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1 se in spine formation as revealed by in vivo two-photon microscopy.
2 es were imaged in intact, live anthers using two-photon microscopy.
3 uring classical conditioning with the use of two-photon microscopy.
4  and imaged their dendritic trees in vivo by two-photon microscopy.
5 e, flow cytometry, fluorescence imaging, and two-photon microscopy.
6 ing whole-cell recordings, optogenetics, and two-photon microscopy.
7 lls were tracked within lymph nodes (LNs) by two-photon microscopy.
8 etwork structure were imaged with the use of two-photon microscopy.
9 al morphology using widefield, confocal, and two-photon microscopy.
10 e quantification of albumin filtration using two-photon microscopy.
11 ing large-volume, high-resolution dual-color two-photon microscopy.
12 ce expressing human WT alpha-synuclein using two-photon microscopy.
13 t in awake mice using subcellular-resolution two-photon microscopy.
14 itic patch-clamp recording with simultaneous two-photon microscopy.
15 ype (WT) and Clcn5 KO mice was determined by two-photon microscopy.
16 expensive, making them promising sources for two-photon microscopy.
17 ambiguity inherent to deep-tissue multifocal two-photon microscopy.
18 g are confocal laser scanning microscopy and two-photon microscopy.
19 iently bright, photostable, and suitable for two-photon microscopy.
20 1,3-diazol-4-yl)-aminoglucose (6-NBDG) using two-photon microscopy.
21 ined viral vector-mediated EGFP transfer and two-photon microscopy.
22 ALS and clustering of Lm-specific T cells by two-photon microscopy.
23  the baboon and human eyes and visualized by two-photon microscopy.
24 aster than point-scanning techniques such as two-photon microscopy.
25  dynamics of immune cells in the meninges by two-photon microscopy.
26          The laser lesions were evaluated by two-photon microscopy.
27 somata, dendrites, and spines as measured by two-photon microscopy.
28 lls at near-physiological temperatures using two-photon microscopy.
29 atures of T cell and DC dynamics observed by two-photon microscopy.
30 s from single neurons in vivo, visualized by two-photon microscopy.
31 t high temporal and spatial resolution using two-photon microscopy.
32 on in adult primary visual cortex by in vivo two-photon microscopy.
33 yte motility and signaling in real time with two-photon microscopy.
34 ampal neurons, using confocal microscopy and two-photon microscopy.
35 d-type or eNMDAR loss-of-function mice using two-photon microscopy.
36 e in acute myeloid leukemia using intravital two-photon microscopy.
37 mained after HS treatment, as highlighted by two-photon microscopy.
38 rons in the mouse primary motor cortex using two-photon microscopy.
39 d autofluorescence emission with traditional two-photon microscopy.
40 6s-labeled neurons beyond the depth limit of two-photon microscopy.
41  order, employing, for example, confocal and two-photon microscopy.
42 ebrafish model of podocyte injury to in vivo two-photon microscopy.
43  not resolved by traditional intensity-based two-photon microscopy.
44 e imaged using epifluorescence, confocal, or two-photon microscopy.
45 issues precisely as a function of time using two-photon microscopy.
46 using conventional intravital microscopy and two-photon microscopy.
47                                              Two-photon microscopy (2PM) has been widely adopted to a
48                       The advent of scanning two-photon microscopy (2PM) has created a fertile new av
49                                              Two-photon microscopy (2PM) imaging in LNs suggests that
50 cal neuronal activation by combining fUS and two-photon microscopy (2PM) in a co-registered single vo
51                                              Two-photon microscopy (2PM) techniques, including two-ph
52                                    Real-time two-photon microscopy allowed the visualization of three
53                                              Two-photon microscopy analysis indicates that chronic al
54 at cellular and subcellular levels combining two-photon microscopy and a genetically encoded calcium
55 which was verified by imaging lymph nodes by two-photon microscopy and by phenotyping migrating cells
56 es invisible to the fly, and compatible with two-photon microscopy and controlled visual stimuli.
