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1 t the surface diffusion coefficient from the mean square displacement.
2  impose tortuosity within the diffusion root mean-square displacement.
3 the high q data were interpreted in terms of mean square displacements.
4 ionally relies on calculating the trajectory mean squared displacement.
5 on that can fit experimental measurements of mean-square displacements.
6 lated the propagation of these errors on the mean-squared displacement.
7 ble surface area (4.09 +/- 0.04 nm) and root mean square displacement (3.51 +/- 0.00261 nm).
8 itatively predicts the rapid increase of the mean-square displacement above approximately 200 K, show
9                                The extracted mean square displacements also reveal a greater motional
10                           We show that image mean square displacement analysis, applied to single pla
11                                              Mean-square displacement analysis of individual trajecto
12 ct on confined molecules because the typical mean-square-displacement analysis does not account for t
13 showed anomalous diffusion, as determined by mean-square-displacement analysis.
14 le quantification of the "hard corona" using mean-squared displacement analysis.
15 s unveiled by the confidence interval of the mean square displacement and by the dynamical functional
16 tin dynamics in real time and determined the mean square displacement and diffusion constant for the
17 ants were determined from linear fits to the mean square displacement and from the mean displacement
18                                     The root mean square displacement and the corresponding absolute
19 sults closely matching experimental plots of mean square displacements and probability density functi
20                             By comparing the mean squared displacement and the response function we d
21 , picosecond timescale, small changes in the mean-square displacement and <k'> are observed, which ar
22 hat captures the power law dependence of the mean-square displacement and can be shown to rigorously
23 ormational space is examined in terms of the mean-square displacement and principal component analysi
24                                              Mean-square displacements and protein resilience on the
25 at equivalent hydration level, GFP dynamics (mean-square displacements and quasielastic intensity) ar
26 ions or nanoparticles in mucus have measured mean-square displacements and reported diffusion coeffic
27  of glassy dynamics, such as plateaus in the mean-squared displacement and the self-intermediate scat
28 hat ensemble-averaged quantities such as the mean-squared displacements and velocity autocorrelation
29 s that includes trajectories, motile speeds, mean squared displacement, and turning angles-while prov
30                       Correlation functions, mean squared displacements, and velocity distributions r
31 re analyzed to yield interaction potentials, mean-square displacements, and colloid-surface associati
32 lowed us to achieve higher resolution in the mean-squared displacement, and thus to increase the accu
33 combine this analysis with the image-derived mean-square displacement approach and gain information o
34 rrors in interparticle separation, angle and mean square displacement are significantly reduced by ap
35                                          The mean square displacements are well described by a stocha
36                          Our results for the mean-square displacement are consistent with a recent ex
37 ega is the frequency, (ii) shear modulus and mean-squared displacement are inversely proportional wit
38 ort and the related anomalous scaling of the mean-squared displacement are regulated by cytoskeleton
39 n averaging of the displacements such as the mean square displacement, are not adapted to the analysi
40  theory is a sigmoid curve of the observable mean square displacement as a function of the ratio of d
41 cales and 2) their inversion to retrieve the mean-squared displacement associated with the process un
42 and also yields the correct amplitude of its mean square displacement at long times.
43 in the gradient with T of the average atomic mean-square displacement at approximately 220 K.
44 alization errors in the determination of the mean-squared displacement by separating the sources of t
45 ent technique applies the calculation of the mean square displacement commonly used in single-molecul
46                                          The mean-squared displacement correlation with time lag had
47 revealed a previously unreported grouping of mean-squared displacement curves at short timescales (<1
48 Average diffusion coefficients obtained from mean square displacement (D(MSD)) data were 20-100% larg
49 als that, in the absence of a net force, the mean squared displacement depends on time as t(0.7), in
50 e of the cell migration, such as cell speed, mean-squared displacement, diffusivity, persistence, spe
51                Anomalous diffusion, in which mean squared displacement does not increase linearly wit
52 iting factors that alter the accuracy of the mean-squared displacement estimation.
53 moved with significantly higher subdiffusive mean square displacement exponents than previously repor
54 an order of magnitude over the perpendicular mean-square displacements for both surfaces.
