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The quenching data was quantified by Stern-Volmer equation <img src="http://journals.plos.org/plosone/article/asset?id=info?doi/10.1371/journal.pone.0018333.e002.PNG" class= inline-graphic"/> where Fo and F are the fluorescence intensities in the absence and in the presence of the quencher, respectively.
Data was quantified by least square means and corresponding standard error.
The apoptosis array data was quantified by scanning the membrane on a Biospectrum AC ChemiHR 40 (UVP, Upland, CA, USA) and analysis of the array image file was performed using image analysis software according to the manufacturer's instructions.
First, the correlation between the expression of survival-associated gene groups and survival data was quantified by a multivariate Cox proportional hazards model; then, the protein-protein interaction (PPI) network was used to preselect the gene groups obtained by the first step.
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The data were quantified by measuring the mean activation in two different grids placed over auditory cortex.
Data were quantified by measuring the peak amplitude of average of 15 20 EPSCs for each type of EPSC response.
Data were quantified by comparing peak areas against those of a four-point calibration of DA standards (0, 1, 5 and 10 pg/µl).
The data were quantified by using ΔΔCT = ΔCTESCC-ΔCTNormal.
The data were quantified by using ΔΔCT = ΔCTIEN-ΔCTNormal.
Data were quantified by blinded digital image analysis (NIS-Elements).
The Western-blot data were quantified by densitometry analysis.
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