ライフサイエンスコーパス: Mauthner cell

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 n/notch1a (des) gene result in supernumerary Mauthner cells.

10 fiber neurons in fish and amphibians called Mauthner cells.

11 the integration of audiovisual inputs in the Mauthner cell, a command neuron necessary and sufficient

12 lectrical and chemical) contacts on goldfish Mauthner cells, a model synapse for the study of vertebr

13 tion of the lateral dendrite of the goldfish Mauthner cells, a pair of large reticulospinal neurons i

14 Killing just the Mauthner cell affected escapes from tail-directed but no

15 Acoustic stimuli that activate ASR-command Mauthner cells also activate dorsal raphe nucleus (DRN)

16 Both Mauthner cell and motor neurons were highly active, each

17 eurons, which project to the vicinity of the Mauthner cells and their inputs.

18 pses between auditory afferents and goldfish Mauthner cells are constructed by apposition of hemichan

19 s indicate that the homeotically transformed Mauthner cells are fully functional in the escape circui

20 "large myelinated club endings" on goldfish Mauthner cells are identifiable "mixed" (electrical and

21 hese data support the hypothesis that excess Mauthner cells are incorporated into the escape-response

22 Mauthner cells are the largest neurons in the hindbrain

23 ntified descending brain neurons (Muller and Mauthner cells) are capable of axonal regeneration.

24 le single synaptic contacts on the zebrafish Mauthner cells, at which gap junctions coexist with spec

25 rescence microscopy to observe the growth of Mauthner cell axons and their postsynaptic targets, the

26 o in the goldfish reticulospinal neuron, the Mauthner cell, can be evoked by afferent tetanization or

27 contrast, the two segmental homologs of the Mauthner cell, cells MiD2cm and MiD3cm, showed axon coll

28 w differential attenuation properties in the Mauthner cell dendrites arising at least partly from dif

29 en a zebrafish makes a fast escape response, Mauthner cells directly activate contralateral spinal in

30 of visual information on the morphologies of Mauthner cells during developmental and evolutionary tim

31 Previous fills of the Mauthner cell had revealed short, knob-like collaterals.

32 that these neurons may have evolved from the Mauthner cell in the medulla of teleost fish, although N

33 The length of ventral dendrites of Mauthner cells in dark-raised surface fish larvae were l

34 ivated form of Notch decreased the number of Mauthner cells in des mutants indicating that des functi

35 Calcium imaging revealed that all Mauthner cells in desb420 mutants were active during an

36 The activity of the paired Mauthner cells in rhombomere 4 (r4) has been shown to be

37 We compared the structure of Mauthner cells in surface fish raised under daily light

38 olishes electrical transmission and disrupts Mauthner cell-initiated escape responses.

39 gest that excitatory bias is provided to the Mauthner cell ipsilateral to approached barriers, either

40 The hindbrain Mauthner cell is an essential component of this circuit.

41 rade spread of signals from the postsynaptic Mauthner cell is dramatically enhanced by depolarization

42 between auditory afferents and the goldfish Mauthner cell is mediated by coexisting gap junctions an

43 amatergic) synaptic terminals on the teleost Mauthner cell known as "Club endings" constitute because

44 rical and chemical) synaptic contacts on the Mauthner cells, known as Club endings, constitute a valu

45 l components of the mixed EPSP evoked in the Mauthner cell lateral dendrite by a single stimulus to t

46 uditory afferent synapses terminating on the Mauthner cell lateral dendrite.

47 The Mauthner cell (M-cell) is a command-like neuron in teleo

48 Studies on the Mauthner cell (M-cell) of goldfish, Carassius auratus, h

49 roperties and synaptic sound response of the Mauthner cell (M-cell), the decision-making neuron of th

50 m with electrophysiological responses of the Mauthner cell (M-cell), the threshold detector that init

51 l circuits, we examined the roles of ectopic Mauthner cells (M-cells) in the escape response of larva

52 For that, we studied the Mauthner cells (M-cells) in the goldfish startle circuit

53 The reticulospinal Mauthner cells (M-cells) of the startle circuit have bee

54 synapses between auditory afferents and the Mauthner cell, may ensure efficient communication betwee

55 erially homologous reticulospinal cells (the Mauthner cell, MID2cm, and MID3cm) during behavior.

56 f three repeated reticulospinal neurons--the Mauthner cell, MiD2cm, and MiD3cm--is thought to produce

57 The Mauthner cell of goldfish receives auditory and visual i

58 out of primary neurons, including the unique Mauthner cell on each side of the hindbrain, depends on

59 1 3' segment of 60 nucleotides did not enter Mauthner cell processes to any significant extent.

60 r of three hindbrain reticulospinal neurons: Mauthner cells, RoL2 cells, and MiD3cm cells.

61 by feinting with their body, triggering the Mauthner cell that is furthest from their head milliseco

62 rded at glycinergic junctions on the teleost Mauthner cell (time to peak approximately 0.3-0.4 ms and

63 s, enhancing synaptic communication from the Mauthner cells to the auditory afferents where electrica

64 the main morphological change in Muller and Mauthner cells was an increase in soma size.

65 cialization in neighbouring dendrites of the Mauthner cell, we report cross-modal dendritic interacti

66 rical and chemical) synapses on the goldfish Mauthner cell, we show here that gap junction hemichanne

67 Using model electrical synapses in zebrafish Mauthner cells, we demonstrated that ZO1 is required for

68 by converging on the lateral dendrite of the Mauthner cell, whereas projections from secondary neurom

69 he mGi may represent a mammalian analogue to Mauthner cells, with a separation of function for neuron