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1 oorly understood high-pass filtering seen in electrosensory afferents and downstream neurons.
2                                  Retinal and electrosensory afferents elicit local monosynaptic excit
3 y electric fish, probability coding (P-type) electrosensory afferents encode amplitude modulations of
4 nges in the frequency response properties of electrosensory afferents enhance mate detection by male
5 sed a lateral line placode-derived system of electrosensory ampullary organs and mechanosensory neuro
6 em, comprising mechanosensory neuromasts and electrosensory ampullary organs, is a useful model for i
7 se temporal coding is a hallmark of both the electrosensory and auditory systems.
8 in-like immunoreactivity was examined in the electrosensory and electromotor systems of the two famil
9               Recordings were made from fish electrosensory and monkey vestibular sensory neurons.
10 sory and electromotor command system, or the electrosensory and trigeminal motor command.
11  are many anastomoses between the peripheral electrosensory and trigeminal nerves, but these senses r
12 rest in the possible connections between the electrosensory and trigeminal systems.
13  to nP, TS, and tectum modulate responses to electrosensory and/or visual motion and, in particular,
14                                    Auditory, electrosensory, and mechanosensory responses are dominat
15 field potentials evoked by auditory, visual, electrosensory, and water displacement stimuli in this w
16 ss the implications of preglomerular/pallial electrosensory-associated afferents with respect to a ma
17                                        Thus, electrosensory behavior may be used as a model system fo
18 tion of amphid sensory neurons also disrupts electrosensory behavior.
19  this circuit in relation to newly described electrosensory behaviors, including prey capture, social
20 we call this dominance of the electric sense electrosensory capture.
21 erinacea) and functionally couple to mediate electrosensory cell membrane voltage oscillations, which
22 (BK) channel are preferentially expressed by electrosensory cells in little skate (Leucoraja erinacea
23 ltaneous single unit recordings of principal electrosensory cells show that an increase in the spatia
24                                              Electrosensory cells within these ampullae can discrimin
25 ment and evolution of the mechanosensory and electrosensory components of the lateral line must be di
26                 We provide evidence that the electrosensory consequences of tail bending are opposed
27 y processing generate negative images of the electrosensory consequences of the animal's own behavior
28 rmed into negative images of the predictable electrosensory consequences of the fish's motor commands
29 lus motion triggers paradoxical responses to electrosensory contrast.
30 t 'sensory conflict' when mechanosensory and electrosensory cues are separated, striking first toward
31 ronotus leptorhynchus can capture prey using electrosensory cues that are dominated by low temporal f
32 ates, but the effect of gonadal androgens on electrosensory encoding during the reproductive season i
33         The nP is a central component of all electrosensory feedback pathways to the electrosensory l
34 location shows, for the first time, that the electrosensory flow contains behaviorally relevant infor
35 reconstruction of sensory input, we show how electrosensory flow is actively created during highly pa
36 ith their mammalian orthologues that support electrosensory functions: structural adaptations in CaV1
37 age-gated cation channels in a population of electrosensory hair cells.
38                                       In the electrosensory hindbrain, a corollary discharge that sig
39 se neurons also showed low-pass filtering of electrosensory information but with larger maximum decli
40                       Adaptive processing of electrosensory information occurs in the cerebellum-like
41 iform cells are efferent neurons that convey electrosensory information to higher stages of the syste
42             The responses of cells in ELL to electrosensory input are strongly affected by corollary
43 ry system, the statistical properties of the electrosensory input evoked by natural swimming movement
44                       Analyzing the afferent electrosensory input shows that a significant gain in in
45 L) receives diencephalic inputs representing electrosensory input utilized for communication and navi
46                 Using a model to compute the electrosensory input, we show that these behavioral adju
47 " that act to cancel predictable patterns of electrosensory input.
48 tectal neurons receive converging visual and electrosensory inputs, as investigated in the lamprey -
49 al dynamics of motor corollary discharge and electrosensory inputs.
50 ectroreceptor pathway; in the nucleus of the electrosensory lateral line lobe (ELL) and the big cells
51  comparison mechanisms was identified in the electrosensory lateral line lobe (ELL) in the hindbrain
52                 Phase-locking neurons in the electrosensory lateral line lobe (ELL) of a weakly elect
53  Differential-phase-sensitive neurons in the electrosensory lateral line lobe (ELL) of the African el
54 odulation of information transmission in the electrosensory lateral line lobe (ELL) of the hindbrain.
55  this report, we describe correlations among electrosensory lateral line lobe (ELL) pyramidal cells'
56 nts and E- and I-type pyramidal cells in the electrosensory lateral line lobe (ELL) to random distort
57 omatotopically ordered hindbrain maps of the electrosensory lateral line lobe (ELL), the dorsolateral
58 st brain station for central processing, the electrosensory lateral line lobe (ELL), were investigate
59 isparity thresholds of output neurons of the electrosensory lateral line lobe (ELL), where the repres
60  all electrosensory feedback pathways to the electrosensory lateral line lobe (ELL).
