ライフサイエンスコーパス: theoretical model

1 why this could be in light of the IH and our theoretical model.

2 attering morphology combined with a suitable theoretical model.

3 f 0.48(3)pi is in excellent agreement with a theoretical model.

4 collision frequency calculated by using the theoretical model.

5 d agreement with the predicted values by the theoretical model.

6 atches per nanoparticle, in agreement with a theoretical model.

7 n of mRNA copy-number to the prediction of a theoretical model.

8 mapping observed brain network data onto the theoretical model.

9 n exceeds the hyperfine, in agreement with a theoretical model.

10 Experimental data agree with a theoretical model.

11 pling strength, which is in agreement with a theoretical model.

12 ly improved by including convection into the theoretical model.

13 -based computer simulation derived from that theoretical model.

14 re not predicted by the latest generation of theoretical models.

15 cribe movement, and forms the basis for many theoretical models.

16 upon this angle, thereby satisfying earlier theoretical models.

17 ck of suitable calibration data or validated theoretical models.

18 Data are compared with various theoretical models.

19 ural information without the need to rely on theoretical models.

20 ions cannot be reliably predicted by current theoretical models.

21 ty risk, an important factor in evolutionary theoretical models.

22 motion detection that is a hybrid of classic theoretical models.

23 were previously found prone to extinction in theoretical models.

24 xperimental data, numerical simulations, and theoretical modeling.

25 ase separation, we combined biochemistry and theoretical modeling.

26 Additionally, although theoretical models address how language control mechanis

27 We also built a theoretical model aimed at exploring the role of life-hi

28 self-referencing (calibration) with a robust theoretical model allows for the analysis of local surfa

29 the experimental data with a newly developed theoretical model allows us to quantify the thermodynami

30 Comparing with theoretical models also retaining full wavenumber-depend

31 We present a theoretical model and a set of experiments showing how s

32 tween the contact stiffness predicted by the theoretical model and by the analogous experimental resu

33 Using a general theoretical model and experimental evolution, we tease a

34 ain the mechanism of wave generation using a theoretical model and numerical simulations, which show

35 nanospheres, and compared our results with a theoretical model and prior studies.

36 with experimental results, a combination of theoretical modeling and atomistic simulations indicates

37 Both the theoretical modeling and atomistic simulations predict t

38 Using theoretical modeling and experimentation, we show that c

39 terials and ultrathin device designs through theoretical modeling and finite element analysis.

40 no diffusional effect, which simplifies the theoretical modeling and quantitative analysis of the vo

41 Theoretical modelling and experiments demonstrate that f

42 Theoretical modelling and laboratory experiments demonst

43 Theoretical models and methods for analyzing nano-phenom

44 Theoretical models and numerical simulations are in very

45 Theoretical models and observational studies suggest sel

46 ch advances have been driven not only by new theoretical models and pharmacological applications of a

47 how closely the physical system matches the theoretical models and prevents attacks due to discrepan

48 ignals in PPS is of particular relevance for theoretical models and simulations of BSC and eventually

49 Theoretical models and sparse laboratory observations ha

50 We have developed theoretical models and statistical tools that assist in

51 perimental results have been analyzed with a theoretical model based on the Boltzmann kinetic equatio

52 However, to reconcile theoretical models based on this mechanism with experime

53 id bioaccessibility was predicted by using a theoretical model, based on almond particle size and cel

54 ular uptake of nanoparticles through various theoretical models before comparing this with observatio

55 nd evolution, and researchers have developed theoretical models, both verbal and mathematical, to fac

56 es have been conducted for most elements and theoretical modelling can be performed to high precision

57 ations of DNA, as well as to the belief that theoretical models can substitute experimental ones in s

58 In our theoretical model, cells synthesize and secrete autoindu

59 Thus, the presented theoretical model clarifies some molecular aspects of th

60 Theoretical modeling confirms a frustrated aggregation p

61 A theoretical model considering for two-point coupling suc

62 A theoretical model considering the valley-dependent optic

63 Our theoretical model culminates in phase diagrams that accu

64 of thermal fluctuations consistent with our theoretical modeling, demonstrating the efficacy in comb

