ライフサイエンスコーパス: bursting activity

1 terns, application of either blocker induced bursting activity.

2 k plateau potential generation, also affects bursting activity.

3 rtical activity exhibits rhythmic population bursting activity.

4 ulate nucleus, GABA suppresses ganglion cell bursting activity.

5 eously active, showing both single spike and bursting activity.

6 are found to undergo correlated spontaneous bursting activity.

7 modulated during lactation to support short bursting activity.

8 ctivating cation currents also did not alter bursting activity.

9 egulated appear to be phase relationships of bursting activity.

10 zed oscillations in the form of seizure-like bursting activity.

11 and dopamine a key regulator, of spontaneous bursting activity.

12 hey express more highly correlated, rhythmic bursting activity.

13 esigned for the digitization and analysis of bursting activity.

14 shock by increasing spontaneous activity and bursting activity.

15 ere was a significant reduction in organized bursting activity.

16 contractions first appear with the onset of bursting activity 17 hours after egg laying.

17 efficacy by completely blocking spontaneous bursting activity, along with potency greater than that

18 Blockade or slowing of rhythmic bursting activity also prevents the normal expression pa

19 loping neural circuits generate synchronized bursting activity among neighboring neurons, a pattern t

20 Both during normal bursting activity and antidromic nerve stimulation, the

21 olved in cellular responses such as neuronal bursting activity and cardiac rhythm.

22 zation, leading to the generation of plateau-bursting activity and facilitated Ca(2+) entry.

23 el system leads to the generation of plateau-bursting activity and high-amplitude Ca(2+) transients.

24 ugh voltage-gated Ca channels often supports bursting activity and mediates graded transmitter releas

25 Graphene electrodes record high-frequency bursting activity and slow synaptic potentials that are

26 e in the afferent control of dopamine neuron bursting activity and that this control is exerted via a

27 on is to increase the likelihood of extended bursting activity and thus markedly augment Ca(2+) relea

28 oot stimulation could evoke regular rhythmic bursting activity, and our data suggested that capsaicin

29 te consisted of initial large spikes, cyclic bursting activity, and small spikes lasting up to a minu

30 ous, highly rhythmic episodes of propagating bursting activity are present early during the developme

31 ltricial rodents and that apical IHCs showed bursting activity as opposed to more sustained firing in

32 es that Cav3.3 may be the most important for bursting activity associated with the GnRH/LH (luteinizi

33 revious studies suggest that the spontaneous bursting activity, asynchronous between the two eyes, co

34 potential depolarisation and high-frequency bursting activity at preferred whisker angles.

35 , which explains the pump's contributions to bursting activity based on Na(+) dynamics.

36 neous recordings demonstrated a delay in the bursting activity between different segments, with great

37 that a moderate decrease in the frequency of bursting activity, caused by in ovo application of the G

38 ability (P(o)) of the InsP(3)R-1 and induced bursting activity, characterized by extended periods of

39 tory synaptic drives involved in spontaneous bursting activity, contribute differentially to the spat

40 of dopamine neurons in normal mice included bursting activity, DD mice recordings showed only a sing

41 However, the precise frequency of bursting activity differentially affects the two major p

42 pontaneously generates a pattern of rhythmic bursting activity during the period when the connectivit

43 ight exhibit similar patterns of spontaneous bursting activity early in development but later develop

44 e stimulated with trains of pulses mimicking bursting activity, EJPs facilitated more in individuals

45 olve an increase in spontaneous asynchronous bursting activity (epileptiform activity) induced either

46 ockers, which produced three rates of spinal bursting activity: fast, intermediate, and slow.

47 mportant cellular responses such as neuronal bursting activity, fluid secretion, and cardiac rhythmic

48 one group showed a transient increase in the bursting activity, followed by a decrease and cessation

49 photoreceptor drive but rather some form of bursting activity generated in the inner retina, as a re

50 ution of the Na(+)/K(+) pump current to such bursting activity has not been well studied.

51 )-free perifusion medium induced oscillatory bursting activity in all sixty-nine cells displaying bot

52 Bursting activity in B51 was associated with, and predic

53 We found that bursting activity in cell B51 contributed significantly

54 ed video-rate calcium imaging of spontaneous bursting activity in chick embryonic retinal ganglion ce

55 ristic of immature synaptic connections, and bursting activity in developing spinal neurons may promo

56 onic firing pattern with very few exhibiting bursting activity in elevated K(+).

57 itatory neurotransmission driving correlated bursting activity in ganglion cells is not fixed but und

58 y play a prominent role in modulating phasic bursting activity in guinea pig vasopressin neurones.

59 supported by the finding of an increased MN bursting activity in immature SOD1(G93A) spinal cords an

60 methods to show that synchronous infra-slow bursting activity in mitral cells of the mouse accessory

61 is a key determining factor for the onset of bursting activity in mouse ventricular myocytes.

