1 via T-type Ca(2+) channels, as indicated by
two-photon imaging.
2 antial reductions in motion artifacts during
two-photon imaging.
3 ated at the fine spatial scale observed with
two-photon imaging.
4 multiple cortical layers in awake mice using
two-photon imaging.
5 table by both MRI and near-infrared excited,
two-photon imaging.
6 ing submicron-resolution, three-dimensional,
two-photon imaging.
7 ding plate reading, cell sorting and one- or
two-photon imaging.
8 measured neural activity using widefield and
two-photon imaging.
9 l neurons to visual stimuli, as confirmed by
two-photon imaging.
10 Under
two-photon imaging,
a single GAC generated rectified loc
11 By providing
two-photon imaging access to cortical neuronal populatio
12 unctional mapping; and functionally targeted
two-photon imaging across all cortical layers in awake m
13 Furthermore, biochemical and
two-photon imaging analyses identified elevated and imba
14 Two-photon imaging analysis revealed in Munc18b-depleted
15 Here, using fast 3D
two-photon imaging and a caged glutamate, we challenge t
16 Here we used in vivo
two-photon imaging and a unique analysis method to rigor
17 rioration in adolescence as shown by in vivo
two-photon imaging and ameliorated a behavioral deficit
18 thyl (AM) ester version of Cal-590, combined
two-photon imaging and cell-attached recordings revealed
19 Here, using longitudinal in vivo
two-photon imaging and correlated electron microscopy of
20 Here, we used conventional and
two-photon imaging and electron microscopy to show that
21 rodent whisker system using a combination of
two-photon imaging and electrophysiology during active t
22 Using a combination of
two-photon imaging and electrophysiology in awake head-r
23 Here, we have used
two-photon imaging and electrophysiology to investigate
24 Two-photon imaging and flow cytometry revealed in kidney
25 Here we use
two-photon imaging and focused ion beam-scanning electro
26 a novel combination of high-throughput live
two-photon imaging and gene expression profiling to stud
27 Electrophysiological,
two-photon imaging and glutamate uncaging, and electron
28 tic integration in CA3 pyramidal cells using
two-photon imaging and glutamate uncaging.
29 hair cells in vivo using electrophysiology,
two-photon imaging and immunostaining applied to wild-ty
30 By using microfluidics, intravital
two-photon imaging and long-term-engraftment assays, we
31 glia is used in combination with label-free,
two-photon imaging and microRNA studies to characterize
32 n a mouse model of neuropathic pain, in vivo
two-photon imaging and patch clamp recording showed init
33 Here we implemented combined
two-photon imaging and photolysis in vivo to monitor and
34 axons that innervate BA (VTA(DA->BA)) using
two-photon imaging and photometry in behaving mice.
35 bility to adaptively patch, under continuous
two-photon imaging and real-time analysis, fluorophore-e
36 d -2 homodimers and heterodimers obtained by
two-photon imaging and spectroscopy fluorescence resonan
37 andpass optical filters enables simultaneous
two-photon imaging and visual stimulation over a large r
38 nd defect in motility (measured by real-time
two-photon imaging)
and that these cells have a decrease
39 ivity, we combined molecular identification,
two-photon imaging,
and electrophysiological recordings
40 Using a new, non-invasive, intravital
two-photon imaging approach we study physiological hair-
41 The lateral and axial resolutions for
two-photon imaging are 0.8 and 10 mum, respectively.
42 observations of spiking activity produced by
two-photon imaging are temporally blurred and noisy.
43 ntum sized clusters making them suitable for
two-photon imaging as well as other applications such as
44 our knowledge, quantitative high-resolution
two-photon imaging at 100 MPa of living microbes from al
45 din backbone can be optimized for intravital
two-photon imaging by installing a red fluorophore.
46 We also show two-step and
two-photon imaging can be combined to give quartic non-l
47 ng chemogenetics and optogenetics, live cell
two-photon imaging,
cell fate reprogramming and human pl
48 By integrating in vivo
two-photon imaging co-registered with electron microscop
49 Here, using electrophysiology,
two-photon imaging,
cognitive tasks, and mathematical mo
50 Two-photon imaging confirmed that basophils did not inte
51 Immunohistochemical studies and in vivo
two-photon imaging confirmed that there is no significan
52 rom fictively behaving larval zebrafish, and
two-photon imaging data from behaving mouse.