65 Here, we develop a theoretical model describing ParA/ParB-mediated motility

66 In this work, we develop a theoretical model describing the physical mechanism of a

67 e, be used to discriminate between different theoretical models describing the molecular mechanism of

68 geometries, which can be designed using the theoretical model developed here.Forcing a DNA molecule

69 Using spectroscopic measurements and theoretical modelling, Draguta and Sharia et al. quantit

70 transmission electron microscopy imaging and theoretical modeling elucidate the nanometer-scale mecha

71 Here, we show that theoretical models emphasizing different biological fact

72 bjective of this investigation is to provide theoretical models enabling design of remineralization b

73 Neural resonance theory (NRT) provides a theoretical model explaining how an internal periodic re

74 We report a theoretical model for chromatin (Minimal Chromatin Model

75 We develop a theoretical model for field reconstruction and verify it

76 Using a theoretical model for membrane mechanics and membrane pr

77 e a new, physically motivated, generalisable theoretical model for mtDNA populations during developme

78 horylation sensor, and provide a mechanistic theoretical model for spatial regulation of Aurora B pho

79 ent spectra are interpreted by introducing a theoretical model for the description of the coupling of

80 ectroscopic experimental investigation and a theoretical model for the interfacial field at the junct

81 ctral evolution is explained by developing a theoretical model for the power spectral density of tunn

82 A theoretical model for the proposed actuator is developed

83 with membranes of various types, we employ a theoretical model for the shape and thermodynamics of in

84 We propose a unified theoretical model for the thermal resistance analysis by

85 We developed a theoretical model for the transduction of chemical energ

86 In particular, our current understanding and theoretical models for amplified or multiple energy tran

87 While theoretical models for computing properties given the mi

88 ides valuable benchmarks for comparison with theoretical models for gas-surface reactivity aiding in

89 Such behavior agrees with common theoretical models for nanoparticle dielectrophoresis.

90 ft, bears a resemblance to those proposed in theoretical models for rodent head direction cells.

91 (-1) K(-2) putting strong constraints on the theoretical models for the Fermi surface reconstruction.

92 Minimal theoretical models for various materials are presented.

93 less in autistic children than predicted by theoretical modelling, given their poor temporal resolut

94 are interpreted with the aid of a high-level theoretical model giving excellent agreement with the ex

95 A long tradition of theoretical modeling has sought ultimate evolutionary ex

96 ical nature of the Solar System predicted by theoretical models has yet to be rigorously confirmed by

97 Theoretical models have attributed this limit to formati

98 Several theoretical models have been proposed, but experimental

99 While a number of theoretical models have been proposed, the lack of advan

100 Theoretical models have been used to argue that seasonal

101 Although theoretical models have demonstrated that predator-prey

102 Long-standing theoretical models have made predictions about the compu

103 However, few theoretical models have tried to explain these facts com

104 Comparison to a theoretical model (hexagonal centered pattern) ensured t

105 ically focus on studying, through a stylized theoretical model, how stochasticity in water availabili

106 remes is consistent with a recently proposed theoretical model in which CAPE depends on the influence

107 this article analyzes the assumptions of the theoretical models in the field.

108 Here, we combine a theoretical model, in vitro, and in vivo experiments rev

109 e compute hole mobility with three different theoretical models incorporating increasing measures of

110 Theoretical modelling indicated that growth-independent

111 Theoretical model indicates that disclination lines are

112 Our theoretical model indicates that this represents close t

113 Theoretical modeling indicates that strong dispersion fo

114 Theoretical modelling indicates that this is due to nona

115 We further show that the theoretical model is able to account for the climatologi

116 The theoretical model is based on an approach applied previo

117 The proposed theoretical model is beneficial for the design and appli

118 A theoretical model is developed to account for this hinde

119 Based on the experimental results, a theoretical model is developed, which shows that the opt

120 st the polarization state of THz waves and a theoretical model is established to describe the relatio

121 A theoretical model is presented to determine optimal curr

122 A theoretical model is proposed for the prediction of wett

123 A theoretical model is proposed to predict the total ion f

124 A theoretical model is then developed to account for this

125 A theoretical model is used to decipher how transcription

126 The theoretical modeling is revisited here, and it is shown

127 :YAG cavity, and quantitative agreement with theoretical models is found.

