ライフサイエンスコーパス: dynamic

1 re often part of a bigger community assembly dynamic.

2 fibres does not depend on calcium influx or dynamics.

3 , reward-dependent reorganization of control dynamics.

4 quiescent glasses and relate them to glassy dynamics.

5 lifetime and sharply dependent on crosslink dynamics.

6 c coupling, are suggested to be the limiting dynamics.

7 r size and the underlying immune recruitment dynamics.

8 cin uptake and predict subsequent population dynamics.

9 ng microscopy (STM), and ab initio molecular dynamics.

10 ffects of different formulations on backbone dynamics.

11 tion, correlating with the excited nanoscale dynamics.

12 consequences for population and evolutionary dynamics.

13 ces shaping range edges and to predict their dynamics.

14 eloped dimer-scale computational model of MT dynamics.

15 ific influences on molecular plasma membrane dynamics.

16 oving our understanding of spatial community dynamics.

17 lizing and determining protein stability and dynamics.

18 ad predicted by the stability of their brain dynamics.

19 of data analytics and modeling of biological dynamics.

20 r in this game-hinges on the game's learning dynamics.

21 al diffusion process and stochastic Langevin dynamics.

22 rategies that mine data to reveal underlying dynamics.

23 e our understanding of ancient DNA breakdown dynamics.

24 eration dynamics play out in long-term stand dynamics.

25 nt body of evidence suggests that the highly dynamic Abeta oligomers are the main causal agent associ

26 second bright pipi* state, which affects the dynamics, acting mainly as a "doorway" state for the nOp

27 signaling dynamics, and, in turn, signaling dynamics affects inhibitor responses, we investigated as

28 odel shows promise for predicting population dynamics after multiple disturbance events and for manag

29 Ab initio molecular dynamics (AIMD) simulations and molecular beam vacuum-UV

30 Ab initio molecular dynamics (AIMD)-informed EXAFS analysis was employed to

31 Here, we study stochastic evolutionary dynamics along these equilibrium paths.

32 reflects a capacity to contract and support dynamic alteration of DT caliber and resistance analogou

33 es exhibited greater variation in population dynamics among tissues and cell populations over the cou

34 sors are most commonly applied for real-time dynamic analysis and measurement of interactions in bio-

35 nd/or type of cancer, which demonstrated the dynamic and conditional miRNA regulation during cancer p

36 distinct T-cell subsets and by definition is dynamic and responsive to an ever-changing environment a

37 During S-phase, dynamic and stable interactions decreased considerably c

38 ysis revealed significant changes in several dynamic and static gait parameters resulting in overall

39 ion but show that the direction of change is dynamic and unpredictable.

40 e of vacuole-related proteins in BR receptor dynamics and BR responses remains elusive.

41 dynamics engine, such as standard molecular dynamics and cell-modeling packages.

42 applied to interrogate intestinal epithelial dynamics and characterize situations in which processes

43 ondrial dysfunction, maintains mitochondrial dynamics and enhances mitochondrial biogenesis and synap

44 We developed a genetic toolkit to study MT dynamics and function in diverse cells.

45 We use classical molecular dynamics and hybrid quantum mechanics/molecular mechanic

46 pp, polyP has an additive effect on nucleoid dynamics and organization during starvation.

47 Population dynamics and species persistence are often mediated by s

48 nd respiratory motion phases, contrast-agent dynamics, and blood flow velocity fields.

49 oviding valuable probes for local structure, dynamics, and ligand binding.

50 s kinase inhibitors interfere with signaling dynamics, and, in turn, signaling dynamics affects inhib

51 tress-induced behavioral disorders, and that dynamics are a critical axis of manipulation for causal

52 cates coherent phase space regions where the dynamics are approximately linear from those that are st

53 In numerous physical models on networks, dynamics are based on interactions that exclusively invo

54 omputational analysis showed that the output dynamics are controlled in a complex way by the concentr

55 of true population change for species whose dynamics are driven by stochastic processes.Adelie pengu

56 shows that both conformational rigidity and dynamics are essential for controlling protein activity.

