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1 mic capillary diameter: 5.1 +/- 0.1 microns (bright field, 39 capillaries in 10 animals) and 5.1 +/-
2 ization methodology composed of quantitative bright-field absorbance microscopy (QBAM) and deep neura
3 on the human expert analysis of conventional bright-field and birefringence images were performed.
4 res was confirmed by particle size analysis, bright-field and cryogenic transmission electron microsc
5                                              Bright-field and dark-field illumination techniques for
6 havior are identified for further study from bright-field and dark-field light-microscopy modes, resp
7 ce expressing only human HbC were studied by bright-field and differential interference contrast vide
8 alized proteins using immunofluorescence and bright-field and electron microscopy.
9                                              Bright-field and epifluorescence microscopy and CLSM sho
10 opically as follows: (i) in wet mounts (with bright-field and epifluorescence microscopy), (ii) in mo
11  and protobiofilm in the feedwater stream by bright-field and epifluorescence microscopy.
12                           The instrument has bright-field and fluorescence microscopy capabilities in
13                                              Bright-field and fluorescence microscopy provided simila
14  images collected from the same sample using bright-field and fluorescence microscopy.
15 lls were measured blinded to diagnosis using bright-field and fluorescent microscopy.
16 gh-spatial-resolution ex vivo MR imaging and bright-field and immunofluorescent histologic examinatio
17 the ATX1 catalytic domain (atx1setm) through bright-field and long-term time-lapse confocal microscop
18 icrovasculature was imaged non-invasively by bright-field and multi-photon laser microscopy, and opti
19 h complementary studies also performed using bright-field and polarised light microscopy, small-angle
20 as a function of mesogen concentration using bright-field and polarized optical microscopy.
21                                              Bright-field and scanning electron microscopy establishe
22           Photon-upconversion, fluorescence, bright-field, and dark-field microscopy techniques have
23 lt microscope to record large field-of-view, bright-field, and fluorescence images of samples that ar
24  the cost of targeting the N-terminus, while bright field APP C-terminus studies were performed for 1
25 ual label immunofluorescent and single label bright-field approaches.
26                              Validation of a bright-field assay for assessment of HER-2/neu gene ampl
27 in situ hybridization represents a promising bright-field assay for the assessment of HER-2/neu gene
28                                              Bright field (BF) optical microscopy is regarded as a po
29                                          The bright-field (BF) optical microscope is a traditional bi
30               Streamers can be visualized in bright field by phase imaging, and fluorescence-staining
31 ic information theoretic approach to segment bright field defocused images.
32 e in extracting information from microscopic bright field defocused images.
33 lysis of cellular processes with microscopic bright field defocused imaging has the advantage of low
34   We present an integrative method combining bright-field dual-colour chromogenic and silver ISH assa
35 algorithm through simulated and experimental bright-field electron tomography data, showing significa
36                               We used axial (bright-field) electron tomography in the scanning transm
37 e is successfully applied to phase contrast, bright field, fluorescence microscopy and binary images.
38 ns: multimodal FACED imaging flow cytometry (bright-field, fluorescence and second-harmonic generatio
39 irmed using 3 different types of microscopy (bright-field, fluorescence, and electron), 2 additional
40 nsemble learning model to detect whether any bright-field frame showed an embryo before or after onse
41   Streptavidin-Nanogold was used to generate bright-field gene copy signals using GoldEnhance gold-ba
42 th high-angle annular dark-field and annular bright-field (HAADF and ABF) imaging and nanoscale compo
43  whose tumors were resected with traditional bright-field illumination only.
44 ., intrinsic UV fluorescence, birefringence, bright-field image analysis, etc.) is often complicated
45 into their Gram-stained equivalents matching bright-field image contrast.
46                                              Bright-field image retinal maps and fluorescent images w
47 nsic tissue phase map and the standard color bright-field image, familiar to the pathologist.
48                                      However bright field images lack the contrast and nuclei reporti
49                                              Bright field images of the splitting processes at the ju
50                         The combination with bright-field images and monitoring of highly abundant en
51 sistent with those of Bragg fringe widths in bright-field images obtained at lower magnification.
52 tions into images that are equivalent to the bright-field images of histologically stained versions o
53 D archives multi-wavelength fluorescence and bright-field images of tissue microarrays for scoring an
54  and nuclear morphology from fluorescence or bright-field images using the VAMPIRE algorithm.
55 e flow cytometer can extract high-resolution bright-field images with a spatial resolution <700 nm us
56 , and is applicable to both fluorescence and bright-field images, and requires little to no prior kno
57  subdermal blood vessels by using intravital bright-field images, hyperspectral imaging, fluorescence
58                                              Bright field imaging of biological samples stained with
59                      Simultaneous high-speed bright field imaging of cavitation and measurements of t
60                  Here we apply hyperspectral bright field imaging to collect computed tomographic ima
61 ble automated identification of particles by bright field imaging, followed by classification by SHG.
62 entification of the head of the animal under bright field imaging.
63           Here, we report a time-lapse-based bright-field imaging analysis system that allows us to i
64 ply, as the only experimental step comprises bright-field imaging of culture-media samples followed b
65   Specifically, we performed high-throughput bright-field imaging of numerous drug-treated and -untre
66                    A combination of FLIM and bright-field imaging pinpoints limitations in catalyst s
67 mples in the presence of aberrations using a bright-field imaging setup operating with a source of sp
68 itative mathematical analysis of the dynamic bright-field imaging shows that defect clusters preferen
69                                          Via bright-field imaging with an ultrafast electron microsco
70 lular drug responses only by high-throughput bright-field imaging with the aid of machine learning al
71 copy (e.g., multicolor fluorescence imaging, bright-field imaging), cell focusing, cell sorting, and
72 rtilization wild-type embryos, and uses only bright-field imaging, circumventing requirement for anes
73 , using fluorescence-activated cell sorting, bright-field imaging, immunofluorescence, and RNA analys
74 of the immobilized cell were monitored using bright-field imaging.
