Exact(4)
The effects of alcohol and PTH on cancellous and cortical bone mass, architecture and turnover were determined by densitometry and histomorphometry.
The effects of TNF alpha and gamma-IFN on sphingomyelin turnover were determined, and the specificity and role of sphingomyelin hydrolysis in HL-60 human promyelocytic leukemia cells with 20% hydrolysis of sphingomyelin at 15 min, 40% hydrolysis at 30-60 min, and return to base line at 2 h.
Biochemical markers of bone turnover were determined in order to evaluate the rate of bone formation and resorption as predictors of periprosthetic bone loss.
Initial velocities for substrate turnover were determined by use of various substrate concentrations (0.1 4 m m) in reaction mixtures (0.8 mL) each containing an aliquot of enzyme (OYE2, final protein concentration 100 μg mL−1) in Tris ⋅HCl buffer solution (50 m m, pH 7.5) with NADH (15 m m).
Similar(56)
Income effects as a function of turnover are determined for each of the value chain steps; in addition to the data on income, this method also provides results on employment effects.
During those 24 hours, protein turnover was determined by means of the [15N]-glycine end-product technique [30].
The amount of substrate turnover was determined calorimetrically by measuring the absorbance which is proportional to IL-1β concentration.
The dissociation constant of MtBPL for its ligands was high relative to EcBirA (Table 4, Figure 4), hence enzyme turnover was determined by steady state kinetics.
Synaptic protein abundance and turnover are determined by de novo protein synthesis and proteasome activity [32]; the latter was previously demonstrated to be essential for Aβ-induced degradation of PSD-95 [21].
The substrate turnover was determined colorimetrically by measuring the absorbance, which was proportional to the MMP-3 concentration.
The amount of substrate turnover was determined colorimetrically by measuring the absorbance, which was proportional to the PG concentration.
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