1 antial reductions in motion artifacts during
two-photon imaging.
2 ated at the fine spatial scale observed with
two-photon imaging.
3 table by both MRI and near-infrared excited,
two-photon imaging.
4 ing submicron-resolution, three-dimensional,
two-photon imaging.
5 l neurons to visual stimuli, as confirmed by
two-photon imaging.
6 via T-type Ca(2+) channels, as indicated by
two-photon imaging.
7 Under
two-photon imaging,
a single GAC generated rectified loc
8 By providing
two-photon imaging access to cortical neuronal populatio
9 unctional mapping; and functionally targeted
two-photon imaging across all cortical layers in awake m
10 Furthermore, biochemical and
two-photon imaging analyses identified elevated and imba
11 Two-photon imaging analysis revealed in Munc18b-depleted
12 Here, using fast 3D
two-photon imaging and a caged glutamate, we challenge t
13 Here we used in vivo
two-photon imaging and a unique analysis method to rigor
14 rioration in adolescence as shown by in vivo
two-photon imaging and ameliorated a behavioral deficit
15 thyl (AM) ester version of Cal-590, combined
two-photon imaging and cell-attached recordings revealed
16 Here, we used conventional and
two-photon imaging and electron microscopy to show that
17 rodent whisker system using a combination of
two-photon imaging and electrophysiology during active t
18 Using a combination of
two-photon imaging and electrophysiology in awake head-r
19 Two-photon imaging and flow cytometry revealed in kidney
20 Here we use
two-photon imaging and focused ion beam-scanning electro
21 a novel combination of high-throughput live
two-photon imaging and gene expression profiling to stud
22 Electrophysiological,
two-photon imaging and glutamate uncaging, and electron
23 tic integration in CA3 pyramidal cells using
two-photon imaging and glutamate uncaging.
24 n a mouse model of neuropathic pain, in vivo
two-photon imaging and patch clamp recording showed init
25 Here we implemented combined
two-photon imaging and photolysis in vivo to monitor and
26 bility to adaptively patch, under continuous
two-photon imaging and real-time analysis, fluorophore-e
27 d -2 homodimers and heterodimers obtained by
two-photon imaging and spectroscopy fluorescence resonan
28 nd defect in motility (measured by real-time
two-photon imaging)
and that these cells have a decrease
29 ivity, we combined molecular identification,
two-photon imaging,
and electrophysiological recordings
30 Using a new, non-invasive, intravital
two-photon imaging approach we study physiological hair-
31 The lateral and axial resolutions for
two-photon imaging are 0.8 and 10 mum, respectively.
32 ntum sized clusters making them suitable for
two-photon imaging as well as other applications such as
33 We also show two-step and
two-photon imaging can be combined to give quartic non-l
34 ng chemogenetics and optogenetics, live cell
two-photon imaging,
cell fate reprogramming and human pl
35 Two-photon imaging confirmed that basophils did not inte
36 rom fictively behaving larval zebrafish, and
two-photon imaging data from behaving mouse.
37 We measured Ca(2+) transients by
two-photon imaging dendrites while recording neuronal so
38 l glutamate uncaging, voltage-sensitive dye,
two-photon imaging,
electrophysiology, and immunohistoch
39 Two-photon imaging experiments revealed that antiviral C
40 oton imaging and illustrate the potential of
two-photon imaging for use in studying helical macromole
41 Here, we extend
two-photon imaging from anesthetized, head-stabilized to
42 We next used in vivo
two-photon imaging from individual neurons and epifluore
43 Using
two-photon imaging,
Golgi staining, immunohistochemistry
44 Here, we established
two-photon imaging guided cell-attached recordings from
45 Finally,
two-photon imaging guided recordings from parvalbumin-po
46 escent protein in neocortical cells in 2000,
two-photon imaging has enabled the dynamics of individua
47 techniques such as multielectrode arrays and
two-photon imaging has made it easier to measure correla
48 Using
two-photon imaging in acute rat brain slices and glomeru
49 Using high-resolution confocal and in vivo
two-photon imaging in AD mouse models, we demonstrate th
50 Using optogenetic stimulation and in vivo
two-photon imaging in adolescent mice, we found that pha
51 Our studies demonstrate the utility of
two-photon imaging in answering questions in the pre-imp
52 Here we report techniques for long-term
two-photon imaging in awake macaque monkeys.