53 bipolar cell from the mouse retina based on
two-photon imaging data.
54 In vivo
two-photon imaging demonstrated that surveillance behavi
55 We measured Ca(2+) transients by
two-photon imaging dendrites while recording neuronal so
56 d, combinatorial spectral compatibility, and
two-photon imaging depth.
57 nhanced Scan Engines for Large field-of-view
Two-Photon imaging (
Diesel2p).
58 Clonal analysis and longitudinal intravital
two-photon imaging directly demonstrate that Klf9 functi
59 Here, we use in vivo
two-photon imaging during hyperspectral visual stimulati
60 l glutamate uncaging, voltage-sensitive dye,
two-photon imaging,
electrophysiology, and immunohistoch
61 Two-photon imaging experiments revealed that antiviral C
62 ombine transparent microelectrode arrays and
two-photon imaging for longitudinal, multimodal monitori
63 oton imaging and illustrate the potential of
two-photon imaging for use in studying helical macromole
64 Here, we extend
two-photon imaging from anesthetized, head-stabilized to
65 We next used in vivo
two-photon imaging from individual neurons and epifluore
66 Using
two-photon imaging,
Golgi staining, immunohistochemistry
67 Here, we established
two-photon imaging guided cell-attached recordings from
68 Finally,
two-photon imaging guided recordings from parvalbumin-po
69 orescence, but more sensitive to motion, and
two photon imaging has always required anchoring the mic
70 escent protein in neocortical cells in 2000,
two-photon imaging has enabled the dynamics of individua
71 techniques such as multielectrode arrays and
two-photon imaging has made it easier to measure correla
72 Comparative studies utilizing
two-photon imaging have indicated that substrates contai
73 Calcium imaging techniques, such as
two-photon imaging,
have become a powerful tool to explo
74 For
two-photon imaging,
however, the effects of hemodynamic
75 Here, we performed time lapse in vivo
two photon imaging in somatosensory cortex of adult mice
76 ed neuronal ATP homeostasis during SDs using
two-photon imaging in acute brain slices from adult mice
77 Using
two-photon imaging in acute rat brain slices and glomeru
78 Using high-resolution confocal and in vivo
two-photon imaging in AD mouse models, we demonstrate th
79 Using optogenetic stimulation and in vivo
two-photon imaging in adolescent mice, we found that pha
80 d odorant sampling on MTC responses, we used
two-photon imaging in anesthetized male and female mice
81 Our studies demonstrate the utility of
two-photon imaging in answering questions in the pre-imp
82 Here we report techniques for long-term
two-photon imaging in awake macaque monkeys.
83 Here, by using
two-photon imaging in awake macaques and systematically
84 d by higher-resolution electrophysiology and
two-photon imaging in awake macaques.
85 Here, we use longitudinal
two-photon imaging in awake mice and single-cell transcr
86 Here, using in vivo
two-photon imaging in awake mice, we found that learning
87 Using chronic
two-photon imaging in awake mice, we observed spontaneou
88 patch-clamp recording, flash photolysis, and
two-photon imaging in brain slices from 4-5-week-old mic
89 adult mice (P40-P61), using chronic in vivo
two-photon imaging in different sensory areas.
90 We use
two-photon imaging in Drosophila to characterize a first
91 Using in vivo
two-photon imaging in female mice, we show that mPOA(Nts
92 ing of light-evoked Ca(2)(+) responses using
two-photon imaging in individual cone photoreceptor term
93 and red (jRGECO1a) Ca(2+) indicators, using
two-photon imaging in isolated mouse spinal cord with at
94 Two-photon imaging in layer 2/3 of the primary somatosen
95 ssments of tetramethylammonium diffusion and
two-photon imaging in live mice, we show that natural sl
96 high-resolution fixed-tissue microscopy and
two-photon imaging in living mice we observed that a lar
97 In this study, we used
two-photon imaging in macaque monkey V1 to demonstrate t
98 We used volumetric
two-photon imaging in mice expressing GCaMP6s and nuclea
99 By utilizing in vivo
two-photon imaging in mice, we found that cell-type-spec
100 spike-related calcium signals recorded with
two-photon imaging in motor and somatosensory cortex.
