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1  of hydrazine in live fruit-fly larvae using epifluorescence microscopy.
2 ric field-induced behavior to be followed by epifluorescence microscopy.
3  mitochondrial [Ca(2+)] were monitored using epifluorescence microscopy.
4 c nerves in the ventricles using whole mount epifluorescence microscopy.
5 ned by culture on selective agar media or by epifluorescence microscopy.
6 rons at kilohertz frame rates using standard epifluorescence microscopy.
7  planar transparent materials using standard epifluorescence microscopy.
8 smic shuttling event that can be measured by epifluorescence microscopy.
9 ing exposure to FLC using flow cytometry and epifluorescence microscopy.
10 iochemical analysis and real-time imaging by epifluorescence microscopy.
11 ual protein-DNA complexes by single-molecule epifluorescence microscopy.
12 l screens for ERAD modifiers using widefield epifluorescence microscopy.
13  in the feedwater stream by bright-field and epifluorescence microscopy.
14 sly injected after injury and detected using epifluorescence microscopy.
15 oteins and oligonucleotides were observed by epifluorescence microscopy.
16 n and particle dispersion are measured using epifluorescence microscopy.
17 (3.83 x 10(7) VLP ml(-1)) when observed with epifluorescence microscopy.
18 ts and population kinetics were observed via epifluorescence microscopy.
19  by their bilayer-substrate distance d using epifluorescence microscopy.
20 ere studied with atomic force microscopy and epifluorescence microscopy.
21 th visual recovery also noted through use of epifluorescence microscopy.
22  alpha, VEGF, and IGFBP-3, and visualized by epifluorescence microscopy.
23 using differential interference contrast and epifluorescence microscopy.
24 r application of caffeine or carbachol using epifluorescence microscopy.
25 1) receptor in the rat brain was examined by epifluorescence microscopy.
26 vice, the T-sensor, by means of conventional epifluorescence microscopy.
27 allow PPIs to be interrogated using standard epifluorescence microscopy.
28 ast, differential interference contrast, and epifluorescence microscopy.
29 are observed in planar-supported bilayers by epifluorescence microscopy.
30 ytes of microperfused IBDUs were detected by epifluorescence microscopy and a fluorescence assay, res
31 rs in films of pulmonary surfactant, we used epifluorescence microscopy and Brewster angle microscopy
32                             Bright-field and epifluorescence microscopy and CLSM showed that biofilm
33 ferential Interference Contrast coupled with Epifluorescence Microscopy and Confocal Laser Scanning M
34 bidopsis thaliana cells using variable-angle epifluorescence microscopy and developed a set of inform
35 ce microscopy, scanning electron microscopy, epifluorescence microscopy and ellipsometry.
36 s of protein uptake in Jurkat lymphocytes by epifluorescence microscopy and flow cytometry revealed i
37                                        Using epifluorescence microscopy and flow cytometry, we have c
38 of certain phospholipids with cholesterol by epifluorescence microscopy and measurement of cholestero
39                Combining this technique with epifluorescence microscopy and quantitative image analys
40  supported lipid bilayer is characterized by epifluorescence microscopy and the long-range lateral mo
41 y increased both cytoplasmic calcium (fura-2 epifluorescence microscopy) and ciliary beat frequency (
42 imental techniques, including pi-A isotherm, epifluorescence microscopy, and absorption and emission
43 f SPTRX3 was evaluated by flow cytometry and epifluorescence microscopy, and correlated with clinical
44 valuated by cell culture, flow-cytometry and epifluorescence microscopy, and further assayed with a b
45 transfer-based assays, video edge detection, epifluorescence microscopy, and L-type Ca2(+) current me
46 bcellular resolution, even when using simple epifluorescence microscopy, and located the chief sites
47 re followed by total internal reflection and epifluorescence microscopy, and the lateral diffusion of
48 ities: two-photon laser-scanning microscopy, epifluorescence microscopy, and total internal reflectio
49 ngmuir film properties, UV-vis spectroscopy, epifluorescence microscopy, and transmission electron mi
50                           Using confocal and epifluorescence microscopy, as well as biochemical assay
51  fusions have been created and visualized by epifluorescence microscopy, both in transgenic Arabidops
52                                              Epifluorescence microscopy confirmed the specific intera
53 ual drops using OCD RT-qPCR and imaged using epifluorescence microscopy correlate with amplification
54                                              Epifluorescence microscopy demonstrated a positive corre
55 ays, transmission electron microscopy (TEM), epifluorescence microscopy (EFM), and flow cytometry (FC
56 rboring a GFP marker gene were visualized by epifluorescence microscopy, either directly in situ or a
57                                  Large field epifluorescence microscopy enabled in situ and real-time
58                                              Epifluorescence microscopy established that the bilayer
59 arged lipids using supported lipid bilayers, epifluorescence microscopy, fluorescence recovery after
60      The slides were stained and examined by epifluorescence microscopy for the presence of C. tracho
61       The phase diagram was determined using epifluorescence microscopy for vesicle populations with
62                    In support of this, video epifluorescence microscopy found that OMTs in solution d
63  have developed such a technique in confocal epifluorescence microscopy, giving access to new regions
64 icroscopy, such viruses can be visualized by epifluorescence microscopy if stained brightly.