55         For 28 computed structures, the root mean squared displacement from the average structure exc
56 denotes random molecular motion in which the mean square displacements grow as a power law in time wi
57      The movement is superballistic with the mean square displacement growing with time as [Formula:
58 opulations has shown evidence of diffusion - mean squared displacements growing linearly in time - an
59              We calculate an imaging-derived Mean Squared Displacement (iMSD), which simultaneously p
60 ge Correlation Spectroscopy (RICS) and image-Means Square Displacement (iMSD) were applied to quantif
61 ed from the temperature dependence of atomic mean-squared displacements in molecular dynamics simulat
62  higher diffusion coefficient, and increased mean-squared displacements in neutron scattering experim
63  give both the rate at which single-particle mean square displacements increase and the rate at which
64  reveal unusual Brownian motion in which the mean square displacement increases as a fractional power
65                  In classical diffusion, the mean-square displacement increases linearly with time.
66 ch media foster anomalous subdiffusion (with mean-squared displacement increasing less than linearly
67  anomalous diffusion may occur, in which the mean-square displacement is proportional to a nonintegra
68 ents using single-particle tracking in which mean-square displacement is simply proportional to time
69 oves with a constant intermediate speed, the mean-square displacement is strongly enhanced.
70 meters and compute key observables-including mean square displacement, kinetic energy, potential ener
71 fusion models defined by arbitrary nonlinear mean-squared displacement &lt;x2> versus time relations.
72 h fluids are differentiated by measuring the mean-squared-displacement &lt;Deltar(2)> of embedded tracer
73 t exposure levels are very low and the image mean square displacement method does not require calibra
74 and dynamic properties often evaluated using mean square displacement (MSD) analysis.
75 alyses of random walks traditionally use the mean square displacement (MSD) as an order parameter cha
76                        The ensemble-averaged mean square displacement (MSD) exhibits superdiffusive b
77  of the mixtures were investigated using the mean square displacement (MSD) of the centers of mass of
78           A three-stage dynamics governs the mean square displacement (MSD) of water molecules, with
79                           The combination of mean squared displacement (MSD) and cumulative distribut
80 so predicts the subdiffusive behavior of the mean squared displacement (MSD) on short, intermediate t
81 y densifying glass and measure the resulting mean squared displacement (MSD).
82 of particles in mucus, based on the measured mean squared displacements (MSD).
83 ansient subdiffusive temporal scaling of the mean-square displacement (MSD proportional, variant tau
84                                 Conventional mean-square displacement (MSD) analysis of single-partic
85                                      A local mean-square displacement (MSD) analysis separates ballis
86 lding/nonfolding dynamics is examined by the mean-square displacement (MSD) and the fractional diffus
87 usion at short timescales (t<7 s) with their mean-square displacement (MSD) Deltax(t)2 scaling as t1.
88 nserved waters reflected substantially lower mean-square displacement (msd) in all simulations, excep
89 mpare the distribution of the time-dependent mean-square displacement (MSD) of polystyrene microspher
90 es inside the cell from a tracked particle's mean-square displacement (MSD).
91               Here, we demonstrate, by using mean-square displacements (msd) from Mossbauer and neutr
92 iculate trajectory data have been limited to mean-squared displacement (MSD) analysis.
93 ion and 30Hz temporal resolution, from which mean-squared displacement (MSD) and viscosity distributi
94 urth equation, the usual characterization of mean-squared displacement (MSD) curves for migrating cel
95                                              Mean-squared displacements (MSD) and protein resilience
96 lective scattering significantly affects DWS mean-square displacements (MSDs) in dense colloidal emul
97  alpha, which is typically obtained from the mean-square displacements (MSDs).
98 ion rate constant is shown to scale with the mean square displacement of a receptor-ligand complex.
