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1 cts on representations of a second modality (audition).
2 lanation for this central issue in music and audition.
3 l and functional role for dopamine in normal audition.
4 ns onto regions concerned with olfaction and audition.
5 t of the relative influence of vision versus audition.
6 g an extensive reexamination of invertebrate audition.
7 ncy selectivity and sensitivity in mammalian audition.
8 t of phonological representations depends on audition.
9 ge to traditional models of neural coding in audition.
10 s than during localization in both touch and audition.
11 tion within the mammalian cochlea to enhance audition.
12 A similar phenomenon has been documented in audition.
13 imuli into electrical impulses that subserve audition.
14 es in the MGv perform different functions in audition.
15 s between acoustic elements are important in audition.
16 y during attention shifts between vision and audition.
17 oluntary attention shifts between vision and audition.
18 the temporal bone play an important role in audition.
19 of sensory functions including olfaction and audition.
20 n and movement, can be perceived by touch or audition.
22 contains the sensory organs specialised for audition and balance, develops from an ectodermal placod
24 experiments how information originating from audition and imagery affects the brain activity patterns
25 ound, and touch), the location of a speaker (audition and sight), and the rhythm or duration of an ev
26 sampled by two of the major sensory systems, audition and touch, notwithstanding that these signals a
29 simple duration-detection mechanisms across audition and touch; these systems were chosen because fi
33 mic sensory signals, such as occurs in human audition, and as a means to lock an intrinsic rhythm to
37 r the monkey's cerebral memory mechanisms in audition are intrinsically different from those in other
38 ems (vision, olfaction, somatosensation, and audition) are thought to use different but partially ove
39 arly in embryonic development, maturation of audition around the time of hatching suggested that syna
41 euronal information processing in vision and audition, but the principle of SAT is still debated in o
43 , most importantly, the speed of response of audition compared with other senses means that we have n
45 ut to a striatothalamic pathway important to audition-dependent vocal plasticity, and changes in spin
47 omplex sounds is a crucial function of human audition, especially in music and speech processing.
48 ral regulatory lineage being under stringent audition for interaction with MHC class II/self-peptide.
61 nducted, the direct influence of compromised audition on the auditory cortex and the potential impact
63 administered to 3 groups of participants in audition-only, vision-only, and auditory-visual conditio
64 es have shown that manipulating frequency in audition or touch can have a significant cross-sensory i
65 recently surged in the neural mechanisms of audition, particularly with regard to functional imaging
66 indicate that monkeys perform serial DMS in audition remarkably poorly and that whatever success the
68 vant modality-they fully combined vision and audition such that they perceived equal numbers of flash
72 m multiple sensory sources (e.g., vision and audition) to maximize an organism's ability to identify
73 ce a common color percept termed "white." In audition, two mixtures, each containing an independent s
74 Therefore, standard steady-state studies in audition, using sinusoidal AM, may not be sensitive to a
77 thoroughly explored in interactions between audition, vision, and touch may also explain the combina
80 y modalities, is particularly challenging in audition, where sounds from various sources and localiza
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