Sentence examples for log percentage from inspiring English sources

Exact(7)

Most simply, this is the change in the log percentage of adults ages 15 to 49 with HIV for a unit change in the independent variable.

The slope of the linear regression from log percentage remaining vs. incubation time relationships (−kel) was used in the conversion to in vitro T1/2, values by in vitro T1/2 = 0.693/ kel.

Two-way ANOVAs with blocking were performed on log percentage of cells in each phase of the cell cycle to assess the significance of the NO effect, cAMP effect, and their interaction (Fig. 4B).

The only variables that remained significant after multivariable modeling were prior use of any cephalosporin (odds ratio [OR] 4.0, 95% confidence interval [CI] 1.2 to 13.6, p = 0.029), and log percentage of residents with a gastrostomy tube (OR 3.9, 95% CI 1.3 to 12.0, p = 0.016).

The graph for Korsmeyer-Peppas model was plotted between log time and log percentage drug remaining and the correlation coefficient was found (r) 0.947 for in vitro drug release, that is, almost unity for lorazepam NP and release exponent value (n) 0.460; therefore the best fit model for nanoparticles was Korsmeyer-Peppas model.

The graph for Korsmeyer-Peppas model was plotted between log time and log percentage drug remaining and the correlation coefficient was found (r) 0.891 for ex vivo drug release, that is, almost unity for lorazepam NP and release exponent value (n) 0.43; therefore the best fit model for nanoparticles was Korsmeyer-Peppas model.

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Similar(5)

Log percentages of naïve and PMA-differentiated U937 cells in each phase of the cell cycle were compared by paired t-tests, unadjusted for multiple comparisons (Fig. 4A).

The relationship between EV protein levels and WML volume (expressed as log transformed percentage of intracranial volume) and BPF (expressed percentage of intracranial volume) on 1.5 T brain MRI was assessed with multivariable linear regression modelling.

To study the drug release kinetics, data obtained from in vitro permeation studies were fitted in various kinetic models: zero order as the cumulative percent of drug permeated versus time, first order as the log cumulative percentage of drug remaining versus time, and Higuchi's model as the cumulative percent drug permeated versus square root of time.

The logarithm of the conditional stability constant (Log K), percentage of fluorophores that correspond to metal binding (% f) were measured by using this equation.

Figure 8 Histograms of natural log of percentage error of thickness measurements determined using cluster analysis (top left), as deviation from expected thickness decay (middle and right hand panels) as a function of distance from source and using field measurements (shown in red).

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