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1 e to a modifiable pattern that is subject to self-organization.
2 ly broken by an emergent process of cellular self-organization.
3 s an important mechanism underlying cellular self-organization.
4  populations with slow dynamics; and spatial self-organization.
5 ems, especially in relation to multicellular self-organization.
6  extreme frictional conditions which trigger self-organization.
7 odulation of force and contribute to spindle self-organization.
8  form as the result of externally controlled self-organization.
9 des with small molecules undergo aggregation/self-organization.
10 ecome an important model system for studying self-organization.
11  steric interactions between them, drive the self-organization.
12  based on spontaneous processes of inorganic self-organization.
13 therapeutics or fabrication methods based on self-organization.
14 system, the basic neural circuitry undergoes self-organization.
15  interplay between genetic specification and self-organization.
16 tant but poorly understood role in molecular self-organization.
17 ity is not necessary for this type of atomic self-organization.
18 esis, near-unity purification, and nanoscale self-organization.
19 derived components that polymerize driven by self-organization.
20 aptability, directed motion, regulation, and self-organization.
21 ions each, represents an astonishing feat of self-organization.
22 ith defects in either tubulin recruitment or self-organization.
23 ts for pattern transformation, an example of self-organization.
24 S-blastoids) through lineage segregation and self-organization.
25  integrate multiple mechanisms of ecological self-organization.
26 igate fundamental mechanisms behind cellular self-organization.
27 o the nanoscale, and are proposed to reflect self-organization, a characteristic of living systems th
28 tems, and provides a means to detect spatial self-organization against physical template heterogeneit
29                  This form of nonequilibrium self-organization allows the creation of structures that
30 alangeal pattern, it has been suggested that self-organization alone could be sufficient.
31 ing forebrain organoids that enables ordered self-organization along dorso-ventral and antero-posteri
32 of a natural phase transition in the dynamic self-organization among N individuals within a social sy
33                        High-level 'rules' of self-organization and assembly are increasingly used to
34 hemotactic interactions to generate emergent self-organization and collective behaviours reminiscent
35  we quantify missing information, emergence, self-organization and complexity for a collective motion
36 nimals exhibit a higher degree of emergence, self-organization and complexity over time.
37 ons to achieve certain degrees of emergence, self-organization and complexity.
38           We investigate computationally the self-organization and contraction of an initially random
39              The model used is an example of self-organization and could be more widely applicable to
40 ences of a neurophysiological fingerprint of self-organization and criticality in sleep- and wake-rel
41 r and such behavior is often associated with self-organization and dynamics occurring near critical t
42 amatergic neuronal synapse, inducing spatial self-organization and embryonic cell specification.
43 f biological fitness and chemical stability, self-organization and emergence, and ultimately to disco
44 tu study of dislocation structure formation, self-organization and evolution in the bulk.
45            Here, we review the principles of self-organization and how they set cells in motion to cr
46 filament arrays and provide insight into the self-organization and mechanics of cytoskeletal assembli
47 esults from interplay between adhesion-based self-organization and morphogen-directed patterning.
48                                  Controlling self-organization and morphology of chemical architectur
49                           Although molecular self-organization and pattern formation are key features
50  networks lead to large-scale nonequilibrium self-organization and pattern formation in life is a maj
51                                              Self-organization and pattern formation in network-organ
52  this organism is for biophysical studies of self-organization and pattern formation.
53        TLSs thus reveal an advanced level of self-organization and provide a powerful platform for in
54  We first introduce nanoscale self-assembly, self-organization and reaction-diffusion processes as es
55 esign pathways for active materials based on self-organization and reconfigurability.
56 ion mammalian embryo is a paradigm of tissue self-organization and regulative development; however, t
57 ular cytoplasm has a remarkable capacity for self-organization and that introduction of such macromol
58 logical, demonstrates complex spatiotemporal self-organization and the emergence of collective behavi
59 use different sources of energy to carry out self-organization and the performance of work in their e
60 rch on regeneration, organ morphogenesis and self-organization - and the links between these fields.
61 ith a high propensity towards supramolecular self-organization, and describe the pathway through whic
62 (e.g., on cooperation, multilevel selection, self-organization, and development) and thereby help int
63 t conditions this heterogeneity can arise by self-organization, and what information it can convey.
