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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                             To do so we used carbocyanine dye tracing from the callosum, the internal
23                                              Carbocyanine dye tracing in Pax6 heterozygotes (Pax6(+/-
24                                              Carbocyanine dye tracing of the thalamocortical fiber pa
25 ed a combination of immunohistochemistry and carbocyanine dye tracing to study neurons and their proc
26 fish (Danio rerio) were examined by means of carbocyanine dye tracing.
27 x following Lucifer yellow microinjection or carbocyanine dye tracing.
28       Using DTMRI, immunohistochemistry, and carbocyanine dye tract-tracing studies, we analyzed the
29 tricle of hamsters by using two methods: the carbocyanine dye, 1,1'dioctadecyl-3,3'-tetramethylindoca
30                                   Lipophilic carbocyanine dye, DiI (1, 1'-dioctodecyl-3,3,3',3'-tetra
31 carbocyanine perchlorate (DiI), a lipophilic carbocyanine dye, which incorporates into endothelial ce
32 elation maps in a photosynthetic protein and carbocyanine dye.
33 ated in bromodeoxyuridine or injected with a carbocyanine dye.
34  These data suggest that certain symmetrical carbocyanine dyes can modulate tau aggregation in the sl
35        The present study used the lipophilic carbocyanine dyes DiI and DiD to examine the ipsilateral
36                           By using different carbocyanine dyes injected into either the cingulate cor
37                                 We have used carbocyanine dyes to fate map the primitive streak in th
38 >20 months) were labelled DiOlistically with carbocyanine dyes to quantify changes in dendritic tree
39   Accordingly, we conjugated fluorescein and carbocyanine dyes to somatostatin and bombesin receptor-
40 ections from multiple targets with different carbocyanine dyes we identified subplate cells with mult
41                        The use of lipophilic carbocyanine dyes, combined with particle-mediated bioli
42 Phaseolus vulgaris leucoagglutinin(PHA-L) or carbocyanine dyes, we characterize the POm thalamocortic
43  penetration characteristics superior to the carbocyanine dyes.
44 eoylphosphatidylcholine, were labeled with a carbocyanine fluorophore.
45  resonance energy transfer acceptor from the carbocyanine fluorophore.
46 trachloro-1,1',3,3'-tetraethylbenzimidazolyl-carbocyanine iodide (JC-1).
47 trachloro-1,1',3, 3'-tetraethylbenzimidazole carbocyanine iodide (JC-1).
48 trachloro 1,1',3,3'-tetraethylbenzimidazolyl-carbocyanine iodide) staining, using live cell confocal
49 nance energy transfer (FRET) between matched carbocyanine lipid analogs in the plasma membrane outer
50 d probe, with the biomembranes delineated by carbocyanine lipid reporters.
51 near hexapeptide GRDSPK with a near-infrared carbocyanine molecular probe (Cypate) yielded a previous
52 a 1,1'-dioctadecyl-3,3,3' 3'-tetramethylindo-carbocyanine perchlorate (Di-1) cell-labeling method.
53 e 1,1'-dioctadecyl-3,3,3',3'-tetramethylindo-carbocyanine perchlorate (DiI).
54 be 1,1'-dioctadecyl-3,3,3'3'-tetramethylindo-carbocyanine perchlorate showed that pCRLPs are taken up
55 yl ester (CFSE), dioctadecyl-tetramethylindo carbocyanine perchlorate, or chloromethyl tetramethylrho
56 turgeon were therefore examined by using the carbocyanine probe DiI, biocytin, and biotinylated dextr

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