ライフサイエンスコーパス: in behaving

1 this issue, we used chronic calcium imaging in behaving adult mice to examine the activity of indivi

2 multiple cortical and subcortical structures in behaving and anesthetized animals.

3 haracterizations of neuronal firing patterns in behaving animals and humans have suggested how neural

4 extended the exploration of neuroplasticity in behaving animals and humans.

5 of theta generation that operate in parallel in behaving animals and link them to anxiolytic drug act

6 ytotic dopamine release as a key AMPH action in behaving animals and support a unified mechanism of a

7 ology and plasticity of hippocampal circuits in behaving animals and that these changes have importan

8 reversible manipulations of neural activity in behaving animals are transforming our understanding o

9 The functional properties of neurons in behaving animals are typically assessed over time per

10 is of themedial entorhinal cortex, and which in behaving animals could support generation of grid-lik

11 cking a temporal pattern of their activation in behaving animals during auditory fear conditioning re

12 Key prospective usages include brain imaging in behaving animals for relating cellular dynamics to an

13 Information processing in behaving animals has been the target of many studies

14 neously record from large numbers of neurons in behaving animals has ushered in a new era for the stu

15 Unit recordings in behaving animals have revealed the transformation of

16 ly induced at the peak of local theta rhythm in behaving animals in region CA1 and that LTD was found

17 antifying the metabolism of the intact brain in behaving animals is clearly of interest.

18 Neural activity recorded in behaving animals is nonstationary, making it difficul

19 by developing birds; single-unit physiology in behaving animals is providing important clues about s

20 bute to cognition, their response properties in behaving animals is unclear.

21 ing, activation, and inactivation of neurons in behaving animals promise to revolutionize studies of

22 ence for an inverted U at the cellular level in behaving animals promises to bridge in vitro molecula

23 ted, the specific function of these circuits in behaving animals remains unknown.

24 In vivo recordings in behaving animals revealed that MD-PFC beta-range sync

25 Studies in behaving animals suggest that neurones located in the

26 this, we observe with large-scale recordings in behaving animals that the relative contribution of PV

27 his study used extracellular unit recordings in behaving animals to evaluate thalamocortical response

28 h of these techniques are broadly applicable in behaving animals to test hypotheses about the biophys

29 ese regions for study at cellular resolution in behaving animals using a rapidly expanding palette of

30 off, we optically recorded circuit activity in behaving animals while manipulating circuit function

31 llations (0.5-2 Hz in anesthetized, 0.5-4 Hz in behaving animals) and supratheta (6-10 Hz in anesthet

32 upratheta (6-10 Hz in anesthetized, 10-25 Hz in behaving animals) bands.

33 m of longitudinal analysis of brain activity in behaving animals, allowing dissociation of the roles

34 efficiently relay information to the cortex in behaving animals, but have markedly different consequ

35 minent feature of neuronal activity recorded in behaving animals, but the mechanism by which it occur

36 each type of processing relates to the other in behaving animals, despite their common substrate.

37 h caused thermal and mechanical hyperalgesia in behaving animals, induced an enhancement of transmiss

38 In behaving animals, local inhibition of PKMzeta disrupt

39 of LC activity, similar to those that occur in behaving animals, may be more effective in increasing

40 these fluctuations was twofold smaller than in behaving animals, passive animals had the same patter

41 me sequential agonist and antagonist methods in behaving animals, we demonstrate that the conditioned

42 ng and calcium imaging of egg-laying muscles in behaving animals, we found that the muscles appear to

43 cell-type-specific optogenetic manipulations in behaving animals, we show that dendrite-targeting som

44 hroughput long-term extracellular recordings in behaving animals.

45 al control of neuronal activity and circuits in behaving animals.

46 tigated the functional contributions of FSIs in behaving animals.

47 iming rule for cue-reward learning paradigms in behaving animals.

48 in layer II of the medial entorhinal cortex in behaving animals.

49 terneurons contribute to cerebellar function in behaving animals.

50 as been characterized electrophysiologically in behaving animals.

51 these cells has not previously been studied in behaving animals.

52 tissue organization and signaling mechanisms in behaving animals.

53 e fluctuations similar in many ways to those in behaving animals.

54 the firing properties of CA1 and CA3 neurons in behaving animals.

55 se as transgenically encoded calcium sensors in behaving animals.

56 ation for odor discrimination and adaptation in behaving animals.

57 f biophysical control mechanisms are evident in behaving animals.

58 ntial, ultimately, to study these properties in behaving animals.

59 e involvement of MAPK in learning and memory in behaving animals.

