ライフサイエンスコーパス: theory

1 ing were calculated using density functional theory.

2 We complement our data by a quantitative theory.

3 studied carefully by means of experiment and theory.

4 r an alternative perspective: semantic space theory.

5 lowest energy scales by the Luttinger liquid theory.

6 use that space has not yet been described in theory.

7 ns about prices and quantities from economic theory.

8 rvival but not in the direction predicted by theory.

9 d that need to be incorporated into existing theory.

10 esentations of gist at its core, fuzzy-trace theory.

11 horizontally transferred gene to prove this theory.

12 simplicity, which is fundamental to Gestalt theory.

13 and is well described by a phenomenological theory.

14 trajectories, using principles from control theory.

15 xical within the framework of optimal choice theory.

16 um salts is explored with density functional theory.

17 tablished principles of electrophysiological theory.

18 slower than expectations based on simplified theory.

19 ocess set out within constructivist grounded theory.

20 ely data driven and agnostic to evolutionary theory.

21 ates is not controllable in terms of control theory.

22 temperature dependence predicted by the LKSR theory.

23 show us the way to integrate simulation with theory.

24 parameter at the core of Density Functional Theory.

25 copies that exist, along with the results of theory.

26 onal details required to validate speciation theory.

27 intuitive local pictures and simple analytic theory.

28 an important but separate role in validating theories.

29 se, and conceptual developments and a priori theories.

30 matter fields in context of the Gauss-Bonnet theories.

31 ies in patients inconsistently support these theories.

32 ognition develops needs to be central to our theories.

33 of the relevant biological and computational theories.

34 antum many-body ground states that challenge theory(2).

35 MUSTACHE employs scale-space theory, a technical advance in computer vision, to detec

36 n or parents) with dynamic and bidirectional theories about the interdependence of children and paren

37 Yet people can have various theories about what peace "is." In this study, we examin

38 Drawing on ideas from information theory, an efficient retinal code could be defined as on

39 gent properties that escape a standard group theory analysis.

40 cesses, thereby enriching both sociocultural theories and Bayesian accounts of cognition.

41 Most theories and hypotheses in psychology are verbal in natu

42 ss this question empirically, we bridged art theory and cognitive research and designed an experiment

43 ere remains a significant disconnect between theory and empirical research.

44 Whilst theory and empirical work suggests that song may become

45 Through this confluence of theory and experiment, we unify the existing body of str

46 Using concepts of probability theory and inferential statistics, we present a comprehe

47 will advance the development of range limit theory and its applications to biodiversity conservation

48 dehyde to NO(2) (HCHO/NO(2)), developed from theory and modeling, has previously been used to indicat

49 n the computational side, density functional theory and noncovalent interaction analysis reveal that

50 Additionally, EIS's underlying theory and potential surface modification techniques are

51 ariations in ecological rates of change, the theory and practice of managing ecological systems shoul

52 To contribute more fully to theory and practice, these reported experiences must be

53 earch and localizes O-glycosites using graph theory and probability-based localization.

54 Herein, qualitative theory and quantum chemical calculations are used to dev

55 At the intersection of quantum theory and relativity lies the possibility of a clock ex

56 l developmental science framework integrates theory and research on single-generation development (i.

57 ications of the work carried out to date for theory and research, and points toward next steps for ad

58 ll help to bridge the gap between ecological theory and the complex dynamics observed in metagenomic

59 Due to the core assumptions of kinetic theory and the drive toward realizing reproducible gas-p

60 iology that combines the proteome allocation theory and the structural model of cell division.

61 Here, we extend metabolic scaling theory and use global simulation models to demonstrate t

62 powered studies, publication bias, imprecise theories, and inadequate statistical procedures.

