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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.
57                   Through the calculation of experimental data, 3D local resolution evaluation algori
58                         By cross-referencing experimental data, a good selectivity (up to 66%) for on
59    It is shown that the models reproduce the experimental data accurately, indicating that both of th
60                                          The experimental data acquired in this study revealed not on
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
63                                              Experimental data also demonstrate the ability for all o
64  appropriate parameter choices and (iv) post-experimental data analysis.
65                    Our model is validated by experimental data and allows predicting the phase change
66 database for metabolomics studies, their raw experimental data and associated metadata.
67  transducing mechanical signals, we combined experimental data and computational simulations to evalu
68           DFT calculations fully support the experimental data and demonstrate the crucial roles of t
69 was to provide clinical translation to these experimental data and determine if DAP+BL combination th
70                We further show, by combining experimental data and DFT calculations, as a proof of co
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
74                    Our method relies only on experimental data and might be of wide application and i
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
78                                          The experimental data and simulation results suggest that me
79                        Taken together, these experimental data and simulations indicate that the heli
80  of the presented numerical platform against experimental data and then results and discussion, highl
81                                              Experimental data and theoretical calculations are in go
82                                         Both experimental data and theory modeling show that the peri
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
92                                              Experimental data are analyzed using general time course
93 two approaches, the similarities between the experimental data are assessed by means of the Euclidean
94 xotic materials properties, but little to no experimental data are available on these materials.
95                                              Experimental data are consistent with a mechanism in whi
96 t the brain's fluid transport systems, where experimental data are lacking, and what is still debated
97                                  Using these experimental data as restraints, we adopted an integrati
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
104                  Analytical modelling of the experimental data, based on Hill-Langmuir adsorption cha
105 al network simulations, until further direct experimental data become available.SIGNIFICANCE STATEMEN
106 the robustness of REDCRAFT in utilizing less experimental data both in quality and quantity.
107 onceptual framework to integrate and analyze experimental data, but also making testable predictions.
108              Thus, a vast amount of valuable experimental data can be acquired, which can help in und
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
112 undle, and we compare these constraints with experimental data collected from the literature.
113 ontrolled approach for handling metadata and experimental data collection, collation and linkage in t
114                                              Experimental data comprised three animal models of breas
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
117                                          The experimental data constructed to test this hypothesis sh
118           SSIPe was evaluated on large-scale experimental data containing 2204 mutations from 177 pro
119                                              Experimental data corroborated by theoretical calculatio
120     The scattering matrix we obtain from the experimental data delivers an ultra-sensitive benchmark
121                                 The obtained experimental data demonstrate a highly sensitive and rel
122                                              Experimental data demonstrated a significantly higher (P
123                     Stochastic modelling and experimental data demonstrated the feedback loop to act
124                                              Experimental data demonstrated ~ 8.5 psi is the threshol
125       The models were validated by analyzing experimental data demonstrating the effects of agonists
126                             In line with the experimental data, during concurrent 4-AP therapy, degen
127                         More than one set of experimental data, each related to a specific stereoisom
128 plain the observed potential transients, and experimental data fit theory well.
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
131                                              Experimental data for a variable path length (0-60 mm) H
132  RosettaDEER can effectively leverage sparse experimental data for a wide array of modeling applicati
133 on is accurately obeyed over a wide range of experimental data for aluminum and copper.
134             Here we show that a large set of experimental data for different rocks can be described b
135 % and (iii) the structural interpretation of experimental data for dynamic RNAs is highly complex, ev
136        An IKs computational model was fit to experimental data for each mutation, and the impact of e
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
140                               By fitting the experimental data for the length-diameter dependence to
141 nd accuracy, and 3) integrate simulation and experimental data for training disparate datasets to lea
142 notechnology research has generated numerous experimental data for various nanomaterials.
143                    In addition, we deposited experimental data for ~ 2500 compounds in the PubChem bi
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
147                                              Experimental data from atomic force microscopy single-mo
148 is competition and validated the theory with experimental data from continuous cultures reported in t
149 ding of 27 drugs and compared the results to experimental data from conventional methods.
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)
153                            In the absence of experimental data from physiologically relevant animal m
154 es of ART on simulated data sets, as well as experimental data from real metabolic engineering projec
155 ramagnetic resonance experiments and analyze experimental data from recent literature.
156 s-based C models by comparing simulations to experimental data from seven long-term bare-fallow (vege
157            Our theoretical model matches the experimental data from the water window to the keV x-ray
158                        Using simulations and experimental data from three different types of memristi
159               After calibrating the model on experimental data from two circuits, we demonstrate clos
160                                              Experimental data from various microbial fuel cell studi
161                     Fitting the model to the experimental data gave an association constant (K(A)) of
162 e metadata collection and linkage of related experimental data generated locally by vendor software.
163              Application of best practice in experimental data generation and predictive methodologie
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
166                                              Experimental data have identified the modulation of inna
167                                              Experimental data have proved that GORE-TEX has a 2.5-fo
168 s crucially on the amount and quality of the experimental data, how it is integrated, and if it suppo
169                  Simulations and analysis of experimental data identified a moving median filter as a
170 i) an unprecedented tight quality control of experimental data, (ii) the automated identification of
171                          Epidemiological and experimental data implicate cutaneous human papillomavir
172 olated limit of detection of 2.2 CFU/ml from experimental data in buffer solution with no sample prep
173 ties of the LFTFs are derived from available experimental data in literature.
174 e features of this work is that it relies on experimental data in reaction rate computations.
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)
177 logy annotations that were obtained from the experimental data in the literature.
