ライフサイエンスコーパス: calcium imaging

1 sponses to 5-HT were determined by live cell calcium imaging.

2 sinophil activation as we show by intravital calcium imaging.

3 ectrode voltage-clamp electrophysiology, and calcium imaging.

4 cortex, recorded simultaneously by widefield calcium imaging.

5 tive in the hemicord, which was confirmed by calcium imaging.

6 ellular activity in the DMS astrocytes using calcium imaging.

7 antly assessed through behavioral assays and calcium imaging.

8 MP6 mice from both sexes by using mesoscopic calcium imaging.

9 tool for examining these structures has been calcium imaging.

10 of OT neurons in awake mice using two-photon calcium imaging.

11 lls of the mouse barrel cortex using in vivo calcium imaging.

12 rding local network activity with two-photon calcium imaging.

13 fixed sucrose preference task and two-photon calcium imaging.

14 strocytes appeared dormant during time-lapse calcium imaging, a subgroup displayed persistent, rhythm

15 for simultaneous optogenetic stimulation and calcium imaging across wide areas of brain slice enables

16 Using two-photon calcium imaging and electrophysiological recordings in t

17 ndplates and muscle fibers is confirmed with calcium imaging and electrophysiological recordings.

18 dge, we recorded PPC activity using 2-photon calcium imaging and electrophysiology during a visual od

19 Here, we use two-photon calcium imaging and electrophysiology in head-fixed walk

20 of all-atom molecular dynamics simulations, calcium imaging and electrophysiology, we identify an al

21 e effects on single neurons using two-photon calcium imaging and found that the increase in response

22 neurons of the lateral OFC using two-photon calcium imaging and investigated how OFC dynamically int

23 monitored FSI activity with fiber photometry calcium imaging and manipulated FSI activity with chemog

24 of the focus using bihemispheric wide-field calcium imaging and multielectrode arrays.

25 By means of time-lapse in vivo calcium imaging and neural activity manipulation in free

26 Using two-photon calcium imaging and Neuropixels probe recordings of Purk

27 Applying 2-photon calcium imaging and optogenetic manipulation of anatomic

28 Projection-specific two-photon calcium imaging and optogenetic manipulations show that

29 r and flow in individual brain microvessels, calcium imaging and optogenetics allow the investigation

30 We used calcium imaging and optogenetics in a sequential decisio

31 Here we combine two-photon calcium imaging and optogenetics in tethered flying flie

32 Ac) by combining patch-clamp recordings with calcium imaging and optogenetics.

33 Calcium imaging and optrode recording showed that they a

34 By combining two-photon calcium imaging and patch-clamp electrophysiological rec

35 Calcium imaging and patch-clamp experiments show that G2

36 We combined optogenetics with calcium imaging and pharmacology to demonstrate that sti

37 6 weeks) were used for live-cell fluorescent calcium imaging and qRT-PCR to determine the expression

38 application of optogenetics, chemogenetics, calcium imaging and related approaches.

39 METHODS AND The CRESCENT trial (Calcium Imaging and Selective CT Angiography in Comparis

40 ntifying integrator neurons using two-photon calcium imaging and then reconstructing the same neurons

41 d computational methods, based on two-photon calcium imaging and two-photon optogenetics, to detect,

42 ical' combination of simultaneous two-photon calcium imaging and two-photon optogenetics, we identifi

43 Recently, several studies using two-photon calcium imaging and virtual navigation have identified "

44 ISPR-Cas9), electrophysiological recordings, calcium imaging, and behavioral analyses, we demonstrate

45 ope, quantitative polymerase chain reaction, calcium imaging, and DREADD (designer receptor exclusive

46 We use confocal microscopy, calcium imaging, and electrophysiology to show that in e

47 assays using patch-clamp electrophysiology, calcium imaging, and multielectrode array (MEA) experime

48 slice electrophysiology, in vivo two-photon calcium imaging, and optical imaging of intrinsic signal

49 ue utilizing behavioral modeling, two-photon calcium imaging, and optogenetic inactivation in mice.