101 with GFP expression using both widefield and
two-photon imaging in mouse cortex.
102 Using in vivo
two-photon imaging in mouse models, we found that two di
103 Using
two-photon imaging in prefrontal brain slices, we show t
104 ng a combination of whole-cell recording and
two-photon imaging in rat mPFC slices, we were able to c
105 Here we use
two-photon imaging in visual cortex as mice learn a visu
106 Using
two-photon imaging in vivo, we show that pMBP-eGFP-NTR t
107 Two-photon imaging indicates that ADLumin-1 can efficien
108 We used
two-photon imaging,
infrared-differential interference c
109 In vivo
two-photon imaging is a valuable technique for studies o
110 e penetration depth and reduced photodamage,
two-photon imaging is an highly promising technique for
111 otobleaching tendency, their applications in
two-photon imaging is highly limited.
112 rate that the combination of ASAP2s and fast
two-photon imaging methods enables detection of neural e
113 We combined
two-photon imaging microscopy in brain slices with in vi
114 ing influenza virus-infected lung in vivo by
two-photon imaging microscopy.
115 visual cortex using a combination of in vivo
two-photon imaging,
morphological reconstruction, immuno
116 neurovascular function in awake mice, using
two photon imaging of individual neurons and vessels and
117 onic mechanisms is quantitative and combined
two-photon imaging of [Cl(-)]i and pHi, but this has nev
118 Here we combine two-photon uncaging with
two-photon imaging of a fluorescent label of surface AMP
119 lutamate release from mouse bipolar cells by
two-photon imaging of a glutamate sensor (iGluSnFR) expr
120 2 neurons during rotarod learning by in vivo
two-photon imaging of a knockin reporter.
121 Here we show, using
two-photon imaging of a near-infrared 2-deoxyglucose ana
122 Using
two-photon imaging of a newly developed ventral spinal c
123 Here we report video-rate,
two-photon imaging of a physiologically intact preparati
124 Using in vivo
two-photon imaging of bacterial artificial chromosome tr
125 of the cortical metabolic rate of oxygen and
two-photon imaging of blood vessel diameter in a rat mod
126 Intravital
two-photon imaging of bone tissues showed that a potent
127 Using in vivo
two-photon imaging of both awake and anesthetized mice,
128 Two-photon imaging of CA1 neurons expressing enhanced gr
129 lowed by targeted loose-patch recordings and
two-photon imaging of calcium responses in vivo to chara
130 signal imaging through the intact skull and
two-photon imaging of calcium signals in single neurons.
131 We used
two-photon imaging of calcium signals in the ferret visu
132 In this study we used in vivo
two-photon imaging of calcium signals to further explore
133 Here we used simultaneous two-channel,
two-photon imaging of CBF axons and auditory cortical ne
134 In vivo
two-photon imaging of cerebral blood vessels revealed su
135 Two-photon imaging of cortical neurons in vivo has provi
136 nt and mature mice, and combine longitudinal
two-photon imaging of cortical synapses with repeated be
137 icted pattern of calcium influx, we combined
two-photon imaging of dendritic [Ca2+] dynamics with den
138 Here, we perform fast
two-photon imaging of dendritic and somatic membrane pot
139 Here, using
two-photon imaging of dendritic Ca(2+) signals, electric
140 We used time-lapse
two-photon imaging of dendritic spine motility in acutel
141 First, we performed time-lapse
two-photon imaging of dendritic spine motility of layer
142 We used chronic in vivo
two-photon imaging of dendritic spines and axonal bouton
143 TTEBC and concurrent map plasticity, we used
two-photon imaging of dendritic spines in barrel cortex
144 high-resolution microlenses, and illustrate
two-photon imaging of dendritic spines on hippocampal ne
145 Here, we combined chronic in vivo
two-photon imaging of dendritic spines with auditory-cue
146 We employ long-term, rapid light-sheet and
two-photon imaging of early zebrafish retinogenesis to t
147 Finally, using
two-photon imaging of extracellular glutamate, we find t
148 Here, we used
two-photon imaging of Fluo-4-loaded rat brain slices to
149 Two-photon imaging of fluorescence in brain enables anal
150 l imaging of head-fixed, behaving mice using
two-photon imaging of fluorescent activity reporters has
151 By using
two-photon imaging of fluorescent biosensors and dyes in
152 ration of the adult mouse brain that enabled
two-photon imaging of fluorescently labeled CA1 pyramida
153 We developed an optical technique based on
two-photon imaging of fluorescently labeled extracellula
154 Using
two-photon imaging of FM 1-43, a fluorescent marker of s
155 mossy fibre presynaptic boutons, we used (i)
two-photon imaging of FM1-43 vesicular release in rat hi
156 Here we perform
two-photon imaging of GABA release in the inner plexifor
157 shrew (Tupaia belangeri) visual cortex using
two-photon imaging of GCaMP6 calcium signals.