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
180                                 Modeling and experimental data indicate that scaling relies on the co
181                                      Current experimental data indicates that RAGE is a critical medi
182                                          The experimental data indicates the behavior of 4 and P towa
183 plague locust, for which excellent field and experimental data is available.
184 ccur through larger rearrangements, but here experimental data is extremely limited.
185 del that can predict NN thermodynamics where experimental data is scarce or absent.
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,
192             However, when informed by mosaic experimental data model predictions greatly vary illustr
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
198           It was validated using preclinical experimental data of antibody-mediated (213)Bi and (225)
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
204                                          New experimental data of the size-dependence of particle vis
205                                  We analyzed experimental data on 183 unique single point mutations t
206 acterize the SND conditions by incorporating experimental data on AF-induced electrical remodelling,
207                            A comparison with experimental data on bacteria allows us to evaluate the
208  understanding of this factor is crucial for experimental data on disease modifiers and their transla
209                                          Our experimental data on E. coli liquid cultures demonstrate
210  KS oligosaccharide-loaded galectins support experimental data on Gal-3 and -7, and extend the scope
211                             Validation using experimental data on miRNA-disease associations demonstr
212 ur derivation results with computational and experimental data on mutant protein stabilities across a
213 tions of existing methods in species without experimental data on PAS.
214 Pitx2-knockout atria by incorporating recent experimental data on Pitx2-induced electrical and struct
215                                        While experimental data on the boundaries of membrane-embedded
216                    A new model to synthesize experimental data on the effects of transfluthrin on Aed
217                                  However, no experimental data on the identity of complexes related t
218                  The expression captures the experimental data on the LFP for different fluids under
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.
221                                  However, no experimental data or models define the binding mode of T
222 sed studies can aid in the interpretation of experimental data or provide a spark for the discovery o
223                          Consistent with the experimental data, our complementary first-principles DF
224 ragg-Williams approximation) to describe the experimental data over a wide range of acetone partial p
225 488 growth conditions corresponding to 3,221 experimental data points were simulated.
226                                        Novel experimental data presented here validates our model, wh
227                The published high-throughput experimental data provide an opportunity to analyze posi
228 ree-dimensional structures associated to the experimental data provided by Hi-C maps.
229 lexity bottleneck, with quantitative fits to experimental data rapidly becoming computationally intra
230       Traditionally, methods to analyze such experimental data rely on tracking embedded or endogenou
231 etailed ab initio calculations, supported by experimental data, render a substantially different mode
232                                              Experimental data reveal that the CIE coordinates within
233 e 200 ns simulations, validated by available experimental data, reveal processes and mechanisms by wh
234                Additionally, analysis of the experimental data reveals 29 cases of cross-stress prote
235 s of antibiotics and to generate the largest experimental data set of selective effect concentrations
236                    Here, we obtain a diverse experimental data set of the Ebola virus infection in vi
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
239  the applicability of these methods to three experimental data sets.
240                                              Experimental data show that between 95% (4-iodophenol) a
241  RNA has adopted its tertiary structure, new experimental data show that L11 binds to Mg(2+)-dependen
242                              CLT is based on experimental data showing that psychologically distant e
243                  Our results closely reflect experimental data, showing that small founding populatio
244 model accounts for the phenotypes of several experimental data (single and multiple mutations).
245 ture, and sympathetic nervous system, recent experimental data suggest that immune cells may play a r
246                                              Experimental data suggest that IRE ablation produces lar
247                                              Experimental data suggest that sugars could play a role
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
251         Agreement with such a diverse set of experimental data suggests that details of the generated
252                                          Our experimental data support a model in which SurA binds uO
253                                              Experimental data supported major predictions of the eff
254                                    These new experimental data, supported by computational and cataly
255                                          The experimental data, supported by simulations, establish a
256 view goes through the available clinical and experimental data supporting a role for cardiac lymphati
257                 However, there is no in vivo experimental data supporting these two theoretical predi
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
260              We then re-analysed a subset of experimental data that included only ecologically realis
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
264  and were found to be in good agreement with experimental data, thus corroborating our method.
265                                  Fitting the experimental data to a NEURON model revealed that the sp
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
269                    Here we provide the first experimental data to investigate the capacity of SARS-Co
270                                  We compared experimental data to mathematical models of spreading me
271 ted promoter states are fit by comparison of experimental data to model predictions.
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-
274        However, there are some contradictory experimental data to this assumption.
275 a workflow for the robust fitting of OMAM to experimental data using derived equations.
276                               We analyze the experimental data using single-cell tracking to calculat
277                                              Experimental data was generated by Definitive-Screening-
278 a decrease in recombinase expression and new experimental data was generated that confirms this relat
279                                         This experimental data was used to validate a numerical model
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
282                     Using both simulated and experimental data, we demonstrate that these advances al
283      By comparing with ground truth data and experimental data, we demonstrated that SMIS is useful t
284             Comparing simulation results and experimental data, we determine the Poisson ratio of the
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
287                      Using recently acquired experimental data, we present and validate a computation
288 by fitting a hidden Markov model of EMT with experimental data, we propose a statistical mechanism fo
289                     Using both simulated and experimental data, we show that this model improves both
290                                 Based on our experimental data, we suggest structural models for the
291                                              Experimental data were further compared with the couplin
292                                          The experimental data were integrated in a mathematical mode
293 tably-logistic models failed to describe the experimental data whereas the Gompertz model generated v
294                     Computations support the experimental data, which indicate that it is necessary t
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.
298                                 By combining experimental data with predictions from models we descri
299  binding can be learned from high-throughput experimental data without the need for target structural
300                    Optimizing the model with experimental data yields conformational protection as we

 
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