63 It is well understood that this free theory, and even interacting integrable models, can supp

64 cialty care prevention settings, discuss the theory- and practice-based criteria of a rapid diet scre

65 Graph theory approaches to understanding decision-making in si

66 The results of the analytic theory are compared with simulation results obtained by

67 mon B3LYP/6-31G* level of density functional theory are in excellent agreement with reactivity determ

68 ations for the resulting [Formula: see text] theory are obtained and show that particles follow non-g

69 This has resulted in complex theories as to how these receptors are activated in vivo

70 previously evaluated by developing a kinetic theory based on a simplified one-dimensional model for O

71 Our signal-detection-theory-based model accurately replicated behavioral outc

72 The serving algorithm of discrete field theories belongs to the family of structure-preserving g

73 ing levels of influence has been proposed in theory but blocked by data limitations in the United Sta

74 The purpose of replication is to advance theory by confronting existing understanding with new ev

75 ested prediction of Cultural Group Selection theory, by assessing whether readiness to cooperate betw

76 r dynamics simulation and density functional theory calculation, showing a unique chemical recognitio

77 Based on density functional theory calculations and experiments on multiple push-pul

78 Density functional theory calculations and symmetry analysis of the large u

79 n principles supported by density functional theory calculations for engineering analogs of this clas

80 gles) are consistent with density functional theory calculations for these FeS(x) phases.

81 Density-functional theory calculations further suggested that, compared wit

82 Density functional theory calculations herein reveal that lowering *CO(2) c

83 Density functional theory calculations identify the thiophene units and cya

84 Density functional theory calculations indicate that P promotes hydrogenati

85 Density functional theory calculations indicates that NFS locate at an inte

86 n denaturation and simple density functional theory calculations of flavin dimers.

87 Static density functional theory calculations of the benzene-to-phenyl hydride lan

88 Density functional theory calculations showed that (*)OH oxidizes 6:2 FTS b

89 Density-functional theory calculations suggest that the formation of the hi

90 ture characterization and density functional theory calculations suggest that the interaction between

91 tic resonance studies and density functional theory calculations were carried out on the substrate-Fe

92 Density functional theory calculations, combined with second-generation abs

93 surfaces as confirmed by density functional theory calculations, demonstrating the potential of poro

94 In combination with density functional theory calculations, first insights into a long-lived ex

95 Revealed by density functional theory calculations, the selenium vacancy in ReSe(2) cry

96 h agree with density functional perturbation theory calculations.

97 1)H NMR spectroscopy, and density functional theory calculations.

98 lved photoluminescence, and density function theory calculations.

99 it using first-principles density functional theory calculations.

100 principles modeling using density functional theory calculations.

101 sonance spectroscopy, and density functional theory calculations.

102 Least-cost optimality theory can be used to predict the acclimation of photosy

103 the synergy between far-IR spectroscopy and theory can provide an unprecedented picture of the struc

104 Current theories cannot resolve this apparent contradiction.

105 ominently from conceptual density functional theory (CDFT)-of the relative importance of electrostati

106 As informed by chemical graph theory (CGT), the vast majority of species observed in t

107 ned an experiment leveraging construal level theory (CLT).

108 ecipitation in North America, and models and theory consistently suggest continued increases with fut

109 show that the original elements of the codon theory continue to make important predictions for cerebe

110 w live in middle-income democracies that, in theory, could use their resources to end extreme poverty

111 nits, identified by using density functional theory coupled with an evolutionary structure-predicting

112 trates that the unique status of CSBs is not theory-dependent.

113 In this perspective, we extend the theory developed for species diversity to further our un

114 In all cases, density functional theory (DFT) and higher-level methods for electronic str

115 Spin-polarized periodic density functional theory (DFT) and nonperiodic DFT calculations are deploy

116 s of these reactions with density functional theory (DFT) and show that they involve ambimodal [6+4]/

117 Density functional theory (DFT) calculations indicate that, in addition to

118 Density functional theory (DFT) calculations of the electronic structures r

119 O), which we propose from density functional theory (DFT) calculations predisposes the copper active

120 Density functional theory (DFT) calculations reveal that the C/MoS(2) inter

121 solid-state structure and density functional theory (DFT) calculations revealed that the Si=C bonds a

122 hly puzzling, as previous density functional theory (DFT) calculations showed that all the possible s

123 Density functional theory (DFT) calculations showed that approximately half

124 titration experiments and density functional theory (DFT) calculations support the results obtained f

125 In this work, we use density functional theory (DFT) calculations to examine the electronic prop

126 Density functional theory (DFT) calculations were performed to explain the

127 Supported by density functional theory (DFT) calculations, redox disproportionation form

128 d data, in agreement with density-functional theory (DFT) calculations, shows continuous red-shifts a

129 Combined with density functional theory (DFT) calculations, the results demonstrate that

130 diffraction coupled with density functional theory (DFT) calculations.