64 ks regulating Cdc42 oscillations and spatial self-organization appear to provide a flexible mechanism
65                                 Ordering and self-organization are critical in determining the dynami
66                    Multiple accounts of this self-organization are currently influential and in this
67           The patterning events driving this self-organization are currently unknown.
68                        Pattern formation and self-organization are fascinating phenomena found widely
69 where plant-plant interactions and community self-organization are important.
70 ; however the mechanical principles for such self-organization are not understood.
71 hallenge to unraveling principles underlying self-organization around criticality in biological recur
72                  The extent to which de novo self-organization, as opposed to inheritance of an alrea
73  and their rotational movement drive spindle self-organization, as well as how the forces acting in t
74  cell-cell correlations, showing evidence of self-organization at the onset of aggregation (as oppose
75                        The self-assembly and self-organization behavior of uracil-conjugated enantiop
76 rue through a variety of fluctuation-driven, self-organization behaviors exhibited by out-of-equilibr
77  zebrafish explants do not undergo bona fide self-organization, but rather display features of geneti
78 teria is a fascinating case of multicellular self-organization by bacteria.
79 al for understanding the oscillation pattern self-organization by MinD-MinE interaction dynamics on t
80 anes within cyanobacteria could disrupt this self-organization by sterically occluding or sequesterin
81                   However, it is unclear how self-organization by this mechanism remains robust when
82 erplay of these principles in the context of self-organization can account for the emergence of struc
83 is study provides experimental evidence that self-organization can be paramount to enhancing ecosyste
84                        In vitro, Min protein self-organization can be reconstituted in the presence o
85  indicate that this intrinsic propensity for self-organization can even extend to the formation of co
86 ro-posterior positional values is curtailed, self-organization can then produce several digits with t
87 a, suggesting that Hydra's wound-healing and self-organization capabilities may employ similar mechan
88  paradigms not only demonstrate the enormous self-organization capacity of neural stem cells, they al
89  is unclear how to reconcile this remarkable self-organization capacity with classical experiments de
90                          As a result of this self-organization, cells drive fluid flows that circulat
91 eties per molecule, commonly exhibit typical self-organization characteristics, which promotes the fo
92 ids, characterized by this kind of nonlinear self-organization, defines a new class of turbulent flow
93 rk information flow, network robustness, and self-organization degree.
94 T(FBTTh2)2 can achieve exceptional levels of self-organization directly via solution deposition.
95  work supports a cooperative process of ring self-organization driven by the interaction between acti
96                                         This self-organization, driven by asymmetric fitness effects
97 nt at an autonomous process of microfilament self-organization driving the formation of streaming pat
98 , where the inherent anisotropy drives motor self-organization, droplet deformation, and division int
99                       We show that dynamical self-organization during growth can create a coherent in
100  broad variety of dissipative structures and self-organization effects, have drawn significant resear
101                                  During such self-organization, energy distributed in a broadband of
102      Our results revealed that both forms of self-organization enhanced the persistence of the constr
103 x networks can be explained as the result of self-organization, even in the absence of synaptic reinf
104  in vitro, it is yet unclear how these basic self-organization events are modulated by the crowded in
105 ns and peptides, it is yet unclear how these self-organization events are precisely modulated by micr
106 enabling abiotic soft tissue with multiscale self-organization for effective load bearing and energy
107 dicate that centrosomal MTs complement Golgi self-organization for proper Golgi assembly and motile-c
108 characteristic shapes, but the mechanisms of self-organization for robust morphological maintenance r
109 g in the mammary gland, we reconstituted its self-organization from aggregates of primary cells in vi
110            These dynamic patterns emerge via self-organization from an activator-inhibitor network, i
111               Here, we demonstrate a form of self-organization from nonequilibrium driving forces in
112 cal micro environments that promote cellular self-organization have enhanced the ability to recapitul
113 tructures, and dynamics of proteins, such as self-organization, hydration forces and ionic interactio
114      Our model highlights a novel pattern of self-organization in a bacterial biofilm.
115  chiral springs and helices on the colloidal self-organization in a nematic liquid crystal using lase
116 tration of EPSs are important factors in the self-organization in a nonequilibrium growing colony.
117 ys that could have brought about features of self-organization in a peptide world are considered in t
118 es a striking example of irradiation-induced self-organization in a quantum system.
119  bacteria or flocks of birds are examples of self-organization in active living matter.
