ライフサイエンスコーパス: theoretical model

1 y, theory of planned behaviour and the trans-theoretical model).

2 ial magnetic field are in agreement with our theoretical model.

3 relationships between variables guided by a theoretical model.

4 )/6-311++G(2df,2p)//UMP2(full)/6-311++G(d,p) theoretical model.

5 straining diffusion and implementing a creep theoretical model.

6 which both find excellent agreement with our theoretical model.

7 stretching and rupturing, corroborating the theoretical model.

8 methods on data simulated according to some theoretical model.

9 recombination length, neglected by previous theoretical models.

10 n and growth behaviors based on the existing theoretical models.

11 lways much better than predicted by existing theoretical models.

12 etailed and framed in the context of several theoretical models.

13 ystallography, single-molecular imaging, and theoretical models.

14 t modeling approach involving three distinct theoretical models.

15 provided empirical support for complementary theoretical models.

16 pacitance, and confirm the measurements with theoretical models.

17 cted from currently accepted biochemical and theoretical models.

18 on fault mechanics is mainly conjectured by theoretical models.

19 en limited but is critical to fully validate theoretical models.

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

21 e interactions are currently the two leading theoretical models.

22 ich reveal the remarkable foresight of these theoretical models.

23 question of how recorded activity relates to theoretical models.

24 e groundwork for quantitative comparisons to theoretical models.

25 although this is now reinforced by extensive theoretical modeling.

26 n bulk samples, by combined experimental and theoretical modeling.

27 roscopy and light-scattering techniques with theoretical modeling.

28 tory experiments, numerical simulations, and theoretical modeling.

29 imaging with quantitative image analysis and theoretical modeling.

30 luated using atomic force microscopy and the theoretical modeling.

31 sotopically enriched solutions combined with theoretical modeling.

32 pmental stage creates an extra challenge for theoretical modelling.

33 iffraction measurements, optical studies and theoretical modelling.

34 Additionally, although theoretical models address how language control mechanis

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

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

37 e reconstituted from a linear combination of theoretical models, although this procedure carries a si

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

39 We also show, both by analyzing a revised theoretical model and by experimentally following single

40 ich is analyzed and predicted by an advanced theoretical model and further confirmed by experimental

41 Detailed experiments, supported by theoretical modeling and analysis, reveal that the quasi

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

43 Both the theoretical modeling and atomistic simulations predict t

44 Here, through theoretical modeling and characterization of bubble beha

45 Here, we use theoretical modeling and coarse-grained simulation to ex

46 This work is a theoretical modeling and experimental demonstration of e

47 TiO3 NCs and devices based on BaTiO3 NCs via theoretical modeling and experimental piezoresponse forc

48 Using a combination of theoretical modeling and quantitative live-cell imaging

49 Here we show, based on detailed theoretical modelling and rigorous simulations, that it

50 empirical modelling may be overcome through theoretical modelling and simulation that consider under

51 e electromagnetic field in the holes both by theoretical modelling and spectroscopic measurements.

52 ynthesis dynamics has been studied both with theoretical models and by profiling ribosome footprints,

53 rate in extensive experiments, together with theoretical models and computational analysis, the robus

54 These results provide strong validation of theoretical models and demonstrate that critical slowing

55 a tool to bridge the gap between multi-level theoretical models and Edisonian trial-and-error approac

56 are encounters, (2) contribute to developing theoretical models and empirical research to refine ante

57 Similarly, theoretical models and experiments have shown that punis

58 Theoretical models and experiments suggest that social n

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

60 Speciation is typically studied via theoretical models and snapshot tests in natural populat

61 With the help of theoretical models and spectroscopic/diffractometric stu

62 In this review, we trace the history of the theoretical models and the experimental work that led up

63 Consistent with theoretical models and the known functions of the dentat

64 Hall voltage noise is in good agreement with theoretical models and we demonstrate that minimum detec

65 or attributes of the concept, and identify a theoretical model, and can also lead to new perspectives

66 tegies concerning electrochemical reactions, theoretical model, and in situ characterization are disc

67 Technical details, theoretical modeling, and new experimental methods are a

68 g small-angle X-ray/neutron scattering data, theoretical modelling, and computer simulations, sodium

69 odels built from long-term demographic data, theoretical models, and methods that leverage widely ava

70 Here, we use a theoretical modeling approach to investigate the hypothe

71 The main features of the theoretical model are confirmed, especially the abrupt d

72 simulations with current computer power and theoretical models are now in an excellent position to a

73 Theoretical models are used to explain the shielding mec

74 Intuitively, this suggests-and prominent theoretical models argue-that memory interference is bes

75 y in situ Raman spectro-electrochemistry and theoretical modeling as well as contrast catalytic tests

76 explained within the framework of a minimal theoretical model based on "mitogen competition." We pro

77 A theoretical model based on electrostatic and surface ene

78 Using a theoretical model based on hydrodynamic singularities, w

79 A theoretical model based on kinetic Wulff construction th

80 e rationalise experimental results through a theoretical model based on Mie theory.

