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1 ulture and caspase 3 activity was quantified fluorometrically.
2 d in situ by confocal microscopy or measured fluorometrically.
3 ition of a molar excess of EDTA and followed fluorometrically.
4 on root shavings and sections were measured fluorometrically.
5 formance liquid chromatography, and detected fluorometrically.
6 lity to adhere to a variety of BRG materials fluorometrically.
7 rbed to tissue culture plastic was evaluated fluorometrically.
8 ed fluorescence that could then be monitored fluorometrically.
9 s state is distinguishable topologically and fluorometrically.
10 Fluorescein was quantified fluorometrically.
11 Tracer was quantified fluorometrically.
12 suited than ASP(+) to study hSERT transport fluorometrically.
13 rypsin-like proteasome activity was measured fluorometrically.
17 embrane content of dipyridamole was measured fluorometrically and correlated with sickling-induced fl
18 ct (stable for at least 7 days) was detected fluorometrically and quantitated by direct integration o
19 of association and dissociation were studied fluorometrically, and the kinetic parameters for the two
20 The product of the reaction was confirmed fluorometrically as the magnesium chelate of the porphyr
21 multilamellar vesicles have been determined fluorometrically at 37 degrees C using approximately 0.3
22 tors with bactericidal activity (as measured fluorometrically by using a metabolizable dye) when stim
26 ions which can determine the biofilm acidity fluorometrically due to carbonate removal in acidic envi
30 Trans-sarcolemmal Ca2+ entries were measured fluorometrically in myocytes during depolarizing steps t
32 NA repair proteins are active and the use of fluorometrically labeled oligonucleotide substrates cont
33 e LightCycler is a rapid thermal cycler that fluorometrically monitors real-time formation of amplico
35 all three oxidation states either determined fluorometrically or calculated using thermodynamic cycle
37 measure of lipid peroxidation) were measured fluorometrically using propidium iodide and chloromethyl
39 utoanalyzer (Roche) was used to measure NADH fluorometrically when rArDH and NAD were added to serum
40 ed MCD assay monitors the production of NADH fluorometrically, which is not ideal for library screeni