1 associative learning over days using chronic
two-photon calcium imaging.
2 response to a range of visual stimuli using
two-photon calcium imaging.
3 itecture of glomerular modules using in vivo
two-photon calcium imaging.
4 eously recording local network activity with
two-photon calcium imaging.
5 recipient neuronal populations using in vivo
two-photon calcium imaging.
6 roughout the entire population using in vivo
two-photon calcium imaging.
7 novel head-fixed sucrose preference task and
two-photon calcium imaging.
8 al areas, measured using large-field-of-view
two-photon calcium imaging.
9 ges while neural activity was recorded using
two-photon calcium imaging.
10 dark exposure in awake head-fixed mice using
two-photon calcium imaging.
11 nal ganglion cell axon boutons using in vivo
two-photon calcium imaging.
12 nd excitatory pyramidal neurons with chronic
two-photon calcium imaging.
13 ead-fixed mice in a moving environment using
two-photon calcium imaging.
14 ral cerebellum during a Pavlovian task using
two-photon calcium imaging.
15 recording of OT neurons in awake mice using
two-photon calcium imaging.
16 ex in vivo while measuring their output with
two-photon calcium imaging.
17 ing learning over a week, using longitudinal
two-photon calcium imaging.
18 sory and visual cortices of awake mice using
two-photon calcium imaging across cortical layers.
19 Here, using
two-photon calcium imaging across six experimental parad
20 Two-photon calcium imaging allows the activity of indivi
21 We used
two-photon calcium imaging,
an optical method, to circum
22 Two-photon calcium imaging and convolutional neural netw
23 Using in vivo
two-photon calcium imaging and electrophysiological reco
24 Using
two-photon calcium imaging and electrophysiological reco
25 Here, we use
two-photon calcium imaging and electrophysiology in head
26 Using
two-photon calcium imaging and electrophysiology, we rec
27 fic glomerulus and recorded PN activity with
two-photon calcium imaging and electrophysiology.
28 Using
two-photon calcium imaging and ex vivo electrophysiology
29 We measured neural activity using
two-photon calcium imaging and extracellular recordings.
30 red the same effects on single neurons using
two-photon calcium imaging and found that the increase i
31 e, we use patch-clamp electrophysiology, and
two-photon calcium imaging and glutamate uncaging, to sh
32 te line-attractor-contributing neurons using
two-photon calcium imaging and holographic optogenetic p
33 activity of neurons of the lateral OFC using
two-photon calcium imaging and investigated how OFC dyna
34 Using volumetric
two-photon calcium imaging and local field potentials in
35 Using
two-photon calcium imaging and Neuropixels probe recordi
36 Projection-specific
two-photon calcium imaging and optogenetic manipulations
37 Using
two-photon calcium imaging and optogenetic manipulations
38 Here we demonstrate using
two-photon calcium imaging and optogenetics in mice that
39 Here we combine
two-photon calcium imaging and optogenetics in tethered
40 Two-photon calcium imaging and optogenetics revealed tha
41 By combining
two-photon calcium imaging and patch-clamp electrophysio
42 orizontal cells (HCs) using a combination of
two-photon calcium imaging and pharmacology at the level
43 erebral ischaemia combined with fast in vivo
two-photon calcium imaging and selective microglial mani
44 Using in vivo
two-photon calcium imaging and SF-iGluSnFR-based glutama
45 Two-photon calcium imaging and spike recordings reveal a
46 Two-photon calcium imaging and tail tracking showed that
47 Here, we used population
two-photon calcium imaging and targeted two-photon optog
48 for perceptual decision-making, we combined
two-photon calcium imaging and targeted two-photon optog
49 y first identifying integrator neurons using
two-photon calcium imaging and then reconstructing the s
