ライフサイエンスコーパス: barrage

1 stematically with the magnitude of the input barrages.

2 king is associated with increased inhibitory barrages and narrower visually evoked synaptic potential

3 activity, independent of ascending afferent barrage, and enlarged receptive fields.

4 The inhibitory barrages are effectively nullified at low doses of picro

5 Here, we injected EPSC barrages at the soma and at the proximal, middle, and di

6 4.4 mV for the IPSP and 3.0 mV for the EPSP barrage, because of temporal summation and/or facilitati

7 isted after interruption of ascending spinal barrage by spinal cord transection above the level of th

8 This barrage consisted of postsynaptic responses to spiking a

9 membrane potential (e.g., -65 mV), these PSP barrages could result in the activation of a low-thresho

10 dendritic and somatic EPSPs were identical, barrages delivered to the dendrite generated much higher

11 tal event, the number of preictal inhibitory barrages dropped, and in parallel with this change, the

12 In the distal dendrites, EPSC barrages evoked repetitive bursts of action potentials,

13 Beyond these clues, the mechanisms of barrage firing are unknown.

14 on of one interneuron in some cases triggers barrage firing in a nearby, unstimulated interneuron.

15 Together, these findings suggest that barrage firing is probably triggered by a multicellular

16 Induction of barrage firing was blocked by lowering extracellular cal

17 Finally, barrage firing was normal in mice with deletion of the p

18 Despite its calcium dependence, barrage firing was not prevented by inhibiting chemical

19 it here as 'retroaxonal barrage firing', or 'barrage firing' for short.

20 firing, we refer to it here as 'retroaxonal barrage firing', or 'barrage firing' for short.

21 ecorded interneuron with BAPTA did not block barrage firing, suggesting that the required calcium ent

22 nced virus transmission, but did not prevent barrage formation associated with mycelial incompatibili

23 ractions between two tightly linked genes in barrage formation, heterokaryon formation, and asymmetri

24 The enhanced afferent barrage from these neurons sensitizes spinal neurons and

25 oked plateau potentials in SGCs and synaptic barrages in downstream hilar neurons without blocking fa

26 These observations suggest that ectopic barrages in the injured IAN contribute more to the devel

27 are thought to reflect a sustained synaptic barrage, involving the coordination of hundreds of pyram

28 effects of different components of synaptic barrages (namely, depolarization, increase in membrane c

29 that one or more cometary airbursts/impacts barraged North America approximately 12,900 cal yr B.P.

30 When present, however, these inhibitory barrages occlude an intense excitatory synaptic drive th

31 tens of seconds to minutes produces a sudden barrage of action potentials lasting about a minute beyo

32 During the barrage of antidromic spikes, high-frequency firing will

33 ynchronous release component is reduced, the barrage of asynchronous GABA release from CCK interneuro

34 sensory input to the olfactory bulb evokes a barrage of asynchronous synaptic excitation and highly r

35 The barrage of comets and asteroids that produced many young

36 120-gp41) with CD4 and coreceptors trigger a barrage of conformational changes in Env that drive the

37 us synaptic bombardment, receiving a complex barrage of excitatory and inhibitory inputs.

38 By introducing a barrage of excitatory and inhibitory synaptic conductanc

39 nd stereotyped temporal sequence: an initial barrage of excitatory input was rapidly quenched by inhi

40 an olfactory nerve stimulation with a short barrage of excitatory inputs mediated by mitral, tufted,

41 neurons experience a significant spontaneous barrage of fast, amino-acid-mediate synaptic transmissio

42 work both types of neurone received a phasic barrage of gamma frequency excitatory inputs but, due to

43 n-specific firing despite receiving a steady barrage of heterogeneously tuned excitatory inputs that

44 (ii) The barrage of impulses that came from the peripheral nocice

45 (iii) The barrage of impulses that came from the sensitized second

46 d peptides attributable to an injury-induced barrage of impulses.

47 tion provides a means of selecting among the barrage of information reaching the retina and of enhanc

48 This persistence of firing during a constant barrage of inhibition raises the question of what patter

49 put from many PCs, resulting in a continuous barrage of inhibitory inputs.

