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The application of different diagnostic criteria derived for deposition processes allowed us to observe a simple nucleation/growth process in HClO4 media (OPD) and an adsorption/nucleation process at pH > pKa1 of the oxalic acid (UPD).
The efficient production of DV1 RSPs by HeLa-prME cell line and the fact that RSPs could mimic the maturation and secretion processes allowed us setting up an assay to study the interaction between DV and host cells during egress, a step which has received little attention in comparison to DV viral entry and replication [40], [41], [42], [43].
These processes allowed us to identify PIP for inclusion in the study and alternative therapy options.
Our approach of observing several sub-cellular processes allowed us to analyse differences in the kinome requirement for multiple subcellular processes.
These processes allowed us to examine the data and then reflect on it until definitive patterns emerged and saturation achieved [ 22].
This grouping of all processes into two sets (fast and slow processes) allowed us to reduce the initial complexity of the catalytic cycle and derive rate equations describing the operation of 5-LO according to the methods described in [ 27].
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Although tedious time is still required for these procedures, the end-results obtained through the selection/amplification processes allow us to use stable cMAbs.
This process allowed us to use a mixture of deductive and inductive analysis [ 24].
The use of relatively simple mathematical models (such as vector-autoregressive processes) allows us to distil the essential dynamics of complex temporal processes in biological systems.
Cellular biology processes allow us to choose between embryonic stem cells or adult stem cells for regenerative medicine.
Derivational morphological processes allow us to create new words (e.g. punish (V) to noun (N) punishment) from base forms.
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Justyna Jupowicz-Kozak
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