128 range of experimental features, supported by theoretical modelling, it is found that the main ingredi

129 Competing theoretical models make different predictions on which l

130 of morphology and information obtained from theoretical modeling may aid in developing an optimized

131 We developed a theoretical model named niche-efficiency to integrate ni

132 Thus, neither a physically correct theoretical model nor a comprehensive climate model supp

133 y of scientific disciplines commented on the theoretical model of CLimate, Aggression, and Self-contr

134 We propose a revised theoretical model of decision making related to pain ass

135 We use a recent theoretical model of deep fluids that includes ions, to

136 he rotational mechanism, we have developed a theoretical model of dilute photonic crystal, based on M

137 A theoretical model of elastically coupled reactions is pr

138 Here, we present a data-driven decision-theoretical model of feeding in Caenorhabditis elegans O

139 relevance, an experimentally tested, general theoretical model of phototaxis seems unavailable to dat

140 measure signal transduction and implement a theoretical model of signaling dynamics to predict how t

141 ng coefficient of variation estimates into a theoretical model of statistical variability, we also pr

142 We present a theoretical model of stem cell fate computation that is

143 mental results are verified according to the theoretical model of the coupled metronomes.

144 A theoretical model of the process suggests that fluctuati

145 A theoretical model of the supramolecular barrel-rosette,

146 tions and quantum-chemical calculations of a theoretical model of the tethered TEMPO system.

147 These results are fully consistent with a theoretical model of valley magnetoelectricity driven by

148 onic conditions by advancing a comprehensive theoretical model of vesicle dynamics.

149 We combine theoretical modeling of cell migration in a tail-bud-lik

150 lations, quantum chemistry calculations, and theoretical modeling of collective dipole interactions i

151 the electrochemical characterization and the theoretical modeling of electron traps in nanocrystallin

152 Corresponding theoretical modeling of the CsPbBr3 NC density of states

153 In the theoretical modeling of these structures, we adopt a hie

154 Theoretical modeling of this behavior reveals the pushin

155 gas-phase measurements offer support for the theoretical modeling of this chiroptical effect.

156 Quantitative analysis and theoretical modelling of spatial variations in the movie

157 The source is best described by theoretical models of a kilonova consisting of radioacti

158 paired footshock, an effect not predicted by theoretical models of associative learning.

159 e data to evolutionary trees generated using theoretical models of biodiversity.

160 into fundamental network alterations, graph theoretical models of brain networks were derived.

161 iding valuable new constraints against which theoretical models of catastrophe induction can be teste

162 Initial predictions were based on simple theoretical models of DNA.

163 Our results not only highlight the need for theoretical models of graphene to take into account this

164 w these physiological results have motivated theoretical models of how the brain selects actions, reg

165 Here, we review theoretical models of lingering place cell excitability

166 This article provides an overview of theoretical models of multistable perception, a review o

167 One of the most prominent theoretical models of neural sequence generation is the

168 Motor protein phenomena have inspired theoretical models of one-dimensional transport, crowdin

169 Simulating several theoretical models of place-cells suggested that combini

170 These findings support theoretical models of pneumococcal competition and antib

171 with the presence of internal friction, and theoretical models of polymer dynamics provide a framewo

172 Some theoretical models of population growth, however, predic

173 The late-time component is consistent with theoretical models of r-process-enriched neutron star ej

174 onization in the theta range is common among theoretical models of recollection, direct evidence supp

175 A review of recent theoretical models of resource provisioning and infectio

176 Recent theoretical models of schizophrenia posit that dysfuncti

177 While ISR has been described in theoretical models of single neurons, here we provide th

178 These results challenge current theoretical models of sperm locomotion.

179 e quantitative experimental data for testing theoretical models of stability, supporting models that

180 Here we study two complementary theoretical models of the adult Drosophila midgut, a ste

181 Previous theoretical models of the effect of sexual selection on

182 ons correlates with beta power, in line with theoretical models of the neural instantiation of predic

183 Theoretical models of transcription often incorporate th

184 capsid yield, with potential applications to theoretical models of viral evolution.

