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1 s were analyzed in comparison with available experimental data.
2 resource models of ecosystems is suitable to experimental data.
3 est compounds and agreed reasonably with the experimental data.
4 on of the final morphology in agreement with experimental data.
5 ults, and then computer simulations based on experimental data.
6 integrates inference from these models with experimental data.
7 onstrate that there is a good agreement with experimental data.
8 ides an improved fit to previously published experimental data.
9 l) have not been sufficiently validated with experimental data.
10 with relaxed lattice constants matching the experimental data.
11 (NS) and cryo-electron tomography (cryo-ET) experimental data.
12 ics and isotherms were evaluated against the experimental data.
13 ons of our theory were in agreement with the experimental data.
14 ombining molecular dynamics simulations with experimental data.
15 solve a conflict between different types of experimental data.
16 y than the static one for both synthetic and experimental data.
17 nty sites, and found good agreement with the experimental data.
18 , restricting analysis and interpretation of experimental data.
19 is further refined by being trained with the experimental data.
20 ges have practical implications for relevant experimental data.
21 et engagement and equilibrium constants from experimental data.
22 alues were then computed and compared to the experimental data.
23 The values for model A were consistent with experimental data.
24 odel parameters were assessed from published experimental data.
25 was assessed through a set of simulated and experimental data.
26 Theoretical calculations help supporting the experimental data.
27 using an advanced physical model to the fit experimental data.
28 ing high throughput experiments on available experimental data.
29 gans, five of which are already supported by experimental data.
30 veloped and parameters aligned with previous experimental data.
31 required for the accurate description of the experimental data.
32 er of breeding birds using observational and experimental data.
33 , and the results obtained nicely agree with experimental data.
34 ors are in excellent agreement with existing experimental data.
35 ic reproductive number, R(0), estimated from experimental data.
36 to perform docking studies rationalizing the experimental data.
37 us that is calibrated with existing in vitro experimental data.
38 (TE) was shown to be associated with UOC in experimental data.
39 nation of computational results with certain experimental data.
40 tools necessary to apply this perspective to experimental data.
41 imensional parameters, which agree well with experimental data.
42 differences between them and to support the experimental data.
43 rmance in a simulation study and apply it to experimental data.
44 apacitive currents, combining simulation and experimental data.
45 the molecular structure without the need for experimental data.
46 rmined by fitting mathematical models to the experimental data.
47 ty and infer tumor evolutionary history from experimental data.
48 g dynamics of biological systems from sparse experimental data.
49 to uniquely correlate with several types of experimental data.
50 half octave below CF, in accordance with the experimental data.
51 uare lattice provide the best agreement with experimental data.
52 functional theory (DFT) to compare with the experimental data.
53 erimental apparatus, for comparison with the experimental data.
54 mostly literature data supplemented with new experimental data.
55 iagnostic differences between calculated and experimental data.
56 that generates root anatomical networks from experimental data.
59 It is shown that the models reproduce the experimental data accurately, indicating that both of th
61 results in reasonable accord with available experimental data, after correcting for differences in n
62 position, and demonstrate its application on experimental data aimed at the determination of four pol
67 transducing mechanical signals, we combined experimental data and computational simulations to evalu
69 was to provide clinical translation to these experimental data and determine if DAP+BL combination th
71 been rationalized based on a combination of experimental data and DFT calculations, which suggests t
72 ary flow model revealed great alignment with experimental data and greater correlation to viscosity t
73 ach presents a promising avenue to integrate experimental data and make regional-scale predictions of
75 range of viscoelastic solids for predicting experimental data and responses with improved accuracy.
