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1 activity is direction specific and graded by turning angle.
2 d angular deviation, apparent speed and mean turning angle.
3 id not affect bifurcation but rather altered turning angles.
4 uring the food gathered by the agents as the turning angle and hop length noise widths are varied.
5 es the observed statistical distributions of turning angle and speed derived from time-lapse studies
6 apsular region was 38% slower and had higher turning angles and arrest coefficients than naive T lymp
7  with other prisms to obtain a wide range of turning angles and expansion ratios.
8 l maneuverability, as indicated by decreased turning angles and increased flight speed.
9 all components of slug movement (mean speed, turning angles and movement/resting times) were signific
10 ify strong temporal correlations between the turning angles and speed that preclude the case of a sim
11 k on area-restricted search (ARS) that links turning-angle and step-size changes to geographically lo
12 ed by intermediate step lengths and variable turning angles, and (3) Traveling mode, characterized by
13 meters such as hop lengths, pause times, and turning angles are typically reported as probability den
14 mode, characterized by long step lengths and turning angles around 0(o).
15 ode, characterized by short step lengths and turning angles around 180(o); (2) Moderately active (or
16  T cell motion including speed, persistence, turning angle, directionality, and confinement of T cell
17 displacement probability distribution or the turning angle distribution.
18 tigate how two different features related to turning angle distributions influence encounter success:
19 dels using a proper choice of representative turning angle distributions of the recently proposed Jon
20 can be reached by means of distinctly shaped turning angle distributions, provided that the resulting
21 y than slugs released individually and their turning angle has a clear anticlockwise bias.
22 vement modes with different step lengths and turning angles in a hypothetical ungulate population wit
23 athematical explanation for why average axon turning angles in gradients in vitro saturate very rapid
24           Patterns with a prescribed zig-zag turning angle less than 90 degrees are obtained upon seq
25 orward and backward swimming with an average turning angle of 150 degrees .
26                           We assume that the turning angle of a worker is individually specific and n
27                          To a lesser extent, turning angles of varphi2 = 0 degrees are also found.
28 y, distance from home), spatial shape (total turning angle, segment complexity), and temporal charact
29                           In both owls, head-turning angles varied as a sinusoidal function of ITD.
30 rface duration, horizontal displacement, and turning angle were used to identify travelling, resting
31  Two components of movement (move length and turning angle) were not associated with density, nor was
32 otile speeds, mean squared displacement, and turning angles-while providing a variety of visualizatio