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1 go red binding, crystal violet staining, and confocal laser scanning microscopy.
2 ateral to the stimulated side and studied by confocal laser scanning microscopy.
3 dition, the biofilms were examined following confocal laser scanning microscopy.
4 alization in human prostate cancer tissue by confocal laser scanning microscopy.
5 contacts (putative synapses) was counted by confocal laser scanning microscopy.
6 scein conjugates for 10-14 h, then imaged by confocal laser scanning microscopy.
7 teins were colocalized to the nucleoplasm by confocal laser scanning microscopy.
8 ith conventional fluorescence microscopy and confocal laser scanning microscopy.
9 ) by immunofluorescence and semiquantitative confocal laser scanning microscopy.
10 g was measured by staining with fluo3-AM and confocal laser scanning microscopy.
11 the DNA stain 4',6-diamino-phenylindole, and confocal laser scanning microscopy.
12 ble label immunohistochemistry combined with confocal laser scanning microscopy.
13 ualized, and pellicle thickness measured, by confocal laser scanning microscopy.
14 re studied using conventional microscopy and confocal laser scanning microscopy.
15 These sections were examined by confocal laser scanning microscopy.
16 ion of ligand, concentration, and time using confocal laser scanning microscopy.
17 in-1 receptor and examined with three-colour confocal laser scanning microscopy.
18 ng the fluorescent Ca2+ indicator fluo-3 and confocal laser scanning microscopy.
19 All the specimens were examined under Zeiss confocal laser scanning microscopy.
20 were examined and analyzed using time-lapse confocal laser scanning microscopy.
21 subunit-specific antibodies and quantitative confocal laser scanning microscopy.
22 in single optical sections with three-colour confocal laser scanning microscopy.
23 ed and examined for microbial vitality using confocal laser scanning microscopy.
24 in the ER of living HeLa cells, as imaged by confocal laser scanning microscopy.
25 growth was characterized using electron and confocal laser scanning microscopy.
26 of the dye in phloem and xylem tissues using confocal laser scanning microscopy.
27 was embedded in a protein matrix as shown by confocal laser scanning microscopy.
28 aining method followed by flow cytometry and confocal laser scanning microscopy.
29 Expression of F-actin was determined using confocal laser scanning microscopy.
30 and nucleus, as shown by immunofluorescence confocal laser scanning microscopy.
31 evaluated by immunocytochemistry followed by confocal laser scanning microscopy.
32 qualitative analysis was also carried out by confocal laser scanning microscopy.
33 stem cell compromise confirmed with in vivo confocal laser scanning microscopy.
34 regates and phase separation as confirmed by confocal laser scanning microscopy.
35 monitored LTP-GFP in developing anthers with confocal laser scanning microscopy.
36 sualization of podocyte foot processes using confocal laser scanning microscopy.
37 scular structures at higher resolutions than confocal laser scanning microscopy.
38 cted by transmission electron microscopy and confocal laser scanning microscopy.
39 Microstructure was characterised by confocal laser scanning microscopy.
40 obtained from single cell images captured by confocal laser scanning microscopy.
41 lated differential scanning calorimetry, and confocal laser scanning microscopy.
42 rties and microstructure of the butter using confocal laser scanning microscopy.
43 fluorescent protein in mammalian cells using confocal laser scanning microscopy.
44 veral thousand particles that were imaged by confocal laser scanning microscopy.
45 d on titanium implants in vitro, detected by confocal laser scanning microscopy.
46 in continuous-flow biofilms and analyzed by confocal laser scanning microscopy.
47 ected randomly and imaged digitally by using confocal laser-scanning microscopy.
48 ion and less photo-bleaching, as compared to confocal laser-scanning microscopy.
49 studied in the PnO by immunofluorescence and confocal, laser scanning microscopy.