50 l motion capture, in vivo electrophysiology, calcium imaging, and optogenetics, we demonstrate a nove

51 Using rabies tracing, calcium imaging, and patch-clamp recordings, we show tha

52 nsgenic mouse brain slice model that enables calcium imaging as a quantitative readout of neuronal ac

53 vation was evaluated by c-Fos expression and calcium imaging at one minute after the anesthetic admin

54 e model for the optimization of three-photon calcium imaging based on experimentally tractable parame

55 Our approach highlights how two-color calcium imaging can help identify and localize the origi

56 Concurrent with SWR recordings, we performed calcium imaging, cell-attached, and whole-cell recording

57 ng, immunohistochemistry, optogenetic (GCaMP calcium imaging, channelrhodopsin), and colon motility s

58 ogy research for performing in vivo neuronal calcium imaging, colocalization of fluorescent labels, n

59 build on recent improvements in single-cell calcium imaging combined with optogenetics to test the c

60 neous intracellular recording and two-photon calcium imaging confirm that fluorescence activity is li

61 h at a rate of 0.66 +/- 0.02 um h(-1) pN(-1) Calcium imaging confirmed the strong increase in elongat

62 targeted, three-dimensional (3D) two-photon calcium imaging coupled with immunohistochemistry-based

63 e present CaImAn, an open-source library for calcium imaging data analysis.

64 ctivity of each neuron from raw fluorescence calcium imaging data is a nontrivial problem.

65 Synthetic calcium imaging data showed that, compared to uncorrecte

66 Neuroanatomical analysis and two-photon calcium imaging demonstrate that DALcl1 and DALcl2 form

67 Wide-field, cellular-resolution GCamP7b calcium imaging demonstrated similar initial patterns of

68 In vivo calcium imaging demonstrates that, as their shape predic

69 Two-photon calcium imaging during decision making revealed that the

70 Calcium imaging during valence-based learning exhibited

71 Here, we use in vivo calcium imaging, electrophysiology, and behavior to unde

72 Using immunohistochemistry, calcium imaging, electrophysiology, impedance measuremen

73 Widefield calcium imaging enables recording of large-scale neural

74 y performing perforated patch recordings and calcium imaging experiments in rats (male and female), w

75 Calcium imaging experiments in the mosquito AL revealed

76 ecific contacts with FRU-expressing neurons; calcium imaging experiments reveal bidirectional functio

77 We performed calcium imaging experiments to evaluate responses of ent

78 e dorsal raphe nucleus (DRN) with wide-field calcium imaging, extracellular recordings, and iontophor

79 ing, for example, to smart FISH, large-scale calcium imaging from cortex and deep brain structures, c

80 We performed combined in vivo 2-photon calcium imaging from different targeted neuronal subpopu

81 See-Shells allow calcium imaging from multiple, non-contiguous regions ac

82 Using in vivo multiphoton calcium imaging from transgenic PUb-GCaMP6s mosquitoes,

83 Targeted recordings and in vivo calcium imaging further revealed that neurons adapt thei

84 While calcium imaging has become a mainstay of modern neurosci

85 1300 nm three-photon calcium imaging has emerged as a useful technique to all

86 however, combining an atlas with whole-brain calcium imaging has yet to be performed in vivo in adult

87 Although optical probes for intracellular calcium imaging have been available for decades, the dev

88 Recent studies using calcium imaging have measured neural activity at high sp

89 Trans-synaptic tracing and calcium imaging identified dopaminergic neurons projecti

90 Using cellular calcium imaging in a virtual reality (VR)-based locomoti

91 Stimulation and calcium imaging in acute slices showed that there is loc

92 scale physiological recording and two-photon calcium imaging in adult male and female mice, we show t

93 We performed in vivo two-photon calcium imaging in an experimental model of Dravet syndr

94 Using calcium imaging in awake mice of both sexes, we show tha

95 Using two-photon calcium imaging in awake mice, we show that the encoding

96 l and tufted cells, using chronic two-photon calcium imaging in awake mice.

97 Two-photon calcium imaging in awake mouse models showed that nicoti

98 etinal axons using wide-field and two-photon calcium imaging in awake mouse thalamus across arousal s

99 We used calcium imaging in awake zebrafish during optokinetic be

100 ng novel transgenic lines, optogenetics, and calcium imaging in behaving larval zebrafish.