57 uctures calculated using classical molecular dynamics are in excellent agreement with the orientation

58 dies and big-data approaches assessing sleep dynamics are lacking.

59 interacting signals, finding that signaling dynamics are largely robust to interference.

60 In cells, actin dynamics are regulated by kinases, such as the LIM domai

61 In ephemeral pond ecosystems, temporal dynamics are relatively more important than in many syst

62 g of oscillations (limit cycles) though this dynamics are the typical response of many natural system

63 eal highly variable and heterogeneous oxygen dynamics at a high, quasi-continuous resolution across b

64 rning the depth and amplitude of large-scale dynamics at extratropical latitudes.

65 determining species abundance and community dynamics at multiple spatial scales.

66 To study its dynamics at multiple time scales in response to inputs a

67 FRET) to resolve single-molecule association dynamics at up to millimolar concentrations of fluoresce

68 nt approach: we propose a model for language dynamics based on the principles of cellular automata/ag

69 ring static interaction networks): it builds dynamic (based on ordinary differential equation) models

70 Results indicate that dissolution dynamics become increasingly important with increasing a

71 Here, we investigate the dynamic behaviors of the entropic uncertainty relation o

72 rous gold as a case study to demonstrate the dynamic behaviour of bimetallic systems during activatio

73 may play an important role in mitochondrial dynamics by mediating mitochondrial fission.

74 luable to prepare and probe transition-state dynamics by the photodetachment of anions with an equili

75 The simulations reveal that the evolutionary dynamics can be collapsed onto master curves governed by

76 w that agonist-induced intracellular calcium dynamics can be modified by changing the levels of SERCA

77 how that violation of ergodicity in the fast dynamics can drive the whole system to equilibrium.

78 chromatin tethers, together with microtubule dynamics, can mobilize the genome in response to DNA dam

79 , this method offers an avenue to understand dynamic cell behavior, including processes such as induc

80 e role of glutamate, ion concentrations, and dynamics cell volume in other brain pathologies and norm

81 Tissue regeneration requires dynamic cellular adaptation to the wound environment.

82 hemodynamic effects via computational fluid dynamics (CFD).

83 These data suggest that the dynamic CGs we identify are not specific to the Col-Cvi

84 This dynamic change in B cell survival mechanisms is unique t

85 t over 5000 distal noncoding regions exhibit dynamic changes in chromatin accessibility between devel

86 An illustrative patient with dynamic changes in ctDNA content during therapy and a re

87 s macaques under various conditions, finding dynamic changes in each state.

88 We tested this hypothesis by documenting dynamic changes in the tomato (Solanum lycopersicum) nuc

89 sorghum, and Brachypodium revealed rapid and dynamic changes only occurring to the Ae. tauschii Gli-2

90 he different disease courses, supporting the dynamic CNS damage hypothesis to explain MS heterogeneit

91 Its dynamic CO2 uptake also matched well with its static con

92 present OpenRBC, a coarse-grained molecular dynamics code, which is capable of performing an unprece

93 st use of thiosemicarbazone exchange to form dynamic combinatorial libraries.

94 emergence of a novel self-replicator from a dynamic combinatorial library made from a threonine cont

95 d selectivity, yet little is known about the dynamic compositional and structural changes that these

96 Our results reveal for the first time the dynamic connection between FTO RNA binding and demethyla

97 none (PQQ)-based biosensor were evaluated by dynamic constant potential amperometry at 1.3V under non

98 ible and orthogonal elements for predictable dynamic control of gene expression.

99 voltage step is less than 100 mus, allowing dynamic control of the induced motion.

100 Specific parameters of signaling dynamics correlated strongly with drug sensitivity for 1

101 The dynamic couplings between regions separated by large gen

102 we introduce silyl ether linkage as a novel dynamic covalent motif for dynamic material design.

