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1  be immediately examined by conventional and confocal fluorescence microscopy.
2 mmunohistochemistry, isolectin staining, and confocal fluorescence microscopy.
3 were co-localized with iNOS as determined by confocal fluorescence microscopy.
4 rface TGF-beta on Foxp3+CD4+CD25+ T cells in confocal fluorescence microscopy.
5 nd their subcellular locations determined by confocal fluorescence microscopy.
6 ed of DOPC/DPPC or DLPC/DPPC are observed by confocal fluorescence microscopy.
7 NA also could be detected over background by confocal fluorescence microscopy.
8 he detection of single protein molecules via confocal fluorescence microscopy.
9 neously in live explants using spinning disk confocal fluorescence microscopy.
10 ther beta1AR trafficked to lysosomes we used confocal fluorescence microscopy.
11 issues were imaged using epifluorescence and confocal fluorescence microscopy.
12 immunoprecipitation assays and visualized by confocal fluorescence microscopy.
13 utophagosome marker, by Western blotting and confocal fluorescence microscopy.
14 single-photon counting coupled with scanning confocal fluorescence microscopy.
15 fluorescent protein translocation assays and confocal fluorescence microscopy.
16 protein on the plasma membrane, as judged by confocal fluorescence microscopy.
17 o study their trafficking pattern in vivo by confocal fluorescence microscopy.
18 ullary collecting duct (IMCD) segments using confocal fluorescence microscopy.
19  by subcellular fractionation studies and by confocal fluorescence microscopy.
20 llary is directly imaged with laser scanning confocal fluorescence microscopy.
21 er of hippocampal synapses using FM 1-43 and confocal fluorescence microscopy.
22 and localization patterns monitored by using confocal fluorescence microscopy.
23 ofluorometer, and the cells were examined by confocal fluorescence microscopy.
24 f IL-12, as determined by flow cytometry and confocal fluorescence microscopy.
25 jacent to the plasma membrane as detected by confocal fluorescence microscopy.
26 distribution of this receptor as detected by confocal fluorescence microscopy.
27 were partially colocalized, as determined by confocal fluorescence microscopy.
28 L-2, altered actin morphology as assessed by confocal fluorescence microscopy.
29 elease as demonstrated by flow cytometry and confocal fluorescence microscopy.
30 nals from single neurons with laser scanning confocal fluorescence microscopy.
31 on of dyes and imaging of tagged proteins by confocal fluorescence microscopy.
32 pressing DsRed (Discosoma sp.) and imaged by confocal fluorescence microscopy.
33 cal actin dynamics simultaneously by AFM and confocal fluorescence microscopy.
34 rmed by transmission electron microscopy and confocal fluorescence microscopy.
35 stallites are also estimated with the use of confocal fluorescence microscopy.
36  with respect to those of Min as revealed by confocal fluorescence microscopy.
37 or metastasis, and results were confirmed by confocal fluorescence microscopy.
38 of the transmembrane protein was analyzed by confocal fluorescence microscopy.
39 cribe a protocol for interfacing 3D-MTC with confocal fluorescence microscopy.
40 intracellular localization was evaluated via confocal fluorescence microscopy.
41 vidual live DM1 model cells using time-lapse confocal fluorescence microscopy.
42 ative extracellular oxidant distributions by confocal fluorescence microscopy.
43 heir cellular localization was visualized by confocal fluorescence microscopy.
44 complex was illustrated through live imaging confocal fluorescence microscopy.
45 sformation of 1 to 2 inside such cells using confocal fluorescence microscopy.
46 ecies inside the cells has been evaluated by confocal fluorescence microscopy.
47 racellular bioorthogonal probe, as judged by confocal fluorescence microscopy.
48 e corroborated with immunohistochemistry and confocal fluorescence microscopy.
49 les was examined in real time wide-field and confocal fluorescence microscopy.
50  in endothelial F-actin was determined using confocal fluorescence microscopy.
51 on of DnaA in living cells was visualized by confocal fluorescence microscopy.
52                     The films were imaged by confocal fluorescence microscopy.
53 lls (L1210FR leukemia cell line) by means of confocal fluorescence microscopy.
54 os and FG in CeA neurons was visualized with confocal-fluorescence microscopy.