50 Recent advances combining
two-photon calcium imaging and two-photon optogenetics w
51 an 'all-optical' combination of simultaneous
two-photon calcium imaging and two-photon optogenetics,
52 optical and computational methods, based on
two-photon calcium imaging and two-photon optogenetics,
53 Here we used
two-photon calcium imaging and two-tone stimuli with var
54 Recently, several studies using
two-photon calcium imaging and virtual navigation have i
55 Here, we used
two-photon calcium imaging and whole-cell recordings in
56 Here, we combined axonal tracing,
two-photon calcium imaging,
and chemogenetic manipulatio
57 Using viral tracing,
two-photon calcium imaging,
and computational modeling,
58 bination of slice electrophysiology, in vivo
two-photon calcium imaging,
and optical imaging of intri
59 ed this issue utilizing behavioral modeling,
two-photon calcium imaging,
and optogenetic inactivation
60 bination of electrophysiological approaches,
two-photon calcium imaging,
and protein biochemistry in
61 Extracellular electrophysiology and
two-photon calcium imaging are widely used methods for m
62 Two-photon calcium imaging can monitor activity of spati
63 Here, we leverage
two-photon calcium imaging combined with single-cell hol
64 Simultaneous intracellular recording and
two-photon calcium imaging confirm that fluorescence act
65 e use fast, targeted, three-dimensional (3D)
two-photon calcium imaging coupled with immunohistochemi
66 However, analysis of
two-photon calcium imaging data from tethered flies walk
67 Two-photon calcium imaging data show that this facilitat
68 Applying DeepInterpolation to
two-photon calcium imaging data yielded up to six times
69 Neuroanatomical analysis and
two-photon calcium imaging demonstrate that DALcl1 and D
70 Two-photon calcium imaging demonstrated that enhancing t
71 In vivo
two-photon calcium imaging demonstrates that Ndnf-INs in
72 Two-photon calcium imaging during decision making reveal
73 Using in vivo longitudinal
two-photon calcium imaging during the period that preced
74 tical neurons in awake mice using volumetric
two-photon calcium imaging during visual stimulation.
75 We further show with in vivo
two-photon calcium imaging,
ex vivo calcium imaging, and
76 or-like activity, patch-clamp recordings and
two-photon calcium imaging experiments show that approxi
77 In line with these findings,
two-photon calcium imaging experiments showed that the p
78 Using
two-photon calcium imaging,
flash photolysis of caged gl
79 Chronic
two-photon calcium imaging from ACtx pyramidal neurons (
80 social sensory information processing using
two-photon calcium imaging from hippocampal CA2 pyramida
81 ns in ensembles in experiments using in vivo
two-photon calcium imaging from primary visual cortex of
82 dLGN and V1, both with electrophysiology and
two-photon calcium imaging,
have described receptive fie
83 Here we combined virtual-reality behaviour,
two-photon calcium imaging,
high-throughput electron mic
84 se, we used whole-cell electrophysiology and
two-photon calcium imaging in acute slices from male and
85 ming large-scale physiological recording and
two-photon calcium imaging in adult male and female mice
86 We combined this approach with
two-photon calcium imaging in an all-optical method to i
87 We performed in vivo
two-photon calcium imaging in an experimental model of D
88 ere we combined intracellular recordings and
two-photon calcium imaging in anesthetized adult zebra f
89 We used
two-photon calcium imaging in anesthetized and awake mic
90 mplex motion patterns known as plaids, using
two-photon calcium imaging in awake male and female mice
91 Here, we used
two-photon calcium imaging in awake mice to compare visu
92 Using
two-photon calcium imaging in awake mice, we show that t
93 (OB), mitral and tufted cells, using chronic
two-photon calcium imaging in awake mice.