60 emerged as a suitable method for such tasks in behaving animals.

61 cordings of spontaneous cholinergic dynamics in behaving animals.

62 ver, on the coding of odors among OT neurons in behaving animals.

63 llenges with closed-loop optogenetic control in behaving animals.

64 imaging of cortical function and dysfunction in behaving animals.

65 thus it has remained challenging to perform in behaving animals.

66 ether they occur or what their role might be in behaving animals.

67 sibly reduce the firing of serotonin neurons in behaving animals.

68 es of individual miRNAs have been elucidated in behaving animals.

69 of MEC neurons, such as grid cells, recorded in behaving animals.

70 We confirmed both of these hypotheses in behaving animals.

71 the selection of a target among distractors in behaving animals.

72 ns comes from recordings of individual cells in behaving animals; however, it is notoriously difficul

73 n vivo, we show fluorescence voltage sensing in behaving Caenorhabditis elegans.

74 Here we show that in behaving cats, thalamocortical neurons in the lateral

75 ivation of parvalbumin-positive interneurons in behaving ChR2-EYFP reporter mice.

76 he ability to perform patch-clamp recordings in behaving Drosophila promises to help unify the unders

77 cordings from genetically identified neurons in behaving Drosophila.

78 d a rapid tonic firing during tonic seizures in behaving GEPR-9s, suggesting that the MGB may be impl

79 tigate neural correlates of visual attention in behaving honeybees (Apis mellifera).

80 synaptic signaling by specific ion channels in behaving humans.

81 rnal circuitry of the motor cortex for study in behaving humans.

82 saturation via multi-wavelength irradiation in behaving hyperoxic rats.

83 nic lines, optogenetics, and calcium imaging in behaving larval zebrafish.

84 Stimulation of the MRN in behaving malnourished animals may markedly affect the

85 rol of nociception and central sensitization in behaving mammals and enables selective activation of

86 t progress and future directions for imaging in behaving mammals from a systems engineering perspecti

87 the causal impact of biochemical signalling in behaving mammals, in a targetable and temporally prec

88 g capabilities for recording neural dynamics in behaving mammals, including the means to monitor hund

89 ctivate these neurons at different intervals in behaving mice and were able to fragment sleep without

90 New electrophysiological recordings in behaving mice by Luo, Fee and Katz reveal aspects of

91 Microdialysis in behaving mice confirmed that EE normalized increases

92 Intracellular recordings in behaving mice demonstrate that bimodal excitation dri

93 macological disruption of glucagon signaling in behaving mice indicated a critical role for glucagon

94 n of BF cholinergic or glutamatergic neurons in behaving mice produced significant effects on state c

95 releasing parafacial zone (PZ(Vgat)) neurons in behaving mice produces slow-wave-sleep (SWS), even in

96 ortex (V1) and lateromedial (LM) visual area in behaving mice revealed that the variability in LM neu

97 ity of large populations of cortical neurons in behaving mice subject to visual stimuli.

98 Here we show for the first time in behaving mice that the somatostatin-expressing neuron

99 ciative learning tasks), we decided to study in behaving mice the putative changes in strength taking

100 multi-channel epidural ERP characterization in behaving mice with high precision, reliability and co

101 mulation, neural recording and drug delivery in behaving mice with high resolution.

102 In behaving mice with unilateral SCI, four consecutive 2

103 In behaving mice, cholinergic stimulation was less effec

104 In behaving mice, the same peptides function as individu

105 Using in vivo intracellular recordings in behaving mice, we find that excitatory neurons in the

106 g optogenetics and multi-electrode recording in behaving mice, we found that brief selective drive of

107 surement of neuronal and glial cell activity in behaving mice, we have developed fluorescence imaging

108 Here, using two-photon calcium imaging in behaving mice, we show that granule cells convey info

109 and cell type-specific deep-brain recordings in behaving mice, we show that orexin cell activation ra

110 ed with optogenetic and molecular techniques in behaving mice, we show that SOM(+) CeL neurons are ac

111 By recording and labeling individual neurons in behaving mice, we show that the representation of bri

112 the hippocampus with subcellular resolution in behaving mice.

113 iated with decreased sweet taste sensitivity in behaving mice.

114 it dynamics and alter spatial working memory in behaving mice.

115 ing fear learning and extinction over 6 days in behaving mice.

116 vioural, hormonal and dopaminergic responses in behaving mice.

117 d large-scale recording of neuronal activity in behaving mice.

118 maintain SWS or EEG slow-wave activity (SWA) in behaving mice.

119 layer-specific modulation of their activity in behaving mice.