81 We use a theoretical model based on scanning electron microscope

82 he analyses have been here corroborated by a theoretical model based on the diffusion equation.

83 onclusions are additionally supported by the theoretical model based on the Gross-Pitaevskii equation

84 A theoretical model based on this proposal describes quant

85 etween these two alterations is suggested by theoretical models based on striatal dopamine's topograp

86 results are consistent with predictions from theoretical models based primarily on evidence from lang

87 methods bridge statistical, data-driven and theoretical, model-based neurosciences at the level of s

88 validate our experimental results against a theoretical model built using finite element analysis an

89 Theoretical modeling calculations corroborate and explai

90 field optical microscopy (THz s-SNOM) with a theoretical model can quantitatively measure and image s

91 t the presented force-probing assays and the theoretical model can serve a combined testbed to invest

92 Using data simulated from a theoretical model can substantially impact the results o

93 When inferring causality, four nonexclusive theoretical models can account for this association: 1)

94 Additionally, our theoretical model captures behavioral differences result

95 Theoretical modelling confirmed the existence of acid an

96 Further energy breakdown analysis based on a theoretical model confirms that the improved energy effi

97 sults are in quantitative agreement with our theoretical model derived from classical nucleation theo

98 The goal of this study was to develop a theoretical model describing injury-related ATP and ADP

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

100 This heterogeneity was not captured by theoretical models describing curiosity as a desire to l

101 The traditional theoretical models did not reproduce the wavelength scal

102 Theoretical models distinguish between neural responses

103 The analysis of the experimental data by theoretical modeling elucidates the thermodynamic parame

104 demic are successfully described by the same theoretical model, even though the two events are caused

105 We present the theoretical modeling, experimental characterization, and

106 udied in terms of lattice distortion using a theoretical model, first-principles calculations, synchr

107 We develop a theoretical model for magnetic manipulation of graphite

108 When interpreted using a theoretical model for mRNA dynamics, the single-cell dat

109 In the context of a theoretical model for regulation of Chlamydomonas multip

110 A theoretical model for released iceberg energy supports t

111 The application of a theoretical model for solid state voltammetry to the exp

112 Here we develop a theoretical model for surface plasmons of interacting na

113 aggregation of mechanosensors and develop a theoretical model for the clustering of mechanosensors i

114 We explore a game theoretical model for the evolution of mind-reading stra

115 his relocation is still elusive, we devise a theoretical model for the molecular-motor-driven motion

116 By referring to existing theoretical models for membrane PD, we found that while

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

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

119 Although numerous theoretical models for sequential action generation have

120 Theoretical models for the aging dynamics need to be rev

121 produce, guiding the development of accurate theoretical models for the interaction of H(2) with a so

122 were compared with simulated images for four theoretical model geometries, including possible bond-an

123 Furthermore, the theoretical model goes beyond the experimental results b

124 A theoretical model has been developed to predict the ampl

125 g release at zero-order rates, empirical and theoretical modelling have been extensively employed and

126 has focused on kin-discriminating behaviour, theoretical models have assumed indiscriminating behavio

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

128 y means of quantum-chemical calculations and theoretical modeling, how chemical substitution affects

129 The VMA has been predicted through theoretical models, however few studies have investigate

130 We propose a theoretical model in which social processes (both social

131 ntal data agree quantitatively with a simple theoretical model in which the new phase results from SO

132 These phenomena can be described by a theoretical model in which the periodic moire potential

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

134 al platform that closely resembles idealized theoretical models in the quantum Hall regime.

135 Rather than generate data from a theoretical model, in this paper we develop methods to a

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

137 revisit of various experimental findings and theoretical models--including those of our own--in the f

138 A theoretical model incorporating enzymatic rate expressio

139 Furthermore, our empirical data and theoretical model indicate that increased connectance re

140 Although theoretical models indicate that the presence of sociall

141 g the (U)MPWB1K/cc-pVTZ//(U)MPWB1K/6-311G(d) theoretical model, indicated a large singlet-triplet ene

142 Theoretical model indicates that disclination lines are

143 Application of a theoretical model indicates that the evolutionary load i

144 A theoretical model is derived describing the mass uptake

145 A new theoretical model is formulated for the quantitative ana

146 A constitutive theoretical model is proposed that, despite its simplici

147 d largely from animal models, and associated theoretical modelling, it is demonstrated that inter-hem