185 These findings have implications for theoretical models of visual awareness and for the rehab

186 markable field experiment has both validated theoretical models of Wolbachia population dynamics and

187 Theoretical models on the evolution of quantitative char

188 ctroscopy, Raman spectroscopy, together with theoretical modeling, on both precursor 2 and product 1,

189 Comparing four categories of theoretical models, only Fisher's geometrical model (FGM

190 In fact, a theoretical model originally developed for force-driven,

191 Despite extensive theoretical modelling, our knowledge of this state of ma

192 een shown to precede critical transitions in theoretical models, paleo-climate time series, and in la

193 table than mutualisms among generalists, and theoretical models predict that in many mutualisms, part

194 ring in how variable they are over time, and theoretical models predict that this consistency can be

195 tal structure is supported by a perturbative theoretical model predicting the frequency band-gaps of

196 Whilst there have been many theoretical models predicting structural and electrical

197 bservation is in sharp contrast with general theoretical models, predicting the initiation of intragr

198 Theoretical model predictions are thereby validated agai

199 Recent theoretical models propose that working memory is mediat

200 A theoretical model relating the experimental bending radi

201 perimental data are very scarce so that many theoretical models remain untested.

202 Despite the known importance of self climb, theoretical models require a typically unknown activatio

203 Moreover, complementary theoretical modeling results also corroborate this chang

204 absorption, hydrogen evolution kinetics and theoretical modelling reveal a non-monotonic behaviour w

205 Our theoretical models reveal an odd-even effect where even-

206 Kinetic measurements guided by theoretical modeling revealed that Pex15 molecules at mi

207 Theoretical modelling revealed myosin-mediated cytoskele

208 A theoretical model reveals that this network has self-reg

209 Resolution of this fact, using a theoretical model, reveals that the attraction between D

210 Simulations and theoretical modelling show that the ensuing particle dyn

211 Theoretical models show that communities are relatively

212 Our theoretical modeling shows that the interaction between

213 Our theoretical modelling shows that asymmetric potential ba

214 Theoretical modelling shows that the matter that is expe

215 Combined theoretical modeling, spectroscopic analysis, and electr

216 To perform a theoretical modeling study to identify whether large, cl

217 Empirical studies and theoretical modeling suggest that 7 was formed via a six

218 Experimental evidence and theoretical modeling suggest that piles of confined, hig

219 Theoretical models suggest that genetic mechanisms inhib

220 Theoretical models suggest that polarity can arise from

221 Theoretical models suggest that these outflows originate

222 Our theoretical model suggests that feedback among membrane

223 An influential theoretical model suggests that the speed and rate at wh

224 Theoretical modeling suggests a 30-40% lowered flexural

225 Theoretical modeling supports the experimental results a

226 Here, we apply a simple theoretical model, taken from signal detection theory, t

227 A general theoretical model that accounts for viscous dissipation,

228 Based on this analysis, we have created a theoretical model that captures the key features of the

229 We develop a theoretical model that captures these features, building

230 Here, we develop a new theoretical model that explores how coherent delocalized

231 By using a theoretical model that includes a bridging fibre, we sho

232 d photon counts matched those predicted by a theoretical model that incorporated the photophysical pr

233 We developed the first theoretical model that is capable of simulating the effe

234 e distribution of products, and we develop a theoretical model that predicts many of our experimental

235 tical analysis of the data based on a recent theoretical model that predicts the amplitude of the flu

236 In this work we describe a theoretical model that predicts the interfacial contact

237 Finally, we derive a theoretical model that quantitatively describes the kine

238 We present a theoretical model that shows it is optimal to store more

239 preted within the framework of a transparent theoretical model that starts from a well-known partial

240 a framework for researchers to identify the theoretical model that they purport to use, the antecede

241 highlight some principles from evolutionary theoretical models that can deepen our understanding of

242 esults provide empirical support for current theoretical models that emphasize the importance of gene

243 We develop theoretical models that explain why adaptation to a wide

244 sociation fraction of 65 +/- 15%, supporting theoretical models that LMH is an atomic metallic liquid