101 Here, using two-photon calcium imaging in behaving mice, we show that granule c

102 ty and movement, we used in vivo, two-photon calcium imaging in CA1 of male and female mice, as anima

103 Using two-photon calcium imaging in CA1 while mice performed an olfactory

104 Here, we use brain-wide calcium imaging in combination with microfluidic stimula

105 g has emerged as a useful technique to allow calcium imaging in deep brain regions.

106 We used two-photon calcium imaging in female mice to characterize the dispa

107 We develop methods for stable hindbrain calcium imaging in free-moving mice, which show that per

108 Using in vivo calcium imaging in freely behaving mice, we found that i

109 Calcium imaging in freely exploring mice revealed a gene

110 Here, we employed single-photon calcium imaging in freely moving mice to investigate the

111 Using calcium imaging in freely moving mice, we decoded an ani

112 We combined two-photon calcium imaging in head-fixed flying flies with optogene

113 sm on TRPM2 using whole-cell patch clamp and Calcium imaging in human embryonic kidney 293 cells with

114 Using two-photon calcium imaging in identified cell types in awake, head-

115 is question using two-photon and light-sheet calcium imaging in intact, behaving zebrafish larvae.

116 Using two-photon calcium imaging in layers 2/3, we found that local varia

117 Calcium imaging in live nerves and cultured Schwann cell

118 We used fast in vivo two-photon calcium imaging in male mouse neocortex to reconstruct,

119 rs of the motor cortex and performed in vivo calcium imaging in mice during locomotion.

120 Two-photon calcium imaging in mice has confirmed the presence of th

121 vity and movement through in vivo two-photon calcium imaging in mice learning a lever-press task.

122 Calcium imaging in mice performing a delayed Go or No-Go

123 Using chronic two-photon calcium imaging in mice performing random foraging or go

124 yer 2/3 (L2/3) and L5 of barrel cortex using calcium imaging in mice running in a tactile virtual rea

125 Using longitudinal calcium imaging in mice, multiple large virtual environm

126 Using microendoscopic calcium imaging in mice, we find that sex information is

127 To address this, using in vivo two-photon calcium imaging in mice, we tracked the response evoluti

128 seizures.SIGNIFICANCE STATEMENT We have used calcium imaging in mouse sensory cortex in vivo to recon

129 Here the authors employ widefield calcium imaging in mouse visual areas to demonstrate tha

130 We performed in vivo two-photon calcium imaging in neocortex during temperature-induced

131 Here we used 2-photon calcium imaging in neuronal birthdate-labeled Mash1-CreE

132 By simultaneously performing microendoscopic calcium imaging in pairs of socially interacting mice, w

133 Furthermore, we image nerve activity via calcium imaging in real time to demonstrate that electri

134 Calcium imaging in semi-intact mouse colon preparations

135 For example, calcium imaging in the zebrafish brain recently revealed

136 Using longitudinal in vivo calcium imaging in un-anesthetized mouse pups, we show t

137 neurons during REM sleep, we use deep-brain calcium imaging in unrestrained mice to map the activity

138 In vivo population calcium imaging in vibrissa primary somatosensory cortex

139 ophysiological recording and high-throughput calcium imaging in vivo.

140 Ex vivo calcium imaging indicates that AstC directly inhibits a

141 Despite major advances, calcium imaging is still limited by the biophysical prop

142 es, such as optogenetics, chemogenetics, and calcium imaging, manipulating social engrams will likely

143 ons using stereoscopy (vTwINS), a volumetric calcium imaging method that uses an elongated, V-shaped

144 Calcium imaging microscopy of dissociated OSNs revealed

145 ull spatiotemporal information in two-photon calcium imaging movies, we propose a 3D convolutional ne

146 , chemogenetic stimulation (n = 44), in vivo calcium imaging (n = 20), ex vivo electrophysiology (n =

147 simultaneous cellular-resolution two-photon calcium imaging of a local microcircuit and mesoscopic w

148 Two-photon calcium imaging of abducens neurons in control and dscam

149 Here, combining daily calcium imaging of CA1 sequence dynamics in running head

150 Using calcium imaging of cellular responses in awake mice, we

151 Longitudinal in vivo calcium imaging of DLS SST-INs in awake, behaving mice i

152 We applied the technology to calcium imaging of entire dendritic spans of neurons as

153 d natural scene representation, we performed calcium imaging of excitatory neurons in the primary vis

154 his with the cnidarian Hydra vulgaris, using calcium imaging of genetically engineered animals to mea

155 By performing two-photon calcium imaging of head-fixed male and female mice runni

156 uperior capacity of BPI for optogenetics and calcium imaging of human neurons.