55                         Using laser scanning confocal fluorescence microscopy, alternans of electrica
56 hromaffin granule exocytosis were studied by confocal fluorescence microscopy, amperometry, and cell-
57                                              Confocal fluorescence microscopy and a lymphoid enhancer
58                                        Using confocal fluorescence microscopy and analysis of oligosa
59 n analyte dispersion was characterized using confocal fluorescence microscopy and electrochemical det
60 ngle living cells has been achieved by using confocal fluorescence microscopy and externally tagged p
61                                  We then use confocal fluorescence microscopy and flow cytometry to d
62                                              Confocal fluorescence microscopy and fluorescence resona
63 luding atomic force microscopy combined with confocal fluorescence microscopy and Fourier transform i
64                                 Standard and confocal fluorescence microscopy and image analysis were
65                                              Confocal fluorescence microscopy and immunohistochemistr
66                    Further investigations by confocal fluorescence microscopy and immunoprecipitation
67                                     Scanning confocal fluorescence microscopy and multiphoton fluores
68                                              Confocal fluorescence microscopy and proliferation/viabi
69 ic-field-induced mechanical stimulation with confocal fluorescence microscopy and provides an optiona
70 nity reagents suitable for western blotting, confocal fluorescence microscopy and pull-down applicati
71 ased in the Vit D-preconditioned cultures by confocal fluorescence microscopy and semiquantitative im
72 sh medial giant axons (MGAs) with time-lapse confocal fluorescence microscopy and showed that many in
73  endogenous syntaxin 6 as determined both by confocal fluorescence microscopy and subcellular fractio
74  are consistent with similar measurements by confocal fluorescence microscopy and subcellular fractio
75                                 Quantitative confocal fluorescence microscopy and surface biotinylati
76                          GUVs were imaged by confocal fluorescence microscopy and then analyzed for c
77                                Hyperspectral confocal fluorescence microscopy and three-dimensional s
78                                              Confocal fluorescence microscopy and uptake kinetic anal
79 the dye barrier, were assessed by time-lapse confocal, fluorescence microscopy and by electron micros
80                                 We used TEM, confocal fluorescence microscopy, and a novel correlativ
81 attering, differential scanning calorimetry, confocal fluorescence microscopy, and atomic force micro
82  a combination of yeast two-hybrid analysis, confocal fluorescence microscopy, and fluorescence reson
83  ex vivo MRI, x-ray fluorescence microscopy, confocal fluorescence microscopy, and histological analy
84 llography, isothermal titration calorimetry, confocal fluorescence microscopy, and in vivo photoactiv
85 monstrated using atomic force microscopy and confocal fluorescence microscopy, and possible explanati
86 imultaneous confocal reflectance microscopy, confocal fluorescence microscopy, and rheology.
87 trated by nanopore formation experiments and confocal fluorescence microscopy, and they can act as co
88                                            A confocal fluorescence microscopy-based assay was used fo
89 ed that we could indeed realize multichannel confocal fluorescence microscopy by utilizing the freque
90 ndocytosis (RME) based on flow cytometry and confocal fluorescence microscopy (CFM) analyses, which e
91 rmation reported by the two techniques, with confocal fluorescence microscopy (CFM) used to supplemen
92 ECs) using atomic force microscopy (AFM) and confocal fluorescence microscopy (CFM).
93 ith confocal reflection microscopy (CRM) and confocal fluorescence microscopy (CFM).
94 confocal reflectance microscopy (CRM) and/or confocal fluorescence microscopy (CFM).
95                                              Confocal fluorescence microscopy combined with internal
96                                      We used confocal fluorescence microscopy correlated with scannin
97                                              Confocal fluorescence microscopy demonstrated that MIP i
98 a complex with IL-13Ralpha1 in solution, and confocal fluorescence microscopy demonstrated that these
99                                              Confocal fluorescence microscopy demonstrated that, for
100                                      Rather, confocal fluorescence microscopy demonstrated the loss o
101                                     Further, confocal fluorescence microscopy demonstrates that C. ko
102                                              Confocal fluorescence microscopy demonstrates that Fre6:
103                                              Confocal fluorescence microscopy demonstrates that Slob
104 h a combination of three imaging modalities: confocal fluorescence microscopy, direct stochastic opti
105 n using both stimulated Raman scattering and confocal fluorescence microscopy established rhabduscin'
106  after magnetic field exposure using fibered confocal fluorescence microscopy (FCFM).