158 valanche dynamics, using in vivo whole-brain
two-photon imaging of GCaMP6s larval zebrafish (males an
159 By combining confocal and
two-photon imaging of genetically encoded pH reporters w
160 Here, we use in vivo
two-photon imaging of genetically encoded voltage and ca
161 Time-lapse
two-photon imaging of GFP-labeled microglia demonstrates
162 gical manipulations, glutamate uncaging, and
two-photon imaging of GFP-transfected hippocampal pyrami
163 We also show that ASAP2s enables
two-photon imaging of graded potentials in organotypic s
164 Here we demonstrate chronic
two-photon imaging of granule cell population activity i
165 Here, to test this possibility, we performed
two-photon imaging of hippocampal CA1 as mice navigated
166 neuron-pair operant conditioning task using
two-photon imaging of IN subtypes expressing GCaMP6f.
167 n in a mouse model of acute lung injury with
two-photon imaging of intact lung tissue.
168 that use the emerging technique of real-time
two-photon imaging of intact lymphoid organs began to di
169 Using in vivo
two-photon imaging of intracellular calcium signals, we
170 By an approach combining
two-photon imaging of isolated renal tubules, physiologi
171 Using
two-photon imaging of large groups of neurons, we show t
172 ual cortex, we demonstrate that high-quality
two-photon imaging of large neuronal populations can be
173 To understand this diversity, we use
two-photon imaging of layer 5 neocortical pyramidal cell
174 flow cytometry, conventional microscopy, and
two-photon imaging of live cells.
175 Two-photon imaging of live exposed cortex showed that se
176 By using
two-photon imaging of live zebrafish embryos, we observe
177 Here,
two-photon imaging of living T cells in explanted lymph
178 In vivo
two-photon imaging of microglia in the intact brain has
179 Two-photon imaging of migrating T cells in the steady-st
180 Dual-color in vivo
two-photon imaging of mouse ACx showed pathway-specific
181 We performed in vivo
two-photon imaging of myelin sheaths along single axons
182 well as cellular and subcellular resolution
two-photon imaging of neural structures up to 600 um dee
183 Stable one- and
two-photon imaging of neuronal activity in awake, behavi
184 system capable of chronic, motion-stabilized
two-photon imaging of neuronal calcium signals from maca
185 Two-photon imaging of neuronal population activity showe
186 Here, we introduce volumetric
two-photon imaging of neurons using stereoscopy (vTwINS)
187 We use in vivo,
two-photon imaging of novel genetically encoded voltage
188 etically targeted single-unit recordings and
two-photon imaging of Ntsr1-Cre+ L6 CT neurons in the pr
189 of identified Schaffer collateral axons with
two-photon imaging of postsynaptic calcium signals and f
190 the present study, we used fluorescence and
two-photon imaging of presynaptic terminals with the flu
191 -principle correlative experiments combining
two-photon imaging of protein distributions and 3D EM.
