ライフサイエンスコーパス: self-organization

1 extreme frictional conditions which trigger self-organization.

2 odulation of force and contribute to spindle self-organization.

3 form as the result of externally controlled self-organization.

4 des with small molecules undergo aggregation/self-organization.

5 ecome an important model system for studying self-organization.

6 steric interactions between them, drive the self-organization.

7 based on spontaneous processes of inorganic self-organization.

8 therapeutics or fabrication methods based on self-organization.

9 igate fundamental mechanisms behind cellular self-organization.

10 system, the basic neural circuitry undergoes self-organization.

11 tant but poorly understood role in molecular self-organization.

12 esis, near-unity purification, and nanoscale self-organization.

13 derived components that polymerize driven by self-organization.

14 alogous materials that lack the capacity for self-organization.

15 ucture are impressive examples of biological self-organization.

16 e to a modifiable pattern that is subject to self-organization.

17 PPT) showing how seasonality affects spatial self-organization.

18 bility to encapsulate guest molecules during self-organization.

19 integrate multiple mechanisms of ecological self-organization.

20 ly broken by an emergent process of cellular self-organization.

21 s an important mechanism underlying cellular self-organization.

22 populations with slow dynamics; and spatial self-organization.

23 ems, especially in relation to multicellular self-organization.

24 natural question: Can origami arise through self-organization?

25 We show that the motor-driven self-organization activities associated with NuMA (i.e.,

26 tems, and provides a means to detect spatial self-organization against physical template heterogeneit

27 This form of nonequilibrium self-organization allows the creation of structures that

28 alangeal pattern, it has been suggested that self-organization alone could be sufficient.

29 entry, acting as a switch that triggers the self-organization and activation of STIM1-ORAI1 clusters

30 High-level 'rules' of self-organization and assembly are increasingly used to

31 The self-organization and biomechanical functions of tendon

32 we quantify missing information, emergence, self-organization and complexity for a collective motion

33 nimals exhibit a higher degree of emergence, self-organization and complexity over time.

34 ons to achieve certain degrees of emergence, self-organization and complexity.

35 We investigate computationally the self-organization and contraction of an initially random

36 The model used is an example of self-organization and could be more widely applicable to

37 r and such behavior is often associated with self-organization and dynamics occurring near critical t

38 f biological fitness and chemical stability, self-organization and emergence, and ultimately to disco

39 tu study of dislocation structure formation, self-organization and evolution in the bulk.

40 ppreciation for the principles governing the self-organization and functional characteristics of comp

41 filament arrays and provide insight into the self-organization and mechanics of cytoskeletal assembli

42 Controlling self-organization and morphology of chemical architectur

43 networks lead to large-scale nonequilibrium self-organization and pattern formation in life is a maj

44 Self-organization and pattern formation in network-organ

45 this organism is for biophysical studies of self-organization and pattern formation.

46 Complex systems display self-organization and predictive behavior along a range

47 l variations in the resource, especially for self-organization and productivity.

48 We first introduce nanoscale self-assembly, self-organization and reaction-diffusion processes as es

49 ion mammalian embryo is a paradigm of tissue self-organization and regulative development; however, t

50 significantly influence the tendon fibrils' self-organization and self-healing and therefore contrib

51 ular cytoplasm has a remarkable capacity for self-organization and that introduction of such macromol

52 use different sources of energy to carry out self-organization and the performance of work in their e

53 rch on regeneration, organ morphogenesis and self-organization - and the links between these fields.

54 ith a high propensity towards supramolecular self-organization, and describe the pathway through whic

55 (e.g., on cooperation, multilevel selection, self-organization, and development) and thereby help int

56 t conditions this heterogeneity can arise by self-organization, and what information it can convey.

57 ks regulating Cdc42 oscillations and spatial self-organization appear to provide a flexible mechanism

58 Multiple accounts of this self-organization are currently influential and in this

59 The patterning events driving this self-organization are currently unknown.

60 Pattern formation and self-organization are fascinating phenomena found widely

61 where plant-plant interactions and community self-organization are important.

62 The principles of self-assembly and self-organization are major tenets of molecular and cell

63 ; however the mechanical principles for such self-organization are not understood.