120 y multicellular systems, including microbial self-organization in biofilms, embryogenesis, wound heal
121 to investigate simple physical mechanisms of self-organization in biological assemblies.
122 deciphering the mechanisms of spatiotemporal self-organization in cells.
123  encourage the emergence of coordination via self-organization in children with DCD.
124 est that simple physical principles underlie self-organization in complex biological assemblies and i
125 ed support the analysis of complex bacterial self-organization in confined volumes.
126 the principles controlling self-assembly and self-organization in CSD grown oxides.
127 of these lineages, providing a framework for self-organization in development.
128 ocesses, and detect and evaluate the role of self-organization in driving such patterns.
129 he prevailing theoretical outlook on spatial self-organization in ecology must expand to incorporate
130 ction by extending the spatial range of cell self-organization in emerging model systems such as orga
131 roperties are owed in part to their specific self-organization in hierarchical molecular structures,
132 best-understood examples of emergent protein self-organization in nature.
133 tures facilitated by cell death may underlie self-organization in other developmental systems, and co
134                                              Self-organization in the cell relies on the rapid and sp
135 sustaining elongation, and the triggering of self-organization in the form of lamellar fingers.
136 nchronously--instead they display a striking self-organization in the form of metachronal waves (MCWs
137 ces this modular structure through dynamical self-organization in the MEC.
138               The level of self-assembly and self-organization in the SAFs is unprecedented for a des
139 bility of such structures beckons control of self-organization in the temporal regimes.
140 ea that the membrane itself mediates protein self-organization in these processes through minimizatio
141 sess the functional importance of keratin IF self-organization in vivo.
142 led 'Regeneration of Organs: Programming and Self-Organization' in March, 2014.
143               Here we discuss the process of self-organization into patterns on the bacterial nucleoi
144 hear of a granular material leads to dynamic self-organization into several phases with different spa
145 ility to break symmetry and polarize through self-organization is a fundamental feature of cellular s
146          We also find that this mechanism of self-organization is conserved in the human prostate.
147                                 We find that self-organization is dominated by the interfacial energy
148                                The resulting self-organization is easily understood in terms of motor
149   In the mammalian embryo, the potential for self-organization is manifested in its extraordinary dev
150 cell cohesion, we show that this strategy of self-organization is robust to severe perturbations affe
151                                              Self-organization is the spontaneous formation of spatia
152  Together with rapid component turnover, the self-organization mechanism continuously reassembles and
153 ness of this process suggests that a similar self-organization mechanism may contribute to the reorga
154 ns new perspectives for the understanding of self-organization mechanisms.
155                              Such mesophasic self-organization might allow synapses to achieve a 'Gol
156 f the key dynamic traits of complex systems: self-organization, modularity and structural properties.
157 -tailed size distribution that is typical of self-organization near a critical point.
158        Our mathematical model shows that the self-organization observed in our experiments is control
159                      A complementary form of self-organization occurs among swarming insects, flockin
160                             We show that the self organization of vortices into lattices is accompani
161 operties of the early embryo and mediate the self-organization of "gastrulation-like" nodes in cultur
162 providing a previously unidentified route to self-organization of a many-body system.
163                                 The emergent self-organization of a neuronal network in a developing
164 erve cooperation between individuals and the self-organization of a sustained trust network, which fa
165                                          The self-organization of active particles is governed by the
166 is experimentally demonstrated, based on the self-organization of Ag nanoclusters under an electric f
167 -1-coated 2D substrates of ~1 kPa results in self-organization of all three germ layers: ectoderm on
168 yst and then with the glycosyl donor enables self-organization of an ordered transition-state.
169 hes have revealed how T4P dynamics influence self-organization of bacteria, how bacteria respond to e
170 t with regard to memory but also extended to self-organization of behavior.
171                      Rational control of the self-organization of beta-peptides sequences to adopt re
172 ithin complex chemical mixtures, wherein the self-organization of biomolecules allows them to form "a
173 lease units via Ca-induced Ca release causes self-organization of Ca spark clusters.
174 y will have implications in problems such as self-organization of cell tissues or the design of capil
175  carbon-resource, controls the emergence and self-organization of cells exhibiting the glycolytic sta
176  observations have revealed that large-scale self-organization of cells in actively expanding biofilm
177                                          The self-organization of colloidal particles is a promising
178                                              Self-organization of colloidal Pt nanocubes into two typ
179 al tissue scaffolds, and they were formed by self-organization of coplanar reticular networks with bu
180   Overall, these results reveal a remarkable self-organization of corticofugal and callosal tracts wi
181 al theories have been developed to study the self-organization of cytoskeletal filaments in in vitro
182 n budgeting, thereby driving the biochemical self-organization of distinct cell states.