75 ted in rat-tendon cryosections using SHG and bright-field imaging.
76 mple experimental setup, based on a standard bright-field inverted microscope (no fluorescence requir
77 nt also altered the pattern of mu-ORi at the bright-field light microscopic level.
78 n and the concomitant aggregation of LDLs by bright-field light microscopy and cryogenic transmission
79 e molecular binding events under an ordinary bright-field microscope and serve as a diffraction grati
80        Its system is identical to a standard bright-field microscope with a lamp and a camera - no la
81            This technique uses an unmodified bright-field microscope, an array of microlenses, and a
82 e parameters per sample, using a traditional bright-field microscope-based flow assay allows only one
83 n can expand the functionality of commercial bright field microscopes, provide easy field detection o
84 les, by taking advantage of data analysis of bright field microscopy images.
85 roduce the XFEL DFXM setup with simultaneous bright field microscopy to probe density changes within
86  severe to mild lymphocytic infiltrations by bright field microscopy were examined in parallel with i
87 ion, (e) distorted posterior suture lines by bright field microscopy, and (f) development of a mild a
88 l immunofluorescent microscopy, single label bright field microscopy, and electron microscopy (EM).
89                                           In bright field microscopy, each cell contains a bright yel
90 small angle neutron scattering, rheology and bright field microscopy, we identify the coexistence of
91  Cell growth and viability were evaluated by bright field microscopy.
92  traps and analyzed for > 30 mold taxa using bright field microscopy.
93                  Diameter was observed using bright field microscopy.
94        For phenotypic analysis, we performed bright-field microscopy and Aliziran Red S staining to a
95  Schaub and colleagues combined quantitative bright-field microscopy and artificial intelligence (dee
96 -positive cells were counted by conventional bright-field microscopy and confirmed by confocal micros
97     This method is based on fluorescence and bright-field microscopy and on a custom MATLAB program t
98  methods to trace impregnated dendrites from bright-field microscopy images that enabled accurate 3-d
99                                      In-line bright-field microscopy images were captured for each sa
100                                     Although bright-field microscopy is a simple and robust method of
101 is using clinical histopathology is based on bright-field microscopy of thinly sliced tissue specimen
102                                              Bright-field microscopy provides a blurred visualization
103                                 Conventional bright-field microscopy provides contrast based on atten
104 om an aqueous stream into plugs, (iii) using bright-field microscopy to detect the formation of a fib
105 ective under different recording conditions (bright-field microscopy with simultaneous patch-clamp re
106 bserving wound closure with fluorescence and bright-field microscopy, (2) histology to quantify infla
107 s, which is currently performed manually via bright-field microscopy, and toward the development of a
108                               Gram staining, bright-field microscopy, hematoxylin and eosin, periodic
109 vide a means of locating single molecules by bright-field microscopy, prior to single-molecule detect
110 he sections were imaged with fluorescence or bright-field microscopy.
111 f chromosomal translocations by conventional bright-field microscopy.
112  NT-proBNP immunocomplexes and recorded with bright-field microscopy.
113 ycine were counted in a masked fashion under bright-field microscopy.
114 ification of subcellular debris particles in bright-field-microscopy images.
115 llows switching between epifluorescence/TIRF/bright field modes without adjustments or objective repl
116                    We assembled a dataset of bright-field movie frames from 8-cell-stage embryos, sid
117 with neural networks trained on conventional bright-field or fluorescence microscopy images.
118  sample debris, previously not possible with bright-field or scanning ion imaging.
119 a task that has not been routine with either bright-field or TOF-SIMS.
120 g a diverse range of microscopic techniques (bright field, phase contrast, differential interference
121 ening drug discovery platforms, for example, bright-field, phase contrast, and fluorescence microscop
122 the contributions of light microscopy, i.e., bright-field, polarization, differential interference co
123  introduce quantitative image restoration in bright field (QRBF), a digital image processing method t
124 d magnetite by employing a strain-sensitive, bright-field scanning transmission electron microscopy a
125 ls and large organelles using tilt-corrected bright-field scanning transmission electron microscopy c
126 can be rapidly obtained using tilt-corrected bright-field scanning transmission electron microscopy d
127                           The combination of bright-field, scanning ion, and fluorescence microscopy
128 y imaging of the anion sublattice in annular bright-field STEM (ABF-STEM) images.
129 improvement of SIM, compared to conventional bright field system is a factor of 2.
130 animals studied using vertical illumination (bright-field) techniques.
131      The particles appear core-shell like in bright field TEM images.
132                            The images can be bright fields that display position-dependent quantum no
133                                      We used bright-field, time-lapse video, cross-polarized, phase-c
134 ively, is discussed as well as comparison to bright field transmission electron microscopy imaging th
135 rganization of the crystals were examined by bright-field transmission electron microscopy and electr
136                              High-resolution bright-field transmission electron microscopy and select
137 a much higher contrast than that achieved in bright-field transmission electron microscopy imaging of
138 icroscope, allowing the analysis with simple bright field visualization.

 
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