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1 change and J approximately -290 cm(-1) (-2 J formalism).
2 fraction data within the superspace symmetry formalism.
3 e experiments, based on a mathematical graph formalism.
4 tributed data processing using the MapReduce formalism.
5 n and decision making suffers from a lack of formalism.
6 ation data using the Lipari-Szabo model-free formalism.
7 QSH) effect based upon the scattering matrix formalism.
8  epigenetic landscape through a mathematical formalism.
9  of salt concentration following homopolymer formalism.
10 aluate GB/interface resistance in a Landauer formalism.
11  primary current distribution using Newman's formalism.
12 l binding phenomenon based on an established formalism.
13  a Markov process using a recently developed formalism.
14  between species using combinatorial entropy formalism.
15 (red) and k(ox) predicted by the Marcus-Hush formalism.
16 des in a stoichiometric network, within this formalism.
17 d this apparently very different theoretical formalism.
18 erent approach based on a stochastic kinetic formalism.
19 be explained by a Henderson-Hasselbalch-type formalism.
20 auser effects were analyzed using model-free formalism.
21 c calculations were performed using the MIRD formalism.
22 determined using the Lipari-Szabo model-free formalism.
23 and created visual models using the L-system formalism.
24 c regulatory networks based on the Petri net formalism.
25 d analyze these results using the model-free formalism.
26  genetic network using the S-system modeling formalism.
27 (R(ex)) were obtained using the Lipari-Szabo formalism.
28 ransfer based on the Marcus-Hush (two-state) formalism.
29 n a generalization of the Shockley-Read-Hall formalism.
30 ion obtained by an appropriate thermodynamic formalism.
31 tions within the Green-Kubo phenomenological formalism.
32  terms of experiments and a Landau-de Gennes formalism.
33 waves via the parametrized diastolic filling formalism.
34 transport phenomena within a lattice kinetic formalism.
35  we explain by employing a Landauer-Buttiker formalism.
36 nequilibrium Schwinger-Kadanoff-Baym-Keldysh formalism.
37 nts and morphological outcomes using a graph formalism.
38 ay be untestable without behavioral economic formalisms.
39 ntation of connectomes by using graph theory formalisms.
40 ignificant differences are noted for the two formalisms.
41                                         This formalism allows spin-dependent parameters to be determi
42                                 The proposed formalism allows the transformation of glucose in the co
43                                       The EC formalism allows us to combine information entropy, ener
44 layer and demonstrate a rigorous theoretical formalism and analysis method for computing the induced
45 tion for stochastic effects, no well-defined formalism and associated special named quantities have b
46 alyzed in terms of the Lipari-Szabo dynamics formalism and compared to those of the wild type.
47 TFcP](2+) complexes were analyzed using Hush formalism and found to be of class II (in Robin-Day clas
48 an-field theories like the Poisson-Boltzmann formalism and its approximations, which are routinely us
49 ures are first illustrated by a coupled mode formalism and later verified by employing the Steady-sta
50 of the thermodynamic coupling function (TCF) formalism and Markov state model analysis to a 50-mus da
51 NMR", is based on a largely extended GFT NMR formalism and promises to have a broad impact on project
52 heoretical limitations of the authors' Dirac formalism and suggest the von Neumann open systems appro
53 els and point to potential advances in model formalisms and training procedures that promise to enhan
54 led with use of the Hansen-Coppens multipole formalism, and features associated with both intra- and
55 this work--two based on the generalized Born formalism, and one based on a Gaussian solvent-exclusion
56 rs was incorporated via a reaction-diffusion formalism, and this suggests that ROS may be the primary
57 efront the need for a well-defined dosimetry formalism applicable to deterministic effects that is ac
58     Mathematical formalisms based on a logic formalism are relatively simple but can describe how sig
59 ore properly described using the Marcus-Hush formalism are shown to yield incorrect values of k(0) an
60                                        These formalisms are mostly monotonic and are now known to be
61                              Two theoretical formalisms are widely used in modeling mechanochemical s
62 nalysis of RDCs and holds the classic tensor formalism as a special case.
