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1 as coincidence detectors for measurement of interaural time difference.
2 ons depended on the neurons' selectivity for interaural time difference.
3 a shift in the tuning of tectal neurons for interaural time difference.
4 ns in the nucleus laminaris (NL) that detect interaural time differences.
5 t contributes to sound localization based on interaural timing differences.
6 SCs, thus refining coincidence detection and interaural timing differences.
7 ptive fields (RFs) because of sensitivity to interaural time difference and frequency-specific intera
8 cts in direction (and its underlying cues of interaural time differences and interaural level differe
10 on of a sound's direction by detecting small interaural time differences and visual processing, which
14 of the brain can acquire alternative maps of interaural time difference as a result of abnormal exper
16 ing versus location during the processing of interaural time difference cues in vivoSIGNIFICANCE STAT
17 ever, the first-order central neurons of the interaural time difference detection circuit encode info
18 ects (both sexes) using binaural processing (interaural-time-difference discrimination with simultane
19 of the chicken nucleus laminaris, the first interaural time difference encoder that computes informa
20 nucleus laminaris (NL), the first encoder of interaural time difference for sound localization in bir
21 ween binaural and monaural responses nor the interaural time difference for which nucleus laminaris n
22 ergic inhibition can influence the coding of interaural time differences for sound localization in th
23 ons to the most potent localization cue, the interaural time difference in low-frequency signals (< a
24 mmalian brainstem circuit for computation of interaural time differences is composed of monaural cell
25 y inputs that convey sensitivity to relevant interaural time differences is instructed by the experie
28 h is equivalent to a specific combination of interaural time difference (ITD) and interaural level di
30 NL neurons may exert a dynamic modulation of interaural time difference (ITD) coding in a CF-dependen
36 among the two groups.SIGNIFICANCE STATEMENT Interaural time difference (ITD) is an important cue for
47 tems localize sound sources by computing the interaural time difference (ITD) with submillisecond acc
48 associations between auditory cues, such as interaural time difference (ITD), and locations in visua
49 l neuron in the MSO is tuned to its own best interaural time difference (ITD), indicating the presenc
50 mary cue for localization along the azimuth, interaural time difference (ITD), is based on a cross-co
51 signal-to-noise ratio in the encoding of the interaural time difference (ITD), one of two primary bin
52 mative model of sound source localization by Interaural Time Difference (ITD), that reproduces a weal
54 olive, and these sites were correlated with interaural time difference (ITD)-sensitive responses to
60 erences in the sounds reaching the two ears [interaural time difference (ITD)] to identify where the
61 r implant users do poorly on tasks involving interaural time differences (ITD), a cue that provides i
63 t process different sound localization cues, interaural time differences (ITDs) and level differences
64 of changes in tuning for frequency-specific interaural time differences (ITDs) and level differences
65 ations in the match between their tuning for interaural time differences (ITDs) and the locations of
78 location in the horizontal plane, extracting interaural time differences (ITDs) from the stimulus fin
80 eral CIs, bilateral CI users' sensitivity to interaural time differences (ITDs) is still poorer than
81 laminaris (NL) is involved in computation of interaural time differences (ITDs) that encode the azimu
82 e capable of great accuracy in detecting the interaural time differences (ITDs) that underlie azimuth
84 ns in the medial superior olive (MSO) encode interaural time differences (ITDs) with sustained firing
85 erally implanted human subjects discriminate interaural time differences (ITDs), a major cue for soun
86 a major category of sound localization cue, interaural time differences (ITDs), in juvenile barn owl
87 nteraural intensity or level differences and interaural time differences (ITDs), interact perceptuall
88 athway where cues used to locate sounds, ie, interaural time differences (ITDs), interaural level dif
89 em uses three cues to decode sound location: interaural time differences (ITDs), interaural level dif
90 anipulation altered the relationship between interaural time differences (ITDs), the principal cue us
91 studied example is the computational map of interaural time differences (ITDs), which is essential t
95 binaural sound localization cues, including interaural timing differences (ITDs) and interaural leve
97 such as interaural level differences (ILDs), interaural timing differences (ITDs), and spectral cues.
98 cues can be used to compute sound direction: interaural timing differences (ITDs), interaural level d
100 tal frequency discrimination limens (F0DLs), interaural time differences limens (ITDLs), and attentiv
101 lternative, direct measure of sensitivity to interaural time differences, namely, a following respons
105 previous study, uCDCs were less sensitive to interaural time differences than HCs, resulting in unmod
107 ts to the MSO, which tune the sensitivity to interaural time differences, undergo substantial structu
108 e detectors necessary for the computation of interaural time differences used in sound localization.
109 s are sufficient for estimating the stimulus interaural time difference using responses from single t
110 citatory input to lose their selectivity for interaural time difference when coincidence of impulses
111 had poor cortical sensitivity to changes in interaural time differences, which are critical for loca