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1 h a large red-shift as compared to that of 2-phenylindole.
2 n the acidocalcisomes using 4',6-diamidino-2-phenylindole.
3 dispersed and treated with 4',6-diamidino-2-phenylindole.
4 tion of nuclei stained with 4,6'-diamidino-2-phenylindole.
5 in the dense granules using 4',6-diamidino-2-phenylindole and by its release together with pyrophosph
6 -alpha-tubulin antibody and 4',6-diamidino-2-phenylindole and flow cytometric analysis of Ser(10) pho
7 e sulfonic acid), the DNA stain 4',6-diamino-phenylindole, and confocal laser scanning microscopy.
8 the channel by diminazene, 4',6-diamidino-2-phenylindole, and pentamidine, examine several biophysic
9 dehyde, MDA colorimetrically with N-methyl-2-phenylindole, and taurine by high-performance liquid chr
11 potency/efficacy of GAT211, the prototypic 2-phenylindole-based cannabinoid type-1 receptor (CB1R) ag
12 ic substitution reaction in which N-methyl-2-phenylindole behaves as a good leaving group in the C(sp
18 estigation clearly show that 4,6-diamidino-2 phenylindole (DAPI) is superior to both of these drugs a
19 e ICD of minor-groove-bound 4',6-diamidino-2-phenylindole (DAPI) originates from an intricate interpl
20 (TUNEL) in conjunction with 4'6'-diamidino-2-phenylindole (DAPI) staining and by fluorescence stainin
21 nance imaging, mCherry with 4',6-diamidino-2-phenylindole (DAPI) staining and green fluorescent prote
25 ing compounds, netropsin and 4,6-diamidino-2-phenylindole (DAPI), and a DNA hairpin having the sequen
26 , and staining of cells with 4,6-diamidino-2-phenylindole (DAPI), and the polyP-binding domain of Esc
27 t), connective tissue (CT), 4',6-diamidino-2-phenylindole (DAPI), human gingival epithelial cells (HG
28 hal distending toxin (Cdt), 4',6-diamidino-2-phenylindole (DAPI), human gingival epithelial cells (HG
29 fter labeling in vitro with 4',6-diamidino-2-phenylindole (DAPI), intracellular injection with Lucife
31 y do not stain equally with 4',6-diamidino-2-phenylindole (DAPI), suggesting that byr4 is required fo
32 ited by 5PTB, netropsin and 4',6-diamidino-2-phenylindole (DAPI), two AT-specific minor groove bindin
33 BU), fluorescein (FLU), and 4',6-diamidino-2-phenylindole (DAPI), was achieved with this self-powered
34 es in the fluorescence of a 4',6-diamidino-2-phenylindole (DAPI)-dsDNA complex upon RecA protein bind
36 s of foci have been defined: 4,6-diamidino-2-phenylindole (DAPI)-sensitive foci that are bound to DNA
39 ed on multiphoton imaging of 4',6'-diamino-2-phenylindole (DAPI)-stained tissue to quantify neuron lo
47 ng intact chloroplasts with 4',6-diamidino-2-phenylindole (DAPI); staining at the single-molecule lev
48 bes, single-copy genes, and 4'-6-diamidino-2-phenylindole (DAPI-) and G-banded chromosomes and report
49 amicidin, and a DNA-ligand (4',6-diamidino-2-phenylindole, DAPI) system in this work highlight the ea
50 taining of cellular DNA with 4,6-diamidino-2-phenylindole demonstrated TNF-alpha-induced apoptosis in
52 ined with the nuclear stain 4',6-diamidine-2-phenylindole dihydrochloride (DAPI) and imaged with a fl
53 ent reagents SYPRO Ruby and 4',6-diamidino-2-phenylindole dihydrochloride (DAPI), to detect proteinac
54 g of keratocyte nuclei with 4',6-diaminido-2-phenylindole dihydrochloride (Molecular Probes, Carlsban
55 Apoptosis was evaluated by 4',6-diamidino-2-phenylindole dihydrochloride and terminal deoxynucleotid
57 r apoptosis by using DAPI (4',6-diamindino-2-phenylindole dihydrochloride) and Annexin V staining, al
58 ecules per CPMV using DAPI (4',6-diamidino-2-phenylindole dihydrochloride), propidium iodide (3,8-dia
59 Microbes were enumerated by 4',6-diamidino-2-phenylindole, dihydrochloride (DAPI) staining, and phago
61 ed, using Wright-Giemsa and 4',6-diamidine-2-phenylindole-dihydrochloride staining, that As(2)O(3) bl
62 crotubule immunostaining and 4,6-diamidino-2-phenylindole DNA staining demonstrated that the FTI-2153
63 th markers for nuclei (DAPI; 4',6'-diamino-2-phenylindole), endothelial cells (isolectin IB4), microg
64 as observed with the use of 4,6-diamidino-2-phenylindole-fluorescent staining, and by decreases in t
65 ls were later stained with 4', 6-diamidino-2-phenylindole for simultaneous DNA analysis and immunophe
69 It involves segmenting the 4',6-diamidino-2-phenylindole-labelled image into cells and determining t
70 localization correlated with 4,6-diamidino-2-phenylindole light regions and is excluded from metaphas
72 high levels accumulated in 4',6-diamidino-2-phenylindole-negative zones containing euchromatic (tran
74 the nucleus-specific stain 4',6-diamidino-2-phenylindole, nuclear fragmentation was observed in a ti
75 bes, in addition to inverted 4,6-diamidino-2-phenylindole or conventional G-banding analysis, provide
76 lized red blood cells with 4',6'-diamidino-2-phenylindole or YOYO-1, a sensitive nucleic acid stain,
77 eric DNA binders Hoechst 33258, 4'-diamino-2-phenylindole, pentamidine, berenil, spermine, and spermi
78 that colocalize with DAPI (4',6'-diamidino-2-phenylindole)-positive material and follow DNA movement
80 sis verifies that the FD of 4',6-diamidino-2-phenylindole-stained nuclear structures does not change
83 the acidocalcisomes by using 4',6'-diamino-2-phenylindole staining and identified by using 31P NMR an
86 ed based on the patterns of 4',6-diamidino-2-phenylindole staining of the Nipponbare pachytene chromo
87 e actin cytoskeleton, DNA (4', 6-diamidino-2-phenylindole staining), and calcofluor-staining moieties
88 ation by acridine orange and 4'6-diamidino-2-phenylindole staining, and (3) agarose gel electrophores
90 nick-end labeling (TUNEL), 4',6-diamidino-2-phenylindole staining, and immunohistochemistry for sing
91 clear morphology detected by 4,6-diamidino-2-phenylindole staining, DNA fragmentation assay, and term
92 changes, as demonstrated by 4',6-diamidino-2-phenylindole staining, lack of either DNA laddering, cas
94 the contractile vacuole by 4',6-diamidino-2-phenylindole staining, suggesting, with the immunochemic
100 of cellular DNA, and DAPI (4',6-diamidino-2-phenylindole) staining revealed condensation and fragmen
102 U) pulse-labeling and DAPI (4',6-diamidino-2-phenylindole) staining, which precisely establishes the
103 lls as demonstrated by DAPI (4', 6-diamino-2-phenylindole), TUNEL (terminal deoxynucleotidyl transfer