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1 by PcrA/RepD was followed in real-time using total internal reflection fluorescence microscopy.
2 mbly using both bulk fluorescence assays and total internal reflection fluorescence microscopy.
3 patio-temporally dissociated, as detected by total internal reflection fluorescence microscopy.
4 id bilayer is measured using single-molecule total internal reflection fluorescence microscopy.
5 n components in migrating cells imaged using total internal reflection fluorescence microscopy.
6 gle-virion fusion events are monitored using total internal reflection fluorescence microscopy.
7 re vesicles (LDCVs) in live PC12 cells using total internal reflection fluorescence microscopy.
8 ng conventional far-field epifluorescence or total internal reflection fluorescence microscopy.
9 coded unambiguously using epifluorescence or total internal reflection fluorescence microscopy.
10 rescence microscopy, cell fractionation, and total internal reflection fluorescence microscopy.
11 me, binds and severs MTs via single molecule total internal reflection fluorescence microscopy.
12 re observed in real time via single-molecule total internal reflection fluorescence microscopy.
13 CPs, as determined by quantitative live-cell total internal reflection fluorescence microscopy.
14 splaying ligands for immunoglobulin E, using total internal reflection fluorescence microscopy.
15 -stranded DNA product of the helicase, using total internal reflection fluorescence microscopy.
16 e we used pHluorin-tagged GluA2 subunits and total internal reflection fluorescence microscopy.
17 on of STIM1 can be observed in some cells by total internal reflection fluorescence microscopy.
18 hR beta19'Lys(BODIPYFL), using time-resolved total internal reflection fluorescence microscopy.
19 lambda-repressor CI and its target DNA using total internal reflection fluorescence microscopy.
20 ence resonance energy transfer measured with total internal reflection fluorescence microscopy.
21 interface as a function of temperature using total internal reflection fluorescence microscopy.
22 membranous calcium signal was assessed using total internal reflection fluorescence microscopy.
23 e mechanism of DNA condensation by BAF using total internal reflection fluorescence microscopy.
24 GTP addition when viewed in real time using total internal reflection fluorescence microscopy.
25 single-molecule resolution using time-lapse total internal reflection fluorescence microscopy.
26 g in the presence of VASP and profilin using total internal reflection fluorescence microscopy.
27 microfluidic techniques in conjunction with total internal reflection fluorescence microscopy.
28 ctivity were monitored in real time by using total internal reflection fluorescence microscopy.
29 confirmed in in vitro synaptosomes by using total internal reflection fluorescence microscopy.
30 ging within the evanescent field layer using total internal reflection fluorescence microscopy.
31 a dynamic microtubule assay and examined by total internal reflection fluorescence microscopy.
32 oteins were imaged using epifluorescence and total internal reflection fluorescence microscopy.
33 ion reaches 300 microM is accomplished using total internal reflection fluorescence microscopy.
34 dynamics at the single DNA molecule level by total internal reflection fluorescence microscopy.
35 y observing single muscle actin filaments by total internal reflection fluorescence microscopy.
36 ngths of single molecules were determined by total internal reflection fluorescence microscopy.
37 zation of the plasma membrane plane by using total internal reflection fluorescence microscopy.
38 tin with observations of single filaments by total internal reflection fluorescence microscopy.
39 uorescent protein (GFP-MotB) in the motor by total internal reflection fluorescence microscopy.
40 arious concentrations of MgCl2 solution with total internal reflection fluorescence microscopy.
41 containing structures in live T cells, using total internal reflection fluorescence microscopy.
42 to assay the binding of bacterial toxins via total internal reflection fluorescence microscopy.
43 niques, such as surface plasmon resonance or total internal reflection fluorescence microscopy.
44 The only assay meeting these criteria is total internal reflection fluorescence microscopy.
45 ct signatures upon exocytosis when viewed by total internal reflection fluorescence microscopy.
46 h spatial and temporal resolution similar to total internal reflection fluorescence microscopy.
47 ed in the cell-substratum contact area using total internal reflection fluorescence microscopy.
48 ging within the evanescent field layer using total internal reflection fluorescence microscopy.
