ライフサイエンスコーパス: calcium imaging

1 antly assessed through behavioral assays and calcium imaging.

2 ive for an antibody to TRPV4, as assessed by calcium imaging.

3 act following isolation, revealed by in vivo calcium imaging.

4 g over a week, using longitudinal two-photon calcium imaging.

5 the use of optogenetics in combination with calcium imaging.

6 learning over days using chronic two-photon calcium imaging.

7 cellular recordings from neurons targeted by calcium imaging.

8 ls that are hard to resolve by multicellular calcium imaging.

9 o a range of visual stimuli using two-photon calcium imaging.

10 1 receptor using heterologous expression and calcium imaging.

11 an attractive tool for high-speed volumetric calcium imaging.

12 glomerular modules using in vivo two-photon calcium imaging.

13 article tracking, surface biotinylation, and calcium imaging.

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

15 tool for examining these structures has been calcium imaging.

16 while measuring their output with two-photon calcium imaging.

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

18 wo-photon microscope to perform simultaneous calcium imaging across mouse primary (S1) and secondary

19 RPM7 near or at cell membrane upon IFSS, and calcium imaging analysis demonstrated the transient incr

20 Combining functional calcium imaging and behavioral assays, we show that AWC(

21 Here, we combined calcium imaging and electrophysiological recordings in m

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

23 d memories require sugar receptor Gr43a, and calcium imaging and electrophysiological recordings indi

24 Using calcium imaging and electrophysiological techniques, we

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

26 Using two-photon calcium imaging and electrophysiology, we recorded spont

27 the mechanism of this unusual activity using calcium imaging and electrophysiology.

28 We measured neural activity using two-photon calcium imaging and extracellular recordings.

29 nd mitral cells of the olfactory bulb, using calcium imaging and fast line-scanning microscopy.

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

31 In vitro calcium imaging and immunofluorescence analyses demonstr

32 Using two-photon calcium imaging and optogenetic manipulations of VIP(+)

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

34 ated dorsal root ganglia (DRG) neurons using calcium imaging and patch clamp techniques.

35 Calcium imaging and patch-clamp experiments show that G2

36 ells (HCs) using a combination of two-photon calcium imaging and pharmacology at the level of individ

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

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

39 haemia combined with fast in vivo two-photon calcium imaging and selective microglial manipulation.

40 To fill this gap, we used calcium imaging and single-cell electroporation during o

41 in murine hippocampal slices using confocal calcium imaging and the "added-buffer" approach.

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

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

44 amenable to electrophysiological recording, calcium imaging and viral gene transfer.

45 the basis of electrophysiological-recording, calcium-imaging and behavioural studies, here we report

46 Using in vivo Calcium-imaging and intracellular recordings, we demonst

47 minutes, as assessed by behavior, functional calcium imaging, and electrophysiology of neurons expres

48 pharmacology, Western blotting, single-cell calcium imaging, and electrophysiology were used to exam

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

50 electrophysiological approaches, two-photon calcium imaging, and protein biochemistry in hippocampal

51 ng immunohistochemistry, retrograde tracing, calcium imaging, and whole-cell recordings.

52 gs, optogenetics, and fiber-photometry-based calcium imaging applied to wild-type and conditional tra

53 Here, a combined electrophysiological and calcium imaging approach was developed and used to illum

54 Here, we developed a large-scale calcium-imaging approach coupled with cell labeling to e

55 le- and dual-plane high-speed (up to 160 Hz) calcium imaging as well as in vivo volumetric calcium im

56 These predictions were tested by calcium imaging assays that led to identification of gam

57 g remote stimulation of cells using in vitro calcium imaging assays, electrophysiological recordings

58 In addition, we found that calcium-imaging assays could identify subsets of iSNs th

59 Using calcium-imaging-based unbiased forward genetic screens w

60 aneous two-photon optogenetic activation and calcium imaging by coexpression of a red-shifted opsin a

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

62 Using in vivo calcium imaging combined with genetic silencing, we plac

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

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

65 oard approval and HIPAA compliance, coronary calcium imaging data of 110 consecutive patients (mean a

66 ramework for analysing multi-view, whole-CNS calcium imaging data.

