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1 terns were linked in real-time to high power phase contrast microscopy.
2  imaging techniques such as fluorescence and phase contrast microscopy.
3 the IAS in the basal state was determined by phase contrast microscopy.
4 es were morphologically indistinguishable by phase contrast microscopy.
5 irochete morphogroup were also identified by phase contrast microscopy.
6 The spirochete morphogroup was identified by phase contrast microscopy.
7 grity of the advanced 3D-ET was assessed via phase contrast microscopy.
8 ten requires the use of transmitted light or phase-contrast microscopy.
9 py and the motion of the underlying cells by phase-contrast microscopy.
10  NK cells and FLS were studied by time-lapse phase-contrast microscopy.
11  by trypan blue staining, cell counting, and phase-contrast microscopy.
12   Cell morphology was documented by inverted phase-contrast microscopy.
13                On-going observations were by phase-contrast microscopy.
14 ofilm formed by the wild type over 8 h using phase-contrast microscopy.
15                    Observations were made by phase-contrast microscopy.
16 e ankyrin-3-positive vesicles appear dark on phase-contrast microscopy.
17 moval at 6 weeks by culture, DNA probes, and phase-contrast microscopy.
18          Cell shape change was determined by phase-contrast microscopy.
19 t scattering, as well as by fluorescence and phase-contrast microscopy.
20 ollows: (1) by the morphologic appearance on phase-contrast microscopy; (2) by the levels of aldehyde
21 fixed for study by disseminated interference phase contrast microscopy and electron microscopy.
22 e hydrogel morphology is characterized using phase contrast microscopy and is related to the hydrogel
23 ic acid and Ca(2+) (CaDPA) were monitored by phase contrast microscopy and Raman spectroscopy, respec
24 r matrix protein type-I collagen by means of phase contrast microscopy and rotating disk rheometry.
25       Evaluations were performed by means of phase-contrast microscopy and [3H]thymidine uptake assay
26 logy and cell-cell networks were assessed by phase-contrast microscopy and a cell viability assay, re
27            Neurite outgrowth was assessed by phase-contrast microscopy and calcein AM staining and qu
28 erior vitreous detachment were examined with phase-contrast microscopy and confocal microscopy after
29                    Apoptosis was measured by phase-contrast microscopy and flow cytometry.
30 e periods on the order of weeks by utilizing phase-contrast microscopy and show that these cells acqu
31 ellar motion, visualizing the cell bodies by phase-contrast microscopy and the flagellar filaments by
32                             Time-lapse video phase-contrast microscopy and time-lapse digital confoca
33                                              Phase-contrast microscopy and Wright staining showed mor
34          The experiments were videorecorded (phase-contrast microscopy), and PMN adhesion/migration w
35 as observed by scanning electron microscopy, phase contrast microscopy, and confocal scanning laser m
36 ology that combines fluorescence microscopy, phase contrast microscopy, and laser tweezers Raman spec
37 opy with simultaneous patch-clamp recording, phase contrast microscopy, and traction force microscopy
38 as observed by scanning electron microscopy, phase-contrast microscopy, and fluorescence microscopy.
39 -), as demonstrated by annexin V positivity, phase-contrast microscopy, and in selected cases 4',6'-d
40 fewer attached bacteria, as determined using phase-contrast microscopy, and less biofilm (P < 0.0001)
41 rulent NAP1 strain using optical density and phase-contrast microscopy assays.
42                                              Phase contrast microscopy assesses changes in refractili
43 n vitro on purified type 1 collagen by video phase-contrast microscopy at 22 degrees C.
44                                              Phase-contrast microscopy consistently identified a crea
45                                              Phase contrast microscopy coupled to digital image proce
46                                              Phase-contrast microscopy demonstrated that freshly isol
47 rganoids, pixel-by-pixel, in brightfield and phase-contrast microscopy experiments.
48  specimens were processed as flat mounts for phase-contrast microscopy followed by immunolabeling for
49                                              Phase contrast microscopy has played a central role in t
50 sent a new approach for retrieving halo-free phase contrast microscopy (hfPC) images by upgrading the
51 d measurement of VM structural features from phase-contrast microscopy images.
52 ect diatoms on two-channel (fluorescence and phase-contrast) microscopy images by predicting bounding
53 pseudoholes (14 eyes) using interference and phase-contrast microscopy, immunocytochemistry, and tran
54 wth factor-beta1 (TGF-beta1) was analyzed by phase contrast microscopy, immunofluorescence, quantitat
55 at combines the automated image analysis for phase-contrast microscopy movies with an easy-to-use int
56                                              Phase contrast microscopy of vernix showed multiple cell
57 pted to use multi-trap Raman spectroscopy or phase-contrast microscopy of spores adhered on a cover s
58                                        Under phase contrast microscopy, PDL cells in non-mineralizing
59 d of the rapid drop in spore refractility by phase contrast microscopy, precisely corresponds to the
60 present a methodology that combines external phase contrast microscopy, Raman spectroscopy, and optic
61                             Fluorescence and phase contrast microscopy revealed characteristic apopto
62                                              Phase contrast microscopy revealed identical sperm defec
63                               Examination by phase-contrast microscopy revealed the lytic death of ma
64 ic and phenotypic changes were determined by phase-contrast microscopy, sensitivity to the oxidant te
65 of 3 s data segments of light intensity from phase-contrast microscopy showed no significant delay be
66 e-contrast microscopy, structural details in phase-contrast microscopy, structural details in direct
67  of pressure-sensitive, refractile bodies in phase-contrast microscopy, structural details in phase-c
68                                              Phase-contrast microscopy studies of the entire GBM syst
69  computational imaging systems: differential phase-contrast microscopy, three-dimensional structured
70 l signal, using a custom-made condenser-free phase contrast microscopy to capture the phase change of
71 nveloping membranous structure identified on phase-contrast microscopy to show positive stain results
72 ation and vegetative outgrowth by time lapse phase contrast microscopy, transmission electron microsc
73                                              Phase-contrast microscopy was used to follow biofilm dev
74 ing state-of-the-art integrated differential phase contrast microscopy, we decipher the buckled tetra
75 ifferential interference contrast (DIC), and phase contrast microscopy, we tracked the movement of MT
76                                        Using phase-contrast microscopy, we found that a crc mutant on