49 es with the use of an inducible construct or total internal reflection fluorescence microscopy.
50 of human Cof1, Cof2, and ADF using in vitro total internal reflection fluorescence microscopy.
51 eir behavior at the plasma membrane by using total internal reflection fluorescence microscopy.
52 assays and direct visualization by two-color total internal reflection fluorescence microscopy.
53 y operating single-molecule, objective-type, total internal reflection fluorescence microscopy.
54 using freely in solution were observed using total internal reflection fluorescence microscopy.
55 by vesicle-mediated exocytosis visualized by total internal reflection fluorescence microscopy.
56 teractions near the plasma membrane by using total internal reflection fluorescence microscopy.
57 high-resolution atomic force, confocal, and total internal reflection fluorescence microscopy.
58 ein-p150(Glued) co-complex using dual-colour total internal reflection fluorescence microscopy.
59 t submembrane regions visualized by confocal total internal reflection fluorescence microscopy.
60 nslational modifications were analyzed using total internal reflection fluorescence microscopy.
61 , fluorescence correlation spectroscopy, and total internal reflection fluorescence microscopy.
62 determined by Raman spectroscopy mapping and total internal reflection fluorescence microscopy analys
63 multiscale, live cell imaging (confocal and total internal reflection fluorescence microscopy and a
66 e within the plasma membrane using polarized total internal reflection fluorescence microscopy and am
68 ynthesis and turnover on CME by quantitative total internal reflection fluorescence microscopy and co
69 logy with two complementary imaging methods, total internal reflection fluorescence microscopy and fl
71 n in cultured rat brainstem astrocytes using total internal reflection fluorescence microscopy and fo
73 We had previously developed methods using total internal reflection fluorescence microscopy and im
74 ing dynamic imaging modalities (confocal and total internal reflection fluorescence microscopy and lu
75 obacter crescentus near a glass surface with total internal reflection fluorescence microscopy and ob
76 e focus on recent studies that have employed total internal reflection fluorescence microscopy and ot
79 d actin cytoskeleton within live cells using total internal reflection fluorescence microscopy and si
82 veloped a single molecule system using TIRF (total internal reflection fluorescence) microscopy and p
83 ted using atomic force microscopy, polarized total internal reflection fluorescence microscopy, and N
84 robe illumination volume was minimized using total internal reflection fluorescence microscopy, and P
85 mologs, we applied fluorescence confocal and total internal reflection fluorescence microscopy, and s
86 from the plasma membrane as visualized using total internal reflection fluorescence microscopy, and t
88 e in OAPs; 2) OAPs can be imaged directly by total internal reflection fluorescence microscopy; and 3
90 aining planar membranes are distinguished by total internal reflection fluorescence microscopy as sep
91 P(i)) under zero load in the single-molecule total internal reflection fluorescence microscopy assay.
92 end-residency time, along microtubules in a total internal-reflection fluorescence microscopy assay.
93 ulk actin polymerization and single filament total internal reflection fluorescence microscopy assays
94 concepts of fluorescent speckle microscopy, total internal reflection fluorescence microscopy, atomi
95 Under the same conditions, using total internal reflection fluorescence microscopy, clear
96 in membrane-localized GFP-TRPM7, as seen by total internal reflection fluorescence microscopy, close
97 Immunofluorescence and total internal reflection fluorescence microscopy confir
98 Binding was assayed on planar substrates by total internal reflection fluorescence microscopy down t
99 dy we experimentally tested these views with total internal reflection fluorescence microscopy, elect
100 Live-cell total internal reflection fluorescence microscopy, elect
101 Using total-internal-reflection fluorescence microscopy equipp
102 Fluorescence resonance energy transfer and total internal reflection fluorescence microscopy experi
103 nalysis of mathematical models and live cell total internal reflection fluorescence microscopy experi
104 In real-time total internal reflection fluorescence microscopy experi
105 Moreover, total internal reflection fluorescence microscopy experi
106 Additionally, total internal reflection fluorescence microscopy experi
107 However, total internal reflection fluorescence microscopy experi