107                                              Confocal fluorescence microscopy has established the uti
108       Fluorescence lifetime measurements and confocal fluorescence microscopy have been applied to ob
109                          The method combines confocal-fluorescence-microscopy image stacks of giant u
110                                    Moreover, confocal fluorescence microscopy images of HeLa cells sh
111 s successfully been used to stain and record confocal fluorescence microscopy images of HeLa cells.
112                                              Confocal fluorescence microscopy images of the perpendic
113 s of 5-D (x,y,z,t,channel) and large montage confocal fluorescence microscopy images.
114    We then used flow cytometry and live cell confocal fluorescence microscopy imaging to show that ul
115 cation as stains of vesicle substructures in confocal fluorescence microscopy imaging.
116                                              Confocal fluorescence microscopy, immunocytochemistry an
117 s treated with PAI-1 were subjected to laser confocal fluorescence microscopy, immunoprecipitation an
118 fluorescent tag, was prepared and studied by confocal fluorescence microscopy in human lung adenocarc
119 f tagging with green fluorescent protein and confocal fluorescence microscopy in live cells of the cy
120                             We also utilized confocal fluorescence microscopy in mapped whole mount c
121  more mitochondrial localization as shown by confocal fluorescence microscopy in OVCAR-5 cells, and,
122 e distribution as scored by conventional and confocal fluorescence microscopy in response to an ER ex
123 bution in the liver, they were detectable by confocal fluorescence microscopy in tumor-free tissue an
124 ion of electron microscopy and hyperspectral confocal fluorescence microscopy in wild-type Synechocys
125  fluorescence resonance energy transfer, and confocal fluorescence microscopy) in combination with Mo
126 ng studies against Bacillus subtilis through confocal fluorescence microscopy indicated that Cu NCs s
127          A detailed and systematic polarized confocal fluorescence microscopy investigation is presen
128                                              Confocal fluorescence microscopy is a powerful biologica
129 lular Zn(II) of eukaryotic cells using laser confocal fluorescence microscopy is demonstrated.
130                                              Confocal fluorescence microscopy is often used in brain
131  the utility of the extended FMDV 2A system, confocal fluorescence microscopy is used to demonstrate
132            In this part 3, a third modality, confocal fluorescence microscopy, is added to the techni
133 s of NCAMs were studied using laser scanning confocal fluorescence microscopy (LSCFM).
134 -driven reporter gene expression by in vitro confocal fluorescence microscopy, luciferase assay, 2'-f
135                                              Confocal fluorescence microscopy of Ad-infected NM showe
136 nylated UTP nick end labeling (TUNEL) stain, confocal fluorescence microscopy of ethidium bromide-sta
137                                              Confocal fluorescence microscopy of giant unilamellar ve
138        Differential scanning calorimetry and confocal fluorescence microscopy of giant unilamellar ve
139                                              Confocal fluorescence microscopy of live and fixed HT22
140                                              Confocal fluorescence microscopy of thin-sectioned lymph
141                                              Confocal fluorescence microscopy of tumor cells incubate
142 d biochemical changes in the same cell using confocal fluorescence microscopy or STED.
143                                           By confocal fluorescence microscopy, p85alpha was shown to
144                        By using quantitative confocal fluorescence microscopy, PLF could be scored on
145                                              Confocal fluorescence microscopy proved integrin-mediate
146                                    Live-cell confocal fluorescence microscopy revealed both filamento
147 ges of virus-infected, OVA-treated mice, and confocal fluorescence microscopy revealed colocalization
148                                  Analysis by confocal fluorescence microscopy revealed single-step ph
149 , II, or III InsP3 receptors and analyzed by confocal fluorescence microscopy revealed that all InsP3
150                                              Confocal fluorescence microscopy revealed that HIV-1 pro
151                                              Confocal fluorescence microscopy revealed that internali
152                Subcellular fractionation and confocal fluorescence microscopy revealed that little or
153                                              Confocal fluorescence microscopy revealed that Streptaph
154     Conventional fluorescence microscopy and confocal fluorescence microscopy revealed that the bacil
155                                              Confocal fluorescence microscopy revealed that the BMV 1
156                                              Confocal fluorescence microscopy reveals the accumulatio
157 damine-conjugated phalloidin and analysis by confocal fluorescence microscopy showed disruption of th
158                                              Confocal fluorescence microscopy showed that a fraction
159                                              Confocal fluorescence microscopy showed that both NCoR a
160                                              Confocal fluorescence microscopy showed that P. aerugino
161                                              Confocal fluorescence microscopy showed that Tyr(P)992 r
162                                              Confocal fluorescence microscopy shows a regime of coexi
163                                              Confocal fluorescence microscopy shows colocalization of
164 atment fluorescent labeling of 1 observed by confocal fluorescence microscopy shows nuclear and inten
165                                              Confocal fluorescence microscopy shows that the 6-micron
166                                              Confocal fluorescence microscopy studies demonstrated th
167                                              Confocal fluorescence microscopy studies of human skin p
168                                              Confocal fluorescence microscopy studies revealed that t
169 inus ends were recorded with a spinning-disk confocal fluorescence microscopy system.