67 Our calcium-imaging data show that astrocytic and neuronal c

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

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

70 CaMP6f, and permitting subcellular astrocyte calcium imaging during startle responses in vivo.

71 Using immunohistochemistry, calcium imaging, electrophysiology, impedance measuremen

72 In addition, fluorescent calcium imaging experiments in cultures of DRG cells sho

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

74 Combined optogenetic activation and calcium imaging experiments in vitro, as well as c-Fos a

75 elanopsin-containing ipRGCs was confirmed by calcium imaging experiments on isolated cells in purifie

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

77 Surprisingly, calcium imaging experiments reveal that mitral cell resp

78 This is reflected by our calcium imaging experiments revealing higher responsiven

79 Finally, presynaptic calcium imaging experiments support a model in which a P

80 Through live calcium imaging experiments, we show that these choliner

81 In vivo calcium-imaging experiments showed that the OSNs and PNs

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

83 On the basis of calcium-imaging, genetics, and behavioral studies, here

84 y of traditional imaging technology, in vivo calcium imaging has been limited to superficial brain st

85 A fundamental challenge in calcium imaging has been to infer spike rates of neurons

86 Calcium imaging has been widely applied in this mode, bu

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

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

89 , both with electrophysiology and two-photon calcium imaging, have described receptive fields in anes

90 in vitro electrophysiological recordings and calcium imaging, here we show that the inhibitory GABAer

91 ined intracellular recordings and two-photon calcium imaging in anesthetized adult zebra finches (Tae

92 We used two-photon calcium imaging in anesthetized and awake mice to visual

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

94 In vivo calcium imaging in awake mice reveals that PV cells are

95 unted miniature microscope we confirmed with calcium imaging in awake mice that hM4D activation by CN

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

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

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

99 We used calcium imaging in awake zebrafish during optokinetic be

100 To address this issue, we used chronic calcium imaging in behaving adult mice to examine the ac

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

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

103 ogical and histological analyses, as well as calcium imaging in brain slices of rats, were conducted.

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

105 Using brain-wide calcium imaging in Caenorhabditis elegans, we show that

106 Using calcium imaging in cultured primary murine dorsal root g

107 In fact, using calcium imaging in dissociated VMH neurons showed that k

108 Using in vivo two-photon calcium imaging in Drosophila, we describe direction sel

109 Employing in vivo calcium imaging in freely behaving mice to record activi

110 Here we use two-photon calcium imaging in head-fixed Drosophila melanogaster wa

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

112 Calcium imaging in head-fixed larvae shows that a large

113 Here we use two-photon calcium imaging in head-fixed walking and flying flies t

114 Using in vivo two-photon calcium imaging in layers 2/3 and 4 in mouse V1, we reve

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

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

117 Danielson et al. (2016) use calcium imaging in mice performing a treadmill task to r

118 cells by combining optogenetics and 2-photon calcium imaging in mouse neocortical slices.

119 toring agonist-induced cellular activity via calcium imaging in mouse POMC-EGFP brain slices, which r

120 Using in vivo two-photon calcium imaging in mouse primary visual cortex (V1), we

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

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

123 mbined this approach with in vivo two-photon calcium imaging in order to characterize the RF properti

124 onse biases, we performed chronic two-photon calcium imaging in postrhinal association cortex (POR) a

125 Studying neuronal activity with two-photon calcium imaging in primary visual cortex of mice perform

126 ow using electrophysiological recordings and calcium imaging in rat brain slices that ghrelin stimula

127 Using whole-cell recording and calcium imaging in rat slices, we find that dendritic vo

128 Two-photon calcium imaging in retinal ganglion cell (RGC) axons rev

129 Live calcium imaging in severed zebrafish neurons and tempora

130 Although whole-organism calcium imaging in small and semi-transparent animals ha

131 Using a novel method for calcium imaging in the larval gustatory system, we ident

132 Using in vivo two-photon calcium imaging in the rat barrel cortex during artifici

133 Therefore, we developed a preparation for calcium imaging in the spinal projections of these neuro

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

135 Using calcium imaging in transgenic mice expressing the calciu

136 We used two-photon calcium imaging in V1 of mice performing a stimulus dete

137 r response properties measured by two-photon calcium imaging in vivo in dark-reared mice.

138 Using high-speed two-photon calcium imaging in vivo, we found that responses in mous

139 Live calcium imaging indicates that serotonin inhibits sponta

140 Calcium imaging is a versatile experimental approach cap

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

142 e perforated patch-clamp technique and ratio-calcium-imaging methods, we describe a diffusible second

143 tory synaptogenesis using electrophysiology, calcium imaging, morphological analyses, and modeling.