157 several cell types and apply these tools to calcium imaging of individual neurons and optogenetic ma

158 Using in vivo two-photon calcium imaging of layer 2/3 barrel cortex neurons expre

159 visual cortex (V1), we performed two-photon calcium imaging of layer 2/3 neurons and assessed respon

160 Calcium imaging of layers 2-4 of the barrel cortex revea

161 Two-photon calcium imaging of local cortical populations revealed i

162 nctionally critical C-terminal conformation, calcium imaging of melanopsin mutants including a proxim

163 re, using neural transplantation and in vivo calcium imaging of mouse visual cortex, we investigated

164 Here we use two-photon calcium imaging of neural population dynamics throughout

165 We used in vivo calcium imaging of neural responses to compare projectio

166 We used fast two-photon calcium imaging of neuronal populations (calcium indicat

167 and connect with host systems, we performed calcium imaging of NSPC grafts in SCI sites in vivo and

168 Using in vivo calcium imaging of odor responses, we compared functiona

169 Calcium imaging of S1-S2 neurons, back-labeled via the V

170 Using in vivo two-photon calcium imaging of thalamocortical axons in mice, we sho

171 ombining in vivo 3D random-access two-photon calcium imaging of the dendritic spines of single V1 neu

172 local microcircuit and mesoscopic widefield calcium imaging of the entire cortical mantle in awake m

173 We used in vivo wide-field calcium imaging of the indicator GCaMP6 in head-fixed, a

174 Finally, we demonstrate fast calcium imaging of the larval zebrafish brain and find a

175 tood in vivo Here, we use in vivo two-photon calcium imaging of the vermal cerebellum in awake behavi

176 Here, we use widefield and 2-photon calcium imaging of transgenic mice to measure mesoscale

177 We carried out in vivo confocal calcium imaging of trigeminal ganglia in which neurons e

178 Microendoscopic calcium imaging of VMHdm(SF1) neurons revealed that pers

179 Calcium imaging offers a reasonable surrogate for direct

180 nse to glucose was studied by using in vitro calcium imaging on freshly dissociated MBH neurons.

181 Using a dexterity task, calcium imaging, optogenetic perturbations, and behavior

182 rtual-reality behavioural assays, volumetric calcium imaging, optogenetic stimulation and circuit mod

183 synaptic labeling, ultrastructural analysis, calcium imaging, optogenetics and behavioral analyses, w

184 Here we use in vivo calcium imaging, optogenetics and pharmacological approa

185 d used D2-Cre mice to label D2R+ neurons for calcium imaging or optogenetics.

186 ve injury and combining behavioral analysis, calcium imaging, patch clamping, and pharmacological too

187 luding immunoprecipitation and fluorescence, calcium imaging, phosphate radiolabeling, and a beta-arr

188 rhesus monkey by in vivo electrophysiology, calcium imaging, positron emission tomography, behaviora

189 l profiling of CNS acting compounds based on calcium imaging readouts.

190 Analyzing long-term calcium imaging recordings from posterior parietal corte

191 When applied to whole-brain calcium imaging recordings in freely moving C. elegans,

192 Calcium imaging records large-scale neuronal activity wi

193 Calcium imaging results reveal differentiation at the le

194 Calcium imaging revealed a sensitization of TRPV1-mediat

195 Moreover, calcium imaging revealed elevated neural activity in NI

196 Whole-brain calcium imaging revealed noradrenergic neurons that resp

197 In vivo calcium imaging revealed that different GA drugs activat

198 del of temporal lobe epilepsy, multicellular calcium imaging revealed that disease emergence was acco

