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1 gin has been proposed for cartilaginous fish electroreceptors.
2 dges and migrating primordia, neuromasts and electroreceptors.
3 in appendage, the Schnauzenorgan, is rich in electroreceptors.
4 the central processing of sensory input from electroreceptors.
5 ver, conventional tuning curves predict poor electroreceptor afferent responses to low-frequency stim
7 ach speed can be uniquely determined from an electroreceptor afferent's firing rate, a multiplexed ne
8 Conversely, power law adaptation modifies an electroreceptor afferent's response according to the tim
9 form of spike rate adaptation transforms an electroreceptor afferent's response to "looming" object
10 ystem of weakly electric fish, single P-type electroreceptor afferents accurately encode the time cou
11 esponse properties in tuberous and ampullary electroreceptor afferents of the weakly electric fish Ap
14 This calls into question the homology of electroreceptors and ampullary organs in the two lineage
18 s of ELL that receive input from mormyromast electroreceptors but were absent in the zone of ELL that
22 e hypothesis that lateral line placodes form electroreceptors in cartilaginous fishes by undertaking
23 s between electrosensory signals received by electroreceptors in different parts of the body surface.
27 ne of ELL that receives input from ampullary electroreceptors, indicating markedly different processi
28 Specifically, we recorded from peripheral electroreceptor neurons, which display strong heterogene
29 at innervation is not essential for tuberous electroreceptor organ development, but that it is necess
34 rongest immunoreactivity in the knollenorgan electroreceptor pathway; in the nucleus of the electrose
35 ments had strong effects on the responses of electroreceptors, substantially reducing the amount of i
37 efish (Polyodon spathula), which use passive electroreceptors to detect electrical signals from plank
39 appendage that is covered with thousands of electroreceptors, which makes the fish extremely sensiti
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