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PAT volume was measured in ml using the volume analysis software tool of the Siemens Leonardo Circulation workstation.
Pericardial fat assessment was performed as described previously using the Volume analysis software tool of the Siemens Leonardo Circulation workstation [ 16].
Western blotting data was quantified using the volume analysis tool of QuantityOne 4.6.3 1D Analysis Software (Bio-Rad, Hercules, CA, USA), with Adjusted Volume (Intensity*mm2) as quantitative parameter, and the values expressed as means ± standard errors from two independent sets of data.
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Different post-processing tools were used for the volume analysis, because the individual post-processing tools could only process CT or MR data and not both.
This package uses the finite-volume analysis method.
Due to the variability of physiological systems a flow phantom was used as a proof-of-concept for determining pressure differentials using control volume analysis [ 2].
Larval volumes were quantified from 16-bit grayscale pictures using the Quantity One volume analysis tool (Bio-Rad).
The applied procedures were induction of MS by fructose in drinking water; experimental protocol of walking and running; weighing of body mass and VAT; sacrifice of animals with blood collection and removal of organs and processing of samples for light microscopy using the analysis of volume densities (Vv) of the studied structures.
The LV of each patient was semiautomatically measured using the "liver analysis" function of the volume analyzer SYNAPSE VINCENT (Fuji Film Medical, Tokyo).
The objective of this study was to use control volume analysis and magnetic resonance velocity imaging to non-invasively estimate pressure differentials in vitro.
However, the purpose of this study was to use control volume analysis and phase-contrast magnetic resonance (PC-MR) imaging to non-invasively estimate pressure differentials within a flow phantom as a proof-of-concept prior to in vivo studies.
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