94 Two-photon calcium imaging in awake mouse models showed
95 tivity of retinal axons using wide-field and
two-photon calcium imaging in awake mouse thalamus acros
96 Here, we use
two-photon calcium imaging in awake, behaving mice to mo
97 Here, in vivo
two-photon calcium imaging in awake, behaving mice was u
98 Using
two-photon calcium imaging in behaving mice, we show tha
99 Here, using
two-photon calcium imaging in behaving mice, we show tha
100 uron activity and movement, we used in vivo,
two-photon calcium imaging in CA1 of male and female mic
101 Using
two-photon calcium imaging in CA1 while mice performed a
102 ercome this experimental limitation and used
two-photon calcium imaging in combination with a functio
103 gated these issues using in vivo multineuron
two-photon calcium imaging in combination with informati
104 Using in vivo
two-photon calcium imaging in combination with surface E
105 We used in vivo
two-photon calcium imaging in combination with whole-cel
106 Using
two-photon calcium imaging in dendritic spines, we const
107 Using in vivo
two-photon calcium imaging in Drosophila, we describe di
108 We used
two-photon calcium imaging in female mice to characteriz
109 Here we use
two-photon calcium imaging in head-fixed Drosophila mela
110 We combined
two-photon calcium imaging in head-fixed flying flies wi
111 Here we use
two-photon calcium imaging in head-fixed walking and fly
112 Here, we employ deep-brain
two-photon calcium imaging in heroin self-administering
113 Using
two-photon calcium imaging in identified cell types in a
114 Using in vivo
two-photon calcium imaging in layers 2/3 and 4 in mouse
115 Using
two-photon calcium imaging in layers 2/3, we found that
116 Here we used
two-photon calcium imaging in macaques to examine the fi
117 We used fast in vivo
two-photon calcium imaging in male mouse neocortex to re
118 Using
two-photon calcium imaging in mice exploring a virtual e
119 Two-photon calcium imaging in mice has confirmed the pre
120 neuron activity and movement through in vivo
two-photon calcium imaging in mice learning a lever-pres
121 tigate this coding relationship, we employed
two-photon calcium imaging in mice navigating through di
122 pyramidal neurons in the barrel cortex using
two-photon calcium imaging in mice performing an object-
123 Using chronic
two-photon calcium imaging in mice performing random for
124 To address this question, we performed
two-photon calcium imaging in mice presented with food a
125 Combining single-cell and population
two-photon calcium imaging in mice, we discover that ret
126 To address this, using in vivo
two-photon calcium imaging in mice, we tracked the respo
127 Using in vivo
two-photon calcium imaging in mouse primary visual corte
128 We performed in vivo
two-photon calcium imaging in neocortex during temperatu
129 o postnatal weeks of mouse development using
two-photon calcium imaging in non-anesthetized pups.
130 We combined this approach with in vivo
two-photon calcium imaging in order to characterize the
131 rtical response biases, we performed chronic
two-photon calcium imaging in postrhinal association cor
132 in the mouse ACx and whole-cell recordings,
two-photon calcium imaging in presynaptic terminals, and
133 Here, using chronic
two-photon calcium imaging in primary visual cortex of f
134 Studying neuronal activity with
two-photon calcium imaging in primary visual cortex of m
135 Two-photon calcium imaging in retinal ganglion cell (RGC
136 We combined electrophysiology with in vivo
two-photon calcium imaging in rodents as well as intracr
137 Here we developed
two-photon calcium imaging in the awake echolocating bat
138 Here we present a technique for
two-photon calcium imaging in the central brain of head-
139 les of Hb9 INs in the locomotor CPG, we used
two-photon calcium imaging in the in vitro isolated whol
140 Using in vivo
two-photon calcium imaging in the rat barrel cortex duri
141 Using dual-color
two-photon calcium imaging in the thalamus of awake mice
142 We used
two-photon calcium imaging in V1 of mice performing a st
143 Using
two-photon calcium imaging in vivo and intracellular rec
144 al cortex at different postnatal ages, using
two-photon calcium imaging in vivo and multiple whole-ce
145 tro to their response properties measured by
two-photon calcium imaging in vivo in dark-reared mice.
146 Two-photon calcium imaging in vivo revealed that separat
147 Here we use
two-photon calcium imaging in vivo to determine the micr
148 Using high-speed
two-photon calcium imaging in vivo, we found that respon
149 In a mouse model using
two-photon calcium imaging in vivo, we identify paravent
150 during virtual elevated plus maze test using
two-photon calcium imaging in vivo.
