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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                                              Sodium fluorescein accumulation/clearance was recorded f
5         An ultrasonically atomized and dried sodium fluorescein aerosol was produced with a concentra
6 ement of a vitally injected fluorescent dye (sodium fluorescein) among individual osteocytic lacunae
7 permeability of the BBB to the small tracers sodium fluorescein and biotin.
8 brain barrier permeability to both exogenous sodium fluorescein and endogenous IgG.
9 increased water content and extravasation of sodium fluorescein and Evans blue dyes 24 hours later.
10 function were carried out using diffusion of sodium fluorescein and transcellular electrical resistan
11  are obtained for acetazolamide, riboflavin, sodium fluorescein, and theophylline in 2-hydroxyethyl m
12 9, -0.68, 2.18, 3.12, and 4.02 for mannitol, sodium fluorescein, budesonide, celecoxib, and rhodamine
13 3-, and 40-fold, respectively, for mannitol, sodium fluorescein, budesonide, celecoxib, and rhodamine
14                                        Using sodium fluorescein extravasation, we found that CD2AP(-/
15 elial barrier as evidenced by Evans blue and sodium fluorescein extravasation.
16                        Permeability (Pdc) to sodium fluorescein (F) is a characteristic of the barrie
17 l analytes, 5-carboxyfluorescein (5-FAM) and sodium fluorescein (FL), were experimentally determined.
18 l pharmacokinetics and brain distribution of sodium fluorescein (FL), which is a small molecule marke
19 rabbits were given a periocular injection of sodium fluorescein (fluorescein, 376 Da) or an episclera
20 diffusion apparatus, and its permeability to sodium fluorescein, fluorescein isothiocyanate (FITC)-co
21 solutes, 3H-mannitol (hydrophilic, neutral), sodium fluorescein (hydrophilic, anionic), and rhodamine
22 , and increased paracellular permeability to sodium fluorescein in airway epithelial monolayers.
23 lators of the uptake of the OATP1B substrate sodium fluorescein, in OATP1B1- or 1B3-transfected Chine
24 ran (mol.wt.=10,000 Da; FITC-dextran-10K) or sodium fluorescein (mol.wt.=376; NaFl) in the absence an
25  CA) containing 0%, 0.25%, 1%, 1.5%, or 2.5% sodium fluorescein (Na-Fl).
26          Calibration solutions consisting of sodium fluorescein (Na-Fl; concentration range, 0.01%-2.
27                                          Two sodium fluorescein (NaF) concentrations, 2.5 mg in 0.1 m
28 ed a unilateral 200-muL injection of 2 mg/mL sodium fluorescein (NaF), 25 mg/mL 40-kDa FITC-D, or 25
29          Functional analysis was done by the sodium fluorescein sequestration assay.
30                   The permeability, P(S), to sodium fluorescein (Stokes-Einstein radius = 0.45 nm) ha
31 rmeability to Oregon green dextran (OGD) and sodium fluorescein was measured.
32                     Microneedles coated with sodium fluorescein were then inserted into rabbit cornea

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