199 Furthermore, two-photon calcium imaging revealed that M2 ensemble activity also

200 In vivo calcium imaging revealed that molecularly defined RGCs e

201 In vivo calcium imaging revealed that T4 and T5 neurons encode t

202 on with in vivo electrophysiology and GCAMP7 calcium imaging, revealing a reproducible progression fr

203 In vivo calcium imaging reveals a neuronal subset, predominantly

204 However, the kinds of information that calcium imaging reveals is limited.

205 Two-photon calcium imaging reveals that a thalamic nucleus and a do

206 We report here that ratiometric calcium imaging reveals that Der p1 activates the human

207 were characterized by immunohistochemistry, calcium imaging, RNA sequencing, and quantitative real-t

208 Electrophysiological and calcium imaging SCN recordings demonstrated changes in t

209 ablation, cell-specific genetic rescue, and calcium imaging show that tyra-2 expression in the nocic

210 Calcium imaging showed synchronized activity in groups o

211 evidence of "silencing", intracellular free calcium imaging showed that the cells were still viable.

212 Projection-specific labeling and calcium imaging showed that the great majority of STN-pr

213 [Ca] (i) Simultaneous electrophysiology and calcium imaging showed that the RIIIJ-elicited increase

214 In vivo two-photon calcium imaging shows that DRG neuronal activity is high

215 Calcium imaging shows that the beta-cells in the embryon

216 Here, we used calcium imaging, statistical spike time analysis and a p

217 Finally, in vivo calcium imaging suggests that, as in insect mushroom bod

218 Using calcium imaging techniques to assess IP(3)R channel func

219 Further, we use calcium imaging techniques to identify the olfactory sys

220 siology but not easily detected using modern calcium imaging techniques(9-11), highlighting the power

221 n effective method for volumetric two-photon calcium imaging that increases the number of neurons rec

222 Furthermore, we demonstrated via calcium imaging that the activity of these neurons can b

223 ere, to address this gap, we used two-photon calcium imaging through an implanted lens to record the

224 sed fluorophore-based analysis and live-cell calcium imaging to address the question of whether the b

225 f repetitive whisker stimulation and in vivo calcium imaging to assess tactile defensiveness and barr

226 of visual cortical areas, we used two-photon calcium imaging to characterize the effects of juvenile

227 of cortical maps, we used in vivo two-photon calcium imaging to characterize the properties of thalam

228 ive polymerase chain reaction, and live-cell calcium imaging to define an in vitro phenotype of MRAS-

229 Here, we use calcium imaging to determine how odor identity is encode

230 Here, we rely on calcium imaging to determine how taste and task-related

231 apping; in the present study, we use chronic calcium imaging to examine inhibitory avoidance-induced

232 veloped, high-speed, simultaneous sodium and calcium imaging to examine ion dynamics in spines in hip

233 pping." In the present study, we use chronic calcium imaging to examine remapping during fear retriev

234 Here, we used chemogenetics and in vivo calcium imaging to explore its mechanism.

235 ofiles were also observed using pan-neuronal calcium imaging to identify dimming-responsive neurons i

236 Using calcium imaging to map the activity of the entire epithe

237 rinsic signal optical imaging and two-photon calcium imaging to map visual responses in adult and dev

238 r action potentials in a targeted neuron and calcium imaging to measure the effect on spiking in neig

239 Since the introduction of calcium imaging to monitor neuronal activity with single

240 Here we use in vivo two-photon calcium imaging to monitor the activity of dorsomedial p

241 combine adaptive optics ophthalmoscopy with calcium imaging to optically record optogenetically rest

242 that can be studied with cellular-resolution calcium imaging to potentially include spatial navigatio

243 sed stable GCaMP6f expression and two-photon calcium imaging to probe a very large spatial and chroma

244 To capture these dynamics, we used mesoscale calcium imaging to record neural activity across the dor

245 Here, we used two-photon calcium imaging to record spontaneous activity from the

246 We used local stimulation and volumetric calcium imaging to show that APL inhibits Kenyon cells'

247 iven population events.We applied two-photon calcium imaging to study spontaneous population bursts i