53 Here, by using
two-photon imaging in awake macaques and systematically
54 Here, using in vivo
two-photon imaging in awake mice, we found that learning
55 patch-clamp recording, flash photolysis, and
two-photon imaging in brain slices from 4-5-week-old mic
56 adult mice (P40-P61), using chronic in vivo
two-photon imaging in different sensory areas.
57 We use
two-photon imaging in Drosophila to characterize a first
58 Using in vivo
two-photon imaging in female mice, we show that mPOA(Nts
59 ing of light-evoked Ca(2)(+) responses using
two-photon imaging in individual cone photoreceptor term
60 ssments of tetramethylammonium diffusion and
two-photon imaging in live mice, we show that natural sl
61 high-resolution fixed-tissue microscopy and
two-photon imaging in living mice we observed that a lar
62 In this study, we used
two-photon imaging in macaque monkey V1 to demonstrate t
63 We used volumetric
two-photon imaging in mice expressing GCaMP6s and nuclea
64 spike-related calcium signals recorded with
two-photon imaging in motor and somatosensory cortex.
65 Using in vivo
two-photon imaging in mouse models, we found that two di
66 Using
two-photon imaging in prefrontal brain slices, we show t
67 ng a combination of whole-cell recording and
two-photon imaging in rat mPFC slices, we were able to c
68 Using
two-photon imaging in vivo, we show that pMBP-eGFP-NTR t
69 We used
two-photon imaging,
infrared-differential interference c
70 e penetration depth and reduced photodamage,
two-photon imaging is an highly promising technique for
71 otobleaching tendency, their applications in
two-photon imaging is highly limited.
72 rate that the combination of ASAP2s and fast
two-photon imaging methods enables detection of neural e
73 We combined
two-photon imaging microscopy in brain slices with in vi
74 visual cortex using a combination of in vivo
two-photon imaging,
morphological reconstruction, immuno
75 onic mechanisms is quantitative and combined
two-photon imaging of [Cl(-)]i and pHi, but this has nev
76 Here we combine two-photon uncaging with
two-photon imaging of a fluorescent label of surface AMP
77 lutamate release from mouse bipolar cells by
two-photon imaging of a glutamate sensor (iGluSnFR) expr
78 2 neurons during rotarod learning by in vivo
two-photon imaging of a knockin reporter.
79 Here we show, using
two-photon imaging of a near-infrared 2-deoxyglucose ana
80 Using
two-photon imaging of a newly developed ventral spinal c
81 Here we report video-rate,
two-photon imaging of a physiologically intact preparati
82 Using in vivo
two-photon imaging of bacterial artificial chromosome tr
83 of the cortical metabolic rate of oxygen and
two-photon imaging of blood vessel diameter in a rat mod
84 Intravital
two-photon imaging of bone tissues showed that a potent
85 Using in vivo
two-photon imaging of both awake and anesthetized mice,
86 Two-photon imaging of CA1 neurons expressing enhanced gr
87 lowed by targeted loose-patch recordings and
two-photon imaging of calcium responses in vivo to chara
88 signal imaging through the intact skull and
two-photon imaging of calcium signals in single neurons.
89 We used
two-photon imaging of calcium signals in the ferret visu
90 In this study we used in vivo
two-photon imaging of calcium signals to further explore
91 In vivo
two-photon imaging of cerebral blood vessels revealed su
92 Two-photon imaging of cortical neurons in vivo has provi
93 icted pattern of calcium influx, we combined
two-photon imaging of dendritic [Ca2+] dynamics with den
94 First, we performed time-lapse
two-photon imaging of dendritic spine motility of layer
95 We used chronic in vivo
two-photon imaging of dendritic spines and axonal bouton
96 TTEBC and concurrent map plasticity, we used
two-photon imaging of dendritic spines in barrel cortex
97 high-resolution microlenses, and illustrate
two-photon imaging of dendritic spines on hippocampal ne
98 Here, we combined chronic in vivo
two-photon imaging of dendritic spines with auditory-cue
99 Finally, using
two-photon imaging of extracellular glutamate, we find t
100 Here, we used
two-photon imaging of Fluo-4-loaded rat brain slices to
101 Two-photon imaging of fluorescence in brain enables anal
102 ration of the adult mouse brain that enabled
two-photon imaging of fluorescently labeled CA1 pyramida
103 Using
two-photon imaging of FM 1-43, a fluorescent marker of s
104 mossy fibre presynaptic boutons, we used (i)
two-photon imaging of FM1-43 vesicular release in rat hi
105 shrew (Tupaia belangeri) visual cortex using
two-photon imaging of GCaMP6 calcium signals.