63 the concept of surface plasmons, keeping the formalism as simple as possible by focusing on the quasi
64                              The Marcus-Hush formalism, as exposited by Chidsey, predicts that the va
65 nd were then used to generate a mathematical formalism based on general laws of the disease (i.e., di
66                                      A model formalism based on Voronoi construction is developed to
67                  We have developed a general formalism based on Wigner's original ideas concerning an
68                                 Mathematical formalisms based on a logic formalism are relatively sim
69                                 We outline a formalism, based on a modified Kalman smoother, for usin
70                              The theoretical formalism, based on stochastic path integral weights of
71                                 We develop a formalism, based on the mode expansion method, to descri
72    We illustrate the utility of the proposed formalism by analyzing simulations of unfolding-refoldin
73 electivity extends traditional thermodynamic formalism by including substrate-induced structural alig
74         Flow is determined with Kety-Schmidt formalism by modeling the uptake of gadolinium chelate i
75  can be described with the same mathematical formalism by replacing the electron-phonon coupling para
76 timation and model selection in the Bayesian formalism by using sequential Monte Carlo (SMC) approach
77 e including projector augmented wave (GIPAW) formalism calculations using periodic boundary condition
78 mputers, and (ii) the discovery of a quantum formalism called quantum crystallography and the use of
79 mputers, and (ii) the discovery of a quantum formalism called quantum crystallography and the use of
80 demonstrate how optimizers generated by this formalism can be faster and more effective, while remain
81                                         This formalism can be readily used to evaluate uncertainty in
82                                 The proposed formalism can be used in atomic force microscopy experim
83  Numerical calculations with a Butler-Volmer formalism can estimate the contribution to the OCP mixed
84                                          The formalism combines simulations for each of the relevant
85               We show that a state evolution formalism correctly derives the true sparsity-undersampl
86                                          The formalism covers a broad range of steady-state dynamical
87                          Such a mathematical formalism defines explicit mechanistic hypotheses about
88         Our calculations within the standard formalism demonstrate that the phonon-induced renormaliz
89 tive to tertiary structure, thus the current formalism demonstrates that the Amide I contour may be u
90 1 eV), which could not be predicted by using formalisms derived from effective medium theory.
91                            We show that this formalism derives directly from the physics of RDCs.
92  the Non-equilibrium Green's Function (NEGF) formalism, describe their basic features, and underline
93  approach, when combined with the analytical formalism described here, brings additional sensitivity,
94    The model generated in the bonded cumomer formalism describes key pathways of tumor intermediary m
95                         We present a general formalism describing an additive's tendency to trigger t
96 he exosome concentration in solution using a formalism describing diffusion-limited binding under con
97                                          The formalism developed here is also useful for multiscale f
98 simulate patterns of gene activities using a formalism developed to simulate patterns of memory in ne
99 cient of the redox species), the Marcus-Hush formalism effects a limiting current that can be signifi
100                                          The formalism elucidates the dramatic impacts of initial cel
101                        In the new rule-based formalism, every reactant and product pattern and every
102  Without additional evidence, however, these formalisms fail to explain why a decision-maker would ch
103 e automation is achieved by using a Bayesian formalism for all parameters of the model including the
104 ents show that the Monod, Wyman and Changeux formalism for allosteric proteins, originally developed
105 e of qualitative reasoning (QR) as a unified formalism for both tasks.
106                                 We provide a formalism for calculating the effects upon T2 of tissue
107  analysis within the framework of the Ramsey formalism for chemical shift.
108 ically coupled spiking neurons and present a formalism for computing the network statistics in a pert
109                            We provide here a formalism for dealing with such problems.
110                                    A general formalism for describing and analyzing these diverse sys
111 trode kinetics and the Michaelis-Menten (MM) formalism for enzymatic catalysis, with the BV model acc
112 ent of the protein homeostasis network and a formalism for how this network of competing pathways int
113 al line charges and with the order-parameter formalism for hydration forces.
114 , the sector constraints represent a general formalism for integrating omics data from any experiment
115 ls of polymers and the Poisson-Nernst-Planck formalism for ionic current.
116 orce field based on the charge-equilibration formalism for molecular dynamics simulations of phosphol
117             This article describes a general formalism for obtaining spatially localized ("sparse") s
118            We introduce a maximum likelihood formalism for separating signal from a drifting baseline
119 ysis, co-invented by Reinhart Heinrich, is a formalism for the analysis of biochemical networks, and
120 resent a DEG integration model as a powerful formalism for the analysis of drug-effect relationships
121 nding is modeled using the McGhee-von Hippel formalism for the cooperative binding of ligands to a mo
122 l model, which incorporates the Debye-Huckel formalism for the electrostatics, was used and found to
123  diffuse reflection data in the Kubelka-Munk formalism for the quantitation of contaminants in a comp
124 ive motor proteins, we develop a theoretical formalism for the randomness parameter, a dimensionless
125                                 We present a formalism for unifying the inference of population size
126          To do this we require computational formalisms for both simulation (how according to the mod
127                   Our approach is based on a formalism from machine learning called 'multitask learni
128  doses were calculated according to the MIRD formalism from small-animal PET/CT images.