192 Two-photon imaging of redox-sensitive GFP corroborated t
193 We addressed this question by using
two-photon imaging of resting-state microvascular oxygen
194 In vivo
two-photon imaging of retrovirally labelled adult-born J
195 We have used in vivo time-lapse
two-photon imaging of single motor neuron axons labeled
196 be for the detection of CaMKII activity, and
two-photon imaging of single synapses within identified
197 By in vivo
two-photon imaging of spinal dorsal column sensory axons
198 imaging of mouse visual cortex responses and
two-photon imaging of superficial layer spines on layer
199 Using both
two-photon imaging of synaptic vesicle cycling and elect
200 Measurements of cytokine sensitivity and
two-photon imaging of T cell-dendritic cell (T-DC) inter
201 timuli to larval zebrafish, while performing
two-photon imaging of tectal neurons loaded with a fluor
202 persensitivity (DTH), a convenient model for
two-photon imaging of Tem cell participation in an infla
203 Two-photon imaging of the axon terminals of a single PN
204 Here,
two-photon imaging of the fluorescent serotonin analog 5
205 activity (two-photon glutamate uncaging and
two-photon imaging of the FM 1-43 assay, respectively) a
206 Two-photon imaging of the genetically encoded fluorescen
207 Using
two-photon imaging of the membrane marker FM1-43 in the
208 We used large scale
two-photon imaging of the nodose ganglia from our ex viv
209 living zebrafish larvae, we used time-lapse
two-photon imaging of the presynaptic marker synaptophys
210 Using intravital and kidney slice
two-photon imaging of the three-dimensional structure of
211 Here, we developed an approach for
two-photon imaging of the transverse hippocampal plane i
212 Here we use high-resolution time-lapse
two-photon imaging of transgenic zebrafish to examine ho
213 Using
two-photon imaging of tumor-infiltrating T lymphocytes,
214 O'Herron et al. (2016) perform
two-photon imaging of vascular and neural responses in c
215 By combining computational simulation,
two-photon imaging,
optogenetics, and dual-color uncagin
216 Using fiber photometry recording and
two-photon imaging,
our ACh sensor also enabled sensitiv
217 was required to get sufficient staining for
two-photon imaging,
resulted in typical fluctuations of
218 Electron microscopy and
two-photon imaging reveal that the plasma membrane of mi
219 Two-photon imaging revealed global stimulation-evoked as
220 Concurrently, intravital
two-photon imaging revealed prompt peritubular vasodilat
221 In addition,
two-photon imaging revealed reduced agonist-evoked influ
222 In vivo
two-photon imaging revealed reduced dendritic spine moti
223 In conclusion, hippocampal long-term
two-photon imaging revealed structural plasticity of den
224 Two-photon imaging revealed that the intracellular Ca(2+
225 Two-photon imaging revealed that these cues served as do
226 Two-photon imaging reveals enhanced hue-specific cell cl
227 Real-time
two-photon imaging reveals lymphocyte behaviors that are
228 croscopy-based synaptic reconstruction after
two-photon imaging reveals that, during anesthesia, micr
229 n AD brains combined with repetitive in vivo
two-photon imaging showed focal fibrinogen deposits asso
230 Combined optogenetic activation and
two-photon imaging showed that behavioral effects were a
231 Transcranial
two-photon imaging showed that deficits in extinction le
232 Two-photon imaging showed that many excitatory neurons i
233 Time-lapse in vivo
two-photon imaging showed that OVX-associated reduction
234 However, conventional
two-photon imaging systems are limited in their field of
235 The
two-photon imaging technique promises to offer a facile
236 We developed a
two-photon imaging technique that scans lines of excitat
237 ss this question we developed a transcranial
two-photon imaging technique to follow identified spines
238 l cortex of Fmr1 KO mice with a transcranial
two-photon imaging technique.
239 Using intrinsic and
two-photon imaging techniques in the tree shrew, we asse
240 pansion associated with LTP, as monitored by
two-photon imaging;
this block involved a mechanism iden
241 We used long-term
two-photon imaging through a cranial window, to track in
242 stages of brain AVM formation by time-lapse
two-photon imaging through cranial windows of mice expre
243 Here, we use longitudinal
two-photon imaging through noninvasive thinned skull win
244 imultaneous electrophysiology and time-lapse
two photon imaging to examine how spines change their st
245 We used
two-photon imaging to characterize the motile behavior o
246 hese experiments extend the reach of in vivo
two-photon imaging to chronic, simultaneous monitoring o
247 Here we used in vivo
two-photon imaging to directly assay transport of organe
248 In this study, we utilized in vivo
two-photon imaging to directly monitor the acute structu
249 TP (two-photon targeted patching), that uses
two-photon imaging to guide in vivo whole-cell recording
250 asive, high resolution, endogenous contrast,
two-photon imaging to identify distinct adipose tissue t
251 al as well as dynamic explant and intravital
two-photon imaging to investigate this issue.