50 HL was examined using in situ zymography and confocal laser scanning microscopy after 24 h or 1-y sto
51 on of 299R cells in situ on leaf surfaces by confocal laser scanning microscopy after fluorescence in
52 plasma membrane was detected by quantitative confocal laser-scanning microscopy after beta3 subunit i
54 otypic and cellular distribution of SNAT1 by confocal laser-scanning microscopy alongside other marke
57 aled lamellipodia surrounding gonococci, and confocal laser scanning microscopy analysis showed organ
59 l demineralization models was measured using confocal laser scanning microscopy and analyzed with two
62 actose-specific lectin staining, followed by confocal laser scanning microscopy and electron microsco
67 calization of PS-/SYS-GFP was observed using confocal laser scanning microscopy and gene transcripts
69 grown in flow cells, followed by analysis by confocal laser scanning microscopy and scanning electron
70 dynamic changes in [Ca2+]i levels utilizing confocal laser scanning microscopy and the calcium bindi
72 ques for fluorescence optical sectioning are confocal laser scanning microscopy and two-photon micros
75 thway using immunocytochemistry coupled with confocal laser-scanning microscopy and Western blot anal
78 Subcellular fractionation, flow cytometry, confocal laser scanning microscopy, and immuno-transmiss
80 ay diffraction, infrared imaging microscopy, confocal laser scanning microscopy, and transmission ele
81 n of biotin-labeled Abeta in living cells by confocal laser scanning microscopy; and (iii) transmissi
82 ologies such as microcomputed tomography and confocal laser scanning microscopy are changing how morp
83 histochemistry combined with fluorescence or confocal laser scanning microscopy are common techniques
84 y (ELISA) or immunofluorescent staining with confocal laser scanning microscopy at various time point
86 and dendrites were located with three-colour confocal laser scanning microscopy by examining series o
88 n the bonding interface was then examined by confocal laser scanning microscopy (CLSM) and scanning e
89 e, a 5-amino-fluorescein moiety for FI using confocal laser scanning microscopy (CLSM) as well as a 2
92 airs of co-registered volumetric fluorescent confocal laser scanning microscopy (CLSM) images (z-stac
93 In tissue double-labeled for SS and nNOs, confocal laser scanning microscopy (CLSM) images of SS a
95 n was transiently expressed in CHO-K1 cells; confocal laser scanning microscopy (CLSM) showed localiz
98 with small angle X-ray scattering (SAXS) and confocal laser scanning microscopy (CLSM) studies sugges
101 ctions of bimane-labelled cells collected by confocal laser scanning microscopy (CLSM) with excitatio
102 aracterized by total biomass quantification, confocal laser scanning microscopy (CLSM), and electroki
103 ement (GIC) with dentin have been studied by confocal laser scanning microscopy (CLSM), scanning elec
104 , as determined by differential staining and confocal laser scanning microscopy (CLSM), than the nond
118 We have developed a novel application of confocal laser scanning microscopy coupled to image proc
120 ilm of T. pseudethanolicus on the anode, and confocal laser scanning microscopy demonstrated a maximu
125 Combined reflectance/fluorescence in vivo confocal laser scanning microscopy holds significant pro
126 of orientation, deconvolved high-resolution confocal laser scanning microscopy image stacks of dendr
129 tostatin) were investigated with dual-colour confocal laser scanning microscopy in axons of cervical,
130 marker CD63var, were examined by FACS and by confocal laser scanning microscopy in cell culture and i
131 the nitrocellulose membrane was analyzed by confocal laser scanning microscopy in the "Z" stack mode
133 s expressed 9ORF1 protein and, together with confocal laser scanning microscopy, indicated that this
134 Field emission scanning electron microscopy, confocal laser scanning microscopy, infrared spectroscop
144 mal membrane proteins was investigated using confocal laser scanning microscopy of living cells expre
148 samples were analyzed by epifluorescence and confocal laser scanning microscopy, respectively, using
153 al-labeling immunofluorescence studies using confocal laser scanning microscopy revealed that many (3
164 Virus titration, immunofluorescence and confocal laser scanning microscopy showed virus replicat
165 ammalian cells, and immunocytochemistry with confocal laser-scanning microscopy showed that these two
167 by fluorescence dye adsorption analyzed with confocal laser scanning microscopy that a LPMO (from Neu
170 d indirect immunofluorescence microscopy and confocal laser scanning microscopy to characterize this
174 Here we employed fluorescence microscopy and confocal laser scanning microscopy to investigate how D-
176 of the SiO2@PEI MPs on the damage area using confocal laser scanning microscopy under variable cross-
177 oscopy and the other to obtain specimens for confocal laser scanning microscopy using vital dyes.
178 Neuronal oxidative stress was measured by confocal laser scanning microscopy, using 2,7-dichlorofl
188 ride (EPS):bacteria volume ratio measured by confocal laser scanning microscopy were performed to det
190 aging, and dead:live volume ratio decided by confocal laser scanning microscopy were used to study th
192 ng methods (Scanning Electron Microscopy and Confocal Laser Scanning Microscopy) were employed to obt
193 ormation defect was also readily apparent by confocal laser scanning microscopy when flow cells were
194 ombined high spatial and temporal resolution confocal laser scanning microscopy with advanced image-p
195 fic examination with widefield microscopy or confocal laser scanning microscopy with spectral separat
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