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1 ar fluid 15 minutes after instillation of 1% sodium fluorescein.
2 y bona fide canaliculi, such as sequestering sodium fluorescein.
3 zed piglets using intracarotid injections of sodium fluorescein.
4 plasminogen activator (50 ug in 0.1 mL) with sodium fluorescein (10 ug in 0.1 mL) as an optical label
5 phy (UWFFA), a regimen of half-dose (250 mg) sodium fluorescein (10%) was adopted instead of the full
6 on microscopy to monitor BBB permeability of sodium fluorescein (376 Da), Alexa Fluor (643 Da), and f
7                                              Sodium fluorescein accumulation/clearance was recorded f
8         An ultrasonically atomized and dried sodium fluorescein aerosol was produced with a concentra
9 ement of a vitally injected fluorescent dye (sodium fluorescein) among individual osteocytic lacunae
10 permeability of the BBB to the small tracers sodium fluorescein and biotin.
11 brain barrier permeability to both exogenous sodium fluorescein and endogenous IgG.
12 increased water content and extravasation of sodium fluorescein and Evans blue dyes 24 hours later.
13 (AAV) yields following exposure to 0.1 mg/mL sodium fluorescein and its effects on retinal progenitor
14 function were carried out using diffusion of sodium fluorescein and transcellular electrical resistan
15                           By screening eGFP, sodium fluorescein, and mTagBFP2 for their compatibility
16  are obtained for acetazolamide, riboflavin, sodium fluorescein, and theophylline in 2-hydroxyethyl m
17 (eff) increased by ~ 10% for a small solute, sodium fluorescein, and ~ 120% for larger solutes, BSA a
18 max,MRP2 ), derived from kinetic modeling of sodium fluorescein biliary excretion, showed a significa
19 9, -0.68, 2.18, 3.12, and 4.02 for mannitol, sodium fluorescein, budesonide, celecoxib, and rhodamine
20 3-, and 40-fold, respectively, for mannitol, sodium fluorescein, budesonide, celecoxib, and rhodamine
21                                        Using sodium fluorescein extravasation, we found that CD2AP(-/
22 elial barrier as evidenced by Evans blue and sodium fluorescein extravasation.
23                        Permeability (Pdc) to sodium fluorescein (F) is a characteristic of the barrie
24 l analytes, 5-carboxyfluorescein (5-FAM) and sodium fluorescein (FL), were experimentally determined.
25 l pharmacokinetics and brain distribution of sodium fluorescein (FL), which is a small molecule marke
26 rabbits were given a periocular injection of sodium fluorescein (fluorescein, 376 Da) or an episclera
27 diffusion apparatus, and its permeability to sodium fluorescein, fluorescein isothiocyanate (FITC)-co
28 essed air for 10 s and then dyed with 100-uM sodium fluorescein for 10 s.
29 solutes, 3H-mannitol (hydrophilic, neutral), sodium fluorescein (hydrophilic, anionic), and rhodamine
30 , and increased paracellular permeability to sodium fluorescein in airway epithelial monolayers.
31 hat AAV titers are not affected by 0.1 mg/mL sodium fluorescein in vitro, and viability assays sugges
32 lators of the uptake of the OATP1B substrate sodium fluorescein, in OATP1B1- or 1B3-transfected Chine
33                      These data suggest that sodium fluorescein may be an appropriate means of tracki
34 ran (mol.wt.=10,000 Da; FITC-dextran-10K) or sodium fluorescein (mol.wt.=376; NaFl) in the absence an
35  CA) containing 0%, 0.25%, 1%, 1.5%, or 2.5% sodium fluorescein (Na-Fl).
36          Calibration solutions consisting of sodium fluorescein (Na-Fl; concentration range, 0.01%-2.
37                                          Two sodium fluorescein (NaF) concentrations, 2.5 mg in 0.1 m
38 ed a unilateral 200-muL injection of 2 mg/mL sodium fluorescein (NaF), 25 mg/mL 40-kDa FITC-D, or 25
39 lity to the low molecular weight fluorophore sodium fluorescein (NaFl), whereas diet-induced insulin
40     AAV yields are not affected by 0.1 mg/mL sodium fluorescein, nor is RPC viability.
41            The biliary excretion kinetics of sodium fluorescein reflects MRP2-mediated transport acti
42 ransfer of the water-soluble fluorescent dye sodium fluorescein salt and the drug doxycycline.
43          Functional analysis was done by the sodium fluorescein sequestration assay.
44                   The permeability, P(S), to sodium fluorescein (Stokes-Einstein radius = 0.45 nm) ha
45 rmeability to Oregon green dextran (OGD) and sodium fluorescein was measured.
46                     Microneedles coated with sodium fluorescein were then inserted into rabbit cornea