151 Using electrophysiological recordings and
two-photon calcium imaging in young (6-8 weeks old) 3xTg
152 spiking, using cell-attached recordings and
two-photon calcium imaging,
in the barrel cortex of mice
153 Here, we used a combination of
two-photon calcium imaging,
in vitro signaling assays, a
154 al cells in behaving mice using longitudinal
two-photon calcium imaging integrated with simultaneous
155 er, we combine our novel in vivo spinal cord
two-photon calcium imaging,
mouse genetics, and persiste
156 ploit the full spatiotemporal information in
two-photon calcium imaging movies, we propose a 3D convo
157 n primary somatosensory cortex (S1), we used
two-photon calcium imaging,
neuropharmacology, single-ce
158 method for simultaneous cellular-resolution
two-photon calcium imaging of a local microcircuit and m
159 Two-photon calcium imaging of abducens neurons in contro
160 Instead of enhanced cue representations(8),
two-photon calcium imaging of auditory cortical neurons
161 Using multi-plane
two-photon calcium imaging of CA1 place cell somata, axo
162 Using
two-photon calcium imaging of CA1 pyramidal neurons in r
163 Two-photon calcium imaging of CA3 axonal projections to
164 Here we combined in vivo,
two-photon calcium imaging of complex spikes in microcom
165 Here, we used
two-photon calcium imaging of cortical layer 2/3 neurons
166 rsal lateral geniculate nucleus (dLGN) using
two-photon calcium imaging of dense populations in thala
167 By optimizing microprism-mediated
two-photon calcium imaging of dopamine axon terminals, w
168 To address this gap, we used
two-photon calcium imaging of excitatory interneurons an
169 present results from experiments relying on
two-photon calcium imaging of GC neural activity in mice
170 By performing
two-photon calcium imaging of head-fixed male and female
171 Here we use
two-photon calcium imaging of identified excitatory and
172 Finally,
two-photon calcium imaging of labeled networks of visual
173 Using in vivo
two-photon calcium imaging of layer 2/3 barrel cortex ne
174 use primary visual cortex (V1), we performed
two-photon calcium imaging of layer 2/3 neurons and asse
175 Two-photon calcium imaging of local cortical populations
176 igate the nature of this processing, we used
two-photon calcium imaging of local excitatory auditory
177 Two-photon calcium imaging of motor cortical neurons rev
178 Using
two-photon calcium imaging of mouse hippocampal neurons
179 Here we use
two-photon calcium imaging of mouse neocortical pyramida
180 Here we use in vivo
two-photon calcium imaging of neocortical astrocytes whi
181 erformed whole-brain light-sheet imaging and
two-photon calcium imaging of neural activity in the ret
182 Here we use
two-photon calcium imaging of neural population dynamics
183 We used fast
two-photon calcium imaging of neuronal populations (calc
184 holographic method to simultaneously perform
two-photon calcium imaging of neuronal populations acros
185 OFC terminals in A1 in mice by using in vivo
two-photon calcium imaging of OFC terminals under passiv
186 Here, we performed
two-photon calcium imaging of parvalbumin- and somatosta
187 ical intrinsic activity better, we performed
two-photon calcium imaging of populations of neurons fro
188 Two-photon calcium imaging of retino-recipient midbrain
189 Two-photon calcium imaging of secondary motor cortex (M2
190 Using
two-photon calcium imaging of single neurons in auditory
191 We tested this hypothesis by using
two-photon calcium imaging of spontaneous activity in po
192 Using in vivo
two-photon calcium imaging of thalamocortical axons in m
193 tivity by combining in vivo 3D random-access
two-photon calcium imaging of the dendritic spines of si
194 orly understood in vivo Here, we use in vivo
two-photon calcium imaging of the vermal cerebellum in a
195 Using in vivo
two-photon calcium imaging of visual cortex neurons in G
196 High-speed
two-photon calcium imaging of visual responses showed th
197 Using
two-photon calcium imaging on intact larval zebrafish, w
198 Using in vivo
two-photon calcium imaging or targeted single-unit recor
199 Chronic
two-photon calcium imaging,
population analysis, and com
200 Here we developed a
