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that respond to hormonal or other physico-chemical changes in the cell.
On the other hand, the changes in the cell sizes were not evident.
Electrochemical impedance spectroscopy (EIS) was used to investigate the changes in the cell interfacial characteristics.
This instability may be related to changes in the cell cycle and extracellular matrix degradation.
Changes in the cell population embody the characteristic of cancer plasticity, which could explain how genetic alterations contribute to EGFR or ALK resistance.
During these simulations, certain changes in the cell values (i.e. specific origin to destination traffic volumes) of the estimated OD matrix were incorporated.
The phytochemical saponins interact with the cell membranes, causing changes within the cell membranes, and subsequent changes in the cell wall [63].
In addition, knockdown of MELK with siRNA decreased cell proliferation and caused changes in the cell cycle after radiation or 5-FU treatment.
The morphologic changes in the cell after treatment with compound 3c were assessed by fluorescene microscopy after staining with AO/EB.
However, this culture is a time dependent dynamic process where cells physiology suffers several changes depending on the changes in the cell environment.
The variations in the power conversion efficiencies (PCE) for different DSSCs can be attributed to changes in the cell architecture and fabrication [5 8].
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