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 eous and subrenal capsular space resulted in self-organization of donor-derived vascular networks tha
186 stability, which play a critical role in the self-organization of energy and matter in non-equilibriu
187 BALO) model that allows clonal expansion and self-organization of FACS-sorted bronchioalveolar stem c
188 ffering levels of BMP, WNT and NODAL lead to self-organization of gastruloids into homogenous subpopu
189 ional foams are promising candidates for the self-organization of large photonic networks with combin
190                Many researchers consider the self-organization of lipid and fatty acid molecules into
191            Bottom-up approaches, such as the self-organization of liquid crystals, offer potential ad
192 ween hepatocytes and sinusoids underlies the self-organization of liver tissue.
193 n set-reset latches through the synchronized self-organization of many individual network components.
194 This study unravels the dynamic yet discrete self-organization of mature microglia in the healthy and
195 actions are indeed sufficient to explain the self-organization of MCWs and study beat patterns, stabi
196  mechanistic effects occur in light-mediated self-organization of metal nanoparticles; atoms are repl
197                      The spindle arises from self-organization of microtubules and chromosomes, whose
198                         Here, we studied the self-organization of microtubules growing in the presenc
199                           Here we report the self-organization of motile colloids into a macroscopic
200 ropatterned chip assay, we find that spatial self-organization of mutation-containing progenitor cell
201 s at high gas concentrations can lead to the self-organization of nanobubbles into superlattices with
202    These findings may provide insight to the self-organization of nanoparticles in biomineralization
203 ed with floods is universal, indicating that self-organization of near-critical channels filters the
204 ne morphogenic protein 4 stimulation induced self-organization of neuruloids harboring neural progeni
205 article-based modeling approach to study the self-organization of nonmotile rod-shaped bacterial cell
206 at the colloidal scale, as it can govern the self-organization of particles into hierarchical structu
207 to achieve this goal is based on the spatial self-organization of patches of cell-adhesive molecules
208 as or generate their own niche, enabling the self-organization of patterned tissues.
209               This mechanism of hierarchical self-organization of PBI into supramolecular spheres is
210 teractions of the core proteins required for self-organization of planar polarity.
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 provide a general theoretical foundation for self-organization of social-insect colonies, validated u
217 nd to better understand the forces governing self-organization of soft materials.
218 ple cellular automata model it is shown that self-organization of spatial pattern in a community of s
219 ional roles that twitching might play in the self-organization of spinal and supraspinal sensorimotor
220                     Here, we investigate the self-organization of stabilized microtubules in Xenopus
221 d experiments, supporting the proposition of self-organization of stand structure.
222 speech processing imposes constraints on the self-organization of synchronous cell assemblies and the
223                            Previous study of self-organization of Taxol-stabilized microtubules into
224 ic techniques, we here show evidence of such self-organization of the actin cortex in living HeLa cel
225 olic evolution to the self-amplification and self-organization of the biosphere.
226 tion morphogenesis in which ECM triggers the self-organization of the embryo's stem cells.
227 te that these microarchitectures form due to self-organization of the manifold mineral and organic so
228 nanowire building blocks; third, large-scale self-organization of the mesocrystals and the reduction
229  the influence of spatial confinement on the self-organization of the Min system, a spatial regulator
230 cal properties, which arise from the dynamic self-organization of the nanoparticles under stress.
231 the existence of appropriate rules governing self-organization of the velocity field of a dynamical s
232 cells (protocells) would be dependent on the self-organization of their components and physicochemica
233                                A spontaneous self-organization of these nanostructures is then trigge
234 ntial tool to modulate the global orientated self-organization of these systems.
235    Therefore, in this review, we explore the self-organization of this class of functional molecules
236 ors predictably controlling the strength and self-organization of this facilitation cascade across cr
237 xtracellular matrix (ECM) are crucial to the self-organization of tissues during development.