76 roperties of a-Si that match accurately with experimental data and rival that of the Wooten-Winer-Wea
77 onal simulations of a model system match the experimental data and show how these methods can be adap
80 of the presented numerical platform against experimental data and then results and discussion, highl
83 anner, we apply topological data analysis to experimental data and to results of our numerical simula
84 We have validated the model with independent experimental data and used it to investigate how and to
85 loped models were successfully fitted to the experimental data and used to determine optimal extracti
86 ce input-output transformations that matched experimental data and were poor mediators of intensity-d
87 generating a surrogate model to interpolate experimental data, and a corresponding uncertainty model
88 ctions for the generation of ensembles using experimental data, and extending constraint-based analys
89 to quantify cross-feeding interactions from experimental data, and highlights the importance of meta
90 a birth-death model with both synthetic and experimental data, and show that we can robustly infer m
91 represent novel parcellations resulting from experimental data, and we provide a proof-of-concept for
93 two approaches, the similarities between the experimental data are assessed by means of the Euclidean
96 t the brain's fluid transport systems, where experimental data are lacking, and what is still debated
98 uding limitations of the currently available experimental data as well as potential strategies for ad
99 and rural Uganda, through correlational and experimental data, as well as an instrumental variable a
100 nscript quantification in both simulated and experimental data, as well as the effect on subsequent d
101 ears of observational data from 71 sites and experimental data at 10 sites, we tested two predictions
102 r mechanistic picture is consistent with the experimental data available for Delta(9)D and satisfies
103 ns were performed to support and explain the experimental data based on the predicted physicochemical
105 al network simulations, until further direct experimental data become available.SIGNIFICANCE STATEMEN
107 onceptual framework to integrate and analyze experimental data, but also making testable predictions.
109 Our analysis demonstrates how small-scale experimental data can be leveraged to derive expectation
110 he shift in mEPSC amplitudes observed in the experimental data cannot be reproduced by simulation of
111 to link predictive modeling results with the experimental data characterizing the behavior of the lab
113 ontrolled approach for handling metadata and experimental data collection, collation and linkage in t
115 erved leucine-rich nuclear export signal and experimental data confirmed BEX3 nucleocytoplasmic shutt
116 This integrated model captures all available experimental data connecting the cell proteome compositi
120 The scattering matrix we obtain from the experimental data delivers an ultra-sensitive benchmark
129 (SSD) for thermal stress based on published experimental data for 41 tropical benthic marine species
130 hanges, the same model can also recapitulate experimental data for a different PRE/TRE that allows dy
132 RosettaDEER can effectively leverage sparse experimental data for a wide array of modeling applicati
135 % and (iii) the structural interpretation of experimental data for dynamic RNAs is highly complex, ev
137 demonstrate that RosettaDEER leverages these experimental data for protein fold prediction more effec
138 In each of the spectroscopic methods used, experimental data for the (-)-enantiomer of tert-butylph
139 two models by downhill simplex runs against experimental data for the force-velocity relation and th
141 nd accuracy, and 3) integrate simulation and experimental data for training disparate datasets to lea
144 e applied the combined denoising on a set of experimental data from a lysozyme-silica composite.
145 larly those regarding fats, accord both with experimental data from animals and within-country epidem
146 its six empirical parameters only once using experimental data from any single S(h), and the same set
148 is competition and validated the theory with experimental data from continuous cultures reported in t
150 nd death, all of our knowledge is based upon experimental data from domestic livestock and laboratory
151 e medicine aspects of vitiligo and AA, using experimental data from human, mouse, and in vitro models
152 ld electrospinning (FFES), together with our experimental data from near-field electrospinning (NFES)
154 es of ART on simulated data sets, as well as experimental data from real metabolic engineering projec
156 s-based C models by comparing simulations to experimental data from seven long-term bare-fallow (vege
162 e metadata collection and linkage of related experimental data generated locally by vendor software.
164 ntral for enzyme function, but a scarcity of experimental data has limited our understanding of posit
165 cidence in patients with interferonopathies, experimental data have attested that type-I IFNs affect
168 s crucially on the amount and quality of the experimental data, how it is integrated, and if it suppo
170 i) an unprecedented tight quality control of experimental data, (ii) the automated identification of
172 olated limit of detection of 2.2 CFU/ml from experimental data in buffer solution with no sample prep
175 re reference compounds or large databases of experimental data in related systems and thus can be app
176 The simulation results are validated with experimental data in terms of Single Strand Break (SSB)
178 namics and coupling by interpreting in-vitro experimental data in which the speed of onset can be che
179 il to model and analyse the full spectrum of experimental data, in the statistical power of QTL detec
186 ogeneous components; the wealth of available experimental data is scattered among multiple resources
187 The model, which is supported by existing experimental data, is analyzed using Markov state models
188 corrected PSF images, for both simulated and experimental data, lead to a substantial improvement in
189 ically predicted data with the corresponding experimental data led to the elucidation of the absolute
190 /LC Simulator software and corroborated with experimental data match (overall retention time differen
191 es MassIVE.quant to systematically store raw experimental data, metadata of the experimental design,
193 vanovic isotherm model fitted the adsorption experimental data most with the highest correlation (R(2
194 omes which is, based on human infections and experimental data, now considered a zoonotic pathogen.