103 more detailed data are lacking on dispersal dynamics, demographic processes underpinning population

104 studies has begun to elucidate how signaling dynamics determine cell physiology and represents a para

105 nt an NMR-guided all-atom discrete molecular dynamics (DMD) platform, iFoldNMR, for rapid and accurat

106 The model reproduces intracellular calcium dynamics during control pacing and reveals the high-reso

107 distinct role in the regulation of endosome dynamics during fungal development and plant infection.

108 Regulation of macrophage dynamics during these processes can therefore have a pro

109 e projections as inputs to the deterministic dynamic ecosystem model PnET-BGC.

110 water could be explained via a hypothetical dynamic emission scenario consistent with combined sewer

111 WE software can be used to control any dynamics engine, such as standard molecular dynamics and

112 Proteins are dynamic entities and populate ensembles of conformations

113 Dynamic flux and stochasticity during pre-nucleation ren

114 ic whole-muscle models indicate that maximum dynamic force and power output is 1.35 times higher in a

115 This event is then followed by the dynamic formation of filamentous and branched respirator

116 a high-density electrode array and dopamine dynamics from a carbon-fiber microelectrode.

117 oral soliton bound states and their internal dynamics have escaped direct experimental observation.

118 nd its potential to construct asymmetric and dynamic hetero-vesicle assemblies with complex DNA nano-

119 Charge carrier dynamics in amorphous semiconductors has been a topic of

120 on results in extensive perturbations of the dynamics in both apo- and holo-forms of the HCN4 isoform

121 hlights the important role of SWAP-70 in Cer dynamics in dendritic cells.

122 This study provides a novel tool to study dynamics in ordered and disordered solids and provides n

123 des a framework for understanding resistance dynamics in single cells.

124 ale reproductive tract and peripheral tissue dynamics in single, dual and multiple unit microfluidic

125 account for the discrepancies between growth dynamics in the notch-drives-growth model and real plant

126 enables highly detailed insights into oxygen dynamics in various aquatic and terrestrial environments

127 broadly used to investigate single molecule dynamics in vitro.

128 f the MAPK/ERK pathway mirrors the rapid and dynamic induction of DLL4 transcription and that this pa

129 s tissues of shrews, which would reflect the dynamic infectious status and circulation of MJNV in nat

130 Combining the structural and dynamic investigations, rationales were developed for th

131 revealed through spectroscopic, kinetic, and dynamic investigations.

132 nce that targeting endogenous spatiotemporal dynamics is a potential therapeutic approach for treatin

133 Thus, the study of protein acetylation dynamics is critical for understanding of how this modif

134 , assembly processes and microbial community dynamics is necessary to predict microbial response to p

135 This dynamic kinetic resolution process offers a general appr

136 y obtained through the action of Fe(2+) on a dynamic library of imines generated in situ via condensa

137 nting, photopolymerized and characterized by dynamic light scattering (DLS) and UV/Vis spectroscopy.

138 via, UV-Vis spectroscopy, FTIR spectroscopy, dynamic light scattering and scanning electron microscop

139 r flux across large pore membranes and using dynamic light scattering, with excellent agreement betwe

140 , we report the existence of clearly defined dynamic localized regions of substantially increased str

141 ate podocyte cytoskeleton and slit diaphragm dynamics, MAGI2 mutations have not been described in hum

142 actin cytoskeleton, a process referred to as dynamic mass redistribution (DMR).

143 inkage as a novel dynamic covalent motif for dynamic material design.

144 Investigating telomere dynamics may help us quantify individual variation in th

145 hyperuniform states, driven, nonequilibrium dynamics may.

146 Molecular dynamics (MD) simulations suggest that LSD's slow bindin

147 exchange MS (HDX-MS) methods, and molecular dynamics (MD).

148 ndering this platform amenable to studies of dynamic mechanics on cell behavior across many cell type

149 Nonetheless, the dynamic mechanism leading to the establishment and maint

150 (FEP) coupled with lambda-exchange molecular dynamics method to calculate the binding free energy of

151 Although IBD is dynamic, microbiome studies have primarily focused on si

152 other cellular cargoes by attaching them to dynamic microtubule ends during both polymerization and

153 nein and its accessory complex dynactin with dynamic microtubule plus ends.