248 We also performed real-time calcium imaging to study the effect of BLT1 deficiency i

249 We then use two-photon calcium imaging to track individual cells chronically du

250 Finally, we use two-photon calcium imaging to track the matching process chronicall

251 essing in the VTA and striatum, we have used calcium imaging to visualize instructional signals carri

252 Here, we used random-access two-photon calcium imaging together with electrophysiology in acute

253 We used a deep brain calcium imaging tool to image the intrinsic calcium tran

254 spontaneous activity measured by two-photon calcium imaging using computational methods and graphica

255 ion with electrophysiological recordings and calcium imaging using GCaMP6s, we investigated the facto

256 question by combining whole-brain volumetric calcium imaging using light-field microscopy and an oper

257 Calcium imaging using two-photon scanning microscopy has

258 na vs deeper in the SC), research technique (calcium imaging vs electrophysiology), and stimulus type

259 Live-cell confocal calcium imaging was performed on adult rabbit cardiomyoc

260 activates TRPC channels; then using confocal calcium imaging we demonstrated that Ang II-dependent st

261 Using ensemble calcium imaging, we demonstrate that this reorganization

262 Using calcium imaging, we determined that keratinocyte cold ac

263 study of ferret visual cortex using in vivo calcium imaging, we find evidence for a different develo

264 Here, using in vivo two-photon calcium imaging, we find that PVT neurons projecting to

265 Combining this with calcium imaging, we find that seizure onset rapidly recr

266 Using pan-neuronal calcium imaging, we found that blood is detected by four

267 radioligand analysis, electrophysiology, and calcium imaging, we found that oligoarginine peptides ar

268 Using widefield calcium imaging, we found that performance-related desyn

269 Using calcium imaging, we found that ppk301-expressing cells s

270 Using calcium imaging, we found that these neuron types are no

271 Utilizing genetics, optogenetics, and calcium imaging, we identify a new role for dopamine in

272 Using calcium imaging, we identify olfactory pathways in D. se

273 Using two-photon calcium imaging, we monitored the activity of LC-CA1 fib

274 Using in vivo wide-field calcium imaging, we observed that SCFAs induced altered

275 ing, histology, slice electrophysiology, and calcium imaging, we performed the first functional and m

276 Using fiber photometry calcium imaging, we recorded calcium transients in NAc D

277 Using two-photon calcium imaging, we recorded hippocampal CA1 somatostati

278 Using fast calcium imaging, we show that HCAR1 agonists 3,5-dihydro

279 -Seq, and two-photon glutamate uncaging with calcium imaging, we show that knocking down GluN3A in ra

280 Using genetic labeling and calcium imaging, we show that npvf-expressing neurons in

281 By volumetric calcium imaging, we show that posterior tectal neurons,

282 Finally, using two-photon calcium imaging, we show that SC direction selectivity i

283 Using in vivo two-photon calcium imaging, we studied how MCs responded to odors i

284 quencing and longitudinal in vivo two-photon calcium imaging, we surveyed functional alterations of t

285 Finally, immunohistochemistry and calcium imaging were used to assess potential cellular m

286 disk and nano-tip electrodes, together with calcium imaging, were used to examine the effect of shor

287 By utilizing optical calcium imaging, which records calcium ion flux indicati

288 activity of the mouse brain using wide-field calcium imaging while the mouse learned a motor task ove

289 By combining calcium imaging with a virtual hunting assay, we identif

290 d cerebellar optogenetic stimulation and CA1 calcium imaging with an object-exploration task, and fou

291 Finally, by combining two-photon calcium imaging with birth date labeling of granule neur

292 tracking microscope that enables whole-brain calcium imaging with cellular resolution in freely swimm

293 Calcium imaging with cellular resolution typically requi

294 Calcium imaging with fluorescent protein sensors is wide

295 We combined two-photon calcium imaging with genetic, pharmacological, and singl

296 Calcium imaging with genetically encoded calcium indicat

297 We combined ratiometric calcium imaging with quantitative immunoblotting, immuno

298 bove 1,000 nm and enables improved two-color calcium imaging with red fluorescent protein-based indic

299 sing newly developed simultaneous sodium and calcium imaging with single-spine resolution in pyramida

300 Here we combined two-photon calcium imaging with whole-cell electrophysiology to det