1 recipient neuronal populations using in vivo
two-photon calcium imaging.
2 roughout the entire population using in vivo
two-photon calcium imaging.
3 recipient neuronal populations using in vivo
two-photon calcium imaging.
4 ex in vivo while measuring their output with
two-photon calcium imaging.
5 ing learning over a week, using longitudinal
two-photon calcium imaging.
6 associative learning over days using chronic
two-photon calcium imaging.
7 response to a range of visual stimuli using
two-photon calcium imaging.
8 itecture of glomerular modules using in vivo
two-photon calcium imaging.
9 We used
two-photon calcium imaging,
an optical method, to circum
10 Using
two-photon calcium imaging and electrophysiological reco
11 Using in vivo
two-photon calcium imaging and electrophysiological reco
12 Here, we use
two-photon calcium imaging and electrophysiology in head
13 Using
two-photon calcium imaging and electrophysiology, we rec
14 fic glomerulus and recorded PN activity with
two-photon calcium imaging and electrophysiology.
15 We measured neural activity using
two-photon calcium imaging and extracellular recordings.
16 red the same effects on single neurons using
two-photon calcium imaging and found that the increase i
17 Using
two-photon calcium imaging and optogenetic manipulations
18 orizontal cells (HCs) using a combination of
two-photon calcium imaging and pharmacology at the level
19 erebral ischaemia combined with fast in vivo
two-photon calcium imaging and selective microglial mani
20 y first identifying integrator neurons using
two-photon calcium imaging and then reconstructing the s
21 optical and computational methods, based on
two-photon calcium imaging and two-photon optogenetics,
22 ed this issue utilizing behavioral modeling,
two-photon calcium imaging,
and optogenetic inactivation
23 bination of electrophysiological approaches,
two-photon calcium imaging,
and protein biochemistry in
24 Two-photon calcium imaging can monitor activity of spati
25 Simultaneous intracellular recording and
two-photon calcium imaging confirm that fluorescence act
26 Neuroanatomical analysis and
two-photon calcium imaging demonstrate that DALcl1 and D
27 We further show with in vivo
two-photon calcium imaging,
ex vivo calcium imaging, and
28 or-like activity, patch-clamp recordings and
two-photon calcium imaging experiments show that approxi
29 In line with these findings,
two-photon calcium imaging experiments showed that the p
30 Using
two-photon calcium imaging,
flash photolysis of caged gl
31 dLGN and V1, both with electrophysiology and
two-photon calcium imaging,
have described receptive fie
32 We combined this approach with
two-photon calcium imaging in an all-optical method to i
33 ere we combined intracellular recordings and
two-photon calcium imaging in anesthetized adult zebra f
34 We used
two-photon calcium imaging in anesthetized and awake mic
35 Here, we used
two-photon calcium imaging in awake mice to compare visu
36 Using
two-photon calcium imaging in awake mice, we show that t
37 (OB), mitral and tufted cells, using chronic
two-photon calcium imaging in awake mice.
38 Two-photon calcium imaging in awake mouse models showed
39 Here, using
two-photon calcium imaging in behaving mice, we show tha
40 uron activity and movement, we used in vivo,
two-photon calcium imaging in CA1 of male and female mic
41 ercome this experimental limitation and used
two-photon calcium imaging in combination with a functio
42 gated these issues using in vivo multineuron
two-photon calcium imaging in combination with informati
43 We used in vivo
two-photon calcium imaging in combination with whole-cel
44 Using
two-photon calcium imaging in dendritic spines, we const
45 Using in vivo
two-photon calcium imaging in Drosophila, we describe di
46 Here we use
two-photon calcium imaging in head-fixed Drosophila mela
47 We combined
two-photon calcium imaging in head-fixed flying flies wi
48 Here we use
two-photon calcium imaging in head-fixed walking and fly
49 Using in vivo
two-photon calcium imaging in layers 2/3 and 4 in mouse
50 neuron activity and movement through in vivo
two-photon calcium imaging in mice learning a lever-pres
51 pyramidal neurons in the barrel cortex using
two-photon calcium imaging in mice performing an object-
52 Using in vivo
two-photon calcium imaging in mouse primary visual corte
53 We combined this approach with in vivo
two-photon calcium imaging in order to characterize the
54 rtical response biases, we performed chronic
two-photon calcium imaging in postrhinal association cor
55 in the mouse ACx and whole-cell recordings,
two-photon calcium imaging in presynaptic terminals, and
56 Studying neuronal activity with
two-photon calcium imaging in primary visual cortex of m
57 Two-photon calcium imaging in retinal ganglion cell (RGC
58 Here we present a technique for
two-photon calcium imaging in the central brain of head-
59 les of Hb9 INs in the locomotor CPG, we used
two-photon calcium imaging in the in vitro isolated whol
60 Using in vivo
two-photon calcium imaging in the rat barrel cortex duri
61 We used
two-photon calcium imaging in V1 of mice performing a st
62 Using
two-photon calcium imaging in vivo and intracellular rec
63 al cortex at different postnatal ages, using
two-photon calcium imaging in vivo and multiple whole-ce
64 tro to their response properties measured by
two-photon calcium imaging in vivo in dark-reared mice.