154 Specifically, using a dynamic model implemented on an anatomical brain network

155 a broad class of resource-limited community dynamics models, regardless of parameterization and mode

156 gest of all of the peptidase families, their dynamic motions remain obscure.

157 or this purpose, we introduce the first ever dynamic NA method, DynaMAGNA ++.

158 se engineering approach to infer data-driven dynamic network models of multi-organ gene regulatory in

159 We find that species occupy highly dynamic network positions through time, causing the asse

160 Constitutional dynamic networks (CDNs), composed of exchangeable compon

161 Dynamic networks are important in a number of scenarios.

162 These findings provide evidence for a dynamic neural transformation of low-level speech featur

163 r, they open up new avenues for the study of dynamic neurophysiological correlates of structural cont

164 and segmental isotopic labeling schemes with dynamic nuclear polarization (DNP) NMR.

165 take characteristics in these patients using dynamic O-(2-(18)F-fluoroethyl)-l-tyrosine ((18)F-FET) P

166 This commentary uses the dynamic of identity-protective cognition to pose a frien

167 ith a circuit-based approach to simulate the dynamics of a spin chain and maximise the entanglement g

168 lfactory bulb slices to measure the synaptic dynamics of afferent-evoked input at physiological stimu

169 resolution, and by exploring the structural dynamics of Aqy1 during freezing through molecular dynam

170 as a starting point to explore the nonlinear dynamics of atrial cells and will yield insights into th

171 of our approach to monitor the position and dynamics of both repetitive and non-repetitive genomic r

172 To date, the dynamics of breather solitons in microresonators remains

173 The dynamics of chemical reactions are often governed by tra

174 simultaneous determination of structure and dynamics of conformationally heterogeneous systems by in

175 orescence intermittency, and photoconversion dynamics of Dendra2, a well-known PAFP used in localizat

176 Our study provides a framework to infer the dynamics of differentiation from single cell transcripto

177 tates are often invoked in the excited-state dynamics of donor-acceptor dyads, but their involvement

178 Understanding the ultrafast dynamics of electronically excited BODIPY chromophores c

179 s for ethyl as residue and attributed to the dynamics of elimination reactions.

180 We investigated the population dynamics of exogenous Lactobacillus plantarum and its in

181 Additionally, L1 loop dynamics of fl-p53 in the presence of DNA is revealed, a

182 that as the conformational and translational dynamics of FN increased, the rate of binding, particula

183 define three key epochs in the transcriptome dynamics of human retina from fetal day (D) 52 to 136.

184 ng the structure, intermolecular forces, and dynamics of ionic liquids.

185 atomic structure of T4 is largely known, the dynamics of its fascinating injection machinery is not u

186 tical element for unravelling the structural dynamics of matter.

187 actors, and enhance our understanding of the dynamics of natural populations.

188 We compare the dynamics of novel isoforms based on the number of suppor

189 ty to unidirectional conduction patterns and dynamics of re-entrant excitation waves.

190 d that the behavior of brookite, both in the dynamics of relaxation of photo-generated charges and in

191 e, very little is known about the structural dynamics of ribbons.

192 live imaging, we examined the spatiotemporal dynamics of RNA and LPS in retinal axons during arboriza

193 field modeling to elucidate the delithiation dynamics of single-crystal lithium iron phosphate micror

194 theoretically investigate the full many-body dynamics of the acquisition of angular momentum by a gas

195 min for live cell fluorescent imaging of the dynamics of the bacterial outer membrane as cells divide

196 ma membrane and filopodia, and the 2D and 3D dynamics of the endoplasmic reticulum, in living cells.

197 s were used to characterize the identity and dynamics of the excited states, where singlet and triple

198 The structure and dynamics of the extracellular loops of OprH show distinc

199 The architecture and dynamics of the FG-network have been refractory to chara

200 eriments, we investigated the conformational dynamics of the kinase-substrate interface.