252 Here, we used chronic in vivo
two-photon imaging to longitudinally follow a few thousa
253 Working within the delineated area, we used
two-photon imaging to measure basic taste responses in >
254 We have used high-speed confocal and
two-photon imaging to measure calcium and voltage signal
255 ons for how to leverage fiber photometry and
two-photon imaging to measure dLight1 transients in vivo
256 coded across the mouse visual system, we use
two-photon imaging to measure receptive fields (RFs) and
257 We used
two-photon imaging to monitor intracellular calcium acti
258 ron-specific GCaMP6f mouse line and employed
two-photon imaging to monitor the activity of lumbar mot
259 Here we used
two-photon imaging to record neural activity in the rela
260 ing and diffraction-limited, high-speed spot
two-photon imaging to resolve AP-evoked calcium dynamics
261 We use
two-photon imaging to reveal the functional segregation
262 Here we used mouse models of PD and
two-photon imaging to show that dopamine depletion resul
263 Here, we use
two-photon imaging to simultaneously measure maps of RF
264 we used electrophysiological recordings with
two-photon imaging to study Ca2+ signaling in nontransge
265 Here, we used
two-photon imaging to study neutrophil extravasation fro
266 Here, we used
two-photon imaging to study the patterns of activity of
267 We generated NG2-mEGFP mice and used in vivo
two-photon imaging to study their dynamics in the adult
268 Here, we used in vivo
two-photon imaging to track spines over multiple days in
269 Two-photon imaging together with in situ as well as ex v
270 Next, in vivo
two-photon imaging,
transcriptomics, and computational m
271 Finally,
two-photon imaging using genetically encoded fluorescent
272 two-photon excitation of these particles and
two-photon imaging using these particles are also demons
273 Two-photon imaging was coupled with spike inference to m
274 Single-neuron activity monitored by
two-photon imaging was precisely registered to large-sca
275 Longitudinal in vivo
two-photon imaging was used to track microvessels before
276 Using wide-field epifluorescence and
two-photon imaging we demonstrate a robust modular repre
277 Using
two-photon imaging,
we demonstrate that NMDA spikes evok
278 Using glutamate uncaging and
two-photon imaging,
we demonstrate that the efficacy of
279 Using live
two-photon imaging,
we demonstrate that the microglial r
280 Using
two-photon imaging,
we detected evoked and spontaneous n
281 Using paired recordings and
two-photon imaging,
we determined the properties of the
282 Using repeated in vivo
two-photon imaging,
we find that increases in spine size
283 Using in vivo
two-photon imaging,
we found that experience-dependent e
284 nses to visual stimuli recorded with in vivo
two-photon imaging,
we found that visual detection corre
285 Using
two-photon imaging,
we monitored spontaneous circuit dyn
286 ting this chemogenetic approach with in vivo
two-photon imaging,
we observed that exogenous activatio
287 By neuronal labeling and transcranial
two-photon imaging,
we show in a transgenic mouse model
288 Using in vivo
two-photon imaging,
we show that hypoosmotic stress (20%
289 Using in vivo
two-photon imaging,
we show that locomotion-induced Ca(2
290 a new fluorescent Cu(+) sensor for one- and
two-photon imaging,
we show that neurons and neural tiss
291 Using
two-photon imaging,
we show that T- and R-type voltage-g
292 Here, using longitudinal in vivo
two-photon imaging,
we tracked thousands of corticostria
293 haracterized by novel technologies including
two-photon imaging,
whole-genome transcriptomic and epig
294 Successful application of
two-photon imaging with genetic tools in awake macaque m
295 Using in vivo two-color
two-photon imaging with genetically encoded calcium indi
296 on (Kerlin et al. and Runyan et al.) combine
two-photon imaging with guided electrical recordings to
297 Here, using in vivo
two-photon imaging with laser Doppler and speckle flowme
298 fied mammalian neurons in vivo, by combining
two-photon imaging with single-cell electroporation.
299 demonstrate real-time movement-corrected 3D
two-photon imaging with submicrometer precision.
300 We used
two-photon imaging with the Ca2+-sensitive fluorescent p