64 hallenge to unraveling principles underlying self-organization around criticality in biological recur

65 and their rotational movement drive spindle self-organization, as well as how the forces acting in t

66 cell-cell correlations, showing evidence of self-organization at the onset of aggregation (as oppose

67 The self-assembly and self-organization behavior of uracil-conjugated enantiop

68 rue through a variety of fluctuation-driven, self-organization behaviors exhibited by out-of-equilibr

69 is related to the emergence of coherence-or self-organization-between chromosomal associations and c

70 teria is a fascinating case of multicellular self-organization by bacteria.

71 anes within cyanobacteria could disrupt this self-organization by sterically occluding or sequesterin

72 However, it is unclear how self-organization by this mechanism remains robust when

73 One example of such self-organization, called symmetry breaking, involves sp

74 is study provides experimental evidence that self-organization can be paramount to enhancing ecosyste

75 In vitro, Min protein self-organization can be reconstituted in the presence o

76 indicate that this intrinsic propensity for self-organization can even extend to the formation of co

77 ro-posterior positional values is curtailed, self-organization can then produce several digits with t

78 paradigms not only demonstrate the enormous self-organization capacity of neural stem cells, they al

79 ids, characterized by this kind of nonlinear self-organization, defines a new class of turbulent flow

80 T(FBTTh2)2 can achieve exceptional levels of self-organization directly via solution deposition.

81 work supports a cooperative process of ring self-organization driven by the interaction between acti

82 This self-organization, driven by asymmetric fitness effects

83 nt at an autonomous process of microfilament self-organization driving the formation of streaming pat

84 We show that dynamical self-organization during growth can create a coherent in

85 ure of complex networks and suggest a common self-organization dynamics.

86 broad variety of dissipative structures and self-organization effects, have drawn significant resear

87 Our results revealed that both forms of self-organization enhanced the persistence of the constr

88 x networks can be explained as the result of self-organization, even in the absence of synaptic reinf

89 in vitro, it is yet unclear how these basic self-organization events are modulated by the crowded in

90 ns and peptides, it is yet unclear how these self-organization events are precisely modulated by micr

91 fail to explain the results of the in vitro self-organization experiments.

92 enabling abiotic soft tissue with multiscale self-organization for effective load bearing and energy

93 dicate that centrosomal MTs complement Golgi self-organization for proper Golgi assembly and motile-c

94 characteristic shapes, but the mechanisms of self-organization for robust morphological maintenance r

95 que solvent properties of ionic liquids with self-organization found for liquid crystals.

96 g in the mammary gland, we reconstituted its self-organization from aggregates of primary cells in vi

97 These dynamic patterns emerge via self-organization from an activator-inhibitor network, i

98 Here, we demonstrate a form of self-organization from nonequilibrium driving forces in

99 systems that exhibit lifelike properties of self-organization, growth, and development, and the mode

100 cal micro environments that promote cellular self-organization have enhanced the ability to recapitul

101 tructures, and dynamics of proteins, such as self-organization, hydration forces and ionic interactio

102 This self-organization, if it occurs, results when synchroniz

103 Our model highlights a novel pattern of self-organization in a bacterial biofilm.

104 chiral springs and helices on the colloidal self-organization in a nematic liquid crystal using lase

105 tration of EPSs are important factors in the self-organization in a nonequilibrium growing colony.

106 ys that could have brought about features of self-organization in a peptide world are considered in t

107 es a striking example of irradiation-induced self-organization in a quantum system.

108 We demonstrate patterns of self-organization in abundance distributions emerging as

109 bacteria or flocks of birds are examples of self-organization in active living matter.

110 striking new insights into the mechanisms of self-organization in bacterial cells and indicate how th

111 y multicellular systems, including microbial self-organization in biofilms, embryogenesis, wound heal

112 ic chemistry and for developing new kinds of self-organization in chemically reacting systems.

113 ed support the analysis of complex bacterial self-organization in confined volumes.

114 the principles controlling self-assembly and self-organization in CSD grown oxides.

115 of these lineages, providing a framework for self-organization in development.

116 ocesses, and detect and evaluate the role of self-organization in driving such patterns.

117 he prevailing theoretical outlook on spatial self-organization in ecology must expand to incorporate

118 stem variables that affect the likelihood of self-organization in efforts to achieve a sustainable SE

119 roperties are owed in part to their specific self-organization in hierarchical molecular structures,

120 best-understood examples of emergent protein self-organization in nature.

121 pproach can be expanded and adapted to study self-organization in other cellular systems.

122 tures facilitated by cell death may underlie self-organization in other developmental systems, and co

123 describes a novel mechanism for microtubule self-organization in the absence of centrosomes; this me

124 Self-organization in the cell relies on the rapid and sp

125 sustaining elongation, and the triggering of self-organization in the form of lamellar fingers.

