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1 grams to beyond the diffraction limit of the light microscope.
2 ucleotides, well below the resolution of the light microscope.
3  loss was evaluated morphometrically under a light microscope.
4 olarizer in the optical path of a wide-field light microscope.
5 ere drawn using a drawing tube attached to a light microscope.
6 r of metallic particles were counted under a light microscope.
7 typically convolved in an ordinary polarized light microscope.
8  VL were traced in serial sections under the light microscope.
9 rmined by counting foci of infection under a light microscope.
10 or mappings of proteomes under the lens of a light microscope.
11 ctions and inspected optic nervous under the light microscope.
12 i) the integrity of the sarcolemma under the light microscope.
13 oxin released, and the cell morphology under light microscope.
14 endages of mammalian peripheral nerves using light microscopes.
15 ed by the short optical penetration depth of light microscopes.
16 nt from the imaging response of conventional light microscopes.
17 visualization of brain membranes on ordinary light microscopes.
18 Why can we not see nanoscale objects under a light microscope?
19 e instructions on how to build a modular low-light microscope (1-4 d) by coupling two microscope obje
20 luorophores and image them with conventional light microscopes, acquiring videos in which we analyze
21 rbing the mature biofilms was examined under light microscope and confocal laser scanning microscope.
22 say developed in Peru which uses an inverted light microscope and culture in Middlebrook 7H9 broth to
23 g a conventional wide-field epi-fluorescence light microscope and digital imaging with a low noise co
24 ramatically expanded the capabilities of the light microscope and its usefulness in microbiology rese
25 n were easily identified and counted under a light microscope and many more taste buds, patterned in
26 varicosities that could be identified in the light microscope, and each varicosity made a single syna
27 morphisms, large enough to be visible in the light microscope, and the single nucleotide polymorphism
28 sphine, labeled with ReAsH, monitored in the light microscope, and used to trigger the photoconversio
29 ed with standard light microscopes, confocal light microscopes, and electron microscopes.
30  been defined primarily at the resolution of light microscopes, and the relationship between gamma-H2
31 m and spatial resolution at the limit of the light microscope ( approximately 0.2 micro m).
32 ucleolinus, clearly visible with transmitted light microscopes at 10x magnification, is present in ea
33 n and Arp2/3 complex interact, we employed a light microscope-based assay to visualize actin polymeri
34 f the trapezoid body and documented with the light microscope before being studied with serial-sectio
35 rease the spatial resolution of a wide-field light microscope by a factor of two, with greater resolu
36                                              Light microscopes can now capture data in five dimension
37 orms of microimaging performed with standard light microscopes, confocal light microscopes, and elect
38 f MSU crystals under a compensated polarized light microscope (CPLM) in synovial fluid aspirated from
39 -cellular compartments, imaged with standard light microscopes, do not respond to other nucleotides a
40 hotoelastic modulator based polarimeter in a light microscope, enabling the determination of Stokes p
41   We tested our method using both a standard light microscope equipped with visible and near-ultravio
42                                              Light microscope examination of stained sections showed
43                                   The median light microscope grade of SP mRNA expression in the earl
44         The inherent resolution limit of the light microscope has been a limiting factor in investiga
45                                          The light microscope has long been used to document the loca
46                        Anyone who has used a light microscope has wished that its resolution could be
47 erally bellow the 300nm diffraction limit of light microscopes, has limited most imaging studies to e
48                   We dream of a future where light microscopes have new capabilities: language-guided
49 ocalized to myelin by immunofluorescence and light microscope HRP immunocytochemistry.
50      Here, we use an integrated fluorescence light microscope (iFLM) inside of a focused ion beam and
51 hniques can also improve the resolution of a light microscope image beyond what is achievable with wi
52 human chromosomes 6 and 22 and then examined light microscope images of interphase tertiary chromatin
53                                        Thus, light microscope images of tertiary structure cannot dis
54                      In these model systems, light microscope images reveal fibers or beaded fibers a
55  of neighbouring cells) and arrangement from light microscope images.
