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1 by immunocytochemistry followed by confocal laser scanning microscopy.
2 ve analysis was also carried out by confocal laser scanning microscopy.
3 l compromise confirmed with in vivo confocal laser scanning microscopy.
4 nd phase separation as confirmed by confocal laser scanning microscopy.
5 LTP-GFP in developing anthers with confocal laser scanning microscopy.
6 on of podocyte foot processes using confocal laser scanning microscopy.
7 ransmission electron microscopy and confocal laser scanning microscopy.
8 Microstructure was characterised by confocal laser scanning microscopy.
9 the PnO by immunofluorescence and confocal, laser scanning microscopy.
10 from single cell images captured by confocal laser scanning microscopy.
11 ferential scanning calorimetry, and confocal laser scanning microscopy.
12 microstructure of the butter using confocal laser scanning microscopy.
13 nt protein in mammalian cells using confocal laser scanning microscopy.
14 ransmission electron microscopy and confocal laser scanning microscopy.
15 usand particles that were imaged by confocal laser scanning microscopy.
16 nium implants in vitro, detected by confocal laser scanning microscopy.
17 nuous-flow biofilms and analyzed by confocal laser scanning microscopy.
18 in mice was measured in vivo under 2-photon laser scanning microscopy.
19 number of recent extensions to FCS based on laser scanning microscopy.
20 nding, crystal violet staining, and confocal laser scanning microscopy.
21 the stimulated side and studied by confocal laser scanning microscopy.
22 escence quenching technique with multiphoton laser scanning microscopy.
23 he biofilms were examined following confocal laser scanning microscopy.
24 in human prostate cancer tissue by confocal laser scanning microscopy.
25 ging and Alzheimer's in vivo, using 2-photon laser scanning microscopy.
26 1 to 1 nJ pulses and conventional two-photon laser scanning microscopy.
27 (putative synapses) was counted by confocal laser scanning microscopy.
28 jugates for 10-14 h, then imaged by confocal laser scanning microscopy.
29 isolated cardiomyocytes were imaged using 2P-laser scanning microscopy.
30 their axons in whole mounts with two-photon laser scanning microscopy.
31 e colocalized to the nucleoplasm by confocal laser scanning microscopy.
32 ntional fluorescence microscopy and confocal laser scanning microscopy.
33 ltetrazolium bromide assay and by two-photon laser scanning microscopy.
34 nofluorescence and semiquantitative confocal laser scanning microscopy.
35 sured by staining with fluo3-AM and confocal laser scanning microscopy.
36 tain 4',6-diamino-phenylindole, and confocal laser scanning microscopy.
37 immunohistochemistry combined with confocal laser scanning microscopy.
38 and pellicle thickness measured, by confocal laser scanning microscopy.
39 d using conventional microscopy and confocal laser scanning microscopy.
40 ded in a protein matrix as shown by confocal laser scanning microscopy.
41 ructures at higher resolutions than confocal laser scanning microscopy.
42 amined for microbial vitality using confocal laser scanning microscopy.
43 n solubility, SDS-PAGE pattern, and Confocal Laser Scanning Microscopy.
44 of living HeLa cells, as imaged by confocal laser scanning microscopy.
45 as characterized using electron and confocal laser scanning microscopy.
46 e in phloem and xylem tissues using confocal laser scanning microscopy.
47 thod followed by flow cytometry and confocal laser scanning microscopy.
48 ion of F-actin was determined using confocal laser scanning microscopy.
49 eus, as shown by immunofluorescence confocal laser scanning microscopy.
50 ptic calcium signal recorded with two-photon laser-scanning microscopy.
51 evoked glutamate transients with two-photon laser-scanning microscopy.
52 is regulated during neurotransmission using laser-scanning microscopy.
53 domly and imaged digitally by using confocal laser-scanning microscopy.
56 vessels during behavior, we used two-photon laser scanning microscopy (2PLSM) to measure the diamete
61 amined using in situ zymography and confocal laser scanning microscopy after 24 h or 1-y storage in a
62 R cells in situ on leaf surfaces by confocal laser scanning microscopy after fluorescence in situ hyb
64 Hec6stGFP cross were imaged using two-photon laser scanning microscopy, allowing the simultaneous vis
69 llipodia surrounding gonococci, and confocal laser scanning microscopy analysis showed organisms colo
71 Using an elegant combination of 2-photon laser scanning microscopy and 2-photon uncaging of gluta
72 alization models was measured using confocal laser scanning microscopy and analyzed with two-way ANOV
73 2 complementary imaging techniques: 2-photon laser scanning microscopy and contrast-enhanced ultrasou
76 me-lapse imaging of apoptosis using confocal laser scanning microscopy and demonstrates the utility o
77 mechanism of action study of 12f by confocal laser scanning microscopy and electron microscopy indica
79 ecific lectin staining, followed by confocal laser scanning microscopy and electron microscopy, to sh
83 n of PS-/SYS-GFP was observed using confocal laser scanning microscopy and gene transcripts were dete
85 ing electron microscopy (cryo-SEM), confocal laser scanning microscopy and laser diffraction, where t
86 flow cells, followed by analysis by confocal laser scanning microscopy and scanning electron microsco
88 changes in [Ca2+]i levels utilizing confocal laser scanning microscopy and the calcium binding dye, i
91 l NMDARs in L4 neuron axons using two-photon laser scanning microscopy and two-photon glutamate uncag
93 fluorescence optical sectioning are confocal laser scanning microscopy and two-photon microscopy.
