Sentence examples for mobility of cortical from inspiring English sources

This interpretation, however, does not explain the reduced mobility of cortical granules in β2-syntrophin overexpressing cells.

Furthermore, overexpression of the β2-syntrophin S75D phosphomutant, but not β2-syntrophin S90D enhanced the mobility of cortical granules relative to resting cells overexpressing β2-syntrophin.

Our results support the notion that β2-syntrophin restrains the mobility of cortical granules in insulinoma INS-1 cells, thereby reducing insulin secretion and increasing insulin stores in resting cells, while increasing insulin release upon stimulation.

Conversely, the density and mobility of cortical granules in CgB-mRFP1 INS-1 cells overexpressing either GFP-β2-syntrophin or GFP-β2-syntrophin S90D were similarly reduced relative to cells expressing GFP only.

Analysis by TIRFM further indicated that in resting CgB-mRFP1 INS-1 cells expressing GFP-β2-syntrophin S75D density and mobility of cortical granules were significantly increased by 47.6% (p =  1.65E-10) and 18% (p = 1.7E-04 1.7E-04ctively, respectivelythose exprelativeGFP-β2-syntoophin (Fig. 6C, D and those S2A, B).

Evidence that overexpression of a β2-syntrophin phosphomutant with reduced binding to ICA512 correlated with increased mobility of cortical granules in resting cells is consistent with the hypothesis that phosphorylation of β2-syntrophin affects the ability of the cortical cytoskeleton to restrain granules.

The significant FRET efficiencies detected suggest that direct molecular interactions occur, whereas dynamic experiments using TIRFM revealed that attenuation of cortical F-actin movement clearly diminishes the mobility of SNAP-25 clusters.

Expression of constitutively active mDia1 also rescued the altered mobility of EGFP-caveolin-1 near the plasma membrane, and resulted in the redistribution of caveolin-1, with high levels of cortical staining and colocalization with cortical F-actin.

Stability of the cortical actin cytoskeleton and mobility of BCRs in the plasma membrane depend upon membrane microdomains and the integral membrane proteins adjacent to BCR signaling microclusters.

Intersubject Synchronization of Cortical Activity During Natural Vision.

On the growth and form of cortical convolutions.