120 ays, in slices of mouse dorsal striatum, and in behaving mice.

121 ate single, genetically identified glomeruli in behaving mice.

122 me from two sources: single-neuron recording in behaving monkeys and assessment of the visual abiliti

123 deling, voltage-sensitive dye imaging (VSDI) in behaving monkeys and behavioral measurements in human

124 ngs of the activity of cervical interneurons in behaving monkeys has elucidated their contribution to

125 the firing rates of single neurons recorded in behaving monkeys remain elevated without external cue

126 Studies in behaving monkeys show that neural output from the mot

127 functional properties of the insular cortex in behaving monkeys using intracortical microstimulation

128 In behaving monkeys, Thura and Cisek (2017, in this issu

129 Using functional magnetic resonance imaging in behaving monkeys, we demonstrated a network of cortic

130 Using voltage-sensitive dye imaging in behaving monkeys, we measured neural population respo

131 on in V1 using voltage-sensitive dye imaging in behaving monkeys.

132 t for these mechanisms during motor learning in behaving monkeys.

133 motion artifacts, including calcium dynamics in behaving mouse brain and transient morphology changes

134 dal locomotion with extracellular recordings in behaving NHPs at rest and during locomotion.

135 motor neuronal system present within the MRF in behaving NHPs under normal conditions, in accordance

136 f a locomotor neuronal system within the MRF in behaving NHPs.

137 otor neuroprostheses are widely investigated in behaving non-human primates, but technical constraint

138 ng the responses of tonically active neurons in behaving primates, we found that these correlations h

139 locomotor neuronal circuit within these MRF in behaving primates.

140 Here we show in behaving rabbits that tDCS applied over the somatosen

141 he firing activities of MC neurons, recorded in behaving rabbits, are related to and preceded the ini

142 ) in the acquisition of a trace conditioning in behaving rabbits.

143 ity in motor cortex and basal ganglia output in behaving rats after dopamine cell lesion.

144 the somatosensory area and prefrontal cortex in behaving rats and mice.

145 nhancement of LTP in the VTA and cocaine CPP in behaving rats both require glucocorticoid receptor ac

146 monitoring sensory stimulus-evoked responses in behaving rats by measuring hemodynamic responses in t

147 phetamine-conditioned place preference (CPP) in behaving rats correlates with the magnitude of mGluR-

148 wever, previous electrophysiological studies in behaving rats have reported firing patterns consisten

149 By contrast, studies in behaving rats report pronounced excitation during mov

150 Microinfusions of 2-AG into the PBN in behaving rats robustly stimulated feeding of pellets

151 -specific optogenetics and electrophysiology in behaving rats to search for selective functions of st

152 In behaving rats trained to discriminate between two odo

153 of 94 presumed medium spiny striatal neurons in behaving rats treated with AA or vehicle and examined

154 DLSC neuronal firing changes in behaving rats were subsequently examined, using chron

155 We disrupted OFC activity in behaving rats with a use-dependent NMDA antagonist to

156 In behaving rats, isradipine injected into the VTA suppr

157 We report here a test of this hypothesis in behaving rats, monitoring respiratory activity throug

158 of individual hippocampal principal neurons in behaving rats, such as place fields, theta modulation

159 In behaving rats, thalamic responses were normally small

160 Using multichannel unit recording techniques in behaving rats, we observed sustained conditioned tone

161 linically relevant concentrations of ethanol in behaving rats, without influences from the rest of th

162 esthetized rats and extracellular recordings in behaving rats.

163 noncholinergic basal forebrain (BF) neurons in behaving rats.

164 d the oscillatory synaptic activity detected in behaving rats.

165 1 pyramidal cell burst activity was examined in behaving rats.

166 bility to develop acute tolerance to alcohol in behaving rats.

167 AT) technique is described for brain imaging in behaving rats.

168 ence of local sleep during wake as described in behaving rats.

169 amus (VPMpc) processes gustatory information in behaving rats.

170 bic and infralimbic subdivisions of the mPFC in behaving rats.

171 dings in a motor area of the cerebral cortex in behaving rhesus monkeys (Macaca mulatta) were used to

172 these possibilities, we examined grid cells in behaving rodents as they made long trajectories acros

173 as been the subject of intense investigation in behaving rodents, much less is known on how VPMpc neu

174 how the potential of 3D-wPAT for brain study in behaving rodents.

175 f behaviour requires studying brain activity in behaving subjects using complementary techniques that

176 ntly been imaged with single-cell resolution in behaving vertebrates.

177 to record from 22 neuromodulatory cell types in behaving zebrafish during a reaction-time task that r