62 is supported by the observation of enhanced bursting activity in neurons expressing a gain of functi

63 stonic mice revealed abnormal high-frequency bursting activity in neurons of the deep cerebellar nucl

64 n increase in the frequency and amplitude of bursting activity in neurons with intrinsic bursting pro

65 Glucose triggers bursting activity in pancreatic islets, which mediates t

66 nstrate here that BK channels indeed promote bursting activity in pituitary cells.

67 s correlated, in an Uva dependent manner, to bursting activity in RA, rather than to the respiratory

68 Bursting activity in STN neurones could be induced pharm

69 BAergic transmission to generate correlated, bursting activity in STN neurons.

70 nic activity in the EUS (+56%, n = 7) whilst bursting activity in the EUS became desynchronised.

71 of transient spontaneous and evoked neuronal bursting activity in the formation of functional circuit

72 ntributes to the development of epileptiform bursting activity in the TSC2(+/-) CA3 region of the hip

73 Bursting activity in trigeminal motoneurons is consisten

74 c dysfunction, evident as: an increase in LC bursting activity; in tyrosine hydroxylase expression an

75 ioxolane-linked channels opened in a mode of bursting activity instead of remaining in the open state

76 At 2 d postinjury, intrinsic bursting activity is lost within the intact population.

77 ate that, under our conditions, postsynaptic bursting activity is necessary for associative synaptic

78 ue motoneurons, we conclude that spontaneous bursting activity is not required for the process of nor

79 rizing afterpotential (DAP), which modulates bursting activity, is reduced in isolated GnRH neurons f

80 ing the frequency of episodes of spontaneous bursting activity, known to be important for motor circu

81 polar cells in providing endogenous drive to bursting activity later in development.

82 The nonlinearity of bursting activity might enable pacemaker neurons to faci

83 of inactivity alternating with intervals of bursting activity (mode changes).

84 Bursting activity occurs as the channel shuttles rapidly

85 g GABAA receptors leads to a decrease in the bursting activity of all ganglion cells, suggesting that

86 at HRs exhibit higher basal firing rates and bursting activity of DA neurons in the ventral tegmental

87 In sleeping adult birds, spontaneous bursting activity of forebrain premotor neurons in the r

88 depolarizations correlated with synchronous bursting activity of interneurons.

89 T cholinergic axons selectively enhanced the bursting activity of mesolimbic dopamine neurons that we

90 namics of different ionic currents shape the bursting activity of neurons and networks that control m

91 nteracts with the h-current can regulate the bursting activity of neurons and networks.

92 rter, to examine the role of the pump on the bursting activity of oscillator heart interneurons in le

93 profound and tutor-song-specific changes in bursting activity of RA neurons during the following nig

94 suggesting that they were caused by periodic bursting activity of synaptically coupled cells.

95 he Po predominately by facilitating extended bursting activity of the channel but the underlying biop

96 fusion of glutamate increased the firing and bursting activity of VTA DA neurons.

97 aine injection increases the firing rate and bursting activity of VTA dopamine neurons, and that thes

98 d by perturbation of the normal frequency of bursting activity or interference with GABA(A) receptor

99 increased firing rate, and development of a bursting activity pattern accompany MN-1 respecification

100 eurons display a synchronized high-frequency bursting activity preceding each milk ejection.

101 to assess its role in shaping and modulating bursting activity promoted by pharmacological manipulati

102 ighboring ganglion cells express spontaneous bursting activity (SBA), resulting in propagating waves.

103 le paired STN and GP recordings of tonic and bursting activity show no evidence of coherent activity.

104 e, amplitude, and duration; (2) intermediate bursting activity showed increased rate and duration, bu

105 odulated during c-tsDC stimulation: (1) fast bursting activity showed increased rate, amplitude, and

106 ation, but decreased amplitude; and (3) slow bursting activity showed increased rate, but decreased d

107 e indicated that these models often generate bursting activity that closely resembles epileptic activ

108 the retina generate synchronized patterns of bursting activity that contain information useful for pa

109 lateral caudal (IC) cells, generate inherent bursting activity that depends upon a persistent sodium

110 ellular microelectrode suppresses endogenous bursting activity to account for the discrepancy with re

111 on by channelrhodopsin-2 was used to restore bursting activity to the control frequency.

112 By blocking or slowing this bursting activity, via in ovo drug applications at preci

113 The observed bursting activity was abolished and the spontaneous disc

114 or interspike interval variability of phasic bursting activity was affected.

115 be assessed because when varied individually bursting activity was not maintained.

116 This bursting activity was of the same frequency as the somat

117 In addition, spinal bursting activity was significantly modulated during c-t

118 ance parameters maintaining functional leech bursting activity, we applied Principal Component Analys

119 fine the cellular basis for hypersynchronous bursting activity, we studied the occurrence of paroxysm

120 nces in the robust maintenance of functional bursting activity, we used our existing database of half

121 Characteristics of bursting activity were assessed during c-tsDC stimulatio

122 Rhythmic spontaneous bursting activity, which occurs in many developing neura

123 in creating avalanches--patterns of complex bursting activity with scale-free properties--is examine

124 osed of a few hundred neurons that alternate bursting activity with silent periods, but the mechanism