126 nchronously--instead they display a striking self-organization in the form of metachronal waves (MCWs

127 The level of self-assembly and self-organization in the SAFs is unprecedented for a des

128 bility of such structures beckons control of self-organization in the temporal regimes.

129 sible system for the study of patterning and self-organization in the well-studied model organism Ara

130 ea that the membrane itself mediates protein self-organization in these processes through minimizatio

131 sess the functional importance of keratin IF self-organization in vivo.

132 led 'Regeneration of Organs: Programming and Self-Organization' in March, 2014.

133 Spatial self-organization including striking vegetation patterns

134 Here we discuss the process of self-organization into patterns on the bacterial nucleoi

135 hear of a granular material leads to dynamic self-organization into several phases with different spa

136 ility to break symmetry and polarize through self-organization is a fundamental feature of cellular s

137 We propose that self-organization is a key determinant of the structural

138 We also find that this mechanism of self-organization is conserved in the human prostate.

139 Self-organization is determined independently of polymer

140 We find that self-organization is dominated by the interfacial energy

141 Protein self-organization is essential for the establishment and

142 Here, we show that filament self-organization is mediated by multivalent interaction

143 cell cohesion, we show that this strategy of self-organization is robust to severe perturbations affe

144 Molecular self-organization is thought to drive nuclear body forma

145 rties of atoms and molecules to direct their self-organization, is widely used to make relatively sim

146 Together with rapid component turnover, the self-organization mechanism continuously reassembles and

147 wn to occur through a centrosome-independent self-organization mechanism where microtubule motors cro

148 ns new perspectives for the understanding of self-organization mechanisms.

149 f the key dynamic traits of complex systems: self-organization, modularity and structural properties.

150 -tailed size distribution that is typical of self-organization near a critical point.

151 rrent models of cell signaling, cytoskeletal self-organization, nuclear transport, and the cell cycle

152 Our mathematical model shows that the self-organization observed in our experiments is control

153 A complementary form of self-organization occurs among swarming insects, flockin

154 We show that the self organization of vortices into lattices is accompani

155 activity, and microtubule dynamics drive the self-organization of a bipolar meiotic spindle.

156 switching properties, gelation behavior, and self-organization of a cholesterol-stoppered bistable [2

157 providing a previously unidentified route to self-organization of a many-body system.

158 The emergent self-organization of a neuronal network in a developing

159 erve cooperation between individuals and the self-organization of a sustained trust network, which fa

160 The self-organization of active particles is governed by the

161 is experimentally demonstrated, based on the self-organization of Ag nanoclusters under an electric f

162 -1-coated 2D substrates of ~1 kPa results in self-organization of all three germ layers: ectoderm on

163 se results define minimal parameters for the self-organization of an acentrosomal microtubule network

164 yst and then with the glycosyl donor enables self-organization of an ordered transition-state.

165 Self-organization of aqueous surfactants at a planar gra

166 heoretically in many contexts, including the self-organization of arrays of MTs by motors and the com

167 t with regard to memory but also extended to self-organization of behavior.

168 ithin complex chemical mixtures, wherein the self-organization of biomolecules allows them to form "a

169 opic effect as the main driving-force of the self-organization of BNSLs.

170 rties of the pillars that favor the adhesive self-organization of bundles with pillars wound around e

171 lease units via Ca-induced Ca release causes self-organization of Ca spark clusters.

172 y will have implications in problems such as self-organization of cell tissues or the design of capil

173 observations have revealed that large-scale self-organization of cells in actively expanding biofilm

174 The mechanics of symmetry breaking and the self-organization of cells into fruiting bodies is an ac

175 Self-organization of cellular structures is an emerging

176 entropic forces probably participate in the self-organization of chromosomes within nuclei.

177 The self-organization of colloidal particles is a promising

178 Self-organization of colloidal Pt nanocubes into two typ

179 xquisite fidelity, and is a paradigm for the self-organization of complex macromolecular structures.

180 al tissue scaffolds, and they were formed by self-organization of coplanar reticular networks with bu

181 microtubules plays a predominant role in the self-organization of cortical arrays.