245 Our results support theoretical models that migration should confer survival

246 results thus confirm recent predictions from theoretical models that organisms should combine relevan

247 Our work suggests that in Drosophila, theoretical models that posit that gene duplications are

248 esults provide key physiological support for theoretical models that propose feature-specific, input-

249 Two theoretical models that take into account electrical int

250 Recent work has shown how a theoretical model, the stabilized supralinear network (S

251 Finally, we also establish a theoretical model to analyze the SHGs.

252 Therefore, TBI provides an experimental and theoretical model to examine how metastable dynamics rel

253 By fitting the theoretical model to experimental data, we are able to l

254 We propose a theoretical model to explain the observed reduction of t

255 patial distribution of Mn(III), we propose a theoretical model to explain the structure-performance d

256 ndividual Escherichia coli cells, and used a theoretical model to identify the stochastic activity co

257 We develop a theoretical model to predict the deformation behavior fo

258 Consequently, we derive a theoretical model to simulate the fibre-soil interfacial

259 gical, and laser-dissection experiments with theoretical modeling to characterize forces driving emer

260 ve high-resolution live-cell microscopy with theoretical modeling to explore the mechanistic basis fo

261 ectroscopy, pressed-pellet conductivity, and theoretical modeling to shed light on the key factors re

262 e, we conduct both atomistic simulations and theoretical modeling to show that there in fact exists a

263 numerous applications ranging from abstract theoretical modelling to everyday life devices.

264 the stage for the development of overarching theoretical models to describe the photomechanics in the

265 d compare the temporal spectra with existing theoretical models to gain insights about the underlying

266 on that can be obtained by applying suitable theoretical models to the analysis of these unusually co

267 We have developed the simulation and the theoretical model together, in an iterative manner, with

268 The measurements are reproduced with a theoretical model treating the atoms as coherent, intera

269 Several theoretical models try to explain this feedback system.

270 nal epigenetic variation and briefly present theoretical models under which epimutability is expected

271 Here we discuss the tool, the theoretical model underlying the tool, and the results d

272 A theoretical model underpinning the self-ordering process

273 s introduced by establishing and proving the theoretical model upon hierarchical textures.

274 Combined with theoretical modeling, useful thermodynamic parameters of

275 Validation of a theoretical model using the experimental data was done i

276 A theoretical model was developed for the response of the

277 chemistries by NMR spectroscopy, a DFT-based theoretical model was developed to derive relevant inter

278 A theoretical model was developed to explain how the denat

279 A theoretical model was first developed to determine condi

280 The theoretical model was validated using glycerol reference

281 d in our previous studies and supported by a theoretical model we have recently proposed.

282 Using a theoretical model, we find that, despite invariant richn

283 Using our theoretical model, we predict the transitions from the s

284 ts in conjunction with ensemble assays and a theoretical model, we present a unique case demonstratin

285 tension of liquid droplets predicted from a theoretical model, we proposed a technique to correct th

286 By presenting a simple theoretical model, we quantitatively cast the action of

287 Using theoretical modeling, we can extract the contributions o

288 sing combined spectroscopic measurements and theoretical modeling, we quantitatively rationalize all

289 ion of transient absorption spectroscopy and theoretical modelling, we demonstrate that trapped holes

290 eometry in promoting condensation, and using theoretical modelling, we show how to maximize vapour di

291 Using theoretical models, we attribute this effect to the gene

292 Subsequently, the theoretical models were validated by experiments.

293 Based on these images, a theoretical model which results in good agreement betwee

294 In this paper, we develop a theoretical model which shows that under certain conditi

295 compare these FQH phases with numerical and theoretical models while simultaneously controlling the

296 ly-charged monopoles) does not emerge in our theoretical model, while they are seen in experiments fo

297 We found that behavior corresponded with the theoretical model; while instantaneous threat of punishm

298 ghts into collective chemotaxis by combining theoretical modeling with experimentation.

299 We combined theoretical modeling with experiments to study collectiv

300 y, one property of resilience that builds on theoretical modelling work recognizing that systems clos