129 well established branch of mathematics whose formalism has a vast range of applications from the soci
130 t dynamics of such models, relatively little formalism has been established.
131                                         This formalism has great flexibility, which we show by illust
132 l descriptions such as the Clausius-Mossotti formalism have been used to relate molecular polarizabil
133 a summary metric derived from the hypergraph formalism-hypergraph cardinality-we investigate individu
134                Using probabilistic inference formalisms, I show how all these approaches can be unifi
135            However, each code implements the formalism in a different way, raising questions about th
136 (BN) have been a popular predictive modeling formalism in bioinformatics, but their application in mo
137                       To do so, we develop a formalism in which high-dimensional configurations are n
138 volved with the advent of different modeling formalisms in systems biology and their ability to be ex
139                                          The formalism includes exact treatment of Maxwell's equation
140                                          The formalisms independently developed in the two areas for
141  Analysis of the data in terms of the Marcus formalism indicates that the human glutathione transfera
142 ent) makes coherent and incoherent tunneling formalisms indistinguishable when only one level partici
143 tructed in this paper through a mathematical formalism involving conditional Gaussian mixtures combin
144                            The Hilbert space formalism is a powerful language to express many cogniti
145                             The Mori-Zwanzig formalism is an effective tool to derive differential eq
146                                          The formalism is applied to simulated data obtained from a k
147 ion of the appropriate background theory and formalism is articulated before examining their biosensi
148                  Finally, the Hodgkin-Huxley formalism is central to computational neuroscience to un
149                            A grand canonical formalism is developed to combine discrete simulations f
150                                            A formalism is elaborated to evaluate cell-surface-bound,
151                                          The formalism is exact in that it does not involve any other
152                   The order statistics-based formalism is extended to cover the analysis of correlate
153                                          The formalism is illustrated using the alkaline-induced tran
154 del based on nonequilibrium Green's function formalism is introduced, which explains the observed Fan
155                              The random walk formalism is used across a wide range of applications, f
156                                   While this formalism is well established for amorphous (entropicall
157 alized plasmons and describe the theoretical formalism, its experimental validation and the potential
158     Given that, in a simple transition state formalism: k(u)=K(#)k' (where K(#) describes the equilib
159 idation state, and that the [N(3)](-)/Ru(II) formalism may be more informative.
160 e additional insights gained in the Bayesian formalism more than make up for this cost, especially in
161                               Moreover, this formalism naturally leads to an algorithm to parallelize
162 gle resource has focused on the prescriptive formalism of a necessary niche width and limiting simila
163                                          The formalism of adaptive dynamics reveals two evolutionary
164                        Using a network-based formalism of allostery, we introduced a community-hoppin
165 the electron density distribution within the formalism of Bader's theory (AIM method) reveal that in
166                                   We use the formalism of chemical reaction networks as a 'programmin
167 uid chromatography were studied based on the formalism of classical thermodynamics.
168                               A quantitative formalism of electrochemical surface plasmon resonance (
169                                    Using the formalism of hypergraphs, we identify the presence of gr
170 cal and experimental framework, based on the formalism of information theory, to quantitatively predi
171       In this work, we show how the abstract formalism of quantum theory can be deduced solely from t
172        The connections with the Mori-Zwanzig formalism of statistical physics are discussed, as well
173 ass of self-assembly problems, and using the formalism of stochastic thermodynamics, we derive a set
174  variational model in terms of a generalized formalism of the capillarity scaling theory that assumes
175         In addition, we present a projection formalism of the Mori-Zwanzig type that is applicable to
176 begin by summarizing the basic thermodynamic formalism of thermoelasticity.
177                    However, the mathematical formalism of these mechanisms makes them difficult to co
178 edictable using the preferential interaction formalism of Timasheff.
179 hich cannot be modeled with the conventional formalism of transmission matrices.
180 -linear Schrodinger equation and needs a new formalism of wave kinetics, developed here.
