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1 nt protein in mammalian cells using confocal laser scanning microscopy.
2 usand particles that were imaged by confocal laser scanning microscopy.
3 nium implants in vitro, detected by confocal laser scanning microscopy.
4 nuous-flow biofilms and analyzed by confocal laser scanning microscopy.
5 number of recent extensions to FCS based on laser scanning microscopy.
6 nding, crystal violet staining, and confocal laser scanning microscopy.
7 the stimulated side and studied by confocal laser scanning microscopy.
8 escence quenching technique with multiphoton laser scanning microscopy.
9 he biofilms were examined following confocal laser scanning microscopy.
10 in human prostate cancer tissue by confocal laser scanning microscopy.
11 1 to 1 nJ pulses and conventional two-photon laser scanning microscopy.
12 (putative synapses) was counted by confocal laser scanning microscopy.
13 jugates for 10-14 h, then imaged by confocal laser scanning microscopy.
14 isolated cardiomyocytes were imaged using 2P-laser scanning microscopy.
15 their axons in whole mounts with two-photon laser scanning microscopy.
16 e colocalized to the nucleoplasm by confocal laser scanning microscopy.
17 ntional fluorescence microscopy and confocal laser scanning microscopy.
18 ltetrazolium bromide assay and by two-photon laser scanning microscopy.
19 nofluorescence and semiquantitative confocal laser scanning microscopy.
20 amined for microbial vitality using confocal laser scanning microscopy.
21 sured by staining with fluo3-AM and confocal laser scanning microscopy.
22 tain 4',6-diamino-phenylindole, and confocal laser scanning microscopy.
23 immunohistochemistry combined with confocal laser scanning microscopy.
24 and pellicle thickness measured, by confocal laser scanning microscopy.
25 d using conventional microscopy and confocal laser scanning microscopy.
26 These sections were examined by confocal laser scanning microscopy.
27 gand, concentration, and time using confocal laser scanning microscopy.
28 ptor and examined with three-colour confocal laser scanning microscopy.
29 uorescent Ca2+ indicator fluo-3 and confocal laser scanning microscopy.
30 specimens were examined under Zeiss confocal laser scanning microscopy.
31 mined and analyzed using time-lapse confocal laser scanning microscopy.
32 pecific antibodies and quantitative confocal laser scanning microscopy.
33 optical sections with three-colour confocal laser scanning microscopy.
34 ded in a protein matrix as shown by confocal laser scanning microscopy.
35 of living HeLa cells, as imaged by confocal laser scanning microscopy.
36 as characterized using electron and confocal laser scanning microscopy.
37 e in phloem and xylem tissues using confocal laser scanning microscopy.
38 thod followed by flow cytometry and confocal laser scanning microscopy.
39 ion of F-actin was determined using confocal laser scanning microscopy.
40 eus, as shown by immunofluorescence confocal laser scanning microscopy.
41 by immunocytochemistry followed by confocal laser scanning microscopy.
42 ve analysis was also carried out by confocal laser scanning microscopy.
43 l compromise confirmed with in vivo confocal laser scanning microscopy.
44 nd phase separation as confirmed by confocal laser scanning microscopy.
45 LTP-GFP in developing anthers with confocal laser scanning microscopy.
46 on of podocyte foot processes using confocal laser scanning microscopy.
47 ransmission electron microscopy and confocal laser scanning microscopy.
48 Microstructure was characterised by confocal laser scanning microscopy.
49 the PnO by immunofluorescence and confocal, laser scanning microscopy.
50 from single cell images captured by confocal laser scanning microscopy.
51 ructures at higher resolutions than confocal laser scanning microscopy.
52 ferential scanning calorimetry, and confocal laser scanning microscopy.
53 microstructure of the butter using confocal laser scanning microscopy.
54 is regulated during neurotransmission using laser-scanning microscopy.
55 domly and imaged digitally by using confocal laser-scanning microscopy.
56 ess photo-bleaching, as compared to confocal laser-scanning microscopy.
57 ptic calcium signal recorded with two-photon laser-scanning microscopy.
60 vessels during behavior, we used two-photon laser scanning microscopy (2PLSM) to measure the diamete
65 amined using in situ zymography and confocal laser scanning microscopy after 24 h or 1-y storage in a
66 R cells in situ on leaf surfaces by confocal laser scanning microscopy after fluorescence in situ hyb
67 mbrane was detected by quantitative confocal laser-scanning microscopy after beta3 subunit injection.