131 cofeed measurements, and density functional theory (DFT) calculations.

132 effect of inhibitors, and density functional theory (DFT) calculations.

133 A density functional theory (DFT) computational analysis, using the omegaB97X

134 infrared spectroscopy and density functional theory (DFT) modeling, targeting methanol formation from

135 Density functional theory (DFT) showed water has minor effects on the react

136 Density functional theory (DFT) simulations unveil the crucial role of the

137 ossible, we have employed density functional theory (DFT) to develop a more complete understanding of

138 model was developed using density functional theory (DFT) to potentially predict the titanium oxides

139 Our density functional theory (DFT)-based quantum mechanics/molecular mechanics

140 I define this CLHZ using lipid solubility theory, diving data, and results from animal laboratory

141 l help close the gap between data-driven and theory-driven models of neural dynamics.

142 This theory elaborates on how a particular trait once favoure

143 While well-grounded in the theory, empirical evidence of the trade-off between stre

144 d lengths determined from density functional theory explain the origin of the ferroelectricity, i.e.

145 Brunauer-Emmett-Teller (BET) theory extended Langmuir's ideas to multilayer adsorptio

146 etic approach complemented by a hydrodynamic theory for agents with mixed alignment symmetries, which

147 Our analyses reveal critical data and theory gaps and call for increased efforts to monitor gl

148 This would, in theory, generate aminyl and carboxylate radicals, with t

149 Previous theory has proposed a molecular mechanism of bound-state

150 Recent neurocomputational theories have hypothesized that abnormalities in prior b

151 h as bosons and fermions in a lattice, gauge theories, high-temperature superconductors, quantum spin

152 review, we illustrate the utility of network theory in biological systems and investigate modern tech

153 Systems theories, including network analysis and machine learnin

154 Concepts from dynamical systems theory, including multi-stability, oscillations, robustn

155 Theory indicates that symmetric two-sided loop extrusion

156 advances in plant hydraulics and optimality theory into LSMs, and an alternative to empirical stress

157 tential, and suggest that incorporating such theory into next-generation trait-based terrestrial bios

158 Forty years ago, prospect theory introduced the notion that risky options are eval

159 analyses and the hard-soft acid-base (HSAB) theory is advanced to explain the observed reactivity tr

160 Our theory is based on a minimal model and describes the exp

161 An underlying Lie algebraic theory is developed using the closure of the algebra to

162 Recently introduced [Formula: see text] theory is generalized by adding dependence on the arbitr

163 This mismatch might be because current theory is not clear about the role of behavior in indivi

164 However, direct proof for this theory is still lacking.

165 A key prediction of biological market theory is that individuals can influence resource value

166 This theory is used to rationalize scenarios where predicted

167 Kinetic crystal growth theory is used to show that crystals accelerated from an

168 While translational theories link neurodevelopmental changes in threat learn

169 es, we must design experiments for which the theories make distinct predictions.

170 Supporting this theory, many striatal neurons exhibit such graded change

171 Tests of this theory may combine remote sensing with a generation of n

172 Here we propose that Gestalt theory may explain why rodent islet architecture has his

173 a stronger integration of ideas from network theory may provide insight into metapopulation processes

174 alcogenide compounds, via density-functional-theory molecular-dynamics (DFT-MD) simulations.

175 Density functional theory-molecular dynamics (DFT-MD) simulations of SCN(-)

176 Here, we combined theory, numerical modeling, and field observations to de

177 y of affected connections is consistent with theories of accelerated and/or delayed maturation, but m

178 onsistent with white matter and social-brain theories of ASD.

179 This new evidence can also inform recent theories of binding in visual WM.

180 Through reference to theories of bottlebrush polymer behavior, we demonstrate

181 Recent theories of cortical function construe the brain as perf

182 with systems consolidation and computational theories of episodic memory, evidence from model organis

183 Computational theories of hippocampal function suggest that dentate gy

184 eace "is." In this study, we examine the lay theories of peace of citizens embroiled in a prolonged e

185 ccessive price changes, which test different theories of price dynamics.