182 al theories have been developed to study the self-organization of cytoskeletal filaments in in vitro

183 Diverse myosin II isoforms guide the self-organization of distinct contractile units within i

184 -binding protein sorting is critical for the self-organization of diverse dynamic actin cytoskeleton

185 e necessary and sufficient to facilitate the self-organization of dynamic microtubules into a paralle

186 stability, which play a critical role in the self-organization of energy and matter in non-equilibriu

187 computer model to study lamellipodia via the self-organization of filament orientation patterns.

188 ing of oligonucleotides that is based on the self-organization of half-sliding complementary oligonuc

189 Many researchers consider the self-organization of lipid and fatty acid molecules into

190 Bottom-up approaches, such as the self-organization of liquid crystals, offer potential ad

191 n set-reset latches through the synchronized self-organization of many individual network components.

192 This study unravels the dynamic yet discrete self-organization of mature microglia in the healthy and

193 actions are indeed sufficient to explain the self-organization of MCWs and study beat patterns, stabi

194 mechanistic effects occur in light-mediated self-organization of metal nanoparticles; atoms are repl

195 The motor-driven self-organization of microtubule minus ends at spindle p

196 The spindle arises from self-organization of microtubules and chromosomes, whose

197 Here, we studied the self-organization of microtubules growing in the presenc

198 ly focused bipolar spindles form through the self-organization of microtubules nucleated from chromos

199 elevance network analysis showed a conserved self-organization of modules of interconnected genes wit

200 Here we report the self-organization of motile colloids into a macroscopic

201 igration may be a key physical mechanism for self-organization of nanometer-sized sessile vacancy clu

202 ed with floods is universal, indicating that self-organization of near-critical channels filters the

203 of frontness and backness is responsible for self-organization of neutrophil polarity.

204 article-based modeling approach to study the self-organization of nonmotile rod-shaped bacterial cell

205 at the colloidal scale, as it can govern the self-organization of particles into hierarchical structu

206 to achieve this goal is based on the spatial self-organization of patches of cell-adhesive molecules

207 as or generate their own niche, enabling the self-organization of patterned tissues.

208 This mechanism of hierarchical self-organization of PBI into supramolecular spheres is

209 teractions of the core proteins required for self-organization of planar polarity.

210 The self-organization of polymerizing microtubules (MTs) is

211 ied the effect of spatial confinement on the self-organization of purified motors and microtubules th

212 We demonstrate the self-organization of quasi-one-dimensional nanostructure

213 biological cell to regulate Ca signaling via self-organization of random subcellular events into cell

214 ack loop coordinating cell migration and the self-organization of rosette-shaped sensory organs in th

215 irst analysis of the geometric structure and self-organization of Sc patterns from this network persp

216 he emergence of systems constructed from the self-organization of self-replicating agents acting unde

217 provide a general theoretical foundation for self-organization of social-insect colonies, validated u

218 nd to better understand the forces governing self-organization of soft materials.

219 ple cellular automata model it is shown that self-organization of spatial pattern in a community of s

220 ional roles that twitching might play in the self-organization of spinal and supraspinal sensorimotor

221 erated between antiparallel microtubules, in self-organization of spindle bipolarity and poleward flu

222 esence of these opposing forces promotes the self-organization of spontaneously active neuronal netwo

223 Here, we investigate the self-organization of stabilized microtubules in Xenopus

224 d experiments, supporting the proposition of self-organization of stand structure.

225 speech processing imposes constraints on the self-organization of synchronous cell assemblies and the

226 Previous study of self-organization of Taxol-stabilized microtubules into

227 ic techniques, we here show evidence of such self-organization of the actin cortex in living HeLa cel

228 olic evolution to the self-amplification and self-organization of the biosphere.

229 The self-organization of the dendrimers on the solid substra

230 tion morphogenesis in which ECM triggers the self-organization of the embryo's stem cells.

231 te that these microarchitectures form due to self-organization of the manifold mineral and organic so

232 nanowire building blocks; third, large-scale self-organization of the mesocrystals and the reduction

233 the influence of spatial confinement on the self-organization of the Min system, a spatial regulator

234 cal properties, which arise from the dynamic self-organization of the nanoparticles under stress.

235 in energies show that these forces drive the self-organization of the superlattices.

236 the existence of appropriate rules governing self-organization of the velocity field of a dynamical s

237 cells (protocells) would be dependent on the self-organization of their components and physicochemica

238 actors by these microtubules illustrates how self-organization of these bundles contributes to establ

239 A spontaneous self-organization of these nanostructures is then trigge

240 ntial tool to modulate the global orientated self-organization of these systems.