57  adult V1 with chronic in vivo imaging using two-photon microscopy and determined the spine turnover
58 ing with cellular resolution methods such as two-photon microscopy and electrophysiology is bridging
59                                      We used two-photon microscopy and followed NSCs that were geneti
60  Here, we used the combination of intravital two-photon microscopy and frequency-domain fluorescence
61                    We combined optogenetics, two-photon microscopy and glutamate uncaging to examine
62                                        Using two-photon microscopy and glutamate uncaging to examine
63         To address these issues, we combined two-photon microscopy and laser microsurgery to image th
64 che by various methods, including intravital two-photon microscopy and non-invasive whole-body imagin
65 g modalities, including confocal microscopy, two-photon microscopy and optical coherence tomography,
66 h limit associated with confocal microscopy, two-photon microscopy and optical coherence tomography.
67 r with advanced research techniques, such as two-photon microscopy and optical imaging.
68                                        Using two-photon microscopy and the intrinsic fluorescence of
69 cence imaging of mouse brains by integrating two-photon microscopy and tissue sectioning.
70                                  Here, using two-photon microscopy and whole-cell patch-clamp recordi
71 r sex a combination of whole-cell recording, two-photon microscopy, and spine morphometric analysis t
72          Here, we use whole-cell recordings, two-photon microscopy, and two-photon glutamate uncaging
73 ion in cleared and uncleared specimens using two-photon microscopy; and either manual or semi-automat
74 elated behaviours by using optogenetics with two-photon microscopy, anxiety assays in freely moving m
75                          Here we developed a two-photon microscopy approach to observe thymocytes int
76 imetry, circular dichroism spectroscopy, and two-photon microscopy are used to study the interaction
77 to the realization of a combined single- and two-photon microscopy-based, optogenetics- and imaging-a
78 two-step microscopy, similar in principle to two-photon microscopy but with orders-of-magnitude bette
79 monstrate video-rate multiplane imaging with two-photon microscopy by performing near-instantaneous a
80                       To verify the results, two-photon microscopy combined with a microprism was als
81                          Intravital confocal/two-photon microscopy continuously imaged the surgically
82              Our simulations matched in vivo two-photon microscopy data regarding T cell speed, short
83            Next, the theory is used to model two-photon microscopy data that show, in animals, high r
84                    By utilizing a variety of two-photon microscopy datasets, we show that our method
85 TC penetration from skin surface followed by two-photon microscopy demonstrated a more invasive percu
86                                   Intravital two-photon microscopy demonstrated that LN neutrophils w
87                      In vivo ER imaging with two-photon microscopy detects similar ER enlargement, an
88                            Encoded multisite two-photon microscopy (eMS2PM), a scanless method that a
89                               Point-scanning two-photon microscopy enables high-resolution imaging wi
90 ndogenous CTLs and with intravital live-cell two-photon microscopy evidence for more efficacious CTL-
91                                              Two-photon microscopy experiments demonstrated that the
92  olfactory and visual coupling, we conducted two-photon microscopy experiments in a new GCaMP6s-expre
93 ently, stable labeling techniques and use of two-photon microscopy for deep tissue imaging have enabl
94                                   We advance two-photon microscopy for near-diffraction-limited imagi
95           Here we use whole-cell recordings, two-photon microscopy, GABA uncaging and optogenetics to
96                                              Two-photon microscopy has advanced fluorescence imaging
97                                              Two-Photon Microscopy has become an invaluable tool for
98                                              Two-photon microscopy has provided the first direct obse
99                       Recently, confocal and two-photon microscopy have revealed a proliferation of n
100 ue-green wavelength range are widely used in two-photon microscopy; however, the use of red fluoresce
101                                   Intravital two-photon microscopy imaging of Cxcr6(+/gfp) and Cxcr6(
102  this study, an in vivo model was adapted to two-photon microscopy imaging, and T cell behavior was a
103  large vesicles (2-7 muM) in astrocytes with two-photon microscopy imaging, we found that the exocyto
104 c vesicles, from EC synaptic terminals using two photon microscopy in slices obtained from forebrain
105 rical minimal stimulation, and random-access two-photon microscopy in acute mouse hippocampal slices.