61 eakly labeled inhibitory interneurons in the electrosensory lateral line lobe (ELL).
62 ondary sensory neurons in the nucleus of the electrosensory lateral line lobe (NELL) act as relays of
63                       Pyramidal cells in the electrosensory lateral line lobe burst in response to lo
64 electrosensory nucleus in electric fish, the electrosensory lateral line lobe, resulted in markedly d
65 nd their targets, the pyramidal cells in the electrosensory lateral-line lobe.
66                                          The electrosensory lobe (ELL) of mormyrid electric fish is a
67                                          The electrosensory lobe (ELL) of mormyrid electric fish is o
68                                          The electrosensory lobe (ELL) of mormyrid electric fish is t
69 ing across multiple processing layers in the electrosensory lobe (ELL) of mormyrid fish and report ho
70                                       In the electrosensory lobe (ELL) of mormyrid fish, a main cellu
71       Here, we investigate this issue in the electrosensory lobe (ELL) of weakly electric mormyrid fi
72 rcuit-level account of generalization in the electrosensory lobe (ELL) of weakly electric mormyrid fi
73      Here we demonstrate that neurons in the electrosensory lobe (ELL) of weakly electric mormyrid fi
74 ere we use an advantageous model system--the electrosensory lobe (ELL) of weakly electric mormyrid fi
75  tests the adaptive filter hypothesis in the electrosensory lobe (ELL) of weakly electric mormyrid fi
76                 Medium ganglion cells in the electrosensory lobe create negative images that predict
77        Closed-loop manipulations reveal that electrosensory lobe neurons are capable of simultaneousl
78 show here that such plasticity exists in the electrosensory lobe of mormyrid electric fish and that i
79                                          The electrosensory lobes (ELLs) of mormyrid and gymnotid fis
80 SIGNIFICANCE STATEMENT We show that midbrain electrosensory neurons display correlations between thei
81        We recorded the responses of midbrain electrosensory neurons in the weakly electric fish Apter
82  properties to the temporal selectivities of electrosensory neurons in vivo.
83 tional role of serotonergic innervation onto electrosensory neurons in weakly electric fish by elicit
84 tection thresholds at the level of medullary electrosensory neurons, it seems that the behavior-drive
85 he temporal filtering properties of midbrain electrosensory neurons.
86 to the presence of mAChR3 in the ELL region, electrosensory nuclei including the nucleus praeeminenti
87 by recording evoked potentials from midbrain electrosensory nuclei.
88              Simultaneous recordings from an electrosensory nucleus and electromotor neurons revealed
89 vations of different maps of the first-order electrosensory nucleus in electric fish, the electrosens
90 apture, social signaling and the tracking of electrosensory objects.
91 enes are restricted either to the developing electrosensory or mechanosensory lateral line.
92 ng sharks, rays, and skates, use specialized electrosensory organs called ampullae of Lorenzini to de
93                            We speculate that electrosensory organs may be the 'default' developmental
94 t chitin is prevalent within the specialized electrosensory organs of cartilaginous fishes (Chondrich
95                                       In the electrosensory pathway mediating communication behavior,
96                                In the active electrosensory pathway of mormyrids afferent input is pr
97                                       In the electrosensory pathway that processes communication sign
98                                       In the electrosensory pathway, sensitivity to pauses first aros
99  sensory trigeminal components as well as an electrosensory pathway.
100 omotor pathways and early in the time-coding electrosensory pathways do not follow this hypothesis, a
101                            We reexamined the electrosensory pathways from the periphery to the midbra
102 teins in mormyrid and gymnarchid time-coding electrosensory pathways is consistent with the hypothesi
103 own jamming avoidance response as a probe of electrosensory perception, we show that the ambiguity at
104 primary androgen increase in wild males, the electrosensory primary afferent neurons show an increase
105      In the little skate, Raja erinacea, the electrosensory primary afferents are responsive to elect
106 pike latency is decoded at central stages of electrosensory processing are discussed.
107  implement corollary discharge modulation of electrosensory processing during locomotion.
108                Neurons at the first stage of electrosensory processing generate negative images of th
109 n cerebellum-like structures associated with electrosensory processing in fish.
110  internal model at the first stage of active electrosensory processing in mormyrid fish.
111 ing network model of the first two stages of electrosensory processing replicates this correlation sh
112  the mediolateral axis of the DON, the first electrosensory processing station.
113 and suggest a specific form of modularity in electrosensory processing that can be tested experimenta
114 eurons of the first central nervous stage of electrosensory processing.
