戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 gin has been proposed for cartilaginous fish electroreceptors.
2 dges and migrating primordia, neuromasts and electroreceptors.
3 the central processing of sensory input from electroreceptors.
4 in appendage, the Schnauzenorgan, is rich in electroreceptors.
5 elopmental mechanisms between hair cells and electroreceptors.
6 ver, conventional tuning curves predict poor electroreceptor afferent responses to low-frequency stim
7 by small shifts in the latency of individual electroreceptor afferent spikes after the EOD.
8 ach speed can be uniquely determined from an electroreceptor afferent's firing rate, a multiplexed ne
9 Conversely, power law adaptation modifies an electroreceptor afferent's response according to the tim
10  form of spike rate adaptation transforms an electroreceptor afferent's response to "looming" object
11 ystem of weakly electric fish, single P-type electroreceptor afferents accurately encode the time cou
12                     We measured responses of electroreceptor afferents and constructed a filter-based
13 esponse properties in tuberous and ampullary electroreceptor afferents of the weakly electric fish Ap
14  part of the phase-coding pathway; in S-type electroreceptor afferents.
15           These data confirm the homology of electroreceptors and ampullary organs in cartilaginous a
16     This calls into question the homology of electroreceptors and ampullary organs in the two lineage
17                   We compared the ability of electroreceptors and ELL efferent neurons to encode the
18 l and evolutionary links between non-teleost electroreceptors and hair cells.
19 at lateral line placodes form both ampullary electroreceptors and mechanosensory neuromasts.
20 s of ELL that receive input from mormyromast electroreceptors but were absent in the zone of ELL that
21 ctive sensing that brings objects toward the electroreceptor dense fovea-like head region.
22                       Thousands of cutaneous electroreceptors detect changes in the transdermal poten
23 ene Atoh1 is required for both hair cell and electroreceptor differentiation in sterlet, and for Pou4
24                                     Although electroreceptors displayed relatively homogeneous respon
25 s sharks, skates, and rays, use a network of electroreceptors distributed on their skin to locate adj
26                                          The electroreceptor, enabled by an elastomeric electret, is
27                              Ampullary organ electroreceptors excited by weak cathodal electric field
28 by this ability, we design a soft artificial electroreceptor for sensing approaching targets.
29 e hypothesis that lateral line placodes form electroreceptors in cartilaginous fishes by undertaking
30 s between electrosensory signals received by electroreceptors in different parts of the body surface.
31  non-placodal origins have been proposed for electroreceptors in other taxa.
32 at receives the primary afferent fibers from electroreceptors in the skin.
33                    Spontaneously oscillating electroreceptors in weakly electric fish (Mormyridae) re
34 ne of ELL that receives input from ampullary electroreceptors, indicating markedly different processi
35                          The soft artificial electroreceptor is expected to expand the ways we can pe
36 y species to detect weak electric fields via electroreceptors (modified hair cells) in ampullary orga
37 ked by fields of ampullary organs containing electroreceptors-modified hair cells that respond to wea
38    Specifically, we recorded from peripheral electroreceptor neurons, which display strong heterogene
39            Knollenorgans, among the tuberous electroreceptors of mormyrid electric fish, are modified
40 erties of Knollenorgans, a class of tuberous electroreceptors of mormyrid electric fish.
41 at innervation is not essential for tuberous electroreceptor organ development, but that it is necess
42            Weakly electric fish use tuberous electroreceptor organs to detect their own electric fiel
43                                     Tuberous electroreceptor organs were present in regenerated reinn
44            These fish possess three types of electroreceptor organs.
45 regeneration and differentiation of tuberous electroreceptor organs.
46 rongest immunoreactivity in the knollenorgan electroreceptor pathway; in the nucleus of the electrose
47 erone treatment and found that the timing of electroreceptor responses to self-generated pulses was d
48 ments had strong effects on the responses of electroreceptors, substantially reducing the amount of i
49 localization, we developed a soft artificial electroreceptor that can detect the relative positions o
50                        One class of tuberous electroreceptors, the knollenorgans, plays a critical ro
51 efish (Polyodon spathula), which use passive electroreceptors to detect electrical signals from plank
52           Male stingrays use their ampullary electroreceptors to locate mates, but the effect of gona
53 , representing brain areas downstream of the electroreceptors, to extract the 3D location, size, and
54 ted with the evolution of electrogenesis and electroreceptor type.
55  appendage that is covered with thousands of electroreceptors, which makes the fish extremely sensiti