106                                        Using two-photon microscopy in adolescent mice, we found that
107 combinant adeno-associated virus and in vivo two-photon microscopy in adult macaques, we showed that
108                              We used in vivo two-photon microscopy in adult mice expressing green flu
109                                   Time-lapse two-photon microscopy in adult slices was used to determ
110                       Finally, using in vivo two-photon microscopy in anesthetized or awake-behaving
111                         Here we used in vivo two-photon microscopy in awake head-fixed mice to assess
112 avior of T(FH) cells in GCs in mice, we used two-photon microscopy in combination with a photoactivat
113                                              Two-photon microscopy in combination with fluorescence l
114 e directly observed microglia behaviors with two-photon microscopy in ex vivo spinal cord slices from
115 ion of Abeta within microglia and time-lapse two-photon microscopy in live mice revealed that these c
116  of Drosophila heat shock (HS) genes both by two-photon microscopy in live polytene nuclei and by FIS
117 alian cells, and it can be used with one- or two-photon microscopy in live samples.
118                                              Two-photon microscopy in live transfused animals reveale
119 ith super-resolution imaging techniques, and two-photon microscopy in living knock-ins enables the vi
120                                Using in vivo two-photon microscopy in mouse brain, we quantified mito
121                  Here we use high-resolution two-photon microscopy in organotypic hippocampal slices
122 ow from surrounding capillaries with in vivo two-photon microscopy in peri-infarct cortex before and
123 ond which three-photon microscopy outpeforms two-photon microscopy in recording fidelity.
124 cyamemazine (CYAM) is visualized directly by two-photon microscopy in substantia nigra and striatum b
125                             Using intravital two-photon microscopy in the mouse model of multiple scl
126                        Using chronic in vivo two-photon microscopy in the mouse neocortex, we show th
127                                Using in vivo two-photon microscopy in the mouse somatosensory barrel
128                                      In vivo two-photon microscopy in the peri-contusional cortex was
129 tracer leakage across the BBB in vivo, using two-photon microscopy in the t-MCAO stroke model.
130                                  Here, using two-photon microscopy in vivo in mice, we demonstrate th
131                                        Using two-photon microscopy in vivo, we show that status epile
132 g with GFP-based probes in single-photon and two-photon microscopy, including time-lapse imaging in l
133                                              Two-photon microscopy is a mainstay technique for imagin
134                                              Two-photon microscopy is currently the method of choice
135 a major challenge, as the recording depth of two-photon microscopy is limited because of the scatteri
136 troduced to the field of immunology in 2002, two-photon microscopy is the method of choice for visual
137                                              Two-photon microscopy is used to image neuronal activity
138                                              Two-photon microscopy is widely used to investigate brai
139 int-scanning techniques such as confocal and two-photon microscopy, light-sheet microscopes illuminat
140                 We used a recently developed two-photon microscopy method, based on a novel phosphore
141                                              Two-photon microscopy now enables us to visualize cell m
142                                The advent of two-photon microscopy now reveals unprecedented, detaile
143 mic analysis, immunoelectron microscopy, and two-photon microscopy of astrocytic Ca(2+) signaling in
144                                              Two-photon microscopy of cultured neurons revealed large
145                                      In vivo two-photon microscopy of green fluorescent protein-expre
146  the approach of real-time imaging of GCs by two-photon microscopy of intact lymph nodes has provided
147 ified by immunohistochemistry and intravital two-photon microscopy of kidneys of rats.
148                                      We used two-photon microscopy of live, intact, individual islets
149 ology of astrocytes in 3D images obtained by two-photon microscopy of living APP/PS1 mice and WT litt
150  a mouse infection model in conjunction with two-photon microscopy of living brain tissue and confoca
151                                              Two-photon microscopy of LPL(-/-) lymphocytes revealed r
152                                              Two-photon microscopy of lymph node explants revealed th
153                                        Using two-photon microscopy of lymph nodes we show that tolero
154 T cells using in vitro assays and intravital two-photon microscopy of lymphoid and nonlymphoid tissue
155                        Over the past decade, two-photon microscopy of lymphoid tissues has shed impor
156                                        Using two-photon microscopy of mice in vivo, we showed that th
157 nuclear leukocyte (PMN) migration assay, and two-photon microscopy of mice in vivo.
