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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 e dendrites of TRN neurons to regulate their bursting activity.
10 ilure and a striking reduction in phrenic MN bursting activity.
11 coupled to L-type Ca(2+) channels determines bursting activity.
12 calcium channels determines the promotion of bursting activity.
13 if iMSN and cortical inputs show substantial bursting activity.
14 C-derived networks showed unique patterns of bursting activity.
15 egulated appear to be phase relationships of bursting activity.
16 zed oscillations in the form of seizure-like bursting activity.
17 and dopamine a key regulator, of spontaneous bursting activity.
18 hey express more highly correlated, rhythmic bursting activity.
19 esigned for the digitization and analysis of bursting activity.
20 shock by increasing spontaneous activity and bursting activity.
21 ere was a significant reduction in organized bursting activity.
22  contractions first appear with the onset of bursting activity 17 hours after egg laying.
23 s with wide-spiking pattern showed increased bursting activity along with increased spike timing vari
24  efficacy by completely blocking spontaneous bursting activity, along with potency greater than that
25              Blockade or slowing of rhythmic bursting activity also prevents the normal expression pa
26 loping neural circuits generate synchronized bursting activity among neighboring neurons, a pattern t
27                           Both during normal bursting activity and antidromic nerve stimulation, the
28 olved in cellular responses such as neuronal bursting activity and cardiac rhythm.
29 zation, leading to the generation of plateau-bursting activity and facilitated Ca(2+) entry.
30 el system leads to the generation of plateau-bursting activity and high-amplitude Ca(2+) transients.
31 ugh voltage-gated Ca channels often supports bursting activity and mediates graded transmitter releas
32    Graphene electrodes record high-frequency bursting activity and slow synaptic potentials that are
33 e in the afferent control of dopamine neuron bursting activity and that this control is exerted via a
34 on is to increase the likelihood of extended bursting activity and thus markedly augment Ca(2+) relea
35 oot stimulation could evoke regular rhythmic bursting activity, and our data suggested that capsaicin
36 te consisted of initial large spikes, cyclic bursting activity, and small spikes lasting up to a minu
37 re of coupling, DBS's modulation of cortical bursting activity appeared to amplify the brain signals'
38 ous, highly rhythmic episodes of propagating bursting activity are present early during the developme
39 ltricial rodents and that apical IHCs showed bursting activity as opposed to more sustained firing in
40 es that Cav3.3 may be the most important for bursting activity associated with the GnRH/LH (luteinizi
41 revious studies suggest that the spontaneous bursting activity, asynchronous between the two eyes, co
42  potential depolarisation and high-frequency bursting activity at preferred whisker angles.
43 , which explains the pump's contributions to bursting activity based on Na(+) dynamics.
44 neous recordings demonstrated a delay in the bursting activity between different segments, with great
45 nd h-current expands the range of functional bursting activity by avoiding transitions into nonfuncti
46 that a moderate decrease in the frequency of bursting activity, caused by in ovo application of the G
47 ability (P(o)) of the InsP(3)R-1 and induced bursting activity, characterized by extended periods of
48 tory synaptic drives involved in spontaneous bursting activity, contribute differentially to the spat
49  of dopamine neurons in normal mice included bursting activity, DD mice recordings showed only a sing
50            However, the precise frequency of bursting activity differentially affects the two major p
51 pontaneously generates a pattern of rhythmic bursting activity during the period when the connectivit
52 ight exhibit similar patterns of spontaneous bursting activity early in development but later develop
53 e stimulated with trains of pulses mimicking bursting activity, EJPs facilitated more in individuals
54 olve an increase in spontaneous asynchronous bursting activity (epileptiform activity) induced either
55 ockers, which produced three rates of spinal bursting activity: fast, intermediate, and slow.
56 mportant cellular responses such as neuronal bursting activity, fluid secretion, and cardiac rhythmic
57 one group showed a transient increase in the bursting activity, followed by a decrease and cessation
58  photoreceptor drive but rather some form of bursting activity generated in the inner retina, as a re
59 ution of the Na(+)/K(+) pump current to such bursting activity has not been well studied.
60 )-free perifusion medium induced oscillatory bursting activity in all sixty-nine cells displaying bot
61                                              Bursting activity in B51 was associated with, and predic
62                                We found that bursting activity in cell B51 contributed significantly
63 ed video-rate calcium imaging of spontaneous bursting activity in chick embryonic retinal ganglion ce
64 onist bicuculline had a greater influence on bursting activity in complex versus simple cultures.
65 ristic of immature synaptic connections, and bursting activity in developing spinal neurons may promo
66 onic firing pattern with very few exhibiting bursting activity in elevated K(+).
67 itatory neurotransmission driving correlated bursting activity in ganglion cells is not fixed but und
68 y play a prominent role in modulating phasic bursting activity in guinea pig vasopressin neurones.
69  supported by the finding of an increased MN bursting activity in immature SOD1(G93A) spinal cords an
70  methods to show that synchronous infra-slow bursting activity in mitral cells of the mouse accessory
71 is a key determining factor for the onset of bursting activity in mouse ventricular myocytes.
72  is supported by the observation of enhanced bursting activity in neurons expressing a gain of functi
73 stonic mice revealed abnormal high-frequency bursting activity in neurons of the deep cerebellar nucl
74 n increase in the frequency and amplitude of bursting activity in neurons with intrinsic bursting pro
75                             Glucose triggers bursting activity in pancreatic islets, which mediates t
76 nstrate here that BK channels indeed promote bursting activity in pituitary cells.