144 alcium imaging as well as in vivo volumetric calcium imaging of a mouse cortical column (0.5 mm x 0.5

145 In vivo calcium imaging of behaving animals revealed that locomo

146 Using multi-plane two-photon calcium imaging of CA1 place cell somata, axons and dend

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

148 Here we combined in vivo, two-photon calcium imaging of complex spikes in microcomplexes of P

149 Using both high-speed video recording and calcium imaging of egg-laying muscles in behaving animal

150 GCaMP6 calcium imaging of Eve(+) interneurons in freely moving

151 Electrophysiology and calcium imaging of evoked and endogenous activity near t

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

153 Calcium imaging of granule cell activity 600-800 mum bel

154 operties encode time, we performed brainwide calcium imaging of groups of pacemaker neurons in vivo f

155 Here we use two-photon calcium imaging of identified excitatory and inhibitory

156 Using calcium imaging of input dendrites, we then show that in

157 We performed in vivo calcium imaging of interneurons in the anterior optic tu

158 To address this question, we use calcium imaging of isolated honeybee and Drosophila Keny

159 Using calcium imaging of isolated mouse taste cells, we identi

160 In vivo calcium imaging of L3, combined with neuronal silencing

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

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

163 atants from biopsy specimens was assessed by calcium imaging of mouse dorsal root ganglion neurons.

164 Using two-photon calcium imaging of mouse hippocampal neurons we find tha

165 Here we use two-photon calcium imaging of mouse neocortical pyramidal neurons t

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

167 Using in vivo calcium imaging of multiple neighbouring cerebellar para

168 Here we use in vivo two-photon calcium imaging of neocortical astrocytes while monitori

169 ole-brain light-sheet imaging and two-photon calcium imaging of neural activity in the retina.

170 m and has potential applicability to in vivo calcium imaging of neural tissue, as well as other smoot

171 Sequential calcium imaging of neuronal activity, in the pyramidal c

172 method to simultaneously perform two-photon calcium imaging of neuronal populations across multiple

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

174 sic activity better, we performed two-photon calcium imaging of populations of neurons from the prima

175 Therefore, using in vitro live cell calcium imaging of prelabeled rat hindbrain slices, we c

176 Calcium imaging of primary L cells and the model cell li

177 Using in vivo calcium imaging of projection neurons in the honeybee, w

178 Two-photon calcium imaging of retino-recipient midbrain regions iso

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

180 Two-photon calcium imaging of secondary motor cortex (M2) revealed

181 e tested this hypothesis by using two-photon calcium imaging of spontaneous activity in populations o

182 , was inserted into foveal RGCs, followed by calcium imaging of the displacement of foveal RGCs from

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

184 High-speed two-photon calcium imaging of visual responses showed that the orie

185 Calcium imaging offers a reasonable surrogate for direct

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

187 Using two-photon calcium imaging on intact larval zebrafish, we recorded

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

189 female and male pheromones using anatomical, calcium imaging, optogenetic, and behavioral studies.

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

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

192 els in human embryonic kidney cells and used calcium imaging or whole-cell patch-clamp electrophysiol

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

194 Two-photon calcium imaging provides an optical readout of neuronal

195 ogenetic activation, while simultaneous fast calcium imaging provides high-resolution network-wide re

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

197 Here, we obtained in vivo two-photon calcium imaging recordings from the entire dendritic fie

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

199 We present a modular approach for analyzing calcium imaging recordings of large neuronal ensembles.

200 Multi-channel electrophysiology and calcium imaging reveal that neural activity in premotor

201 Calcium imaging revealed a sensitization of TRPV1-mediat

202 Two-photon calcium imaging revealed a small visual area, AF7, that

203 After one week, calcium imaging revealed moderately synchronous activity

204 Calcium imaging revealed that 55% of the VF neurons were

205 Correspondingly, deep-brain calcium imaging revealed that AGRP neuron activity rapid

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

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

208 Calcium imaging revealed that nMLF activity is correlate

209 Large-scale calcium imaging revealed that V1, PPC, and fMC neurons e

210 In vivo calcium imaging reveals a neuronal subset, predominantly

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

212 te compounds in the mushroom body calyx with calcium imaging reveals sparse, taste-specific and organ