158                                        Using two-photon microscopy of mouse lymph nodes, we revealed
159                                Here, we used two-photon microscopy of peripheral lymph nodes (PLNs) t
160                        In this study, we use two-photon microscopy of the lung parenchyma and note ac
161                                      In vivo two-photon microscopy of the somatosensory cortex of Cdk
162                                      In vivo two-photon microscopy of the somatosensory cortex was pe
163                                    Entangled two-photon microscopy offers nonlinear imaging capabilit
164          Here we used whole-cell recordings, two-photon microscopy, optogenetics and pharmacogenetics
165 l area in awake and freely moving mice using two-photon microscopy or an nVista miniaturized microsco
166 wt1a:eGFP larvae) was observed by intravital two-photon microscopy over extended periods of time.
167 timulus-evoked GCaMP3 responses as imaged by two-photon microscopy permitted functional cell type ann
168                            Here we develop a two-photon microscopy procedure to study marginal zone a
169                                      In vivo two-photon microscopy provides the foundation for an arr
170                                              Two-photon microscopy provides unprecedented sensitivity
171  close proximity, which, in combination with two-photon microscopy, provides a very high spatial reso
172                                              Two-photon microscopy revealed aberrant trafficking of a
173                                   Intravital two-photon microscopy revealed similar glomerular permea
174       Furthermore, the study of microglia by two-photon microscopy revealed that anti-ICAM-1/catalase
175                                              Two-photon microscopy revealed that exocytosis of GLP-1
176 Histological analysis and time-lapse in vivo two-photon microscopy revealed that hyperactivity did no
177 l microscopy and time-lapse studies based on two-photon microscopy revealed that morpholino-based kno
178                 However, recent studies with two-photon microscopy revealed that most cognate interac
179                                              Two-photon microscopy revealed that recipient T cells cl
180                                              Two-photon microscopy revealed that the eyes of the zebr
181                                              Two-photon microscopy revealed that, at the axon, somati
182                                   Intravital two-photon microscopy reveals direct interactions betwee
183 avelength; thus, when imaged by conventional two-photon microscopy, SHG nanoprobes appear to generate
184 acute tubular necrosis (ATN), and intravital two-photon microscopy showed flow abnormalities in the m
185 of alpha-synuclein-GFP transgenic mice using two-photon microscopy showed that NPT100-18A reduced the
186          This addresses the applicability of two photon microscopy studies to understanding actual in
187                  Laser scanning confocal and two-photon microscopy studies reveal that QZ2 is cell-pe
188                      However, we observed by two-photon microscopy that mouse retinas incapable of ph
189   In summary, we show by extended intravital two-photon microscopy that podocytes are stationary cell
190      We used in vivo time-lapse imaging with two-photon microscopy through cranial windows in male an
191                                Using in vivo two-photon microscopy, time-lapse analysis of identified
192 lls to migrate within lymph nodes (LN) using two-photon microscopy to characterize cell velocities an
193                              We used in vivo two-photon microscopy to characterize layer 5 pyramidal
194 ultiple patch-clamp recordings targeted with two-photon microscopy to characterize monosynaptic conne
195                        Here, we used in vivo two-photon microscopy to characterize the dynamics of ax
196   We developed an automated system that uses two-photon microscopy to detect rhythmic neurons from ca
197                                 We have used two-photon microscopy to determine, in a dynamic manner,
198                                      We used two-photon microscopy to elucidate the spatial organizat
199     We applied in vitro confocal and in vivo two-photon microscopy to examine basal calcium levels an
200 ericyte-labeled transgenic mice with in vivo two-photon microscopy to examine the relationship betwee
201                      We used chronic in vivo two-photon microscopy to image dendritic spines and axon
202                                  Here, using two-photon microscopy to image neural activity and vascu