181                           This work develops formalisms of size-topology correlation that are very ge
182 matical representations (based on a discrete formalism) of biological regulatory mechanisms in a modu
183  the Onsager and Machlup action minimization formalism on each side of the transition, thus replacing
184                     On the basis of a recent formalism on the dynamics of metal uptake by complex bio
185 onditional Gaussian Bayesian network (CGBNs) formalism, one appropriate for predicting an outcome of
186 hese relations, in turn, are modeled using a formalism originally developed to treat electron and oth
187 cal modeling and employing the Fokker-Planck formalism, our mathematical analysis suggests that incre
188  was accounted for via the integral equation formalism polarizable continuum model (IEF-PCM) at the H
189 ctrode and a redox couple, the Butler-Volmer formalism predicts that the operative heterogeneous rate
190                                      Several formalisms propose that a representation of noisy eviden
191            Here we build on the mathematical formalism provided by QIT to formulate the quantum H-the
192                                          The formalism provides a mechanistic insight into electronic
193                                This flexible formalism provides an accessible approach for narrowing
194  New structural analysis methods, and a tree formalism re-define and expand the RNA motif concept, un
195 orrectly predicted by a simple thermodynamic formalism relating the oxidation potentials and pKa valu
196  combinations with the sum-over-states (SOS) formalism revealed that the enhancement is due to the st
197 l-free and reduced spectral density function formalisms revealed no evidence of contiguous stretches
198                                This modified formalism should be taken into account when designing ma
199 g RET was derived and an assay based on this formalism, spectral RET (sRET), was developed.
200                                The developed formalism stresses the importance of characterizing nons
201 hes have been widely used for reaction-based formalisms such as SBML.
202          Furthermore, RImmPort supports open formalisms, such as CDISC standards on the open source b
203 0.2 mM according to the Eyring and Arrhenius formalisms suggested that the quantum mechanical nature
204        We can accurately model them by a new formalism, taking into account both the gravity changes
205 ons based on the local-density-approximation formalism, taking into account Coulomb interaction U (LD
206 cal signal, we introduce here a mathematical formalism that (i) accounts for intrinsic changes that i
207 American Chemical Society, provided a simple formalism that allowed investigators to understand fluor
208  different functional phases of the cycle, a formalism that allows the model to be directly compared
209               Here, we develop a theoretical formalism that can accommodate diverse stimuli and behav
210 moothed l(1)-regularized logistic regression formalism that can be cast as a standard convex-optimiza
211                          Here we introduce a formalism that can generate optimizers automatically by
212 f allostery in the context of a quantitative formalism that can reconcile biochemical and biophysical
213 r monomeric alpha-synuclein using a Bayesian formalism that combines data from NMR chemical shifts, R
214         This paper summarizes the scientific formalism that created modern neurology, demonstrates ho
215 s are commonly analyzed using a site binding formalism that includes a parameter, the Hill coefficien
216 les; (b) it uses a parallel constraint-based formalism that is nondirectional; (c) it treats words an
217  HSM we try to propose a hybrid system based formalism that is still sufficiently powerful for descri
218                         Here I present novel formalism that more finely partitions the universe of po
219                  Using a recently introduced formalism that represents heterogeneous local Ca2+ using
220                                  The kinetic formalism that we discuss can describe the cotranslation
221 rectify this using an angular effective mass formalism that we have developed.
222 ified via the parametrized diastolic filling formalism that yields relaxation/viscoelastic (c) and pa
223 mbinatorial cis-regulation and in generating formalisms that accurately predict gene expression from
224 f all possible states and towards rule-based formalisms that allow for implicit model specification,
225  methods based on less effective statistical formalisms that are sensitive to spurious signals in the
226  FAIMS separations in mixtures, derived from formalisms that determine high-field mobilities in heter
227              According to the MIRD committee formalism, the mean absorbed dose to a target is given b
228   By using self-consistent six-band k.p band formalism, the nitride active region consisting of 30 A
229                     We present a concept and formalism, the string graph, which represents all that i
230 emented for the three popular types of model formalisms: the LSODA algorithm for ODE integration, the
231 ased systems is the knowledge representation formalisms they use.
232  addition, the potential utility of the same formalism to (1)H-(1)H cross-relaxation rates is conside
233 guities inherent in transferring the quantum formalism to a less determined realm.
234                       We apply the resulting formalism to a problem from molecular dynamics and show
235 ned with a self-consistent Poisson-Boltzmann formalism to account for ion charge screening in solutio
236 isotropic reorientational eigenmode dynamics formalism to analyze our simulation trajectories, we rep
237                   We applied a thermodynamic formalism to assess the effect of weakly interacting TM
238 choice of an appropriate clear thermodynamic formalism to be used by an interdisciplinary scientific
239 ticle, we use a multiscale nonlinear optical formalism to bring theoretical evidence that anisotropy
240                                We apply this formalism to compute the optimal parameters of low-thres
241                      We present the proposed formalism to construct coarse-grained potential models f
242 e we use the invariant variational bicomplex formalism to derive the first equilibrium equations for
243 y provide sufficiently powerful mathematical formalism to describe biological processes of interest a
244                    Here we present a kinetic formalism to describe cotranslational folding and predic
245 r dynamics simulations, and we propose a new formalism to describe edge functional groups.