106 By combining confocal and
two-photon imaging of genetically encoded pH reporters w
107 Time-lapse
two-photon imaging of GFP-labeled microglia demonstrates
108 gical manipulations, glutamate uncaging, and
two-photon imaging of GFP-transfected hippocampal pyrami
109 We also show that ASAP2s enables
two-photon imaging of graded potentials in organotypic s
110 Here we demonstrate chronic
two-photon imaging of granule cell population activity i
111 neuron-pair operant conditioning task using
two-photon imaging of IN subtypes expressing GCaMP6f.
112 n in a mouse model of acute lung injury with
two-photon imaging of intact lung tissue.
113 that use the emerging technique of real-time
two-photon imaging of intact lymphoid organs began to di
114 Using in vivo
two-photon imaging of intracellular calcium signals, we
115 By an approach combining
two-photon imaging of isolated renal tubules, physiologi
116 Using
two-photon imaging of large groups of neurons, we show t
117 ual cortex, we demonstrate that high-quality
two-photon imaging of large neuronal populations can be
118 To understand this diversity, we use
two-photon imaging of layer 5 neocortical pyramidal cell
119 flow cytometry, conventional microscopy, and
two-photon imaging of live cells.
120 Two-photon imaging of live exposed cortex showed that se
121 By using
two-photon imaging of live zebrafish embryos, we observe
122 Here,
two-photon imaging of living T cells in explanted lymph
123 Two-photon imaging of migrating T cells in the steady-st
124 Dual-color in vivo
two-photon imaging of mouse ACx showed pathway-specific
125 Stable one- and
two-photon imaging of neuronal activity in awake, behavi
126 Two-photon imaging of neuronal population activity showe
127 Here, we introduce volumetric
two-photon imaging of neurons using stereoscopy (vTwINS)
128 We use in vivo,
two-photon imaging of novel genetically encoded voltage
129 of identified Schaffer collateral axons with
two-photon imaging of postsynaptic calcium signals and f
130 the present study, we used fluorescence and
two-photon imaging of presynaptic terminals with the flu
131 Two-photon imaging of redox-sensitive GFP corroborated t
132 In vivo
two-photon imaging of retrovirally labelled adult-born J
133 We have used in vivo time-lapse
two-photon imaging of single motor neuron axons labeled
134 be for the detection of CaMKII activity, and
two-photon imaging of single synapses within identified
135 By in vivo
two-photon imaging of spinal dorsal column sensory axons
136 imaging of mouse visual cortex responses and
two-photon imaging of superficial layer spines on layer
137 Using both
two-photon imaging of synaptic vesicle cycling and elect
138 Measurements of cytokine sensitivity and
two-photon imaging of T cell-dendritic cell (T-DC) inter
139 timuli to larval zebrafish, while performing
two-photon imaging of tectal neurons loaded with a fluor
140 persensitivity (DTH), a convenient model for
two-photon imaging of Tem cell participation in an infla
141 Two-photon imaging of the axon terminals of a single PN
142 Here,
two-photon imaging of the fluorescent serotonin analog 5
143 activity (two-photon glutamate uncaging and
two-photon imaging of the FM 1-43 assay, respectively) a
144 Two-photon imaging of the genetically encoded fluorescen
145 Using
two-photon imaging of the membrane marker FM1-43 in the
146 living zebrafish larvae, we used time-lapse
two-photon imaging of the presynaptic marker synaptophys
147 Using intravital and kidney slice
two-photon imaging of the three-dimensional structure of
148 Here we use high-resolution time-lapse
two-photon imaging of transgenic zebrafish to examine ho
149 Using
two-photon imaging of tumor-infiltrating T lymphocytes,
150 O'Herron et al. (2016) perform
two-photon imaging of vascular and neural responses in c
151 By combining computational simulation,
two-photon imaging,
optogenetics, and dual-color uncagin
152 was required to get sufficient staining for
two-photon imaging,
resulted in typical fluctuations of
153 Electron microscopy and
two-photon imaging reveal that the plasma membrane of mi
154 Two-photon imaging revealed global stimulation-evoked as
155 Concurrently, intravital
two-photon imaging revealed prompt peritubular vasodilat
156 In addition,
two-photon imaging revealed reduced agonist-evoked influ
157 In vivo
two-photon imaging revealed reduced dendritic spine moti
158 In conclusion, hippocampal long-term
two-photon imaging revealed structural plasticity of den
159 Two-photon imaging revealed that the intracellular Ca(2+
160 Real-time
two-photon imaging reveals lymphocyte behaviors that are
161 Two-photon imaging showed that many excitatory neurons i
162 However, conventional
two-photon imaging systems are limited in their field of
163 The
two-photon imaging technique promises to offer a facile
164 ss this question we developed a transcranial
two-photon imaging technique to follow identified spines
165 l cortex of Fmr1 KO mice with a transcranial
two-photon imaging technique.
