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1 in vitro using time-lapse confocal scanning laser microscopy.
2 dynamic light scattering (DLS) and confocal laser microscopy.
3 by scanning electron microscopy and confocal laser microscopy.
4 ometry, as well as fluorescence and confocal laser microscopy.
5 e contrast microscopy, and confocal scanning laser microscopy.
6 telet aggregate) was measured using confocal laser microscopy.
7 e simultaneously evaluated by using confocal laser microscopy.
8 y muscle was determined by confocal scanning laser microscopy.
9 ing the cells in situ with confocal scanning laser microscopy.
10 area was monitored by spinning disc confocal laser microscopy.
11 and quantified by fluorescence and confocal laser microscopy.
12 ling microscopy coupled to confocal scanning laser microscopy.
13 interface by scanning electron and confocal laser microscopy.
14 ysms using high-resolution confocal scanning laser microscopy.
20 detection, but is effective (as are confocal laser microscopy and endocytoscopy) for diagnosis of pol
21 cells and their mitochondria using confocal laser microscopy and in vivo assays of pharmacokinetics,
22 nges on the application of confocal scanning laser microscopy and other advanced microscopic techniqu
23 ponse to hypoxia were determined by confocal laser microscopy and quantitative measurements of NF-kap
24 tum Dot conjugates was monitored by confocal laser microscopy, and colocalization within the endoplas
25 recovery after photobleaching (FRAP) static laser microscopy, and determination of intracellular cal
26 chromoendoscopy with magnification, confocal laser microscopy, and endocytoscopy) allow accurate real
27 aging technologies (cholangioscopy, confocal laser microscopy, and narrow band imaging) have been des
28 -invasively by bright-field and multi-photon laser microscopy, and optical coherence tomography pre-a
29 d fluorescence microscopy, confocal scanning laser microscopy, and transmission and scanning electron
31 ng high-speed videography, confocal scanning laser microscopy (CSLM), and scanning electron microscop
32 hat TLX1 directly binds to CBP, and confocal laser microscopy demonstrated that the two proteins part
33 xpression of the bovine gene was detected in laser microscopy-dissected lymph node lesions from an M.
34 including cell viability studies by confocal laser microscopy, electron microscopy, and measurements
35 sical characteristics that empower nonlinear laser microscopy for biological imaging are described.
36 a novel application of 3D confocal scanning laser microscopy for visualizing the architecture, depos
39 In particular, when combined with two-photon laser microscopy, intravital imaging of surgically expos
44 rcome the limitations of histology, confocal laser microscopy of microdissected whole crypts was used
45 n-responsive PC12 cells, as well as confocal laser microscopy of PC12 immunostained for surface alpha
48 we present a method termed oblique scanning laser microscopy (OSLM) to combine optical coherence tom
50 Using light, electron, and confocal scanning laser microscopy, P. aeruginosa biofilms were visualized
54 der the latter conditions, confocal scanning laser microscopy revealed large clusters of dead P. aeru
56 immunohistofluorescence followed by confocal laser microscopy revealed that subsets of prepubertal LH
57 ventional fluorescence and confocal scanning laser microscopy revealed that the brush border is suppo
58 ne potential as well as microscopy (confocal laser microscopy, scanning and transmission electron mic
59 ectrometry (ATR/FT-IR) and scanning confocal laser microscopy (SCLM) were used to study the role of a
63 sing scanning electron and confocal scanning laser microscopy showed that the presence of PBMCs enhan
65 annexin II antibodies and second by confocal laser microscopy showing co-localization of CEACAM1 with
68 of triple-fluorescence labeling and confocal laser microscopy, terminal fields of the greater superfi
69 these questions, we used two-photon scanning-laser microscopy to examine neutrophil migration in inta
71 ntisera to mGluR1a and mGluR2/3 and confocal laser microscopy to investigate the localization of thes
72 RNA sequencing, flow cytometry, and confocal laser microscopy to map the fibroblast (FB) landscape of
73 ubtilis were analyzed with confocal scanning laser microscopy to reveal a three-dimensional B. subtil
74 e used two-color flow cytometry and confocal laser microscopy to study bacterial uptake by Madin-Darb
77 sing bromouridine incorporation and confocal laser microscopy, we demonstrated that newly synthesized
78 Using an intact cortical mantle and confocal laser microscopy, we examined the spatiotemporal pattern
81 itative biofilm assays and confocal scanning laser microscopy, we observed that glucose inhibited bio
82 ng electron microscopy and confocal scanning laser microscopy were used to further characterize C. du