203                Through these windows we used two-photon microscopy to image odor-evoked Ca(2+) signal
204 microendoscope combined with high-resolution two-photon microscopy to image taste responses from gang
205          To address these questions, we used two-photon microscopy to image the addition of genetical
206                                      We used two-photon microscopy to image vascular architecture, to
207 -responsive fluorescent probes together with two-photon microscopy to image Zn(2+) dynamics mediated
208 nces in axon labeling by viruses and in vivo two-photon microscopy to investigate axon branching and
209           Here, we used longitudinal in vivo two-photon microscopy to investigate dendritic spine dyn
210 Here, we used acute and longitudinal in vivo two-photon microscopy to investigate developmental and e
211       Here, we use patch-clamp recording and two-photon microscopy to investigate morphological and p
212                                        Using two-photon microscopy to measure Ca(2+) excursions, we f
213 esthetized FHM1 mouse model in vivo, we used two-photon microscopy to measure calcium changes in neur
214                                      We used two-photon microscopy to measure dendritic spines in rat
215 orescence correlation spectroscopy (FCS) and two-photon microscopy to measure flow speeds and to quan
216                                 Here we used two-photon microscopy to measure sensory-evoked response
217                Here, we use oxygen-sensitive two-photon microscopy to measure the BOLD-relevant micro
218                                      We used two-photon microscopy to measure the diameters of single
219 al network interactions in vivo by combining two-photon microscopy to monitor astrocyte calcium and e
220                                      We used two-photon microscopy to monitor BBB permeability of sod
221                                      We used two-photon microscopy to monitor ensemble activity durin
222 e sought to address these questions by using two-photon microscopy to monitor interneuron dendritic a
223 is hypothesis, we used dual-color time-lapse two-photon microscopy to monitor rat hippocampal pyramid
224 uilibrium in living cells through the use of two-photon microscopy to observe fluorescence resonance
225                                        Using two-photon microscopy to observe hippocampal neurons lab
226 lidated these reagents by flow cytometry and two-photon microscopy to obtain images at cellular resol
227                     We have employed in vivo two-photon microscopy to produce time-lapse images of se
228 st this possibility physiologically, we used two-photon microscopy to record light stimulus-evoked Ca
229                                 We first use two-photon microscopy to show that GABA(B)Rs inhibit AP
230                                      We used two-photon microscopy to simultaneously track antigen-sp
231                                Here, we used two-photon microscopy to study changes in FUS-mediated B
232 deep-tissue time-lapse imaging based on fast two-photon microscopy to study Drosophila ventral furrow
233                                      We used two-photon microscopy to study the role of ensembles of
234       One solution to this problem is to use two-photon microscopy to target fluorescently labeled ne
235                    The recent application of two-photon microscopy to the visualization of T cell mov
236                          Here we show, using two-photon microscopy to track neural activity over mult
237 lopment and plasticity, we used transcranial two-photon microscopy to track the formation and elimina
238                                     By using two-photon microscopy to visualize bacterium-T-cell cros
239  a chronic hippocampal window approach using two-photon microscopy to visualize dendritic spines thro
240 nd lymphocyte behavior in the brain, we used two-photon microscopy to visualize effector CD8(+) T cel
241 al-time intravital epifluorescence video and two-photon microscopy to visualize malignant T cells fro
242 chanisms governing this segregation, we used two-photon microscopy to visualize migration of purified
243                    Here we used transcranial two-photon microscopy to visualize postsynaptic dendriti
244                                 Here, we use two-photon microscopy to visualize release of the synapt
245                        Here, we used in vivo two-photon microscopy to visualize surface AMPARs in mou
246 of a novel in vivo method we developed using two-photon microscopy to visualize the paravascular spac
247 keletal components and performing intravital two-photon microscopy to visualize TRM cell behavior.
248 site, Toxoplasma gondii, in conjunction with two-photon microscopy, to address this question.
