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1 romasts never make physical contact with the Mauthner cell.
2 t this general organization is absent at the Mauthner cell.
3 ates fast startle reactions triggered by the Mauthner cell.
4 etwork for escape behaviors initiated by the Mauthner cell.
5 chemical) synaptic contacts on the goldfish Mauthner cell.
6 s observed near the lateral dendrites of the Mauthner cell.
7 dial reticular formation (RF), including the Mauthner cell.
8 beyond the specific escape network served by Mauthner cells.
9 fiber neurons in fish and amphibians called Mauthner cells.
10 n/notch1a (des) gene result in supernumerary Mauthner cells.
11 lectrical and chemical) contacts on goldfish Mauthner cells, a model synapse for the study of vertebr
12 tion of the lateral dendrite of the goldfish Mauthner cells, a pair of large reticulospinal neurons i
14 Acoustic stimuli that activate ASR-command Mauthner cells also activate dorsal raphe nucleus (DRN)
17 pses between auditory afferents and goldfish Mauthner cells are constructed by apposition of hemichan
18 s indicate that the homeotically transformed Mauthner cells are fully functional in the escape circui
19 "large myelinated club endings" on goldfish Mauthner cells are identifiable "mixed" (electrical and
20 hese data support the hypothesis that excess Mauthner cells are incorporated into the escape-response
22 rescence microscopy to observe the growth of Mauthner cell axons and their postsynaptic targets, the
23 o in the goldfish reticulospinal neuron, the Mauthner cell, can be evoked by afferent tetanization or
24 contrast, the two segmental homologs of the Mauthner cell, cells MiD2cm and MiD3cm, showed axon coll
25 w differential attenuation properties in the Mauthner cell dendrites arising at least partly from dif
26 en a zebrafish makes a fast escape response, Mauthner cells directly activate contralateral spinal in
28 that these neurons may have evolved from the Mauthner cell in the medulla of teleost fish, although N
29 ivated form of Notch decreased the number of Mauthner cells in des mutants indicating that des functi
33 rade spread of signals from the postsynaptic Mauthner cell is dramatically enhanced by depolarization
34 between auditory afferents and the goldfish Mauthner cell is mediated by coexisting gap junctions an
35 amatergic) synaptic terminals on the teleost Mauthner cell known as "Club endings" constitute because
36 rical and chemical) synaptic contacts on the Mauthner cells, known as Club endings, constitute a valu
37 l components of the mixed EPSP evoked in the Mauthner cell lateral dendrite by a single stimulus to t
41 roperties and synaptic sound response of the Mauthner cell (M-cell), the decision-making neuron of th
42 m with electrophysiological responses of the Mauthner cell (M-cell), the threshold detector that init
43 l circuits, we examined the roles of ectopic Mauthner cells (M-cells) in the escape response of larva
46 synapses between auditory afferents and the Mauthner cell, may ensure efficient communication betwee
48 f three repeated reticulospinal neurons--the Mauthner cell, MiD2cm, and MiD3cm--is thought to produce
50 out of primary neurons, including the unique Mauthner cell on each side of the hindbrain, depends on
53 by feinting with their body, triggering the Mauthner cell that is furthest from their head milliseco
54 rded at glycinergic junctions on the teleost Mauthner cell (time to peak approximately 0.3-0.4 ms and
55 s, enhancing synaptic communication from the Mauthner cells to the auditory afferents where electrica
57 cialization in neighbouring dendrites of the Mauthner cell, we report cross-modal dendritic interacti
58 rical and chemical) synapses on the goldfish Mauthner cell, we show here that gap junction hemichanne
59 by converging on the lateral dendrite of the Mauthner cell, whereas projections from secondary neurom
60 he mGi may represent a mammalian analogue to Mauthner cells, with a separation of function for neuron
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