and the response to phys

184 rs, we identified GEFs that are required for collective migration at large, such as SOS1 and beta-PIX

185 Efficient collective migration depends on a balance between contra

186 nd metastatic melanoma invasion and promotes collective migration in a manner consistent with the inh

187 ove collectively in vortices using a mode of collective migration known as coherent angular motion (C

188 Collective migration of epithelial cells underlies diver

189 (e.g., adhesion and traction forces) to the collective migration of small groups of cells and the ex

190 s with Eph signaling via N-cadherin to drive collective migration of the Schwann cells across the wou

191 However, the actual importance of these to collective migration remains circumstantial.

192 unclear how the different observed modes of collective migration, especially for small groups of cel

193 , when coupled with a mathematical model for collective migration, shows that intracellular contracti

194 We conclude that for effective collective migration, the RHOA-GEFs --> RHOA/C --> actom

195 cell division is crucial for tuning emergent collective migratory behaviors, such as vortical motions

196 The collective mobility of active matter (self-propelled obj

197 A variety of individual and collective mobility patterns such as scaling behaviors a

198 It is shown that at the energy of the collective mode molecules oscillate completely out of ph

199 Biofilms are a collective mode of bacterial life in which a self-produc

200 the tumour-stroma interface that govern the collective mode of migration adopted by carcinoma cells

201 spectroscopy (M-EELS), we studied electronic collective modes in the transition metal dichalcogenide

202 o 200 K via the coherent oscillations of its collective modes, which is reminiscent of that observed

203 regulated biochemical cascade formed by the collective molecular recognition properties and proteoly

204 We attribute its physical nature to collective molecule-molecule interactions leading to a c

205 ated cities in the world, finding that their collective morphology exhibits a directional bias influe

206 om solitary motion and near-wall swimming to collective motility in synchronised swarms and in confin

207 tant regulatory mechanism to coordinate such collective motion.

208 cteria generate and coordinate forces during collective motion.

209 In contrast, the amplitudes of the slower collective motions occurring on the nanosecond (tens to

210 ese motions as fast local motions and slower collective motions of TM helices and of structured loops

211 tterings are driven by a mixture of 0D/1D/2D collective motions.

212 nate individual cell migratory behaviors for collective movement are largely unknown.

213 rt-range chemical gradients lead to coherent collective movement at a macroscopic scale?

214 traveling through heterogeneous landscapes, collective movement can be influenced by both habitat st

215 We show that collective movement decisions guided by individual bison

216 of resource depletion are closely linked to collective movement decisions.

217 o starved Saccharomyces cerevisiae initiates collective NADH dynamics termed glycolytic oscillations.

218 ons may be underestimated when examining the collective national experience.

219 The collective networks display a repeating spatial progress

220 d a framework that links them, revealing how collective neural activity arises from the structure of

221 arch and to focus on DNA methylation and the collective observations of many studies being conducted

222 These collective observations suggest that neuroimmune signali

223 otein-protein interactions sustain conserved collective occupancy.

224 rrelated with the prognosis in 2 independent collectives of patients with tumors.

225 We show that migration of carcinoma collectives on fibrillar FN-rich matrices is achieved th

226 y yield maximum biomass, thereby achieving a collective optimum.

227 Despite lacking the remarkable collective order of other animal ensembles, such as fish

228 y excited, such metal nanostructures feature collective oscillations of electrons (plasmons), providi

229 n in fluorescence intensity and observed the collective particle diffusion over tens of minutes and t

230 with a local group can extend to the global collective, particularly for individuals who are also hi

231 terials that respond to mild stimuli through collective phase transitions and amplify signals could o

232 point; the contributions individuals make to collective phenomena can be quantified; there is heterog

233 ectronic systems that exhibit a multitude of collective phenomena.

234 f network structure and our understanding of collective phenomena.

235 egrees of freedom in graphene, including the collective plasmon modes via the Coulomb interaction, wh

236 Due to the collective plasmonic responses in SNL, these ultrathin 2

237 m) is an order of magnitude greater than the collective polycrystal (K eff /R eff = 10(-5) to 10(-3)

238 w such adaptive versatility manifests in the collective population dynamics and function of cerebral

239 e onset of stimulation, adaptation tunes the collective population dynamics towards a special regime

240 ough an evolutionary game-theoretic model of collective prediction, we investigate the role that ince

241 how that this produces optimal diversity and collective predictive accuracy.