166 Using intrinsic and
two-photon imaging techniques in the tree shrew, we asse
167 We used long-term
two-photon imaging through a cranial window, to track in
168 stages of brain AVM formation by time-lapse
two-photon imaging through cranial windows of mice expre
169 We used
two-photon imaging to characterize the motile behavior o
170 hese experiments extend the reach of in vivo
two-photon imaging to chronic, simultaneous monitoring o
171 Here we used in vivo
two-photon imaging to directly assay transport of organe
172 In this study, we utilized in vivo
two-photon imaging to directly monitor the acute structu
173 TP (two-photon targeted patching), that uses
two-photon imaging to guide in vivo whole-cell recording
174 asive, high resolution, endogenous contrast,
two-photon imaging to identify distinct adipose tissue t
175 al as well as dynamic explant and intravital
two-photon imaging to investigate this issue.
176 Here, we used chronic in vivo
two-photon imaging to longitudinally follow a few thousa
177 Working within the delineated area, we used
two-photon imaging to measure basic taste responses in >
178 We have used high-speed confocal and
two-photon imaging to measure calcium and voltage signal
179 We used
two-photon imaging to monitor intracellular calcium acti
180 ron-specific GCaMP6f mouse line and employed
two-photon imaging to monitor the activity of lumbar mot
181 Here we used
two-photon imaging to record neural activity in the rela
182 We use
two-photon imaging to reveal the functional segregation
183 Here we used mouse models of PD and
two-photon imaging to show that dopamine depletion resul
184 we used electrophysiological recordings with
two-photon imaging to study Ca2+ signaling in nontransge
185 Here, we used
two-photon imaging to study neutrophil extravasation fro
186 Here, we used
two-photon imaging to study the patterns of activity of
187 We generated NG2-mEGFP mice and used in vivo
two-photon imaging to study their dynamics in the adult
188 Here, we used in vivo
two-photon imaging to track spines over multiple days in
189 Two-photon imaging together with in situ as well as ex v
190 two-photon excitation of these particles and
two-photon imaging using these particles are also demons
191 Two-photon imaging was coupled with spike inference to m
192 Single-neuron activity monitored by
two-photon imaging was precisely registered to large-sca
193 Longitudinal in vivo
two-photon imaging was used to track microvessels before
194 Using wide-field epifluorescence and
two-photon imaging we demonstrate a robust modular repre
195 Using
two-photon imaging,
we demonstrate that NMDA spikes evok
196 Using glutamate uncaging and
two-photon imaging,
we demonstrate that the efficacy of
197 Using live
two-photon imaging,
we demonstrate that the microglial r
198 Using paired recordings and
two-photon imaging,
we determined the properties of the
199 Using repeated in vivo
two-photon imaging,
we find that increases in spine size
200 Using in vivo
two-photon imaging,
we found that experience-dependent e
201 nses to visual stimuli recorded with in vivo
two-photon imaging,
we found that visual detection corre
202 Using
two-photon imaging,
we monitored spontaneous circuit dyn
203 By neuronal labeling and transcranial
two-photon imaging,
we show in a transgenic mouse model
204 Using in vivo
two-photon imaging,
we show that hypoosmotic stress (20%
205 a new fluorescent Cu(+) sensor for one- and
two-photon imaging,
we show that neurons and neural tiss
206 Using
two-photon imaging,
we show that T- and R-type voltage-g
207 haracterized by novel technologies including
two-photon imaging,
whole-genome transcriptomic and epig
208 Successful application of
two-photon imaging with genetic tools in awake macaque m
209 Using in vivo two-color
two-photon imaging with genetically encoded calcium indi
210 on (Kerlin et al. and Runyan et al.) combine
two-photon imaging with guided electrical recordings to
211 fied mammalian neurons in vivo, by combining
two-photon imaging with single-cell electroporation.
212 We used
two-photon imaging with the Ca2+-sensitive fluorescent p