108 Here, we combine bulk assays, total internal reflection fluorescence microscopy, fluor
110 Total internal reflection fluorescence microscopy greatl
113 In our study total internal reflection fluorescence microscopy images
114 Here, using multicolor total internal reflection fluorescence microscopy imagin
115 Total internal reflection fluorescence microscopy imagin
116 Total internal reflection fluorescence microscopy imagin
117 Total internal reflection fluorescence microscopy imagin
118 n a membrane using live cell high resolution total internal reflection fluorescence microscopy in con
119 ine triphosphatase) at the cell cortex using total internal reflection fluorescence microscopy in fla
120 ith the use of ecliptic pHluorin-fused ER46, total internal reflection fluorescence microscopy in liv
123 Western blots and single-vesicle imaging by total internal reflection fluorescence microscopy in liv
124 pressed in Chinese hamster ovary cells under total internal reflection fluorescence microscopy in whi
127 tment of which could be directly observed by total internal reflection fluorescence microscopy, in re
128 In the patients' fibroblasts, total internal reflection fluorescence microscopy indica
129 Single-molecule motility assays using total internal reflection fluorescence microscopy indica
130 Biotinylation assays and total internal reflection fluorescence microscopy indica
131 greement with classical measurements made by total internal reflection fluorescence microscopy involv
134 Single molecules of Myo52p, visualized by total internal reflection fluorescence microscopy, moved
135 protease activity at the PM, demonstrated by total internal reflection fluorescence microscopy of a c
143 s investigated using polarization optics and total internal reflection fluorescence microscopy (pTIRF
144 sitive green fluorescent protein tagging and total internal reflection fluorescence microscopy, resol
145 ons, spatial arrangement, and mobility using total internal reflection fluorescence microscopy, reson
146 Total internal reflection fluorescence microscopy reveal
147 Total internal reflection fluorescence microscopy reveal
148 Total internal reflection fluorescence microscopy reveal
149 Total internal reflection fluorescence microscopy reveal
150 eaching experiments and particle tracking by total internal reflection fluorescence microscopy reveal
151 ellular localization studies by confocal and total internal reflection fluorescence microscopy reveal
152 Biochemical analysis and total internal reflection fluorescence microscopy reveal
153 Polarized total internal reflection fluorescence microscopy reveal
154 Real-time total internal reflection fluorescence microscopy reveal
155 Single molecule total internal reflection fluorescence microscopy showed
156 Total internal reflection fluorescence microscopy showed
157 f quantum-dot-labeled AQP4 in live cells and total internal reflection fluorescence microscopy showed
158 ic defects caused by Syn-1A deletion, EM and total internal reflection fluorescence microscopy showed
159 Total internal reflection fluorescence microscopy showed
160 Total internal reflection fluorescence microscopy showed
161 Confocal and live total internal reflection fluorescence microscopy showed
162 By combining total internal reflection fluorescence microscopy, singl
164 Here, we show using patch clamp analysis and total internal reflection fluorescence microscopy, that
169 ination of quantitative live-cell imaging by total internal reflection fluorescence microscopy (TIR-F
171 opy (SIM), ground-state depletion (GSD), and total internal reflection fluorescence microscopy (TIRF)
172 and at the single-particle resolution using total internal reflection fluorescence microscopy (TIRF)
173 nd slow elongating VASP proteins by in vitro total internal reflection fluorescence microscopy (TIRFM
174 eir assembly to make a clot were observed by total internal reflection fluorescence microscopy (TIRFM
175 othelial cells using a unique combination of total internal reflection fluorescence microscopy (TIRFM
176 With the use of single-molecule total internal reflection fluorescence microscopy (TIRFM
177 rder to start addressing this issue, we used total internal reflection fluorescence microscopy (TIRFM
178 s and impaired in type II diabetes, by using total internal reflection fluorescence microscopy (TIRFM
179 Total internal reflection fluorescence microscopy (TIRFM
180 Here we use total internal reflection fluorescence microscopy (TIRFM
181 fficking of DAT to the plasma membrane using total internal reflection fluorescence microscopy (TIRFM
182 We have used total internal reflection fluorescence microscopy (TIRFM
183 Measurements were made by total internal reflection fluorescence microscopy (TIRFM