two-photon calcium imaging preparation to understand int
201 Two-photon calcium imaging provides an optical readout o
202 Here, we obtained in vivo
two-photon calcium imaging recordings from the entire de
203 Perforated-patch recordings and
two-photon calcium imaging reveal that individual SACs h
204 Two-photon calcium imaging revealed a small visual area,
205 Following treatment,
two-photon calcium imaging revealed increases in the num
206 Two-photon calcium imaging revealed sparse coding of con
207 Furthermore,
two-photon calcium imaging revealed that M2 ensemble act
208 Two-photon calcium imaging revealed that serotonin axon
209 nd un-silencing, together with widefield and
two-photon calcium imaging revealed that the anterior ci
210 iking activity of aRSC neurons, estimated by
two-photon calcium imaging,
revealed the existence of tw
211 Two-photon calcium imaging reveals that a thalamic nucle
212 Two-photon calcium imaging reveals that psilocin rapidly
213 In vivo
two-photon calcium imaging reveals that these LC types r
214 Our in vitro patch-clamp recordings and
two-photon calcium imaging show that direction-selective
215 Results from
two-photon calcium imaging show that starvation increase
216 Furthermore, in vivo single-cell
two-photon calcium imaging showed that hippocampal neuro
217 Two-photon calcium imaging shows large strategy-dependen
218 In vivo
two-photon calcium imaging shows that DRG neuronal activ
219 In vivo
two-photon calcium imaging shows the amplitude of food o
220 Using CCD and
two-photon calcium imaging techniques on CA1 pyramidal n
221 Using
two-photon calcium imaging techniques, we found that sin
222 We demonstrate using
two-photon calcium imaging that activation of single syn
223 provides an effective method for volumetric
two-photon calcium imaging that increases the number of
224 Here, to address this gap, we used
two-photon calcium imaging through an implanted lens to
225 performed simultaneous electrophysiology and
two-photon calcium imaging through transparent NeuroGrid
226 We used
two-photon calcium imaging to characterize a functional
227 rentiation of visual cortical areas, we used
two-photon calcium imaging to characterize the effects o
228 To address this issue, we used in vivo
two-photon calcium imaging to characterize the orientati
229 the origin of cortical maps, we used in vivo
two-photon calcium imaging to characterize the propertie
230 Here we use
two-photon calcium imaging to characterize the response
231 We used in vivo
two-photon calcium imaging to demonstrate topographic se
232 In this study, we use mesoscale
two-photon calcium imaging to examine spontaneous activi
233 Here we use chronic
two-photon calcium imaging to explore how wakefulness an
234 We used in vivo
two-photon calcium imaging to independently map ON and O
235 Here, we applied
two-photon calcium imaging to map neuronal tuning for or
236 we used intrinsic signal optical imaging and
two-photon calcium imaging to map visual responses in ad
237 al clones of excitatory neurons, and in vivo
two-photon calcium imaging to measure neuronal response
238 put from primary visual cortex (V1), we used
two-photon calcium imaging to measure responses of axons
239 , we used an auditory "oddball" paradigm and
two-photon calcium imaging to measure responses to simpl
240 mitted in cortical circuits in vivo, we used
two-photon calcium imaging to monitor ensemble activity
241 Here we used awake in vivo
two-photon calcium imaging to monitor neuronal function
242 of Sapap3 KO mice was further explored using
two-photon calcium imaging to monitor striatal output fr
243 Here we use in vivo
two-photon calcium imaging to monitor the activity of do
244 ere we addressed this issue by using in vivo
two-photon calcium imaging to monitor the activity of th
245 Here, we have used
two-photon calcium imaging to monitor the activity of yo
246 By combining
two-photon calcium imaging to obtain dense retinal recor
247 We used stable GCaMP6f expression and
two-photon calcium imaging to probe a very large spatial
248 Here we used large-scale, longitudinal
two-photon calcium imaging to record activity from thous
249 Using
two-photon calcium imaging to record from layer 2/3 neur
250 Using