238 both static compartmentalization and dynamic self-organization of transcriptional apparatus are in ef
239 via acetyldihydropyrans, products of one-pot self-organization of two molecules of ketones and two mo
240               The reaction is based upon the self-organization of two {Te3W38} units around a single
241                                We report the self-organization of universal branching patterns of oil
242                                          The self-organization of Zn(II) complexes on the surface of
243 oning of MinD/ParA proteins is either due to self-organization on a surface or reliance on a landmark
244 ve importance of these two spatial scales of self-organization on mussel bed persistence, we conducte
245  depended on social interactions and spatial self-organization on particle surfaces.
246 of plant functional groups, is the result of self-organization, or the spontaneous emergence of order
247 a well-controlled platform for investigating self-organization phenomena and non-equilibrium critical
248 cosystem, for the view of fairy circles as a self-organization phenomenon driven by water-vegetation
249 te their ubiquity, little is known about the self-organization principles that govern flow statistics
250 le ambient resources arose very early in the self-organization process and dictated the locations of
251                                   Thus, in a self-organization process conjugation may be extended by
252         Coupling photopatterning with either self-organization process provides a powerful route for
253                            Understanding the self-organization process requires not only the in-situ
254 rticles (NPs) is central to comprehension of self-organization processes and a wide spectrum of physi
255 ale deformation regime involving solid-state self-organization processes that lead to efficient energ
256 ng likely being a paradigm for many cellular self-organization processes.
257 with the porphyrin N-core as a new source of self-organization processes.
258 panding toolbox of nanoscale engineering and self-organization provides a chirality-based methodology
259     By controlling the polymer/polymer blend self-organization rate, all-polymer solar cells composed
260                                     However, self-organization realized by the mechanism of spatial f
261  maturation in liver organoids, but organoid self-organization requires cell-to-cell surface contact.
262 bles brain networks with a means of temporal self-organization, resilience, and homeostasis.
263                 The interactions and dynamic self-organization result from the net directional, micel
264 tion of the molecular mechanism of neuruloid self-organization revealed a pulse of pSMAD1 at the edge
265       These studies thus unravel the default self-organization rules governing early embryogenesis an
266     This strategy of asymmetry-driven active self-organization should generalize rationally to other
267 er appreciation of complexity, feedback, and self-organization than her book exhibits.
268 t is an intricate, spatiotemporal process of self-organization that emerges from gene regulatory netw
269  findings present a unique form of bacterial self-organization that influences population structure a
270 such as those found in the nucleolus, show a self-organization that is marked by spatial segregation
271 s, however the mechanisms of non-equilibrium self-organization that may be involved are still poorly
272 scillators is a fascinating manifestation of self-organization that nature uses to orchestrate essent
273                  Here we describe a class of self-organization that operates within densely packed ba
274 cal models and observational studies suggest self-organization, the formation of patterns due to ecol
275 rporates two essential aspects of actomyosin self-organization: the asymmetric load response of indiv
276 anucleosides with the possibility to undergo self-organization through base pairing has been conceptu
277                     Ran-GTP promotes spindle self-organization through the release of importin-bound
278 issipative gas of ultracold potassium atoms: self-organization to a stationary state that is largely
279 terning technologies and directed epithelial self-organization to deliver microparticles to the lumen
280 ion actions that use the emergent effects of self-organization to increase ecosystem resistance to di
281 tablished in the literature, but spontaneous self-organization to prepare such structures has not bee
282                                              Self-organization to the critical state is demonstrated
283                       Here, some examples of self-organization underlying cellular anisotropies at th
284 that lead to such outcomes as self-assembly, self-organization, unique nanostructures, chemical waves
285                      However, the perovskite self-organization upon crystallization and the final ele
286  imply a general thermodynamic mechanism for self-organization via dissipation of absorbed work that
287 ur results reveal a principle for ecological self-organization, where phase separation rather than ac
288                                              Self-organization, where spontaneous orderings occur und
289 y towards a general use of self-assembly and self-organization which can now be widely spread to many
290 for plasma in cancer therapy based on plasma self-organization, which enables adaptive features in pl
291 ls (hESCs) exhibit an intrinsic capacity for self-organization, which motivates their use as a tracta
292 luster tends to decrease indicating to their self-organization, while coupling of thermal effects and
293 aches that are being employed to study their self-organization will also be considered.
294                The ability to tune molecular self-organization with an external stimulus is a main dr
295 ificity, nanoscale synthesis, and long-range self-organization with biomolecular HOSs and opens vast
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

 
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