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

149 Here, we propose a novel theoretical model linking present-focused decision-makin

150 Competing theoretical models make different predictions on which l

151 Our theoretical model matches the experimental data from the

152 An ideal observer is a theoretical model observer that performs a specific sens

153 A theoretical model of a coherent polarization that dephas

154 Here we develop a theoretical model of a haploid population undergoing LGT

155 tacks, and identifying attack onset, a sound theoretical model of a migraine attack, paired with a un

156 Comparing experimental data to a theoretical model of an active nematic reveals that theo

157 Hampered by the absence of evidence and theoretical model of biological semiconductors, the unid

158 ovide the best fit of the measured data to a theoretical model of cavitation bubble dynamics in a Neo

159 eneral conclusions, our work also provides a theoretical model of collective myosin kinetics with a f

160 Here, we propose a theoretical model of coupled modules.

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

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

163 a possible alternative, we present a simple theoretical model of how a non-linearity can arise from

164 st John Hubbard in the 1960s(1), is a simple theoretical model of interacting quantum particles in a

165 titutive immune phenotypes, then developed a theoretical model of our in vitro system, which we fit t

166 The results obtained corroborate a recent theoretical model of SEY reduction as a function of the

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

168 We develop a predictive theoretical model of the physical mechanisms that govern

169 On the other hand, it refers to a particular theoretical model of those things that people do.

170 r systematic studies of catalytic processes, theoretical modeling of complex materials, and model stu

171 Theoretical modeling of the actin network as an active g

172 Following the discussion of theoretical modeling of the piezoelectric materials to c

173 Theoretical modeling of thermal deformations provides a

174 luable input for further improvements in the theoretical modeling of these systems.

175 in the solvents, was investigated through a theoretical modelling of its Hansen solubility parameter

176 Although animal and theoretical models of addiction emphasize the importance

177 The findings support the applicability of theoretical models of addictive behaviors to the social-

178 We tested theoretical models of density-dependent habitat selectio

179 ovel approach that combines data mining with theoretical models of disease dynamics.

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

181 try breaking and axis formation, and current theoretical models of Hydra symmetry breaking use this a

182 e three types of impulsivity, as proposed by theoretical models of impulsivity, and their association

183 These results support several theoretical models of increased exploratory choices in A

184 Theoretical models of memory retrieval have focused on p

185 Here, a summary of theoretical models of nanoparticle dynamics is presented

186 Virtually all existing theoretical models of normal, bright SNIa require the ex

187 n be used to constrain and validate improved theoretical models of pattern formation in Hydra.

188 We review theoretical models of perceptual inference and key suppo

189 phenomenology of perceptual disturbances via theoretical models of perceptual inference.

190 Theoretical models of photosynthetic isotopic discrimina

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

192 and a platform with which to extend and test theoretical models of receptor pharmacology to more accu

193 e ubiquitous in physiology, are described by theoretical models of receptor pharmacology.

194 ent benchmarks to use against other all-atom theoretical models of RNA-ion interactions, interactions

195 Referring to theoretical models of the development of numerical conce

196 ity of liquids and have posed a challenge to theoretical models of the liquid state ever since.

197 e might be useful in validating long-debated theoretical models of the liquid-vapor interface, and en

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

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

200 These observations provide evidence for a theoretical model on speech memory representations and e

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

202 There is currently no theoretical model or hypothesis to explain the interacti

203 hat existing estimates are entirely based on theoretical models or extrapolations from small and bias

204 Supported by a theoretical model, our findings raise questions about wh

205 Theoretical models predict that if the disk is misaligne

206 Theoretical models predict that induced responses can ca

207 Theoretical models predict that information may be limit

208 Theoretical models predict that these planets are more v

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

210 The theoretical model predicts 39% of the variance in chi va

211 The experiments and theoretical model proposed here provide a starting point

212 Simulations of various theoretical models recapitulate final states of natural

213 Theoretical models regarding streaming current/potential

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

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

216 ate limits, simulation results together with theoretical models reveal distinct scaling behavior in f

217 Theoretical modeling revealed that these regulatory stra

218 Theoretical modeling reveals a recurring partially rever

219 Our theoretical modeling reveals that this uniaxial TDM orig

220 Combining vibrational-MCR with emerging theoretical modeling strategies promises synergetic adva

221 al crystal structure matches well with a new theoretical model structure, with carbon atoms inserted

222 The theoretical model successfully explained the lognormal d

223 Prominent theoretical models suggest that cooperation is particula

224 In C(4) plants, theoretical models suggest that leaf carbon isotope comp

225 Recent theoretical models suggest that pair coordination of the

226 Theoretical models suggest that polarity can arise from

227 Theoretical models suggest that such interspecific compe

228 is termed the "area-heterogeneity tradeoff." Theoretical models suggest that the reduction in habitat