242 putation, workload and motivation to work on collective productivity.

243 tes, the catalytic activity arising from the collective properties of graphenes as materials by adsor

244 toms, is a promising approach to realize the collective properties of nanocrystals.

245 The collective properties of tailored Co3O4/Co(OH)2 thin fil

246 elf-assemble into ordered superlattices with collective properties, but the ability for controlling N

247 omena at atomic scales can manifest in their collective properties.

248 bridges the link between their discrete and collective properties.

249 used to demonstrate that oscillations are a collective property of PSM cells that can be actively tr

250 ynergistic effects of the spatial nonuniform collective quantum confinement of sp(2) domains, and the

251 Experimental analyses have explored collective rationality, cognitive capacity, and perceptu

252 Characterizing the collective regulatory impact of genetic variants on comp

253 rganizational social capital is an important collective resource.

254 eta-atom is often generalized to explain the collective response of a metasurface in a manner that ne

255 Collective responses of Pseudomonas PMM/PGM to phosphosu

256 Domain 4 appears central to collective responses to substrate and inhibitor binding.

257 ritical coupling in two-region coupling is a collective result of the coupling at two different coupl

258 We show that these collective results are due to a balance of network elast

259 These collective results explain the unique features of the ae

260 The collective results suggest that learning to produce AG s

261 With our collective results, we suggest that weight variability a

262 sidered consistencies and differences in the collective results.

263 ions of the residues of the beta-barrel as a collective rocking of low amplitude and of hundreds of n

264 mission electron microscopy we show that the collective rotation of the average magnetization proceed

265 and facilitate switches in the direction of collective rotation.

266 sms to unpin contact lines, hence inducing a collective slipping of the colony across the surface.

267 tive matter, and how topology can enrich the collective spatiotemporal dynamics in inherently non-equ

268 Systems hybridising collective spin excitations with microwave photons have

269 A collective state in the neural population, in which neur

270 We show that this collective state is robust to changes in stimulus ensemb

271 real neural population is in a 'structured', collective state.

272 Within the plethora of collective states a complex network can exhibit, we show

273 f a generalized Kuramoto model predicts five collective states as possible long-term modes of organiz

274 through the electromagnetic field, creating collective states that can radiate faster or slower than

275 hastic nanomagnets at GHz speeds through the collective states with an emphasis on the low energy sta

276 The regime of collective strong coupling arises, when various excitati

277 , fostering a debate about the nature of the collective structure of population neural activity.

278 band gap reduction as a result of the BNNSs' collective structure.

279 These collective studies indicate transient BAFFR-Fc-mediated

280 This review provides a collective summary of existing methodological frameworks

281 on programs that promote their individual or collective survival.

282 Collective swimming induced by elasticity may thus facil

283 Here, we report striking collective swimming of bovine sperm in dynamic clusters,

284 ntial applicability is presented through the collective synthesis of several important classes of het

285 ynthesis, which has emerged in parallel with collective synthesis, diverted total synthesis and the p

286 Adaptive collective systems are common in biology and beyond.

287 l traits for plant leaves that represent the collective temperature response of metabolic respiratory

288 We found that these gases alter collective terahertz dipole oscillations in a manner tha

289 hese studies created a paradigm shift in our collective thinking as to why recombinant Envs are ineff

290 Here we show that the collective transition of release channels from an open t

291 provides insight into fundamental aspects of collective transport in active spinner materials and yie

292 Similarly, collective transport in glassy materials is well documen

293 e recovered and distinguished, and that if a collective traveling wave (the metachronal wave) is pres

294 on a remarkable cascade process inducing the collective twofold C-H/threefold C-F bond activations, w

295 over the participation of an individual in a collective U-turn event.

296 Our collective understanding of old and new phagocyte functi

297 ultipotency at the population level reflects collective unipotent cell fate decisions by single stem

298 ions of the two proteins, we first performed collective variable-based steered molecular dynamics (CV

299 of reduced models defined on a small set of collective variables (colvars).

300 The string method in collective variables is used to simulate, without artifa