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

214 Calcium imaging reveals that beta-alanine and histamine

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

216 Functional calcium imaging reveals that NLP-40 and AEX-2/GPCR are b

217 In vivo two-photon calcium imaging reveals that these LC types respond to l

218 Calcium imaging reveals that vPN1 responds preferentiall

219 Electrophysiological and calcium imaging SCN recordings demonstrated changes in t

220 Calcium imaging selectively from OSNs confirmed that thi

221 Calcium imaging showed synchronized activity in groups o

222 Furthermore, in vivo single-cell two-photon calcium imaging showed that hippocampal neuronal activit

223 Indeed, calcium imaging showed that IR40a neurons directly respo

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

225 Calcium imaging showed that these neurons respond to mag

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

227 In vivo two-photon calcium imaging shows the amplitude of food odor-evoked

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

229 By calcium imaging studies, we show that these neurons are

230 Calcium-imaging studies on dissociated dorsal root gangl

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

232 Here we use dendritic recordings and calcium imaging to analyse the role of NMDA spikes in as

233 Here we used calcium imaging to assess how the Kenyon cells in the fl

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

235 come such obstacles, we utilize pan-neuronal calcium imaging to broadly screen the activity of the C.

236 dress this issue, we used in vivo two-photon calcium imaging to characterize the orientation tuning a

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

238 Here we use two-photon calcium imaging to characterize the response properties

239 s, single-neuron labeling, connectomics, and calcium imaging to determine how a set of bona fide line

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

241 of TCR-pMHC-CD8 interaction with concurrent calcium imaging to examine how ligand engagement of TCR

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

243 Here we used molecular genetics and in vivo calcium imaging to investigate the coding of cutaneous t

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

245 Here we use axonal calcium imaging to measure information provided to visua

246 imary visual cortex (V1), we used two-photon calcium imaging to measure responses of axons from V1 ar

247 Here, we use multiphoton calcium imaging to monitor cortical feedback in the olfa

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

249 Here we used awake in vivo two-photon calcium imaging to monitor neuronal function in adult rT

250 O mice was further explored using two-photon calcium imaging to monitor striatal output from the dire

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

252 essed this issue by using in vivo two-photon calcium imaging to monitor the activity of the same popu

253 Here, we have used two-photon calcium imaging to monitor the activity of young abGCs i

254 By combining two-photon calcium imaging to obtain dense retinal recordings and u

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

256 To explore this, we used in vivo two-photon calcium imaging to record the activity of neuronal popul

257 Here we used two-photon calcium imaging to reveal an alternative arrangement for

258 Here we use calcium imaging to reveal how responses across antennal

259 larval zebrafish with two-photon functional calcium imaging to simultaneously monitor neuronal activ

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

261 We used two-photon calcium imaging to study the functional microarchitectur

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

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

264 cally encoded voltage indicators, as well as calcium imaging, to measure sensory stimulus-evoked sign

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

266 We use a combination of calcium imaging, tracer coupling, and electrophysiology

267 Thus, calcium imaging uncovers new similarities between fly an

268 Using fiber photometry calcium imaging we define D1 MSNs as the specific popula

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

270 her with electrophysiological recordings and calcium imaging, we characterize the basic physiological

271 By using live calcium imaging, we compared activation of submucosal ne

272 Using confocal calcium imaging, we demonstrate that the inhibition of S

273 Next, using in vivo calcium imaging, we describe the thermosensory projectio

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

275 ion of patch-clamp recordings and two-photon calcium imaging, we found that Bk strongly sensitizes sp

276 ng, optogenetic circuit mapping, and in vivo calcium imaging, we found that cholinergic axons arising

277 Using ratiometric calcium imaging, we found that increased D1R activity re

278 Using calcium imaging, we found that most olfactory glomerular

279 By in vivo calcium imaging, we found that spiral fiber neurons are

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

281 Using calcium imaging, we identified AI salt-responsive type I

282 Performing extended in vivo calcium imaging, we measure subcellular calcium signals

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

284 Using confocal calcium imaging, we recorded responses to oral stimulati

285 Using in vivo calcium imaging, we revealed training-dependent changes

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

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

288 First, using pharmacogenetics and two-photon calcium imaging, we validate that SACs are necessary for

289 Finally, in single-cell calcium imaging, we validated its selective inhibitory e

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

291 ghtfield microscopy, immunofluorescence, and calcium imaging were used to characterize virally infect

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

293 movement during flight, we combined 2-photon calcium imaging with a machine vision system to simultan

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

295 Calcium imaging with cellular resolution typically requi

296 We combined two-photon calcium imaging with deflection of many whiskers to map

297 on polymerase chain reaction and ratiometric calcium imaging with Fura-2.

298 Dynamic calcium imaging with single-cell resolution revealed the

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

300 Using in vivo calcium imaging with the genetically encoded calcium sen