95 fluorescent protein tracer with multiphoton laser-scanning microscopy and flow cytometry to examine
96 g on a spherical treadmill, using two-photon laser-scanning microscopy and genetically encoded calciu
97 y sedated, responsive mice using multiphoton laser-scanning microscopy and novel genetic tools that e
99 escent protein) and used combined two-photon laser-scanning microscopy and two-photon laser photoacti
100 ation in real time using combined two-photon laser-scanning microscopy and two-photon laser uncaging
101 nd intracellular NO scavenging, confirmed by laser-scanning microscopy and unequivocally validated by
102 ng immunocytochemistry coupled with confocal laser-scanning microscopy and Western blot analysis.
104 a derived from cytotoxicity assays, confocal laser scanning microscopy, and electron microscopy confi
105 ular fractionation, flow cytometry, confocal laser scanning microscopy, and immuno-transmission elect
107 mbination of hyperspectral imaging, confocal laser scanning microscopy, and nanoparticle-based O(2) i
108 ction, infrared imaging microscopy, confocal laser scanning microscopy, and transmission electron mic
109 in-labeled Abeta in living cells by confocal laser scanning microscopy; and (iii) transmission electr
110 uch as microcomputed tomography and confocal laser scanning microscopy are changing how morphology ca
111 istry combined with fluorescence or confocal laser scanning microscopy are common techniques in arthr
113 d glyphosate was assessed employing confocal laser scanning microscopy as well as confocal Raman micr
114 or immunofluorescent staining with confocal laser scanning microscopy at various time points after i
115 ices using Oregon Green BAPTA-1 and 2-photon laser scanning microscopy (BAPTA: 1,2-bis(2-aminophenoxy
117 ve alternative in biological applications of laser scanning microscopy because many problems encounte
118 d is a challenge for conventional two-photon laser-scanning microscopy, because it depends on serial
119 h in conjunction with time-lapse multiphoton laser scanning microscopy by directly observing angiogen
120 ites were located with three-colour confocal laser scanning microscopy by examining series of optical
123 covery after photobleaching (FRAP), confocal laser scanning microscopy (CLSM) and molecular dynamics
124 ding interface was then examined by confocal laser scanning microscopy (CLSM) and scanning electron m
125 ino-fluorescein moiety for FI using confocal laser scanning microscopy (CLSM) as well as a 2-aminoeth
126 nning electron microscopy (SEM) and confocal laser scanning microscopy (CLSM) confirmed that TPI play
129 o-registered volumetric fluorescent confocal laser scanning microscopy (CLSM) images (z-stacks) of st
131 nsiently expressed in CHO-K1 cells; confocal laser scanning microscopy (CLSM) showed localization at
134 l angle X-ray scattering (SAXS) and confocal laser scanning microscopy (CLSM) studies suggested that
136 The application of fluorescence confocal laser scanning microscopy (CLSM) to quantify three-dimen
137 bimane-labelled cells collected by confocal laser scanning microscopy (CLSM) with excitation 442 nm,
138 ed by total biomass quantification, confocal laser scanning microscopy (CLSM), and electrokinetic ana
139 ferent protocols were studied using confocal laser scanning microscopy (CLSM), and the oleosins stabi
140 BM adsorption were elucidated using confocal laser scanning microscopy (CLSM), and the structural cha
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
158 ve developed a novel application of confocal laser scanning microscopy coupled to image processing th
164 pseudethanolicus on the anode, and confocal laser scanning microscopy demonstrated a maximum biofilm
167 ing of FM 1-43 fluorescence using two-photon laser scanning microscopy detected glutamate-induced for
169 different microscopy modalities: two-photon laser-scanning microscopy, epifluorescence microscopy, a
170 PROCEDURE requires a basic understanding of laser-scanning microscopy, experience with handling zebr
172 ic electrode thanks to fluorescence confocal laser scanning microscopy (FCLSM) implemented in situ du
175 aptic dendrites, we have combined two-photon laser scanning microscopy, glutamate uncaging, and whole
176 dition, the recent application of two-photon laser scanning microscopy has made it possible to make r
177 ts to couple phosphorescence with two-photon laser scanning microscopy have faced substantial difficu
178 ed reflectance/fluorescence in vivo confocal laser scanning microscopy holds significant promise for
179 tation, deconvolved high-resolution confocal laser scanning microscopy image stacks of dendritic segm
181 Furthermore, in situ real-time confocal laser scanning microscopy imaging reveals the dynamic pr
182 tracked in the intestine through multiphoton laser scanning microscopy in an ex vivo intestinal model
183 63var, were examined by FACS and by confocal laser scanning microscopy in cell culture and in disease