65 ws: (i) in wet mounts (with bright-field and epifluorescence microscopy), (ii) in modified acid-fast-
66 llular Ca(2+) homeostasis was analyzed using epifluorescence microscopy in Fura-2-loaded cardiomyocyt
67 eins of R-phycoerythrin (RPE) were imaged by epifluorescence microscopy in the nucleoplasm and cytopl
68                                              Epifluorescence microscopy is used measure the partition
69                                              Epifluorescence microscopy is used to determine phase di
70 e measurements compare well with pixel-based epifluorescence microscopy measurements of whole cells w
71 onella, we developed a rapid, nondestructive epifluorescence microscopy method to determine bacteria
72 isease and relapsing fever, were examined by epifluorescence microscopy of bacterial cells embedded i
73                                              Epifluorescence microscopy of fecal samples confirmed th
74                         We used quantitative epifluorescence microscopy of fluorescent nucleotides to
75                  Metabolic radiolabeling and epifluorescence microscopy of Jurkat lymphocytes treated
76                                              Epifluorescence microscopy of living excised corneas rev
77 olipid mixtures have been examined using the epifluorescence microscopy of monolayers at the air-wate
78 ning labeled proteins in microemulsions, and epifluorescence microscopy of plugs and drops generated
79                                              Epifluorescence microscopy of these mutants demonstrates
80 he steps in early hematogenous metastasis by epifluorescence microscopy of tumor cells expressing gre
81 n the grafts was visualized in vivo by using epifluorescence microscopy over 12 weeks.
82 ient of fluorescently labeled particles, and epifluorescence microscopy revealed that upon addition o
83                             Using high-speed epifluorescence microscopy, RhoVR-Halos provide a read-o
84                                              Epifluorescence microscopy studies of mixtures of phosph
85  We demonstrate by intravital two-photon and epifluorescence microscopy that blood monocytes and neut
86                Here, we use metagenomics and epifluorescence microscopy to demonstrate that two commo
87  previously reported the use of narrow-field epifluorescence microscopy to directly monitor cargoes i
88                                      We used epifluorescence microscopy to examine the cell and nucle
89      Here we have used siRNAs and time-lapse epifluorescence microscopy to examine the roles of vario
90     We have used multi-wavelength time-lapse epifluorescence microscopy to image the dynamic interact
91                                        Using epifluorescence microscopy to monitor green fluorescent
92       We combined SDS-PAGE densitometry with epifluorescence microscopy to quantitate HaloTag-labeled
93 on counting histogram method, in tandem with epifluorescence microscopy to quantitatively probe the e
94 yed differential interference microscopy and epifluorescence microscopy to track germinating spores w
95 several biochemical assays along with EM and epifluorescence microscopy, to the best of our knowledge
96 DISCO technique with 1-photon microscopy and epifluorescence microscopy under high power LED illumina
97                  Here, we use variable-angle epifluorescence microscopy (VAEM) to examine the organiz
98  alternative to TIRFM, termed variable-angle epifluorescence microscopy (VAEM), for the visualization
99                                     Standard epifluorescence microscopy was used to detect all three
100                                              Epifluorescence microscopy was used to evaluate corneal
101 nomic sequencing, metabolomic profiling, and epifluorescence microscopy was used to investigate how t
102                              Single-molecule epifluorescence microscopy was used to observe the trans
103                                              Epifluorescence microscopy was used to study peritubular
104                                              Epifluorescence microscopy was used to visualize the org
105 porter was disrupted, by growth analysis and epifluorescence microscopy, we confirmed peptide uptake
106                  For cross-validation, using epifluorescence microscopy, we demonstrated the underlyi
107 ng their positions pairwise in live cells by epifluorescence microscopy, we found that all but rrnC a
108 l as three-dimensional stacks of deconvolved epifluorescence microscopy, we found that inside living
109              Using transmission electron and epifluorescence microscopy, we found that wall thickness
110                                        Using epifluorescence microscopy, we have examined in a model
111                         Utilizing time-lapse epifluorescence microscopy, we observed that the membran
112                           Using confocal and epifluorescence microscopy, we show that baseline TLR ex
113                         Using variable-angle epifluorescence microscopy, we visualized the dynamics o
114 ir interactions with ACs were monitored with epifluorescence microscopy, which revealed a local leafl
115  used in biomedical research for multiplexed epifluorescence microscopy with GFP-based probes, but th
116 neously using video microscopy (for CBF) and epifluorescence microscopy with the pH-sensitive dye BCE
117 d to directly quantify viral production (via epifluorescence microscopy) with minor sample manipulati

 
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