186 o provide detailed benchmarks for predictive theories of roaming.

187 Our results demonstrate that theories of rTPJ function should account for the multifa

188 We argue that the three prominent theories of status allocation-competence-based models, c

189 s how this finding challenges and constrains theories of visual awareness.

190 Object constancies are central constructs in theories of visual phenomenology.

191 Compulsion theory of addiction also has weak support.

192 ominoids, as well as revise the compensation theory of cortical folding.

193 The classic theory of direct-current (DC) insulator-based dielectrop

194 of a search algorithm rooted in the ergodic theory of dynamical systems which can accommodate comple

195 Here, we propose a mechanistic theory of epithelial shells which resemble small-organoi

196 A prominent theory of face recognition holds that the brain computes

197 his open problem, presenting a comprehensive theory of five rational design principles for achieving

198 The replica theory of glasses predicts that in the infinite dimensio

199 The theory of grain boundary (the interface between crystall

200 the fact that Isaac Newton came up with his theory of gravity whilst quarantined during the bubonic

201 al phase changes by pai, as predicted by the theory of half-vortices in a PDW state(6,7).

202 ective host plant defenses and warranted the theory of host specialization for generalist aphids.

203 r sequencing data, we develop a quantitative theory of human T cell dynamics compatible with the stat

204 calculations are in good accordance with the theory of lipid disc micelle vesiculation.

205 Theory of mind plays a fundamental role in human social

206 This suggests a new way of understanding theory of mind-one that is focused on understanding othe

207 with deep implications for neuroscience and theory of neural networks, has no solid theoretical grou

208 Derived from the theory of order statistics, our method controls the fals

209 s with parametric statistical models and the theory of phase transitions in statistical physics.

210 From this redundancy reduction hypothesis, a theory of retinal color coding emerged in which the thre

211 We develop the theory of the method and demonstrate it on an example wi

212 nected recurrent rate networks and develop a theory of the transient sequential activity observed aft

213 Finally, we show how the theory of these domains is unified in four-dimensional s

214 Dynamic energy budget (DEB) theory offers a mechanistic modeling approach to describ

215 We test the predictions of this theory on datasets of pubertal mammary gland tips and em

216 However, current theory on rank orders in biology is somewhat fragmented.

217 within a topological-based bonding evolution theory perspective.

218 Basic stomatal optimality theory posits that stomatal regulation maximizes the car

219 Photosynthetic 'least-cost' theory posits that the optimal trait combination for a g

220 In contrast with theory predicting limitation from a single limiting fact

221 Our theory predicts a set of symmetries of barcode covarianc

222 Search theory predicts that animals evolve efficient movement p

223 Theory predicts that chromosome structures are fluid and

224 The habitual motion path theory predicts that humans tend to maintain their habit

225 Theory predicts that when populations are established by

226 Evolutionary theory predicts that, following successful reproduction

227 Moreover, no theory presently exists to derive city size distribution

228 dings are in line with predictive processing theories proposing that neurons in the deep cortical lay

229 Biological market theory provides a conceptual framework to analyse trade

230 etic) resonance stabilization embedded in VB theory provides a natural and elegant framework for anal

231 Bayesian decision theory provides a simple formal elucidation of some of t

232 electronic properties, and indicate that the theory provides a universal guidance for optimizing phas

233 ond (VB) perspective and demonstrate that VB theory readily enables a clear-cut resolution of both of

234 Contrary to classic theories, recent work (McCormick et al.) has shown that

235 s finding rules out of a majority of current theories related to the crime and proposes diatoms as a

236 that the empirical foundations for prospect theory replicate beyond any reasonable thresholds.

237 According to the now canonical theory, reward predictions are represented as a single s

238 to improve memory, learning, and transfer of theory-rich content.

239 putations at the level of density functional theory show how the terminal OH groups on node vacancies

240 Theory shows that in rapidly evolving populations, such

241 campal subfields, in line with computational theories.SIGNIFICANCE STATEMENT The flexibility of episo

242 ectra with time-dependent density functional theory simulations, we unravel the full relaxation pathw

243 cules using any available combination of DFT theory, solvent model, and NMR-active nuclei, using both

244 The BEF theory states that higher species richness can enhance e

245 tal studies, we performed density functional theory studies on large active site cluster models.