77 s correlated, in an Uva dependent manner, to bursting activity in RA, rather than to the respiratory
78                                              Bursting activity in STN neurones could be induced pharm
79 BAergic transmission to generate correlated, bursting activity in STN neurons.
80 nic activity in the EUS (+56%, n = 7) whilst bursting activity in the EUS became desynchronised.
81 of transient spontaneous and evoked neuronal bursting activity in the formation of functional circuit
82 y throughout the network as well as a robust bursting activity in the thalamus, which is consistent w
83 ntributes to the development of epileptiform bursting activity in the TSC2(+/-) CA3 region of the hip
84                                              Bursting activity in trigeminal motoneurons is consisten
85 c dysfunction, evident as: an increase in LC bursting activity; in tyrosine hydroxylase expression an
86 ioxolane-linked channels opened in a mode of bursting activity instead of remaining in the open state
87                 At 2 d postinjury, intrinsic bursting activity is lost within the intact population.
88 ate that, under our conditions, postsynaptic bursting activity is necessary for associative synaptic
89 ue motoneurons, we conclude that spontaneous bursting activity is not required for the process of nor
90 rizing afterpotential (DAP), which modulates bursting activity, is reduced in isolated GnRH neurons f
91 ing the frequency of episodes of spontaneous bursting activity, known to be important for motor circu
92 polar cells in providing endogenous drive to bursting activity later in development.
93                          The nonlinearity of bursting activity might enable pacemaker neurons to faci
94  of inactivity alternating with intervals of bursting activity (mode changes).
95                                      In STN, bursting activity most commonly preceded the LFP oscilla
96                                              Bursting activity occurs as the channel shuttles rapidly
97 g GABAA receptors leads to a decrease in the bursting activity of all ganglion cells, suggesting that
98 at HRs exhibit higher basal firing rates and bursting activity of DA neurons in the ventral tegmental
99         In sleeping adult birds, spontaneous bursting activity of forebrain premotor neurons in the r
100  depolarizations correlated with synchronous bursting activity of interneurons.
101 T cholinergic axons selectively enhanced the bursting activity of mesolimbic dopamine neurons that we
102 namics of different ionic currents shape the bursting activity of neurons and networks that control m
103 nteracts with the h-current can regulate the bursting activity of neurons and networks.
104 rter, to examine the role of the pump on the bursting activity of oscillator heart interneurons in le
105  profound and tutor-song-specific changes in bursting activity of RA neurons during the following nig
106 suggesting that they were caused by periodic bursting activity of synaptically coupled cells.
107 he Po predominately by facilitating extended bursting activity of the channel but the underlying biop
108 fusion of glutamate increased the firing and bursting activity of VTA DA neurons.
109 aine injection increases the firing rate and bursting activity of VTA dopamine neurons, and that thes
110 d by perturbation of the normal frequency of bursting activity or interference with GABA(A) receptor
111  increased firing rate, and development of a bursting activity pattern accompany MN-1 respecification
112 eurons display a synchronized high-frequency bursting activity preceding each milk ejection.
113 to assess its role in shaping and modulating bursting activity promoted by pharmacological manipulati
114                              The findings of bursting activity, rather than sustained oscillations in
115 ighboring ganglion cells express spontaneous bursting activity (SBA), resulting in propagating waves.
116 le paired STN and GP recordings of tonic and bursting activity show no evidence of coherent activity.
117 e, amplitude, and duration; (2) intermediate bursting activity showed increased rate and duration, bu
118 odulated during c-tsDC stimulation: (1) fast bursting activity showed increased rate, amplitude, and
119 ation, but decreased amplitude; and (3) slow bursting activity showed increased rate, but decreased d
120 Vim, LFP oscillations most commonly preceded bursting activity, suggesting that neuronal firing may b
121 e indicated that these models often generate bursting activity that closely resembles epileptic activ
122 the retina generate synchronized patterns of bursting activity that contain information useful for pa
123 lateral caudal (IC) cells, generate inherent bursting activity that depends upon a persistent sodium
124 y designer drugs (DREADDs) restores rhythmic bursting activity to a previously paralyzed diaphragm wi
125 ellular microelectrode suppresses endogenous bursting activity to account for the discrepancy with re
126 on by channelrhodopsin-2 was used to restore bursting activity to the control frequency.
127 , based on the comparison between the target bursting activity triggered by the teaching signal and t
128                  By blocking or slowing this bursting activity, via in ovo drug applications at preci
129                                 The observed bursting activity was abolished and the spontaneous disc
130 or interspike interval variability of phasic bursting activity was affected.
131 be assessed because when varied individually bursting activity was not maintained.
132                                         This bursting activity was of the same frequency as the somat
133                          In addition, spinal bursting activity was significantly modulated during c-t
134 ance parameters maintaining functional leech bursting activity, we applied Principal Component Analys
135 fine the cellular basis for hypersynchronous bursting activity, we studied the occurrence of paroxysm
136 nces in the robust maintenance of functional bursting activity, we used our existing database of half
137                           Characteristics of bursting activity were assessed during c-tsDC stimulatio
138 ons/organoids, we found increased excitatory bursting activity, which could be explained in part by a
139 v3.2 channels contribute to a high-frequency-bursting activity, which is increased in the spared nerv
140                         Rhythmic spontaneous bursting activity, which occurs in many developing neura
141  in creating avalanches--patterns of complex bursting activity with scale-free properties--is examine
142 osed of a few hundred neurons that alternate bursting activity with silent periods, but the mechanism

 
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