184 Total internal reflection fluorescence microscopy (TIRFM
185 We have used multicolor total internal reflection fluorescence microscopy (TIRFM
186 By using total internal reflection fluorescence microscopy (TIRFM
187 When visualized with total internal reflection fluorescence microscopy (TIRFM
188 In the current study we have used dual color total internal reflection fluorescence microscopy (TIRFM
189 NMDA receptors in rat hippocampal neurons by total internal reflection fluorescence microscopy (TIRFM
190 ned use of atomic force microscopy (AFM) and total internal reflection fluorescence microscopy (TIRFM
191 tribution of fluorophores to be deduced from total internal reflection fluorescence microscopy (TIRFM
192 Total internal reflection fluorescence microscopy (TIRFM
193 We used these nanopores with AFM and total internal reflection fluorescence microscopy (TIRFM
194 Total internal reflection fluorescence microscopy (TIRFM
195 Total internal reflection fluorescence microscopy (TIRFM
196 level of individual endocytic events using a total internal reflection fluorescence microscopy (TIRFM
197 lation on the plasma membrane as revealed by total internal reflection fluorescence microscopy (TIRFM
198 eriments, using a unique method to carry out total internal reflection fluorescence microscopy (TIRFM
199 Total internal reflection fluorescence microscopy (TIRFM
200 Total internal reflection fluorescence microscopy (TIRFM
201 erformed single-particle fusion assays using total internal reflection fluorescence microscopy to com
204 ns of the DNA strand exchange reactions with total internal reflection fluorescence microscopy to det
206 these differences, we used multi-wavelength total internal reflection fluorescence microscopy to dir
208 direct receptor labeling with SNAP-tags and total internal reflection fluorescence microscopy to dyn
209 To address this, we used single molecule total internal reflection fluorescence microscopy to exa
213 we have used fluorescent fusion proteins and total internal reflection fluorescence microscopy to inv
214 sonance energy transfer (FRET) combined with total internal reflection fluorescence microscopy to inv
215 le (SM) fluorescence studies of CYPs, we use total internal reflection fluorescence microscopy to mea
217 8 membrane dye were used in combination with total internal reflection fluorescence microscopy to mea
227 Here we have used patch-clamp recordings and total internal reflection fluorescence microscopy to stu
229 is distinct region of the cell, we have used total internal reflection fluorescence microscopy to stu
230 underlying their cellular functions we used total internal reflection fluorescence microscopy to vis
231 vesicle release in salamander rods by using total internal reflection fluorescence microscopy to vis
232 opy and single actin filament observation in total internal reflection fluorescence microscopy, to ex
234 ropose an improved version of variable-angle total internal reflection fluorescence microscopy (vaTIR
235 el microfluidic strategy in conjunction with total internal reflection fluorescence microscopy was de
241 and membrane-associated vesicles measured by total internal reflection-fluorescence microscopy was de
243 ing microfluidic flow channels combined with total internal reflection fluorescence microscopy, we ap
244 elet-derived growth factor, visualized using total internal reflection fluorescence microscopy, we co
248 ly visualizing actin filament assembly using total internal reflection fluorescence microscopy, we de
249 ing genetically manipulated mouse models and total internal reflection fluorescence microscopy, we de
252 metic assays and single-molecule multi-color total internal reflection fluorescence microscopy, we di
256 ro actin polymerization assay and time-lapse total internal reflection fluorescence microscopy, we fo
257 Furthermore, by use of the triple-color total internal reflection fluorescence microscopy, we fo
266 lasma membrane of live cells is monitored by total internal reflection fluorescence microscopy, we se
267 y using a combination of structural work and total internal reflection fluorescence microscopy, we sh
268 n/retraction and PI3K signaling monitored by total internal reflection fluorescence microscopy, we sh
269 analysis of a novel VLA-4 FRET sensor under total internal reflection fluorescence microscopy, we sh
276 We use multicolor, dual-penetration depth, total internal reflection fluorescence microscopy, which
277 o assess relative subunit stoichiometry with total internal reflection fluorescence microscopy, which
278 ng mechanism in real time, we used polarized total internal reflection fluorescence microscopy with n
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