65 Here we use
two-photon calcium imaging in vivo to determine the micr
66 Using high-speed
two-photon calcium imaging in vivo, we found that respon
67 Using electrophysiological recordings and
two-photon calcium imaging in young (6-8 weeks old) 3xTg
68 spiking, using cell-attached recordings and
two-photon calcium imaging,
in the barrel cortex of mice
69 Using multi-plane
two-photon calcium imaging of CA1 place cell somata, axo
70 Using
two-photon calcium imaging of CA1 pyramidal neurons in r
71 Here we combined in vivo,
two-photon calcium imaging of complex spikes in microcom
72 rsal lateral geniculate nucleus (dLGN) using
two-photon calcium imaging of dense populations in thala
73 Here we use
two-photon calcium imaging of identified excitatory and
74 Using in vivo
two-photon calcium imaging of layer 2/3 barrel cortex ne
75 Two-photon calcium imaging of local cortical populations
76 Using
two-photon calcium imaging of mouse hippocampal neurons
77 Here we use
two-photon calcium imaging of mouse neocortical pyramida
78 Here we use in vivo
two-photon calcium imaging of neocortical astrocytes whi
79 erformed whole-brain light-sheet imaging and
two-photon calcium imaging of neural activity in the ret
80 holographic method to simultaneously perform
two-photon calcium imaging of neuronal populations acros
81 ical intrinsic activity better, we performed
two-photon calcium imaging of populations of neurons fro
82 Two-photon calcium imaging of retino-recipient midbrain
83 Two-photon calcium imaging of secondary motor cortex (M2
84 We tested this hypothesis by using
two-photon calcium imaging of spontaneous activity in po
85 High-speed
two-photon calcium imaging of visual responses showed th
86 Using
two-photon calcium imaging on intact larval zebrafish, w
87 Two-photon calcium imaging provides an optical readout o
88 Here, we obtained in vivo
two-photon calcium imaging recordings from the entire de
89 Perforated-patch recordings and
two-photon calcium imaging reveal that individual SACs h
90 Two-photon calcium imaging revealed a small visual area,
91 Furthermore,
two-photon calcium imaging revealed that M2 ensemble act
92 Two-photon calcium imaging reveals that a thalamic nucle
93 In vivo
two-photon calcium imaging reveals that these LC types r
94 Our in vitro patch-clamp recordings and
two-photon calcium imaging show that direction-selective
95 Results from
two-photon calcium imaging show that starvation increase
96 Furthermore, in vivo single-cell
two-photon calcium imaging showed that hippocampal neuro
97 In vivo
two-photon calcium imaging shows the amplitude of food o
98 Using CCD and
two-photon calcium imaging techniques on CA1 pyramidal n
99 Using
two-photon calcium imaging techniques, we found that sin
100 We demonstrate using
two-photon calcium imaging that activation of single syn
101 provides an effective method for volumetric
two-photon calcium imaging that increases the number of
102 We used
two-photon calcium imaging to characterize a functional
103 To address this issue, we used in vivo
two-photon calcium imaging to characterize the orientati
104 the origin of cortical maps, we used in vivo
two-photon calcium imaging to characterize the propertie
105 Here we use
two-photon calcium imaging to characterize the response
106 We used in vivo
two-photon calcium imaging to demonstrate topographic se
107 Here we use chronic
two-photon calcium imaging to explore how wakefulness an
108 We used in vivo
two-photon calcium imaging to independently map ON and O
109 Here, we applied
two-photon calcium imaging to map neuronal tuning for or
110 we used intrinsic signal optical imaging and
two-photon calcium imaging to map visual responses in ad
111 al clones of excitatory neurons, and in vivo
two-photon calcium imaging to measure neuronal response
112 put from primary visual cortex (V1), we used
two-photon calcium imaging to measure responses of axons
113 mitted in cortical circuits in vivo, we used
two-photon calcium imaging to monitor ensemble activity
114 Here we used awake in vivo
two-photon calcium imaging to monitor neuronal function
115 of Sapap3 KO mice was further explored using
two-photon calcium imaging to monitor striatal output fr
116 Here we use in vivo
two-photon calcium imaging to monitor the activity of do
117 ere we addressed this issue by using in vivo
two-photon calcium imaging to monitor the activity of th
118 Here, we have used
two-photon calcium imaging to monitor the activity of yo
119 By combining
two-photon calcium imaging to obtain dense retinal recor
120 Here we use
two-photon calcium imaging to record the activity of lar
121 To explore this, we used in vivo
two-photon calcium imaging to record the activity of neu
122 Here we used
two-photon calcium imaging to reveal an alternative arra
123 We used
two-photon calcium imaging to sample the response to mon
124 fluorescent retrograde tracing with in vivo
two-photon calcium imaging to simultaneously compare the
125 We used
two-photon calcium imaging to study the functional micro
126 We then use
two-photon calcium imaging to track individual cells chr
127 Finally, we use
two-photon calcium imaging to track the matching process
128 Here, we used random-access
two-photon calcium imaging together with electrophysiolo
129 Using high-speed in vivo
two-photon calcium imaging,
we characterized the recepti
130 ordings from interneurons and TC neurons and
two-photon calcium imaging,
we find that synchronous act
131 a combination of patch-clamp recordings and
two-photon calcium imaging,
we found that Bk strongly se
132 Using
two-photon calcium imaging,
we reconstructed the dynamic
133 Finally, using
two-photon calcium imaging,
we show that SC direction se
134 Using in vivo
two-photon calcium imaging,
we studied how MCs responded
135 First, using pharmacogenetics and
two-photon calcium imaging,
we validate that SACs are ne
136 We combined
two-photon calcium imaging with deflection of many whisk
137 layer neocortical interneurones, we combined
two-photon calcium imaging with whole cell recordings an
138 In this first study, we combined
two-photon calcium imaging with whole-cell recording and
139 In this second study, we have combined
two-photon calcium imaging with whole-cell recording and
140 In vivo
two-photon calcium imaging would benefit from the use of