69 Hec6stGFP cross were imaged using two-photon laser scanning microscopy, allowing the simultaneous vis
74 llipodia surrounding gonococci, and confocal laser scanning microscopy analysis showed organisms colo
76 Using an elegant combination of 2-photon laser scanning microscopy and 2-photon uncaging of gluta
77 alization models was measured using confocal laser scanning microscopy and analyzed with two-way ANOV
78 2 complementary imaging techniques: 2-photon laser scanning microscopy and contrast-enhanced ultrasou
81 mechanism of action study of 12f by confocal laser scanning microscopy and electron microscopy indica
83 ecific lectin staining, followed by confocal laser scanning microscopy and electron microscopy, to sh
87 n of PS-/SYS-GFP was observed using confocal laser scanning microscopy and gene transcripts were dete
88 flow cells, followed by analysis by confocal laser scanning microscopy and scanning electron microsco
90 changes in [Ca2+]i levels utilizing confocal laser scanning microscopy and the calcium binding dye, i
93 l NMDARs in L4 neuron axons using two-photon laser scanning microscopy and two-photon glutamate uncag
95 fluorescence optical sectioning are confocal laser scanning microscopy and two-photon microscopy.
98 fluorescent protein tracer with multiphoton laser-scanning microscopy and flow cytometry to examine
99 g on a spherical treadmill, using two-photon laser-scanning microscopy and genetically encoded calciu
101 y sedated, responsive mice using multiphoton laser-scanning microscopy and novel genetic tools that e
103 escent protein) and used combined two-photon laser-scanning microscopy and two-photon laser photoacti
104 ation in real time using combined two-photon laser-scanning microscopy and two-photon laser uncaging
105 nd intracellular NO scavenging, confirmed by laser-scanning microscopy and unequivocally validated by
106 ng immunocytochemistry coupled with confocal laser-scanning microscopy and Western blot analysis.
108 a derived from cytotoxicity assays, confocal laser scanning microscopy, and electron microscopy confi
109 ular fractionation, flow cytometry, confocal laser scanning microscopy, and immuno-transmission elect
111 ction, infrared imaging microscopy, confocal laser scanning microscopy, and transmission electron mic
112 in-labeled Abeta in living cells by confocal laser scanning microscopy; and (iii) transmission electr
113 uch as microcomputed tomography and confocal laser scanning microscopy are changing how morphology ca
114 istry combined with fluorescence or confocal laser scanning microscopy are common techniques in arthr
116 or immunofluorescent staining with confocal laser scanning microscopy at various time points after i
117 ices using Oregon Green BAPTA-1 and 2-photon laser scanning microscopy (BAPTA: 1,2-bis(2-aminophenoxy
119 ve alternative in biological applications of laser scanning microscopy because many problems encounte
120 d is a challenge for conventional two-photon laser-scanning microscopy, because it depends on serial
121 h in conjunction with time-lapse multiphoton laser scanning microscopy by directly observing angiogen
122 ites were located with three-colour confocal laser scanning microscopy by examining series of optical
123 Here we show that two-photon excitation laser scanning microscopy can penetrate the highly scatt
126 ding interface was then examined by confocal laser scanning microscopy (CLSM) and scanning electron m
127 ino-fluorescein moiety for FI using confocal laser scanning microscopy (CLSM) as well as a 2-aminoeth
130 o-registered volumetric fluorescent confocal laser scanning microscopy (CLSM) images (z-stacks) of st
131 sue double-labeled for SS and nNOs, confocal laser scanning microscopy (CLSM) images of SS and nNOS l
133 nsiently expressed in CHO-K1 cells; confocal laser scanning microscopy (CLSM) showed localization at
136 l angle X-ray scattering (SAXS) and confocal laser scanning microscopy (CLSM) studies suggested that
138 The application of fluorescence confocal laser scanning microscopy (CLSM) to quantify three-dimen
139 bimane-labelled cells collected by confocal laser scanning microscopy (CLSM) with excitation 442 nm,
140 ed by total biomass quantification, confocal laser scanning microscopy (CLSM), and electrokinetic ana
141 C) with dentin have been studied by confocal laser scanning microscopy (CLSM), scanning electron micr
142 rmined by differential staining and confocal laser scanning microscopy (CLSM), than the nondisinfecte
157 ve developed a novel application of confocal laser scanning microscopy coupled to image processing th
163 pseudethanolicus on the anode, and confocal laser scanning microscopy demonstrated a maximum biofilm
165 ing of FM 1-43 fluorescence using two-photon laser scanning microscopy detected glutamate-induced for
167 PROCEDURE requires a basic understanding of laser-scanning microscopy, experience with handling zebr
171 aptic dendrites, we have combined two-photon laser scanning microscopy, glutamate uncaging, and whole
172 dition, the recent application of two-photon laser scanning microscopy has made it possible to make r
173 ts to couple phosphorescence with two-photon laser scanning microscopy have faced substantial difficu
174 ed reflectance/fluorescence in vivo confocal laser scanning microscopy holds significant promise for
175 tation, deconvolved high-resolution confocal laser scanning microscopy image stacks of dendritic segm