246 d on the experimental and density functional theory studies, we propose a catalytic cycle for the pro

247 by detailed computational density functional theory studies, which fully address multi-spin-state rea

248 roscopy) and theoretical (Density Functional Theory) studies reveal that, regardless of the metal ide

249 A density functional theory study is presented here to offer mechanistic insi

250 y a recent spin-polarized density functional theory study.

251 data was described well by electron transfer theory subject to a diffusion-controlled limit.

252 The theory successfully predicts the scaling law [Formula: s

253 According to predictive processing theories, such reversed processing also plays a central

254 too shallow for hydrate formation, existing theories suggest that gas migration occurs via capillary

255 Converging theories suggest that organisms learn and exploit probab

256 vailability models arising from life history theory suggest that socioeconomic conditions influence i

257 ified landscapes, spatial nutrient transport theory suggests that such instabilities can be amplified

258 play in conceptual processing, with embodied theories supporting their direct involvement in processi

259 deled with time-dependent density functional theory (TD-DFT).

260 mechanical time-dependent density functional theory (TDDFT) calculations indicate that the fluorescen

261 Applications of machine learning and graph theory techniques to neuroscience have witnessed an incr

262 BSA methods represent a higher-level scoring theory than docking.

263 d by such observations, we propose a kinetic theory that addresses the nonadiabatic evolution of a ne

264 These results are consistent with the theory that anodal stimulation of the rTPJ increases the

265 Our results contradict the accepted theory that culicine larvae respire via atmospheric gas

266 rge) migrants counters prevailing ecological theory that predicts different traits to be favored unde

267 We provide new evidence supporting the theory that soil-microbe systems are self-organising sta

268 Our network-based approach supports the theory that the position of a start-up within its ecosys

269 Here, we test a recent version of this theory, the internal predictive adaptive response (iPAR)

270 The integration of classical theories through a contemporary lens of consistent indiv

271 the answers of which require applying these theories to metabolomics.

272 this paper, we draw on common-pool resource theory to argue that indigenous territories, when grante

273 l studies applying hybrid density functional theory to cluster models of the bimetallic active sites

274 ) hypothesis provides the most comprehensive theory to date of the biological and cultural evolution

275 Here we combine experiment and theory to examine the mechanistic basis of these differe

276 We use canard theory to explain why enlarging the size of the window r

277 od combines computational geometry and graph theory to measure the degree of order of any packed tiss

278 carry out calculations at various levels of theory to obtain insight into the properties of molecula

279 cs, and we discuss the applicability of this theory to other settings.

280 esis, we extend photosynthetic co-ordination theory to predict the acclimation of R(d) to growth temp

281 muscle capillary numbers with O(2) diffusion theory to propose a novel active role for capillaries th

282 ta delivers an ultra-sensitive benchmark for theory to reproduce, guiding the development of accurate

283 ning probe microscopy and density functional theory to reveal how the generation of S-vacancies withi

284 Here, we develop mathematical theory to show that the rate of such interactions is inh

285 us to apply principles derived from learning theory to understand the evolution of multi-dimensional

286 ntervention, aligned with self-determination theory, trained older adolescent mentors and in-class pe

287 Density functional theory was used to predict structural changes that occur

288 To adjudicate between theories, we must design experiments for which the theor

289 Using density functional theory, we assign the two states to two different perman

290 By means of a perturbative field theory, we derive relevant observables in closed form.

291 Using patch-use theory, we evaluated the rodents' risk-assessment from e

292 Using experiments and theory, we examine the effects of fluctuations, produced

293 Inspired by the evolutionary game theory, we formulated a bi-level optimization framework

294 ethods and quasi-classical and fully quantum theory, we found that a synchronous movement can occur d

295 Drawing on polymer theory, we use this change in lifetime to calculate ster

296 This calls for refinement of the theory which posits that to integrate the senses, the de

297 al systems engineering, and a neurocognitive theory with abstract representations of gist at its core

298 latter loop expansion produces an effective theory with cubic vertices.

299 Our model reconciles the metabolic theory with empirical observations of oxygen limitation

300 Our approach combines optimal mass transport theory with statistical pattern recognition.