50 idal cells resulting from the high frequency barrage of interneurons.

51 t synaptic conductance input, similar to the barrage of noisy synaptic input that cortical neurons ha

52 Unfortunately, the field is complicated by a barrage of overlapping clinical syndromes and histopatho

53 the integrity of the genome from a continual barrage of potentially detrimental insults.

54 stimulated with a computer-generated steady barrage of random inputs, mimicking weak synaptic conduc

55 nder natural conditions, animals encounter a barrage of sensory information from which they must sele

56 We hypothesized that the barrage of signals present in the extracellular milieu o

57 ryonic stages, immune cells are faced with a barrage of signals that will not all be directing the ce

58 rimate chromosomes were compared, creating a barrage of speculation.

59 tive must be accomplished despite a constant barrage of spontaneous DNA double strand breaks.

60 h increased production of cytokines led to a barrage of studies and lively debate on the relative con

61 ed by both a tonic and respiratory-modulated barrage of synaptic events that were blocked by intrathe

62 vent underlying the Up state is a maintained barrage of synaptic excitation, but that the membrane po

63 o increasing concentrations of odorants with barrages of action potentials, and their terminals have

64 or tolbutamide (50-200 microM), we recorded barrages of amperometric events.

65 al cells in vivo and in vitro receive strong barrages of both excitatory and inhibitory postsynaptic

66 fast spiking interneurons, receiving robust barrages of both excitatory and inhibitory synaptic pote

67 The firing evoked by injection of simulated barrages of EPSCs into the proximal dendrite of layer 5

68 ing the generation of spindle waves revealed barrages of EPSPs and IPSPs.

69 ed EPSPs was 4.7-fold greater than identical barrages of EPSPs generated from distal (572 +/- 13 micr

70 Sensory axon stimulation evokes barrages of EPSPs in Blanes cells that trigger long epoc

71 y for evoking action potentials, we injected barrages of EPSPs that simulate the inputs generated by

72 precision, can be achieved through balanced barrages of excitatory and inhibitory synaptic activity.

73 state, in which neurons transiently receive barrages of excitatory and inhibitory synaptic inputs th

74 ortical pyramidal cells receive proportional barrages of excitatory and inhibitory synaptic potential

75 ay be driven by rebound depolarization after barrages of GABA(A) receptor (GABA(A)R)-mediated IPSPs a

76 Pyramidal cells receive barrages of inhibitory inputs in advance of the epilepti

77 on," with the latter resulting from repeated barrages of neural activity from nociceptors.

78 we report that LGN neurons receive periodic barrages of postsynaptic currents from the retina that d

79 on and excitation of interneurons and evoked barrages of postsynaptic GABAergic currents.

80 In contrast, barrages of proximal simulated EPSPs enhanced the rate o

81 Here, the efficacy of barrages of simulated EPSPs generated at known dendritic

82 3 +/- 15 microm from soma; n = 28) dendritic barrages of simulated EPSPs was 4.7-fold greater than id

83 ed patch whole-cell recording, we found that barrages of such events were well coupled in time and gr

84 We first recorded barrages of synaptic conductances from neurons during ep

85 n rat hippocampal slices evoked long-lasting barrages of synaptic inputs in subpopulations of dentate

86 We found that synaptic barrages originate from semilunar granule cells (SGCs),

87 ite this level of excitation, the inhibitory barrages suppress firing, thereby limiting further neuro

88 g flow of excitatory and inhibitory synaptic barrages that not only control participation of neurons

89 g modulated component of the evoked synaptic barrages (the F1 component).

90 Synaptic barrages triggered persistent firing in hilar neurons (h

91 -5/6 received inputs that generated rhythmic barrages (up to 25 Hz) of antidromic spikes during BMPs.

92 llowed by a prolonged (up to 1 sec) synaptic barrage, which fatigued at stimulus repetition rates of

93 Mammalian cells are barraged with endogenous metabolic byproducts and enviro