249 ch as wide-field and confocal one-photon and two-photon microscopy, to compare photochemical and biop
250 ) and CD4(+) T cells in the living spleen by two-photon microscopy (TPM) during the establishment of
251                                              Two-photon microscopy (TPM) has come to occupy a promine
252 ent hydrophobic permeant, using dual-channel two-photon microscopy (TPM) to better understand the tra
253                                              Two-photon microscopy (TPM) was used to observe retinoid
254                                              Two-photon microscopy (TPM), using longer wavelengths th
255 l populations at single-cell resolution with two-photon microscopy up to a depth of 400 microm.
256                         In addition, in vivo two-photon microscopy was performed for the first time o
257                                              Two-photon microscopy was used for imaging of axonal die
258                                              Two-photon microscopy was used to locate DCs in gastric
259                                              Two-photon microscopy was used to observe mitochondrial
260       Using 3D reconstruction and intravital two-photon microscopy we describe the branched organizat
261                                        Using two-photon microscopy we found that Bergmann glia exhibi
262                        Here, using real-time two-photon microscopy we noted rapid delivery of immune
263                                    Thus with two-photon microscopy we probe the bulk minority carrier
264                       Applying our method to two-photon microscopy, we could recover near-diffraction
265                          In combination with two-photon microscopy, we demonstrate that Camuialpha ca
266                                Using in vivo two-photon microscopy, we demonstrate that microglia for
267                                        Using two-photon microscopy, we demonstrate that, in the absen
268                          Applying intravital two-photon microscopy, we demonstrate the gatekeeper fun
269                                Using in vivo two-photon microscopy, we detected improved blood flow a
270                           Using transcranial two-photon microscopy, we examined the effect of visual
271 scent proteins, analysis of mutant mice, and two-photon microscopy, we follow long-range horizontally
272                           Using transcranial two-photon microscopy, we followed apical dendrites of l
273                                        Using two-photon microscopy, we found immature B cells enterin
274                                        Using two-photon microscopy, we found that effector CTL divide
275                                Using in vivo two-photon microscopy, we found that the elimination and
276                                        Using two-photon microscopy, we imaged autonomic ganglia in li
277                           Using transcranial two-photon microscopy, we investigated how neural circui
278 three-color labeling and spectrally resolved two-photon microscopy, we monitor in parallel the daily
279                             Using intravital two-photon microscopy, we observe that sympathetic nerve
280                                        Using two-photon microscopy, we observed stable antigen-specif
281                             Using intravital two-photon microscopy, we observed that local administra
282                                        Using two-photon microscopy, we observed that medullary thymoc
283                                Using in vivo two-photon microscopy, we performed time-lapse imaging o
284                      Using real-time in vivo two-photon microscopy, we quantified mitochondrial fragm
285  yellow fluorescent protein and transcranial two-photon microscopy, we repeatedly imaged dendritic sp
286                       By means of intravital two-photon microscopy, we report that dermal dendritic c
287              Using whole-cell recordings and two-photon microscopy, we show that neurons expressing D
288      Using a combination of optogenetics and two-photon microscopy, we then determine the subcellular
289                                        Using two-photon microscopy, we visualized B cell capture of c
290                                        Using two-photon microscopy, we visualized Ca(2+) signaling an
291                         In this study, using two-photon microscopy, we visualized host NK cell intera
292        Due to the high spatial resolution of two-photon microscopy, we were able to measure a marked
293 as that lie beyond the reach of conventional two-photon microscopy, which is typically limited to ~ 4
294                                        Using two-photon microscopy with 3D reconstruction methodology
295 ating feasibility of in vivo high-resolution two-photon microscopy with continuous wave (CW) excitati
296 culture cells and Xenopus egg extracts using two-photon microscopy with FLIM measurements of FRET.
297 e-organ fluorescence imaging that integrates two-photon microscopy with serial microtome sectioning.
298 se primary visual cortex by using functional two-photon microscopy with single-cell resolution and ge
299 cell-mediated model of EAE combining in vivo two-photon microscopy with two different activation repo
300 ent graphene electrodes by both confocal and two-photon microscopy without causing any light-induced

 
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