115 e fields of neurons within the first central electrosensory-processing region have an antagonistic ce
116 nomyrus brachyistius during stimulation with electrosensory pulse trains.
117 formance by pairs of simultaneously recorded electrosensory pyramidal cells in the hindbrain of weakl
118 that the function of serotonergic input onto electrosensory pyramidal neurons is to render them more
119                  The paddlefish is a passive electrosensory ray-finned fish with a special rostral ap
120 ical tuning allows auditory, vestibular, and electrosensory receptor cells to filter sensory signals
121                  In addition, we showed that electrosensory receptors respond to self-generated EODs
122 shifted corollary discharge optimally blocks electrosensory responses to the fish's own signal.
123 ient increases during navigation to increase electrosensory sampling.
124  in response to each cycle of the sinusoidal electrosensory signal (350-500 Hz) created by the fish's
125 n the presence and absence of self-generated electrosensory signals caused by tail movements.
126 arities on the order of microseconds between electrosensory signals received by electroreceptors in d
127                 Two distinct sensory cues in electrosensory signals, amplitude modulation and differe
128 ization of sudden turns and reversals during electrosensory steering.
129 cellular responses to time-varying (2-30 Hz) electrosensory stimulation and current injection of 27 n
130                                We found that electrosensory stimulation elicited evoked potentials in
131 f the large ganglion cells were inhibited by electrosensory stimuli in the center of their receptive
132  depression was similar to that observed for electrosensory stimuli of the same temporal frequency.
133 t study, sensitivity to temporal patterns of electrosensory stimuli was found to arise within the mid
134 weakly electric fish (Mormyridae) respond to electrosensory stimuli with a phase reset that results i
135                                          For electrosensory stimuli, however, these neurons showed lo
136  in response to continuous and discontinuous electrosensory stimuli.
137 ng the amplitude and phase, respectively, of electrosensory stimuli.
138  misperception of the amplitude and phase of electrosensory stimuli.
139 r sex differences in chirp responsiveness to electrosensory stimuli; males consistently chirp, wherea
140  surface determine responses to second-order electrosensory stimulus features in the weakly electric
141 der did not affect responses to second-order electrosensory stimulus features, other sources of heter
142  decreased in concert with the period of the electrosensory stimulus, whereas in the other four neuro
143 anges after a few minutes of pairing with an electrosensory stimulus.
144           Here, we asked whether the central electrosensory system actually detects the occurrence of
145  using both the natural heterogeneity of the electrosensory system and pharmacological blockade of de
146 No direct connections were found between the electrosensory system and the V motor nucleus but the ce
147            Given the independent loss of the electrosensory system in multiple lineages, the developm
148 ns across multiple sensory maps by using the electrosensory system in weakly electric fish as a model
149                             The elasmobranch electrosensory system is the most thoroughly understood
150 investigated how midbrain neurons within the electrosensory system of Apteronotus leptorhynchus code
151 havior on a spike latency code in the active electrosensory system of mormyrid fish.
152                              Here we use the electrosensory system of mormyrid weakly electric fish t
153                We use the well characterized electrosensory system of weakly electric fish to address
154 within the initial processing station of the electrosensory system of weakly electric fish to shift t
155                                       In the electrosensory system of weakly electric fish, single P-
156  of pairwise spike train correlations in the electrosensory system of weakly electric fish.
157 the relationship to their behaviorally novel electrosensory system remains unclear.
158 on in sharks is not solely performed via the electrosensory system, and that putative magnetoreceptor
159 sults from current lesion experiments in the electrosensory system, however, suggest an alternative p
160 ge about the circuitry and physiology of the electrosensory system, the statistical properties of the
161  mosaic increases are related to evolving an electrosensory system, we should find similar mosaic shi
162 esence evident in specialized regions of the electrosensory system, which suggests an important modul
163 nvironment and is known to be a fovea of the electrosensory system.
164 ost thoroughly understood of the non-teleost electrosensory systems and is useful for studying centra
165                     Progress in the study of electrosensory systems has been facilitated by the syste
166 ined experimental and theoretical studies of electrosensory systems have led to detailed accounts of
167                               Recent work on electrosensory systems in fish has combined traditional
168       These results show that evolving novel electrosensory systems is repeatedly and independently a
169 g this process have come from studies of the electrosensory systems of fish.
170                                          The electrosensory systems of weakly electric fish are recog
171 ntis spp.), which evolved varying aspects of electrosensory systems, independent of mormyroids.
172 A is expressed in deep layers of the dorsal (electrosensory) torus semicircularis (TSd).
173 the diencephalic and mesencephalic nuclei in electrosensory, visual, and acousticolateral functions.
174 ore) project to midbrain regions involved in electrosensory/visual function.

 
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