201 Our data reveal 2D dynamics of the mitochondria, plasma membrane and filopo

202 s been a sustained effort to reconstruct the dynamics of the phosphorus cycle over the past 3.5 billi

203 e catalysis is facilitated by conformational dynamics of the protein scaffold that surrounds the acti

204 model and its complexity is reflected in the dynamics of the relaxation of the system to its ground s

205 lations were used to probe the structure and dynamics of the system at a range of hydration levels.

206 We examined the spatiotemporal dynamics of these complementary processes in a picture n

207 ittle is understood about the morphology and dynamics of these polymer layers.

208 The degree and dynamics of translational control during mammalian devel

209 rovide insight into the clinical and genomic dynamics of tumor evolution with cisplatin-based chemoth

210 light detailed insights in the structure and dynamics of urban segregation that would be otherwise ea

211 , IP3R, and RyR on the intracellular calcium dynamics of VSMC and to understand how variation in prot

212 can amplify stochastic fluctuations in actin dynamics, often resulting in traveling waves of protrusi

213 However, reactivation of mitochondrial dynamics only occurs after transfer to germination condi

214 nterference should occur between alternating dynamics only when the kinematic errors associated with

215 t had exceptional global stability, backbone dynamics, or amide hydrogen exchange rates.

216 The dynamic organization of genes inside the nucleus is an i

217 arning of a static pattern and tracking of a dynamic pattern of up to 4 x 4 pixels are demonstrated,

218 Dynamic PET data were analyzed using the validated two-t

219 Thus, PNUTS and PP1 together fine-tune the dynamic phosphorylation of DNA-PKcs after DNA damage to

220 is a highly complex organ in which multiple dynamic physiological processes are tightly coordinated

221 ogeneity and how its effects on regeneration dynamics play out in long-term stand dynamics.

222 l new tool for large-scale investigations of dynamic PPIs.

223 for mechanistic interpretations and reliable dynamic predictions in new experimental conditions (i.e.

224 (2) the neural substrates that support such dynamic prioritization.

225 aser scanning microscopy imaging reveals the dynamic process of gNP aggregation responses upon biomol

226 The highly dynamic process of nanoparticle collision and oxidation

227 ty of 60S synthesis.Ribosome biogenesis is a dynamic process that involves the ordered assembly of ri

228 ual amino groups could give insight into the dynamic processes occurring at specific locations within

229 findings provide compelling new evidence for dynamic processing of speech sounds in the auditory path

230 y, upregulation of Chd1 restores nucleosomal dynamics, promotes normal induction of protective stress

231 l reaction networks (CRNs) with well-defined dynamic properties.

232 stem to compare their intrinsic assembly and dynamic properties.

233 en variable, in particular when working with dynamic proteins or weakly binding ligands.

234 polymerize head to tail forming tubulin-like dynamic protofilaments, whose organization in the Z-ring

235 cells to directionally migrate over a large dynamic range of chemoattractant.

236 The assay limit of detection (LOD) and dynamic range were determined by spiking B. anthracis DN

237 preserving method accuracy, specificity, and dynamic range.

238 cting cTnT and cTnI in human serum with wide dynamic range.

239 form to create dual-FP biosensors with large dynamic ranges by employing a single FP-cassette, named

240 For the study of dynamic regulation of protein interactions in vivo, ther

241 selectivity (feature vs. eye of origin) and dynamics (relatively slow vs. relatively fast).

242 in situ three-dimensional imaging of defect dynamics remains challenging.

243 Therefore, the modulation of interdomain dynamics represents an important mechanism during antibo

244 isrupting compounds (EDCs) affect population dynamics requires tracking males and females (and sex-re

245 ine the relationship between both static and dynamic retinal vascular caliber and the severity of obs

246 ulting in the rescue of aberrant striatal DA dynamics, reversal of characteristic phenotypic and beha

247 acquisition of high-resolution data sets of dynamic samples.

248 Here we consider a more dynamic scenario in which phage infections give rise to

249 investigated visual working memory in a more dynamic setting, and assessed the following: (1) whether

250 ciations in this study between cell-specific dynamic signaling pathways and drug sensitivity.

