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For immunocytometric analysis, eight panels were defined, dedicated to fine cytometric analyses of the different subsets of cells within the major cellular populations (Table 3).
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Static and dynamic stability margins of FG panels are defined for various volume fractions.
However, in order to facilitate the installation process, a certain minimum distance between the panels is defined.
The GI50 values of the cell lines in the BCell panel were defined as the first point at which the growth curve drops below the 50% level.
A plane rectangular domain of the floor panel is defined as modification domain.
A four-node shear-flexible finiTheelement is selected to compare the results with the present solution.
The characteristic equations of the panel are defined by five highly coupled second and third order partial differential equations in five unknowns, i.e., three displacements, and two rotations.
In this model (Rodrigues et al. 2010), each infill panel is defined by considering four support strut elements, with rigid in-plane behaviour, and a central element, where the in-plane nonlinear hysteretic behaviour is concentrated, as illustrated in Fig. 5a, b.
Negative nuclear (left panel) and prominent cytoplasmic staining (middle panel) of LRP16 were defined as negative, and prominent nuclear staining (right panel) was defined as positive, as described previously [32].
Consensus for the multi-disciplinary panel was defined as >60% agreement (≥17 members in agreement).
We used the option where reference and test panel are defined separately.
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