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1 tion was analyzed by confocal microscopy and spectrofluorometry.
2 lular Ca(2+) concentrations were measured by spectrofluorometry.
3 ve dye fura-2 to monitor [Ca(2+)](i) by bulk spectrofluorometry.
4 goxigenin nick-end labeling and quantitative spectrofluorometry.
5 ifts of NADH were measured by rapid scanning spectrofluorometry.
6 (pyranine), in combination with stopped-flow spectrofluorometry.
7 sample-tissue DNA content was measured with spectrofluorometry.
8 nd displacement were studied by stopped-flow spectrofluorometry.
9 nd by nuclear magnetic resonance spectra and spectrofluorometry.
10 ntent of each dextran type was determined by spectrofluorometry.
13 ted of TL were applied over the corneas, and spectrofluorometry and fluorescent stereomicroscopy were
15 otein (RBP) and transthyretin was studied by spectrofluorometry and size-exclusion chromatography.
16 actility were measured using dual excitation spectrofluorometry and video-edge detection system (Iono
18 ia quartz crystal microbalance, sand column, spectrofluorometry, and dynamic light scattering techniq
19 on and permeability by protease sensitivity, spectrofluorometry, and negative staining electron micro
20 o quantitate intracellular Ca2+ ([Ca2+]i) by spectrofluorometry, and uPAR was aggregated by Ab cross-
21 tracellular Ca2+ concentrations ([Ca2+]i) by spectrofluorometry, and uPAR was aggregated by mAb cross
23 alogue with membrane vesicles was studied by spectrofluorometry, Congo Red binding, and electron micr
24 ellular calcium handling, measured by Rhod 2 spectrofluorometry, demonstrated lower diastolic calcium
25 uorescein fluorescence by flow cytometry and spectrofluorometry, electrophoretic mobility shift assay
26 xXPA for ds undamaged DNA determined in our spectrofluorometry experiments was up to 3 orders of mag
27 the oxidation of 2',7'-dichlorofluorescin by spectrofluorometry, flow cytometry, and confocal microsc
28 (BSA) was investigated by spectrophotometry, spectrofluorometry, FT-IR and circular dichroism (CD) te
29 (Fl-) PEDF and ovalbumin were determined by spectrofluorometry, laser scanning, immunoblotting, epif
30 Rapid mix/chemical quench and stopped-flow spectrofluorometry measurements were carried out with Rh
33 plasts was directly measured by stopped-flow spectrofluorometry using membrane vesicles loaded with t
34 plasts was directly measured by stopped-flow spectrofluorometry using membrane vesicles loaded with t
35 plasts was directly measured by stopped-flow spectrofluorometry using membranes loaded with the Cu(2+
36 acellular calcium [Ca2+]i measured by rhod-2 spectrofluorometry was increased in dopamine-reperfused
38 ermal titration calorimetry and stopped-flow spectrofluorometry, we directly examined metal binding t
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