170 onsistent with a subsequent observation from confocal fluorescence microscopy that aggregates concent
171                            We then show with confocal fluorescence microscopy that incubation of CD4+
172 phospholipids, we found, by conventional and confocal fluorescence microscopy, that transport of wate
173 ayers Percent of ablation was determined via confocal fluorescence microscopy to be approximately 70%
174                                      We used confocal fluorescence microscopy to image the distributi
175    In this work, we have used wide-field and confocal fluorescence microscopy to investigate the spat
176 ring molecular motion in vitro, coupled with confocal fluorescence microscopy to measure the movement
177                           We have undertaken confocal fluorescence microscopy to monitor P-bodies in
178 cytes by using scanning and stationary-point confocal fluorescence microscopy to record Ca2+ signals
179 y we used perforated patch voltage clamp and confocal fluorescence microscopy to study the contributi
180 result, we employed real-time analysis using confocal fluorescence microscopy to study the spatio-tem
181 tographic stationary phase with quantitative confocal fluorescence microscopy under real reversed-pha
182  The reactions were observed in real time by confocal fluorescence microscopy using a Bodipy fluoroge
183 m of infected cells was analyzed by scanning confocal fluorescence microscopy using a newly developed
184 CD205, mPDCA, B220, and GR1) and analyzed by confocal fluorescence microscopy using emission fingerpr
185 l autoradiography, immunohistochemistry, and confocal fluorescence microscopy using human brain speci
186                                              Confocal fluorescence microscopy was used to examine co-
187                              Single molecule confocal fluorescence microscopy was used to perform pho
188              Time-resolved three-dimensional confocal fluorescence microscopy was used to study insul
189                                        Using confocal fluorescence microscopy, we compared tubulin bi
190              Using combined atomic force and confocal fluorescence microscopy, we demonstrate that th
191         Interestingly, by immunoblotting and confocal fluorescence microscopy, we disclosed a robust
192                                        Using confocal fluorescence microscopy, we find that Gab2 is r
193 ceptor-green fluorescent protein chimera and confocal fluorescence microscopy, we found that NF-M red
194                        Using C2C12 cells and confocal fluorescence microscopy, we showed that MyoD an
195                                        Using confocal fluorescence microscopy, we visualized small en
196                             Using time-lapse confocal fluorescence microscopy, we were able to visual
197          siRNAs, co-immunoprecipitation, and confocal fluorescence microscopy were employed to identi
198 cence imaging, histological examination, and confocal fluorescence microscopy were used to identify e
199 aring our estimates with data obtained using confocal fluorescence microscopy, which represents the f
200 tion by immuno-labeling using laser scanning confocal fluorescence microscopy, which revealed an ICI-
201  C1-INH and TagA on the bacterial surface by confocal fluorescence microscopy, which ultimately resul
202         In this study, we used spinning-disk confocal fluorescence microscopy with high temporal and
203 oline (DLPC/DPPC)/cholesterol were imaged by confocal fluorescence microscopy with two fluorescent pr
204 e-contrast microscopy and time-lapse digital confocal-fluorescence microscopy with fluorescent DiI-LD
205  tool, in conjunction with more conventional confocal fluorescence microscopy, with which to image mi
206 ivo was estimated by MRI at 7 Tesla, ex vivo confocal fluorescence microscopy, x-ray fluorescence mic

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