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The time course of cell volume change was followed by fluorescence quenching of the entrapped fluorophore (CF).
The introduction of SrTiO3 and SrZrO3 leads to an expansion of cell volume and refinement of grain size.
To determine the latter, one needs to measure the rate of cell volume changes when placed in anisotonic environment.
To determine cell membrane permeability, one needs to measure the rate of cell volume changes in anisotonic environment.
It has been hypothesized that the change of cell volume is a primary mechanism for cells to perceive the stimuli.
In the mature plant cell, as much as 90 percent of cell volume may be taken up by a single vacuole; immature cells typically contain several smaller vacuoles.
Variation of cell volume in populations of cardiomyocytes can help distinguish their types, while changes in optical thickness during beating cycle identify contraction and relaxation periods and elucidate cell dynamics.
Compression of 2% alginate resulted in cell deformation from a spherical to an oblate ellipsoid morphology with conservation of cell volume.
Since the early days of cell volume regulation research, the role of actin cytoskeleton organization and rearrangement has attracted specific interest.
Microstructural properties of alloy take initial values on annealing at moderate temperatures, i.e., improvement of crystallization and recovery of cell volume.
Empirical descriptions of cell volume regulation (CVR) and pH control were implemented, together with the tubuloglomerular feedback (TGF) system.
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