two-photon calcium imaging to record populations of sing
251 Here, we used
two-photon calcium imaging to record spontaneous activit
252 Here we use
two-photon calcium imaging to record the activity of lar
253 To explore this, we used in vivo
two-photon calcium imaging to record the activity of neu
254 In this study, we used
two-photon calcium imaging to record visually evoked res
255 Here we used
two-photon calcium imaging to reveal an alternative arra
256 We used
two-photon calcium imaging to sample the response to mon
257 fluorescent retrograde tracing with in vivo
two-photon calcium imaging to simultaneously compare the
258 stimulus-driven population events.We applied
two-photon calcium imaging to study spontaneous populati
259 We used
two-photon calcium imaging to study the functional micro
260 used a custom hippocampal microperiscope and
two-photon calcium imaging to track CA1 pyramidal neuron
261 We then use
two-photon calcium imaging to track individual cells chr
262 Finally, we use
two-photon calcium imaging to track the matching process
263 Here, we used random-access
two-photon calcium imaging together with electrophysiolo
264 or studying spontaneous activity measured by
two-photon calcium imaging using computational methods a
265 gy and improve clinical translation, we used
two-photon calcium imaging via a closed cranial window i
266 Using
two-photon calcium imaging,
we assessed if and how the l
267 Using high-speed in vivo
two-photon calcium imaging,
we characterized the recepti
268 Using optogenetics and
two-photon calcium imaging,
we demonstrate that medial P
269 along with in vivo endoscopic one-photon and
two-photon calcium imaging,
we determined that the stria
270 Using in vivo
two-photon calcium imaging,
we find that male and female
271 Here, using in vivo
two-photon calcium imaging,
we find that PVT neurons pro
272 ordings from interneurons and TC neurons and
two-photon calcium imaging,
we find that synchronous act
273 Using
two-photon calcium imaging,
we found altered temporal di
274 a combination of patch-clamp recordings and
two-photon calcium imaging,
we found that Bk strongly se
275 Using
two-photon calcium imaging,
we found that M1(CT) activit
276 Using in vivo
two-photon calcium imaging,
we investigated how drinking
277 Using
two-photon calcium imaging,
we measured DeltaF/F respons
278 Using
two-photon calcium imaging,
we monitored the activity of
279 Using
two-photon calcium imaging,
we observed a small deficit
280 Using
two-photon calcium imaging,
we reconstructed the dynamic
281 Using
two-photon calcium imaging,
we recorded hippocampal CA1
282 -off system combined with immunostaining and
two-photon calcium imaging,
we report that dDG fear engr
283 Here, using
two-photon calcium imaging,
we show that individual neur
284 Lastly, with
two-photon calcium imaging,
we show that inferior olive
285 Finally, using
two-photon calcium imaging,
we show that SC direction se
286 Using in vivo
two-photon calcium imaging,
we studied how MCs responded
287 cell RNA sequencing and longitudinal in vivo
two-photon calcium imaging,
we surveyed functional alter
288 Using
two-photon calcium imaging,
we then investigated how the
289 Additionally, using
two-photon calcium imaging,
we tracked large populations
290 Using
two-photon calcium imaging,
we tracked the same dCA1 and
291 First, using pharmacogenetics and
two-photon calcium imaging,
we validate that SACs are ne
292 Finally, by combining
two-photon calcium imaging with birth date labeling of g
293 We combined
two-photon calcium imaging with deflection of many whisk
294 We combined
two-photon calcium imaging with genetic, pharmacological
295 layer neocortical interneurones, we combined
two-photon calcium imaging with whole cell recordings an
296 Here we combined
two-photon calcium imaging with whole-cell electrophysio
297 In this first study, we combined
two-photon calcium imaging with whole-cell recording and
298 In this second study, we have combined
two-photon calcium imaging with whole-cell recording and
299 horizontal locations (azimuths): volumetric
two-photon calcium imaging with ~700 cells simultaneousl
300 In vivo
two-photon calcium imaging would benefit from the use of