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1 ts spatial-frequency tuning as measured with drifting gratings.
2 of P and 6 % of M cells responded poorly to drifting gratings.
3 ly predict the amplitude of the responses to drifting gratings.
4 were characterized with both white noise and drifting gratings.
5 t were approximately half that evoked by the drifting gratings (1.0% +/- 0.1% versus 2.1% +/- 0.3%, P
6 es of dorsal V2 and dorsal V3, small bars of drifting gratings along the horizontal meridian of the c
7 unmodulated components of spike responses to drifting gratings, an index that forms a bimodal distrib
8 tial resolution of LGN neuronal responses to drifting grating and white noise stimuli when CG neurons
10 discriminate the direction of motion of both drifting gratings and random dot stimuli in their impair
11 minance increments, contrast sensitivity for drifting gratings, and the extraction of motion signal f
12 oral frequencies; (2) plaids composed of two drifting gratings; and (3) gratings masked by full-scree
13 rformance in flicker detection, detection of drifting gratings (at low spatial frequencies), speed di
14 stimuli of differing complexity: sinusoidal drifting gratings, binary dense noise, and natural movie
16 of a direction-selective ganglion cell using drifting gratings can reverse this cell's directional pr
17 rection, SF and TF, and speed in response to drifting gratings in V1 and PM of anesthetized mice.
19 ive fields of single neurons with patches of drifting grating of optimal spatial frequency and orient
20 sented large stimulus sets consisting of (1) drifting gratings of various orientations and spatiotemp
22 plaids--stimuli composed of two orthogonally drifting gratings, presented separately to each eye--in
23 een excitation and inhibition in response to drifting gratings.SIGNIFICANCE STATEMENT The wiring of e
25 ulated firing rates (F1 values) generated by drifting grating stimuli, and their associated interspik
31 -evoked fMRI signal increase associated with drifting-grating stimulus was 1.7% +/- 0.5% (P < 10(-4),
32 r to the preferred orientation measured with drifting gratings than is the orientation preference of
33 lem.' Here we manipulate contrast in several drifting gratings that can be perceived as either indepe
34 in their temporal frequency selectivity for drifting gratings versus the envelope of interference pa
35 aque primary visual cortex V1 in response to drifting grating visual stimuli, were evaluated on coars
36 lectivity of each complex cell measured with drifting gratings was also well predicted by the combina
39 Here, we show that prolonged adaptation with drifting gratings, which alters responses in the early v
41 nd only 12% in PM were tuned to the speed of drifting gratings with PM preferring slower drift rates
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