184 9 was demonstrated by confocal fluorescence laser scanning microscopy in stably transfected HEK293 c
187 ed blood cells were measured with two-photon laser-scanning microscopy in individual subsurface micro
190 odies in the scutellum cells, while confocal laser scanning microscopy indicated oil accumulation in
192 ssion scanning electron microscopy, confocal laser scanning microscopy, infrared spectroscopy and Ram
194 mplex three-dimensional (3D) structures from laser scanning microscopy (LSM) images is increasingly n
195 rescence imaging, but existing methods using laser-scanning microscopy (LSM) are severely limited in
205 ombining whole-cell patch-clamp and 2-photon laser scanning microscopy of basket cells (BCs), we foun
210 ane proteins was investigated using confocal laser scanning microscopy of living cells expressing fus
212 ng protein (L-FABP) by real time multiphoton laser scanning microscopy of novel fluorescent VLC-PUFAs
217 In dendrites visualized with two-photon laser scanning microscopy or electron microscopy, most o
218 When viewed through multiple focal planes by laser scanning microscopy, protein A foci are arranged i
219 ere analyzed by epifluorescence and confocal laser scanning microscopy, respectively, using a green f
221 uared dependence of two-photon excitation in laser scanning microscopy restricts excitation to the fo
223 . and Davalos et al. used in vivo two-photon laser-scanning microscopy reveal that the fine branches
226 ng immunofluorescence studies using confocal laser scanning microscopy revealed that many (30-40%) ty
227 ble immunofluorescence labeling and confocal laser scanning microscopy revealed that MMP-26 was coloc
234 fluorescent in situ hybridization, confocal laser scanning microscopy, scanning electron microscopy,
235 Coinfection experiments examined by confocal laser scanning microscopy show that in communal phagosom
238 s titration, immunofluorescence and confocal laser scanning microscopy showed virus replication signi
239 cells, and immunocytochemistry with confocal laser-scanning microscopy showed that these two proteins
241 scence dye adsorption analyzed with confocal laser scanning microscopy that a LPMO (from Neurospora c
245 al tracing procedure that employs two-photon laser scanning microscopy to activate the photoactivatab
246 t immunofluorescence microscopy and confocal laser scanning microscopy to characterize this structure
248 We used a crystal violet assay and confocal laser scanning microscopy to demonstrate Hms-dependent b
249 l arbors, we have used two-photon excitation laser scanning microscopy to directly image action-poten
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
255 eks old) C57BL6/N mice, followed by confocal laser scanning microscopy to verify TSPO protein in neur
258 dendrites in living animals with two-photon laser-scanning microscopy to determine whether these sei
259 mate to mimic synaptic input and two-photon, laser-scanning microscopy to measure calcium levels in d
263 (CLSM) with excitation 442 nm, or two-photon laser scanning microscopy (TPLSM) with excitation 770 nm
266 t molecules can be achieved using two-photon laser-scanning microscopy (TPLSM) hardware, the integrat
267 his protocol describes the use of two-photon laser-scanning microscopy (TPLSM) to study hair regenera
269 O2@PEI MPs on the damage area using confocal laser scanning microscopy under variable cross-flow rate
270 Pepsin transport was observed by confocal laser scanning microscopy using green fluorescent protei
274 f action potentials in STN neurons, 2-photon laser scanning microscopy was used to guide tight-seal w
283 ng real-time in vitro and in vivo two-photon laser scanning microscopy, we have identified the transp
285 ctivation and, using intravital fluorescence laser scanning microscopy, we reported that the potent s
286 itro migration assays and in vivo two-photon laser scanning microscopy, we showed that CTLA-4 increas
290 ):bacteria volume ratio measured by confocal laser scanning microscopy were performed to determine th
291 e colony forming units (CFU/mL) and confocal laser scanning microscopy were performed to evaluate LTP
293 d dead:live volume ratio decided by confocal laser scanning microscopy were used to study the biomass
295 s (Scanning Electron Microscopy and Confocal Laser Scanning Microscopy) were employed to obtain compl
296 defect was also readily apparent by confocal laser scanning microscopy when flow cells were used to g
297 igh spatial and temporal resolution confocal laser scanning microscopy with advanced image-processing
298 nic social defeat stress and used two-photon laser scanning microscopy with glutamate photo-uncaging
299 nation with widefield microscopy or confocal laser scanning microscopy with spectral separation.
300 as studied as a function of time by confocal laser scanning microscopy, with the dissolved fluorescen