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Bertaccini, E. J., Trudell, J. R. & Lindahl, E. Normal-mode analysis of the glycine alpha1 receptor by three separate methods.
The effect of population structure on the results was assessed by three separate methods and shown to be minimal (genomic control inflation factor 1.04, see Extended Experimental Procedures).
Chromans displaying aliphatic, aryl, vinyl, or silicon substituents at their benzylic sites (4-position) could be prepared by three separate methods (Scheme 5I III).
ATPgammaS-induced proliferation was demonstrated by three separate methods, detection by scintillation counting of [3H]thymidine incorporation, immunocytochemical detection of 5-bromo-2-deoxyuridine incorporation and direct counting of cell numbers.
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The derivation of the expression for R* presented in this paper is given by two separate methods used to develop the previously published expressions, in order to relate the presented and previously published expression to each other.
ZnO nanorods were grown by two separate methods, namely hydrothermal growth (HTG) and vapor transport condensation (VTC) growth.
Cell numbers (from separate plates) were counted by two separate methods.
Stages of nephropathy were classified by two separate methods.
For the microarray, data were normalized by two separate methods each generating comparable results.
The beta errors calculated by two separate methods confirmed a sufficient power of our analyses to detect significant deviations.
Antioxidant activity was evaluated by five separate methods: free radical scavenging, superoxide anion radical scavenging, reducing power, determination of total phenolic compounds and determination of total flavonoid content.
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