246 suggests the adequacy of the Stokes-Einstein formalism to describe RAPs.
247              Here, we use the kinetic theory formalism to describe the dependence of the FRET efficie
248               In this paper we develop a new formalism to detect the equilibrium regimes of an unbran
249                 Here we present a mean-field formalism to estimate the packing density of axisymmetri
250 ng molecular dynamics with a master equation formalism to explain the steady drop in CO diffusion rat
251 an accurate and truly predictive theoretical formalism to explore this remote possibility when intens
252 al groups and thus it provides an ecological formalism to help interpret the present surge in microbi
253                                 We apply our formalism to models of the inositol trisphosphate recept
254  the Keldysh nonequilibrium Green's function formalism to obtain insight into the quantum dynamics of
255  algorithm that extends the Flory-Stockmayer formalism to overcome the limitations of analytic theori
256       We demonstrate the application of this formalism to paramagnetic relaxation enhancement vectors
257 -wise fitting approach, using a mathematical formalism to phenomenologically describe local calcium t
258 estable extension of the quantum probability formalism to psychophysical measures, such as detectabil
259                             The mathematical formalism to quantitatively describe the phenomena is al
260                  We used the Woodhull-Eyring formalism to rationalize the values measured for the ass
261                Here we develop a theoretical formalism to show that a three-dimensional topological i
262                  We use the product operator formalism to show that this oscillatory behavior arises
263               We propose a graph-theoretical formalism to study generic circuit quantum electrodynami
264 entalists, applications of the Butler-Volmer formalism to systems that are more properly described us
265                          We extend here this formalism to the case of the Abeta40 peptide, a 40-resid
266 nal protocol applying the binding polynomial formalism to the constant pH molecular dynamics (CpHMD)
267 dients, we extend the classic Hodgkin-Huxley formalism to uncover a unification of neuronal membrane
268 riment are harnessing the power of landscape formalisms to describe quantitatively the mechanics of f
269       In this work, we combine a logic-based formalism, to describe all the possible regulatory struc
270 periments is related, via the kinetic method formalism, to the enantiomeric composition of the chiral
271 rediction is derived by the Two-State-Vector-Formalism (TSVF) for a particle superposed over three bo
272                              The statistical formalism underlying our approach facilitates supervisin
273  discrete-time models show that the standard formalism used by population genetics ignores forced cha
274 ed with the reduced spectral density mapping formalism using assumed values of the chemical shift ani
275 ted based on 111In imaging data and the MIRD formalism using patient-specific organ masses determined
276                                            A formalism was developed to consistently parameterize the
277                                        Jones formalism was extended to nonlinear optics and was used
278                                   Using this formalism we derive results connecting the stability of
279                                    Thus, the formalism we develop is suitable for describing and pred
280                                       The QR formalism we use is an abstraction of ODEs.
281               Using the generating functions formalism, we analytically solve all the models in the l
282                                   Using this formalism, we analyze 15 empirical fitness landscapes of
283         By resorting to an expanded-ensemble formalism, we are able to determine the free energy requ
284       By adopting a hidden-dynamical-systems formalism, we expressed parameter estimation as an infer
285                        Using a Fokker-Planck formalism, we find no evidence for a feedback mechanism
286         Utilizing the matched molecular pair formalism, we have analyzed patterns of compound promisc
287 oying a plane-wave density functional theory formalism, we investigate the dielectric response of hig
288 operative transition following heteropolymer formalism, whereas secondary structure formation takes p
289 um entropy principle to derive a tensor-free formalism which allows for direct, dynamic analysis of R
290 laxation data is analyzed using a model free formalism which takes into account the very high anisotr
291                                         This formalism, which can also be extended to the flowing ins
292 he structures are estimated using a Bayesian formalism, which provides measures of uncertainty in the
293 ons by combining the standard quasi-chemical formalism with a detailed-balance description that is ap
294 ocess that combines a recombination modifier formalism with a gene-regulatory network model.
295 k that combines the standard genetic linkage formalism with whole-genome molecular-interaction data t
296 species in solution were computed using both formalisms with the Oldham-Zoski approximation.
297                                         This formalism, with its consequent reinforcement and/or inte
298 ed PC12 cells) in light of the heterogeneous formalism yielded independent estimates for the associat
299  be fitted with a Henderson-Hasselbalch-type formalism, yielding pK(a)(2) values of 6.96 +/- 0.04 and
300 he RP equation with CNT based on the Kramers formalism yields an analytical expression for the cavita

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