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1 llary density (FCD), plasma was labeled with fluorescein-isothiocyanate-dextran.
2                   Diffusion coefficients for fluorescein isothiocyanate-dextrans (10-2000 kDa) determ
3 ng transepithelial resistance and passage to fluorescein isothiocyanate-dextran 4 kDa (FD4).
4  electrical resistance, paracellular flux of fluorescein isothiocyanate-dextran 4 kDa, and mRNA expre
5 ectrical resistance and paracellular flux of fluorescein isothiocyanate-dextran (4 kDa) together with
6  TJ barrier permeability was evaluated using fluorescein isothiocyanate-dextran (4 kDa).
7 ferrin in perinuclear endosomes but not with fluorescein isothiocyanate-dextran, a marker for fluid-p
8 sed intestinal permeability, as indicated by fluorescein isothiocyanate-dextran absorption and serum
9  examined by measuring permeability to 4-kDa fluorescein isothiocyanate-dextran and by examining chan
10 e fusion (PL-fusion) was quantified by using fluorescein isothiocyanate-dextran and phase and fluores
11 istance), reduced paracellular permeability (fluorescein isothiocyanate-dextran), and prevented vascu
12 e demonstrated decreased transferrin uptake, fluorescein isothiocyanate-dextran, and horseradish pero
13                                              Fluorescein isothiocyanate-dextran angiography, rat anti
14     Microvascular blood flow was assessed by fluorescein isothiocyanate/dextran angiography, with flu
15  HMGB1 levels, ileal mucosal permeability to fluorescein isothiocyanate dextran, bacterial counts in
16               The pH-sensing layer comprised fluorescein isothiocyanate-dextran conjugate immobilized
17                    Our results indicate that fluorescein isothiocyanate-dextran enters directly into
18 thylene glycol) (PEG) hydrogel incorporating fluorescein isothiocyanate dextran (FITC-dextran) and te
19 d with water-soluble fluorescent dye (42-kDa fluorescein isothiocyanate dextran (FITC-dextran)), to m
20 orated the fluorescent fluid- phase markers, fluorescein isothiocyanate-dextran (FITC-dex) and Lucife
21 plying a flow cytometric technique to detect fluorescein-isothiocyanate-dextran (FITC-dextran) in aci
22 ithelial electrical resistance and increased fluorescein isothiocyanate-dextran flux (P < .05).
23 th mGluR antagonists significantly decreased fluorescein isothiocyanate-dextran flux across the blood
24 acellular permeability was measured by using fluorescein isothiocyanate-dextran flux.
25 ng transepithelial electrical resistance and fluorescein isothiocyanate-dextran flux.
26  mice (105.9 +/- 13.4 vs 59.6 +/- 10.1 mg/mL fluorescein isothiocyanate-dextran flux; P < .05) and im
27 stance and also reduced paracellular flux of fluorescein isothiocyanate-dextran following a calcium s
28                       The SCs of a series of fluorescein isothiocyanate dextrans (four sizes, Mr 16,0
29 sing 376-Da carboxyfluorescein but not 4-kDa fluorescein isothiocyanate-dextran from preloaded liposo
30 ew vessels: high-resolution angiography with fluorescein isothiocyanate-dextran; immunohistochemistry
31 donor cells, previously labeled by injecting fluorescein isothiocyanate-dextran into the zygote, were
32                      Mucosal permeability to fluorescein isothiocyanate dextran (molecular weight 400
33 easuring the mucosal-to-serosal clearance of fluorescein isothiocyanate dextran (molecular weight = 4
34 ophores, calcein (molecular weight: 622) and fluorescein isothiocyanate-dextran (molecular weight: 71
35 d that contraction also stimulates uptake of fluorescein isothiocyanate-dextran molecules from the me
36 ns correlated with increased permeability to fluorescein isothiocyanate-dextran molecules.
37 l endothelial cells in culture to a group of fluorescein isothiocyanate dextrans of different molecul
38    Paracellular permeability was assessed by fluorescein isothiocyanate-dextran passage in both lines
39 ectric cell-substrate impedance sensing, and fluorescein isothiocyanate dextran permeability were ass
40 elial resistance, short circuit current, and fluorescein isothiocyanate-dextran permeability is no di
41 s assessed by apical-to-basal transport of a fluorescein isothiocyanate dextran probe (FD-4).
42 ty at 12 and 24 hours (as assessed by 70-kDa fluorescein isothiocyanate-dextran transmucosal flux); i
43  Intestinal permeability was investigated by fluorescein isothiocyanate-dextran uptake assay, quantit
44 theter was placed and, 30 mins before death, fluorescein isothiocyanate Dextran was injected.
45 This fluorescence appeared more intense when fluorescein isothiocyanate-dextran was used.
46 fined as the extent of vascular filling with fluorescein isothiocyanate/dextran) was significantly de