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Cell growth was measured by modification of the protocol of LDH Cytotoxicity Assay (WST-8 mix reagents, BioCat, Mountain View, CA, USA).
Pgi activity was measured by modification of a coupled assay [47] and followed the production of NADPH at 340 nM in a quartz microtiter plate using an extinction coefficient of 6.2 mM−1 cm−1.
In this report we identified four forms of genomic instability in Drosophila Slbp mutants: an increase in loss of heterozygosity, localized changes in heterochromatin structure as measured by modification of PEV, tetraploidy, and chromosomal breaks.
Plasma lipids (total cholesterol, triglycerides, and HDLc) were measured by modification of the standard Lipid Research Clinics Protocol with enzymatic reagents for lipid determinations (33).
Plasma lipid concentrations (total cholesterol, triglycerides, and HDL cholesterol [HDLc]) were measured by modification of the standard Lipid Research Clinical Protocol by using enzymatic reagents for lipid determination.
Plasma lipid concentrations (including total cholesterol and triglycerides) were measured by modification of the standard lipid research clinics protocol with enzymatic reagents for lipid determination (Myers et al., 2000).
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As in the pivotal trials of galantamine-IR, the primary endpoints were; change in cognition (measured by a modification of the ADAS-cog, the ADAS-cog11) and global rating (CIBIC-plus) from baseline to completion of the trial.
APOP levels were measured by a modification of the method of Witko-Sarsat et al. [23] and Tiwari et al. [24].
β-Galactosidase activity was measured by a modification of the Miller's method [25].
Insulin was measured by a modification of the assay by Snell et al. [ 56].
Hemoglobin was measured by a modification of the Dacie and Lewis method using a dedicated hemoglobinometer.
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