99  agonist activation resulted in a decline in mean square displacement of both receptors, but the drop
100                                Analyzing the mean square displacement of GFP intensity changes in liv
101 pond to the calculation of a certain kind of mean square displacement of the animals relevant to the
102                        Finally, the measured mean square displacement of the optical probes, which is
103  backscattering spectroscopy showed that the mean square displacements of H atoms do exhibit an incre
104 g passive microrheology via videomicroscopy, mean square displacements of tracer particles suspended
105 riterion to fail in 2D in the sense that the mean squared displacement of atoms is not limited.
106 m might be "anomalous" in the sense that the mean squared displacement of particles follows a power l
107 average particle dynamics, quantified by the mean squared displacement of the individual particles, a
108 by the extent and time-lag dependence of the mean squared displacements of thermally excited nanopart
109                      The distribution of the mean squared displacements of these microspheres becomes
110 with a correlation length of 10 A and a root-mean-square displacement of 0.36 A.
111  shows no orientation preference over a root mean-square displacement of 2.5-3.5 microm.
112                   At intermediate times, the mean-square displacement of a diffusing object shows a t
113 diffusion is hindered diffusion in which the mean-square displacement of a diffusing particle is prop
114 eir "native" states, we demonstrate that the mean-square displacement of dihedral angles, defined by
115 e and the rotational diffusion, recovers the mean-square displacement of P. putida if the two distinc
116                                          The mean-square displacement of single, bound proteoglycans
117 ar scattering geometry yielded perpendicular mean-square displacements of 2.7*10(-4) A(2) K(-1) and 3
118 ed, including radial distribution functions, mean-square displacements of lipids and nanoparticle, ch
119                                              Mean-square displacements of localized internal motions
120        Finally, we develop a method based on mean-square-displacement of single particle trajectories
121 lls: the anomalous non-linear scaling of the mean-squared displacement of a 150-nm-diameter particle
122 sing a windowing technique by regressing the mean-squared displacement of cells tracked at high magni
123 s' net incomes as random walks, we study the mean-squared displacement of net income and related quan
124                                          The mean-squared displacement of the resulting trajectories
125         The time-dependent ensemble-averaged mean-squared displacements of all of the particles were
126 tein perdeuteration, we found similar atomic mean-square displacements over a large temperature range
127 regardless of Gaussianity, to retrieve their mean-squared displacement over several orders of magnitu
128 f microscopic displacement, (4) increases in Mean-Squared-Displacement over prolonged time periods ac
129 , mediolateral range (p=0.008), and critical mean square displacement (p=0.012).
130                                    The image-mean square displacement plot obtained is similar to the
131 displacement plot obtained is similar to the mean square displacement plot obtained using the single-
132                         Analysis of the root-mean-squared displacement plots for all of the data reve
133 ns in the cell membrane mostly relies on the mean-squared displacement plots, much information is los
134                       Analyses of the atomic mean-squared displacement, relaxation time, persistence
135 r estimates, as well as the ensemble average mean square displacement reveal subdiffusive behavior at
136  with a subset of CTP scaffolds with an root-mean-square displacement (RMSD) of approximately 0.5 A.
137                                    The image-mean square displacement technique applies the calculati
138 that the technique outperforms the classical mean-square-displacement technique when forces act on co
139 ovements from this experiment showed greater mean squared displacement than predicted by both a simpl
140 m the uncaging spot in all directions with a mean square displacement that varied linearly with time,
141 of competing motion models based on particle mean-square displacements that automatically classifies
142 ed trajectories are exploited to compute the mean-squared displacement that characterizes the dynamic
143   At a gross level, this is characterized by mean-squared displacements that deviate from the standar
144          We explain why fits of subdiffusive mean-square displacements to standard diffusion models m
145 ure times reveals negatively curved plots of mean-square displacement versus time.
146 usion models, suggesting how measurements of mean-squared displacement versus time might generally in
147 ined directly from imaging, in the form of a mean-square displacement vs. time-delay plot, with no ne
148 S. cerevisiae cells and improved analysis of mean square displacements, we quantified DNA motion at t
149 specular angles to characterize the parallel mean-square displacements, which were found to increase
150 lasm-embedded particles are transformed into mean-squared displacements, which are subsequently trans
151 l described by a power-law dependence of the mean-square displacement with observation time.

 
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