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1 ate motor preparation, as reflected in their directional selectivity.
2 ing inputs is critical for the generation of directional selectivity.
3  particular FM direction and thus change its directional selectivity.
4  the null direction, thereby ensuring robust directional selectivity.
5 xist such that nicotinic blockade eliminates directional selectivity.
6 aused even smaller responses, but no loss of directional selectivity.
7 ctively, before and during saccades and with directional selectivity.
8 atterns, with weak theta-modulation and head-directional selectivity.
9 (L4) simple cells, most of which show strong directional selectivity.(18) However, two important ques
10 dentified which neurons are necessary for T4 directional selectivity and ON motion behavioral respons
11 els that also tended to account for both the directional selectivity and responses to coherent motion
12 al functions, including size discrimination, directional selectivity, and looming-evoked escape.
13 latency, contrast sensitivity (C-50 values), directional selectivity, and optimal stimulus velocity.
14  corticothalamic feedback projections on the directional selectivity (angular tuning) of neurons in t
15 ay, the blue cone pathway, and ganglion cell directional selectivity are discussed.
16 tent with a two-asymmetric-pathways model of directional selectivity, but inconsistent with an asymme
17        In the current study, we assessed how directional selectivity changes when reaching movements
18 ge reductions in all measures of spatial and directional selectivity compared with WT neurons.
19 the number of neurons with hemifield and non-directional selectivity curves decreased with increasing
20                                      All 675 directional selectivity curves obtained from 75 IC neuro
21                                          The directional selectivity curves of 45 (60%) neurons did n
22                             A family of nine directional selectivity curves was plotted with a neuron
23                    Among 68 IC neurons whose directional selectivity curves were compared quantitativ
24              The type and sharpness of these directional selectivity curves were then compared in rel
25 ctivity curves were compared quantitatively, directional selectivity determined with sequentially pre
26 athway of binocular animals, the property of directional selectivity (DS) is first exhibited in stria
27                                              Directional selectivity during visually guided hand move
28     This finding explains the high degree of directional selectivity found already in the fly's prima
29 tarburst amacrine cells is the generation of directional selectivity in ON-OFF directionally selectiv
30                     The md-L neurons exhibit directional selectivity in response to mechanical stimul
31 ately one-half of VIP cells show significant directional selectivity in response to optic flow, one-h
32 up II mGluRs have the potential to influence directional selectivity in RGCs by inhibiting transmitte
33 rt that spike threshold can strongly amplify directional selectivity in that the spike directionality
34 ngs, we examine the mechanisms underlying FM directional selectivity in the IC.
35    Application of EGLU alone failed to alter directional selectivity in the RGCs but did reduce the r
36 contrast with previously demonstrated strong directional selectivity in the second, T5-cell, pathway.
37 x (V1) also contains DS neurons, but whether directional selectivity in V1 emerges de novo(11)(,)(12)
38 en show that, in our sample of IC cells, PSP directional selectivity is not created de novo.
39             Exploring retinotopy's impact on directional selectivity leads us to infer that the excit
40 visual functions including motion detection, directional selectivity, local edge detection, looming d
41 y of LGN-DS neurons contributes to the sharp directional selectivity of cortical simple cells.
42                           The hypothesis for directional selectivity of frequency modulations (FMs) i
43 ery cycle may contribute to the variation of directional selectivity of IC neurons with sequential pr
44 locking inhibition significantly reduced the directional selectivity of these neurons, suggesting tha
45 ctural basis for the SACs' ability to confer directional selectivity on postsynaptic neurons is conse
46 esults indicate that, rather than sharpening directional selectivity per se, these circuit elements r
47                          A model for retinal directional selectivity postulates that GABAergic inhibi
48 share similar functional properties, such as directional selectivity, project to similar depths withi
49 he parietofrontal network resumed egocentric directional selectivity, showing higher activation for c
50 nferior occipital gyrus, whereas allocentric directional selectivity (target relative to a visual lan
51                      In addition, egocentric directional selectivity (target relative to gaze) was ob
52 iscovered that nicotinic blockade eliminated directional selectivity to drifting, low spatial frequen
53  extend the range of stimuli that can elicit directional selectivity to include moving textures, that
54 eld bushy T-cells (T4) demonstrate only weak directional selectivity to motion, in striking contrast
55                               This change of directional selectivity was due to the variation in reco
56                                      Second, directional selectivity was minimal in PI neurons belong
57                  To examine the emergence of directional selectivity, we developed genetic driver lin
58 y also maintained visual properties, such as directional selectivity, while increasing response gain
59                         Here we evaluated FM directional selectivity with in vivo whole-cell recordin
60                So far, attempts to eliminate directional selectivity with nicotinic blockade have fai
61 ntal role in the neural circuitry underlying directional selectivity within the retina.