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We have described and evaluated four statistical models (unadjusted, standardized, adjusted, and two-stage) commonly used to assess the effects of lipophilic environmental contaminants on human health when relying on blood specimens for quantifying toxicant concentrations.
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The miniature specimen test technique has been extensively studied for quantifying the properties of bulk materials with greatly reduced volume recently.
For example, an analytical method has been reported for quantifying dl-glufosinate enantiomers in biological specimens using precolumn derivatization and reversed-phase HPLC with a fluorescence detector.
After nucleotide sequencing of all PCR-positive specimens, we developed a specific real-time RT-PCR for quantifying viruses from Brazil (Table 2).
For the PECT system which uses detection coils, a no-reference-needed and more efficient method, for quantifying the wall thickness of the ferromagnetic specimen, should be found.
Two new test methods have been developed for quantifying the resistance to axial cracking of thin-walled tubular specimens.
We developed an efficient, inexpensive assay suitable for quantifying CRP across the physiological range using any blood specimen type.
For quantifying the FCG acceleration, the hydrogen trapping and diffusivity of prestrained specimens were determined.
To describe a method for quantifying patellofemoral joint contact area using magnetic resonance imaging (MRI), we used a repeated measures design using cadaver specimens.
For quantifying cell numbers expressing a marker or an area of positive cells, equal numbers of optical stacks were taken per specimen, collapsed, and quantified using Automeasure in AxioVision (Zeiss, Jena, Germany) or manually.
Molecular methods for quantifying species richness typically exceed estimates made via morphology alone, because molecular methods both reveal cryptic species and permit inclusion of specimens that would otherwise remain unidentified [ 1, 22].
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