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1 nitored by either anionic oxonol or cationic carbocyanine are easily established upon addition of val
2 xpression and suggest the potential of using carbocyanines as optical scaffolds for designing biologi
3        Using these approaches, the resulting carbocyanine derivatives of somatostatin and bombesin an
4                                       Unlike carbocyanine derivatives, the receptor binding of fluore
5 ules was investigated using histological and carbocyanine dye (DiI) tracing techniques.
6   Biotinylated dextran amine and fluorescent carbocyanine dye (DiI) were used to examine connections
7 ing intracortical injections of biocytin and carbocyanine dye (DiI).
8  the gerbil cochlea by using the fluorescent carbocyanine dye 1,1'-dioctadecyl-3,3,3',3'-tetramethyli
9 inal cord of a teleost fish, crystals of the carbocyanine dye 1,1'dioctadecyl-3,3,3',3'-tetramethylin
10  fluorescein isothiocyanate (FITC) or to the carbocyanine dye Cy3 and used to label cytokine-responsi
11 enhancement in the fluorescent signal of the carbocyanine dye Cy5 by using an engineered virus as a s
12 d anterogradely by injecting the fluorescent carbocyanine dye DiA into the dorsal motor nucleus in vi
13  of Oddi (SO) preparations in vitro with the carbocyanine dye DiI revealed that duodenal neurons proj
14 ptor neurons were identified by applying the carbocyanine dye DiI to the adventitia of the aortic arc
15  with aldehyde fixatives and crystals of the carbocyanine dye DiI were placed into the CFR.
16 utinin-horseradish peroxidase (WGA-HRP), the carbocyanine dye DiI, and biocytin) to determine the com
17                              The fluorescent carbocyanine dye diI-C(18)-(3) (diI) has previously been
18 the blastomere: in the first, the lipophilic carbocyanine dye DiIC16 was microinjected directly into
19 elphis domestica by tracing projections with carbocyanine dye in fixed postnatal brains between postn
20 e perinatal development of this pathway with carbocyanine dye labeling in embryonic and early postnat
21                                     Multiple carbocyanine dye placements in the cortical convexity re
22 cence imaging, is composed of a heptamethine carbocyanine dye scaffold for signal generation, a 2-deo
23 15-a commercially available, renally cleared carbocyanine dye sensitive to apoptosis, and with an abs
24                             To do so we used carbocyanine dye tracing from the callosum, the internal
25                                              Carbocyanine dye tracing in Pax6 heterozygotes (Pax6(+/-
26                                              Carbocyanine dye tracing of the thalamocortical fiber pa
27 ed a combination of immunohistochemistry and carbocyanine dye tracing to study neurons and their proc
28 x following Lucifer yellow microinjection or carbocyanine dye tracing.
29 fish (Danio rerio) were examined by means of carbocyanine dye tracing.
30       Using DTMRI, immunohistochemistry, and carbocyanine dye tract-tracing studies, we analyzed the
31 tricle of hamsters by using two methods: the carbocyanine dye, 1,1'dioctadecyl-3,3'-tetramethylindoca
32                                   Lipophilic carbocyanine dye, DiI (1, 1'-dioctodecyl-3,3,3',3'-tetra
33 carbocyanine perchlorate (DiI), a lipophilic carbocyanine dye, which incorporates into endothelial ce
34 ated in bromodeoxyuridine or injected with a carbocyanine dye.
35 elation maps in a photosynthetic protein and carbocyanine dye.
36  These data suggest that certain symmetrical carbocyanine dyes can modulate tau aggregation in the sl
37        The present study used the lipophilic carbocyanine dyes DiI and DiD to examine the ipsilateral
38                           By using different carbocyanine dyes injected into either the cingulate cor
39 d, the rate of indicator reactions involving carbocyanine dyes is measured.
40 long-distance axonal connection tracing with carbocyanine dyes revealed that some Gad65-GFP+ subplate
41                                 We have used carbocyanine dyes to fate map the primitive streak in th
42 >20 months) were labelled DiOlistically with carbocyanine dyes to quantify changes in dendritic tree
43   Accordingly, we conjugated fluorescein and carbocyanine dyes to somatostatin and bombesin receptor-
44 ections from multiple targets with different carbocyanine dyes we identified subplate cells with mult
45 r for 24 h, and introduced into reactions of carbocyanine dyes with H(2)O(2) or hypochlorite.
46                        The use of lipophilic carbocyanine dyes, combined with particle-mediated bioli
47 Phaseolus vulgaris leucoagglutinin(PHA-L) or carbocyanine dyes, we characterize the POm thalamocortic
48  penetration characteristics superior to the carbocyanine dyes.
49 eoylphosphatidylcholine, were labeled with a carbocyanine fluorophore.
50  resonance energy transfer acceptor from the carbocyanine fluorophore.
51 trachloro-1,1',3,3'-tetraethylbenzimidazolyl-carbocyanine iodide (JC-1).
52 trachloro-1,1',3, 3'-tetraethylbenzimidazole carbocyanine iodide (JC-1).
53 trachloro 1,1',3,3'-tetraethylbenzimidazolyl-carbocyanine iodide) staining, using live cell confocal
54 nance energy transfer (FRET) between matched carbocyanine lipid analogs in the plasma membrane outer
55 d probe, with the biomembranes delineated by carbocyanine lipid reporters.
56 near hexapeptide GRDSPK with a near-infrared carbocyanine molecular probe (Cypate) yielded a previous
57 a 1,1'-dioctadecyl-3,3,3' 3'-tetramethylindo-carbocyanine perchlorate (Di-1) cell-labeling method.
58 e 1,1'-dioctadecyl-3,3,3',3'-tetramethylindo-carbocyanine perchlorate (DiI).
59 be 1,1'-dioctadecyl-3,3,3'3'-tetramethylindo-carbocyanine perchlorate showed that pCRLPs are taken up
60 yl ester (CFSE), dioctadecyl-tetramethylindo carbocyanine perchlorate, or chloromethyl tetramethylrho
61 turgeon were therefore examined by using the carbocyanine probe DiI, biocytin, and biotinylated dextr