195 in structure is inconsistent with all of our experimental data obtained with the wild-type sequence.
196 The predicted quantities were compared with experimental data obtained within this study or publishe
197 application also demonstrates agreement with experimental data of [Formula: see text]-H2AX yields for
199 have optimized the algorithms and reanalyzed experimental data of DNA polymerase I diffusing in live
200 parametrized for anionic SNPs and applied to experimental data of four IDP systems with distinctive b
201 to reproduce several qualitative features of experimental data of histone methylation spreading aroun
202 We benchmark our tools against simulated and experimental data of proteins with multiple conformation
203 onstrate this approach on simulated data and experimental data of the kinase Csk and the adaptor PAG
206 acterize the SND conditions by incorporating experimental data on AF-induced electrical remodelling,
208 understanding of this factor is crucial for experimental data on disease modifiers and their transla
210 KS oligosaccharide-loaded galectins support experimental data on Gal-3 and -7, and extend the scope
212 ur derivation results with computational and experimental data on mutant protein stabilities across a
214 Pitx2-knockout atria by incorporating recent experimental data on Pitx2-induced electrical and struct
219 tinuous enzyme kinetic traces resulting from experimental data on the response of the protein lysine
220 ces in estimations are due to differences in experimental data or due to methodological differences.
222 sed studies can aid in the interpretation of experimental data or provide a spark for the discovery o
224 ragg-Williams approximation) to describe the experimental data over a wide range of acetone partial p
229 lexity bottleneck, with quantitative fits to experimental data rapidly becoming computationally intra
231 etailed ab initio calculations, supported by experimental data, render a substantially different mode
233 e 200 ns simulations, validated by available experimental data, reveal processes and mechanisms by wh
235 s of antibiotics and to generate the largest experimental data set of selective effect concentrations
237 , respectively, were trained using the large experimental data set, which enabled the generation of a
238 trained network has been applied to the real experimental data sets from a neutron grating interferom
241 RNA has adopted its tertiary structure, new experimental data show that L11 binds to Mg(2+)-dependen
245 ture, and sympathetic nervous system, recent experimental data suggest that immune cells may play a r
248 e fork geometry was more consistent with the experimental data, suggesting the utility of fork classi
249 ing calculations corroborate and explain the experimental data, suggesting this novel scaffold can be
250 confirmed to be mediated by ion channels and experimental data suggests an insignificant thermal cont
256 view goes through the available clinical and experimental data supporting a role for cardiac lymphati
258 blem to infer accurate Boolean networks from experimental data that are typically short and noisy.
259 cular basis of telomeropathies and highlight experimental data that illustrate how genetic mutations
261 igher affinity for zinc than the monomer and experimental data that suggest coordination in the dimer
262 g reaction kinetics parameters obtained from experimental data, theoretical correlations, and quantum
263 ificance: Merging mathematical modeling with experimental data, this study presents the "TRAMP-based
266 dels were sequentially built and adjusted to experimental data to describe changes in concentration i
267 putationally fitted a continuum model to our experimental data to generate physics-based parameters t
268 cally detailed manner using a diverse set of experimental data to interpret and explain experimental
272 d demonstrate the utility of high-throughput experimental data to refine in silico hiPSC-CM populatio
273 ral bonding orbital analyses correlated with experimental data to reveal the contexts in which short-
278 a decrease in recombinase expression and new experimental data was generated that confirms this relat
280 Based on multiple sources of complementary experimental data, we constructed a spatial model of a H
281 directly fitting a mechanistic model to our experimental data, we demonstrate that the RAD51 polymer
283 By comparing with ground truth data and experimental data, we demonstrated that SMIS is useful t
285 of interglomerular connectivity derived from experimental data, we find that SAC networks, despite th
286 While tuning these networks to recapitulate experimental data, we identified rules governing cell-cl
288 by fitting a hidden Markov model of EMT with experimental data, we propose a statistical mechanism fo
293 tably-logistic models failed to describe the experimental data whereas the Gompertz model generated v
295 -state NMR spectroscopy, and augmented these experimental data with all-atom molecular dynamics simul
296 both allows learning materials physics from experimental data with associated uncertainty quantifica
297 with the invariance properties, we compared experimental data with computational modeling results.
299 binding can be learned from high-throughput experimental data without the need for target structural