177 Furthermore, in situ real-time confocal laser scanning microscopy imaging reveals the dynamic pr
178 tracked in the intestine through multiphoton laser scanning microscopy in an ex vivo intestinal model
179 were investigated with dual-colour confocal laser scanning microscopy in axons of cervical, thoracic
180 63var, were examined by FACS and by confocal laser scanning microscopy in cell culture and in disease
181 9 was demonstrated by confocal fluorescence laser scanning microscopy in stably transfected HEK293 c
184 ed blood cells were measured with two-photon laser-scanning microscopy in individual subsurface micro
188 ed 9ORF1 protein and, together with confocal laser scanning microscopy, indicated that this E4 protei
189 ssion scanning electron microscopy, confocal laser scanning microscopy, infrared spectroscopy and Ram
192 mplex three-dimensional (3D) structures from laser scanning microscopy (LSM) images is increasingly n
193 rescence imaging, but existing methods using laser-scanning microscopy (LSM) are severely limited in
207 ane proteins was investigated using confocal laser scanning microscopy of living cells expressing fus
209 ng protein (L-FABP) by real time multiphoton laser scanning microscopy of novel fluorescent VLC-PUFAs
214 In dendrites visualized with two-photon laser scanning microscopy or electron microscopy, most o
215 When viewed through multiple focal planes by laser scanning microscopy, protein A foci are arranged i
216 ere analyzed by epifluorescence and confocal laser scanning microscopy, respectively, using a green f
218 uared dependence of two-photon excitation in laser scanning microscopy restricts excitation to the fo
221 . and Davalos et al. used in vivo two-photon laser-scanning microscopy reveal that the fine branches
224 ng immunofluorescence studies using confocal laser scanning microscopy revealed that many (30-40%) ty
225 ble immunofluorescence labeling and confocal laser scanning microscopy revealed that MMP-26 was coloc
231 Coinfection experiments examined by confocal laser scanning microscopy show that in communal phagosom
236 s titration, immunofluorescence and confocal laser scanning microscopy showed virus replication signi
237 cells, and immunocytochemistry with confocal laser-scanning microscopy showed that these two proteins
239 scence dye adsorption analyzed with confocal laser scanning microscopy that a LPMO (from Neurospora c
243 al tracing procedure that employs two-photon laser scanning microscopy to activate the photoactivatab
244 t immunofluorescence microscopy and confocal laser scanning microscopy to characterize this structure
246 We used a crystal violet assay and confocal laser scanning microscopy to demonstrate Hms-dependent b
247 We used cellular fractionation and confocal laser scanning microscopy to determine the cellular loca
248 l arbors, we have used two-photon excitation laser scanning microscopy to directly image action-poten
249 blood flow at this level, we used two-photon laser scanning microscopy to image the motion of red blo
250 mployed fluorescence microscopy and confocal laser scanning microscopy to investigate how D-amino aci
251 ion; electrophysiology; and live, two-photon laser scanning microscopy to manipulate both the amount
252 gan culture, we employ time-lapse two-photon laser scanning microscopy to observe proliferative cells
254 ouse hippocampal brain slices and two-photon laser scanning microscopy to study microglial dynamics a
257 dendrites in living animals with two-photon laser-scanning microscopy to determine whether these sei
258 mate to mimic synaptic input and two-photon, laser-scanning microscopy to measure calcium levels in d
261 (CLSM) with excitation 442 nm, or two-photon laser scanning microscopy (TPLSM) with excitation 770 nm
264 t molecules can be achieved using two-photon laser-scanning microscopy (TPLSM) hardware, the integrat
266 his protocol describes the use of two-photon laser-scanning microscopy (TPLSM) to study hair regenera
268 O2@PEI MPs on the damage area using confocal laser scanning microscopy under variable cross-flow rate
270 al oxidative stress was measured by confocal laser scanning microscopy, using 2,7-dichlorofluorescin
273 f action potentials in STN neurons, 2-photon laser scanning microscopy was used to guide tight-seal w
284 ng real-time in vitro and in vivo two-photon laser scanning microscopy, we have identified the transp
286 ctivation and, using intravital fluorescence laser scanning microscopy, we reported that the potent s
287 itro migration assays and in vivo two-photon laser scanning microscopy, we showed that CTLA-4 increas
291 Epifluorescent light microscopy and confocal laser scanning microscopy were employed to visualize the
292 ):bacteria volume ratio measured by confocal laser scanning microscopy were performed to determine th
294 d dead:live volume ratio decided by confocal laser scanning microscopy were used to study the biomass
296 s (Scanning Electron Microscopy and Confocal Laser Scanning Microscopy) were employed to obtain compl
297 defect was also readily apparent by confocal laser scanning microscopy when flow cells were used to g
298 igh spatial and temporal resolution confocal laser scanning microscopy with advanced image-processing
299 nic social defeat stress and used two-photon laser scanning microscopy with glutamate photo-uncaging
300 nation with widefield microscopy or confocal laser scanning microscopy with spectral separation.
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