229 Both experimental results and theoretical models suggest the decisive role of the fill

230 Theoretical models suggest there is no benefit of high a

231 The experimental data and a theoretical model support the proposal that neuronal dif

232 Theoretical modeling supports the experimental results a

233 Consistent with theoretical models, teaching occurs for skills/knowledge

234 A theoretical model that accurately predicts the performan

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

236 Based on a theoretical model that considers two oppositely oriented

237 We present a theoretical model that demonstrates the integral role ch

238 Based on these results, we propose a theoretical model that describes the deformations and mi

239 experimental observations, we built a novel theoretical model that elucidates how CAGE-induced skin

240 ciples behind gliding motility and develop a theoretical model that predicts a 2-regime behavior of t

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

242 ional theory calculations and described by a theoretical model that provides insight into the force-c

243 We present a theoretical model that reproduces the absorption spectru

244 re quantitatively supported by a microscopic theoretical model that reveals how the purely electrical

245 of experimental models easily combined with theoretical models that better elucidate these pathways.

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

247 Theoretical models that have been developed to understan

248 d maximum compressibility is consistent with theoretical models that include detailed electronic stru

249 The relative scarcity of sophisticated theoretical models that include sufficient detail to lin

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

251 malous magnetoresistance are consistent with theoretical models that predict helical edge states with

252 terpret these results in the light of recent theoretical models that predict how ejaculate strategies

253 Here we show, using a theoretical model, that the observed oxygenation steps a

254 NA bases during translocation; and (iii) one theoretical model, the 'B-A scrunchworm', predicts that

255 pectroscopy measurements in combination with theoretical modeling, the nature of the intermolecular i

256 d data are not generated from an unrealistic theoretical model, they exhibit realistic (annoying) att

257 , as real data often exhibit violations from theoretical models, this can result in unsubstantiated c

258 Supported by a theoretical model to account for structural changes in s

259 hared by other cellular enzymes to develop a theoretical model to aid in the design of a novel class

260 Specifically, we develop a game theoretical model to analyse cooperation under defaults

261 Based on these results we apply a simple theoretical model to calculate the circular dichroism sp

262 We present a theoretical model to elucidate how a negative feedback m

263 We develop a theoretical model to explain our experimental observatio

264 A theoretical model to explain the observed hysteretic swi

265 This work demonstrates the ability of the theoretical model to help focus experimental efforts and

266 r the systems fluid dynamics and establish a theoretical model to predict the flow rate in multilayer

267 We develop a theoretical model to quantify the carbon emissions from

268 e we use multiple experimental systems and a theoretical model to show that a combination of nonlinea

269 Here we use a theoretical model to suggest that symbiotic nitrogen-fix

270 We apply this theoretical model to test the possible interactions betw

271 re, we use a combination of experimental and theoretical modeling to reveal the structure-property-pe

272 oscopy and light-scattering experiments with theoretical modeling to show the reversible decrease in

273 We perform theoretical modeling to understand thin film delaminatio

274 ing approach integrates machine learning and theoretical models to explore mechanisms in the macroeco

275 spatial and spectral resolutions and lack of theoretical models to quantitatively analyze near-field

276 Theoretical models to study the interplay between noisy

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

278 This analysis allowed us to evaluate new theoretical models treating the cocrystallization of def

279 A theoretical model underpinning the self-ordering process

280 The theoretical model used here provides a realistic and rem

281 A theoretical model used to simulate the changes in surfac

282 ures of sensors, performance parameters, and theoretical models used to describe CNT sensors.

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

284 Theoretical modeling using discrete anisotropic stress f

285 A theoretical model was first developed to determine condi

286 The theoretical model was validated using glycerol reference

287 Finally, using a theoretical model, we argue that the actin-spectrin skel

288 Using primary survey data and a game-theoretical model, we examine and quantify prosocial beh

289 In the corresponding theoretical model, we treated the proteins as limited-va

290 c-scale electron microscopy observations and theoretical modeling, we delineate the atomic-scale mech

291 Contrary to current theoretical models, we found that the Stx17 N-peptide ap

292 tational tools, experimental techniques, and theoretical models were developed independently.

293 We present a general theoretical model where society is split into subgroups

294 We introduce a theoretical model which considers heat losses due to con

295 r-field electrospinning (NFES), we propose a theoretical model, which can account, phenomenologically

296 Using our theoretical model, which connects geometry to mechanics,

297 mpared with the results of the enhanced ACET theoretical model, which predicts the temperature rise a

298 of pulsation modes that can be compared with theoretical models, which has been done successfully for

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

300 By combining theoretical modeling with experimentation, we show that