56           Live-cell liquid crystal polarized light microscope imaging showed nondisjunction was cause
57 eins phakosin, filensin, and vimentin, using light microscope immunocytochemical methodology.
58 tional thin-section electron microscopy, and light microscope immunocytochemistry to examine and char
59 oid was imaged within the chip using a white light microscope in either transmission or, due to the h
60 first using a cryogenically adapted confocal light microscope in which the specimen is coupled to a h
61 omatic cell counting in which a conventional light microscope is equipped with a web camera to obtain
62                                          The light microscope is traditionally an instrument of subst
63  no structural differences identified at the light microscope level in fascicular/non-fascicular tiss
64  neuropil, perikaryon, and dendrites) at the light microscope level using microdensitometry calibrate
65 c space and stria vascularis observed at the light microscope level were unchanged in either Cx null
66 logically identical to coiled bodies (at the light microscope level) formed in such coilin-depleted e
67 vessels in epoxy resin embedded specimens at light microscope level, and that there is an increase in
68                                       At the light microscope level, neurons of the SN pars reticulat
69                                       At the light microscope level, rich plexuses of NMDAR1-positive
70                                       At the light microscope level, we detect no difference between
71 ing identifiable only as small puncta at the light microscope level, we examined the area with electr
72 three-dimensional analysis techniques at the light microscope level, we quantified the number, length
73  and dfw2J mice was indistinguishable at the light microscope level.
74  obvious changes in lens architecture at the light microscope level.
75 le excrescences within these clusters at the light microscope level.
76 no morphological alterations detected at the light microscope level.
77 on on lens architecture was evaluated at the light-microscope level.
78 eptors (GluR5/6/7) in these laminae by using light microscope (LM) and electron microscope (EM) immun
79 tion, when grown in liquid and examined in a light microscope, lonS mutant cells were extremely long
80 hickness is near the resolution limit of the light microscope, making studies relating cortex thickne
81 uch shorter than the resolution limit of the light microscope, making visualization of this gradient
82 s can be created using a camera mounted on a light microscope, or through whole slide image (WSI) gen
83                                        Under light microscope, predominant lamellar patterns were fou
84  Here, we present an integrated cryo-FIB and light microscope setup called the Photon Ion Electron mi
85  glomeruli were observed in these mice under light microscope, severe proteinuria and albuminuria wer
86                                      Using a light microscope severing assay, cofilin's severing acti
87 hnologies plus the plethora of sophisticated light microscope techniques now available make studying
88                                  We report a light microscope that generates images with translationa
89 ng experimental mouse brain sections under a light microscope-that of correctly identifying the disti
90 e growth cones using a new type of polarized light microscope (the Pol-Scope).
91                              In a polarizing light microscope, these structures exhibit a "Maltese-cr
92 nmotile on motility agar plates, but under a light microscope they exhibited random movement and tumb
93                            In the polarizing light microscope, this antiferroelectric phase shows cha
94 mals and the pontine nuclei examined under a light microscope to detect PHA-L-labeled fibers.
95 TV culture system, was examined daily with a light microscope to identify T. vaginalis.
96  FCS was restricted by the resolution of the light microscope to the micrometer scale.
97 semblies in water from the resolution of the light microscope to the nanometer resolution of the elec
98 olecules allows localization and tracking in light microscopes to a precision about an order of magni
99 n defined using the semiautomated, multimode light microscope, together with a fluorescent analogue o
100 bihelical motility as captured by high-speed light microscope videography.
101                           Morphometry in the light microscope was used to measure loss of rod photore
102                   Under examination with the light microscope, we found that both types of receptors
103                                            A light microscope with a micrometer inset into the eyepie
104 cted by eye or a video camera using a simple light microscope with a proper illuminating system.
105 trate the utility of integrating an inverted light microscope with an ambient ionization source, nano

 
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