Sentence examples for cell advance from inspiring English sources

Consistent with this hypothesis, inverse correlation between cell advance and retrograde flow rate was indeed demonstrated in some cases [11], [17], but not in other cases [17], [18].

The slowed motility later recovered (orange zone of Fig. 3A and Fig. 3D); when the cell advance drastically increased from 3.94 µm/min to 9.28 µm/min, retrograde F-actin flow decreased from 6.75 µm/min to almost zero.

Thirty min after addition of DTT, when the rate of cell advance reduced to 3.89 µm/min, retrograde F-actin flow appeared at a rate of 6.70 µm/min (Fig. 3F).

At key time points (Fig. 3B D), the rates of cell advance were measured by tracing both lamella leading edge (green traces and open triangle) and organelle-rich proximal cytoplasmic domain (blue traces and open triangle), and the rates of concurrent retrograde F-actin flow by the microbeads (red traces and open triangle).

These results suggested that although DTT or MnCl2 could convert the integrins into an active-form conformation that bound to ECM, such chemically activated integrins were unable to re-establish ECM-cytoskeleton coupling, thereby locking retrograde F-actin flow at a persistent slippery state that failed to drive cell advance.

Right after calcium uncaging (red triangle) in the phase of calcium-induced resensitization, forward cell movement initially reduced (yellow zone of Fig. 3A and Fig. 3C); when the rate of cell advance declined from 8.68 µm/min to 5.85 µm/min, the corresponding rate of retrograde F-actin flow increased from 3.21 µm/min to 5.18 µm/min (Fig. 3C).

This focused review will discuss how human iPS cell advances are likely to have an impact on hepatology.

To detect tension within the cell, advances have been made using molecular sensors.

The bleached regions were stationary relative to the substratum as the cell advanced.

In conclusion, in fast-moving Dictyostelium cells, both actin and myosin II filaments remain stationary as the cell advances but show highly dynamic turnover.

Beads attached to the cell were stationary with respect to the substratum but finally accumulated at the rear as the cell advanced.