251 Moreover our NMR, mutagenesis and molecular dynamics simulation studies defined the sequence of the

252 us resistance, HA interaction, and molecular dynamics simulation studies elucidated the binding site

253 Molecular dynamic simulations (MD) of O2 and H2O adsorption energy

254 Molecular dynamics simulations and density-functional methods were

255 ld crystal approach with classical molecular dynamics simulations and quantum-mechanical density func

256 stic fingerprint is also confirmed by direct dynamics simulations for ethyl as residue and attributed

257 Here, we performed molecular dynamics simulations of GLIC in the absence and presence

258 We report atomically detailed molecular dynamics simulations of the permeation of the lethal fac

259 perform classical and accelerated molecular dynamics simulations of vacancy-mediated cation diffusio

260 Kinetics and molecular dynamics simulations on several GalNAc-T2 flexible linke

261 Molecular dynamics simulations revealed that these ligands adopt d

262 Brownian Dynamics simulations suggest that binding asymmetry is a

263 ork, we report multiscale reactive molecular dynamics simulations that characterize the free-energy p

264 We use molecular dynamics simulations to resolve the molecular level reco

265 Molecular dynamics simulations were used to probe the structure an

266 Molecular dynamics simulations with reagent excitation by way of s

267 easurements and from force pulling molecular dynamics simulations, both in water.

268 c modulus of lignin, calculated by molecular dynamics simulations, increases initially with increasin

269 combined with large-scale reactive molecular dynamics simulations, reveal the details of the transfor

270 Using 2D Brownian dynamics simulations, we study a dense, confined mixture

271 cs of Aqy1 during freezing through molecular dynamics simulations.

272 opy, native mass spectrometry, and molecular dynamics simulations.

273 Gammaherpesviruses (gammaHVs) have a dynamic strategy for lifelong persistence, involving pro

274 nd stopped-flow SAXS measurements, revealing dynamic structural changes upon iron binding and core fo

275 Given that synaptic spines are dynamic structures which regulate neuronal plasticity an

276 The wrinkle dynamics (such as reversibility and stability) of human

277 e DYT4 mutation had no impact on microtubule dynamics suggesting a distinct mechanism of action.

278 Thus, dynamic SUMO modification and the presence of SIMs in RC

279 alone promises a route towards increasingly dynamic systems, where the geometry and function of the

280 using FRAP data that captures intracellular dynamics through partial differential equation models.

281 By controlling FN structure and dynamics through tuning surface chemistry, we found that

282 aptive therapy, using patient-specific tumor dynamics to inform on/off treatment cycles, suppresses p

283 ss has challenged efforts to link population dynamics to key drivers.

284 of diverse immune cells and controlling the dynamic transcriptional programs that are a hallmark of

285 This fluidic device allows for the dynamic treatment of spheroids across a semipermeable me

286 Intravital imaging enables to study dynamic tumour-stroma interactions within primary and me

287 Then, we introduce a dynamic two-photon excitation protocol to simultaneously

288 Dynamic ultrasound is crucial in confirming the diagnosi

289 The dynamic underwater chemistry seen in nature is inspiring

290 Inducing this spatiotemporal dynamic using closed-loop optogenetic stimulation is suf

291 of spiking neurons can learn non-linear body dynamics using local, online and stable learning rules i

292 e how the crystal packing alters microsecond dynamics, using solid-state NMR measurements and multi-m

293 Here, we introduce this dynamic utility function to several games.

294 These results provide the first dynamic view of corticostriatal activity during bond for

295 nto the effects of these modifications and a dynamic view of RNA structure changes with increased num

296 HLCA and PEI models, the first-step decision dynamics were initially biased toward the choice represe

297 ext] Although finite temperature equilibrium dynamics will not yield hyperuniform states, driven, non

298 egrating in vivo analysis of gene expression dynamics with a reverse engineering approach to infer da

299 However, protein dynamics within the 3D nucleus are poorly understood.

300 This study provides evidence that the dynamic wound microbiome is indicative of clinical outco