241 Therefore, in this review, we explore the self-organization of this class of functional molecules

242 Self-organization of this type may be important to the f

243 both static compartmentalization and dynamic self-organization of transcriptional apparatus are in ef

244 The reaction is based upon the self-organization of two {Te3W38} units around a single

245 We report the self-organization of universal branching patterns of oil

246 The self-organization of Zn(II) complexes on the surface of

247 oning of MinD/ParA proteins is either due to self-organization on a surface or reliance on a landmark

248 ve importance of these two spatial scales of self-organization on mussel bed persistence, we conducte

249 ystals makes possible the observation of new self-organization phenomena.

250 cosystem, for the view of fairy circles as a self-organization phenomenon driven by water-vegetation

251 n as nongenetic processes, such as molecular self-organization, play an essential and complementary r

252 ucture of the monomers satisfies the amyloid self-organization principle; namely, the low free energy

253 te their ubiquity, little is known about the self-organization principles that govern flow statistics

254 le ambient resources arose very early in the self-organization process and dictated the locations of

255 Thus, in a self-organization process conjugation may be extended by

256 Coupling photopatterning with either self-organization process provides a powerful route for

257 Understanding the self-organization process requires not only the in-situ

258 ic attraction are the driving forces for the self-organization process.

259 rticles (NPs) is central to comprehension of self-organization processes and a wide spectrum of physi

260 ale deformation regime involving solid-state self-organization processes that lead to efficient energ

261 with the porphyrin N-core as a new source of self-organization processes.

262 ng likely being a paradigm for many cellular self-organization processes.

263 By controlling the polymer/polymer blend self-organization rate, all-polymer solar cells composed

264 However, self-organization realized by the mechanism of spatial f

265 Ndel1-dependent microtubule self-organization requires an interaction between Ndel1

266 maturation in liver organoids, but organoid self-organization requires cell-to-cell surface contact.

267 These studies thus unravel the default self-organization rules governing early embryogenesis an

268 This strategy of asymmetry-driven active self-organization should generalize rationally to other

269 y of mathematical biological theories (e.g., self-organization/structure, cladistics/history, and evo

270 These models of self-organization suggest that characteristic patterns s

271 We report a new mechanism of self-organization that can lead to robust surface orderi

272 e mRNA, and this interplay leads to polysome self-organization that drives translation rate to maximu

273 t is an intricate, spatiotemporal process of self-organization that emerges from gene regulatory netw

274 such as those found in the nucleolus, show a self-organization that is marked by spatial segregation

275 scillators is a fascinating manifestation of self-organization that nature uses to orchestrate essent

276 Here we describe a class of self-organization that operates within densely packed ba

277 cal models and observational studies suggest self-organization, the formation of patterns due to ecol

278 rporates two essential aspects of actomyosin self-organization: the asymmetric load response of indiv

279 Ran-GTP promotes spindle self-organization through the release of importin-bound

280 terning technologies and directed epithelial self-organization to deliver microparticles to the lumen

281 ion actions that use the emergent effects of self-organization to increase ecosystem resistance to di

282 tablished in the literature, but spontaneous self-organization to prepare such structures has not bee

283 that lead to such outcomes as self-assembly, self-organization, unique nanostructures, chemical waves

284 However, the perovskite self-organization upon crystallization and the final ele

285 ole of Ndel1 in dynein-dependent microtubule self-organization using Ran-mediated asters in meiotic X

286 imply a general thermodynamic mechanism for self-organization via dissipation of absorbed work that

287 Direct evidence for the self-organization was obtained from AFM investigations w

288 ures not present in the previous cases of NP self-organization were identified and discussed.

289 ur results reveal a principle for ecological self-organization, where phase separation rather than ac

290 Self-organization, where spontaneous orderings occur und

291 y towards a general use of self-assembly and self-organization which can now be widely spread to many

292 for plasma in cancer therapy based on plasma self-organization, which enables adaptive features in pl

293 luster tends to decrease indicating to their self-organization, while coupling of thermal effects and

294 The ability to tune molecular self-organization with an external stimulus is a main dr

295 y of "interactive particle system models for self-organization with birth".

296 pite the possibility to reconstitute protein self-organization with only a few purified components, w

297 Such self-organization (with eight molecules) has only been o

298 nder-appreciated level of intrinsic cellular self-organization, with a focus on the retina and retina

299 we demonstrate that these patterns emerge by self-organization, with no correlation with termite acti

300 sted fibers, thus confirming the presence of self-organization within this series of mixed-hydrazinop