(A and B) Confluent monolayers of the cell lines shown were wounded, and wound closure was monitored for 18h by live imaging microscopy. A: Representative images of vector control, 3XF-VRK1-overexpressing and 3XF-VRK1D177A-overexpressing cells are shown at 0 and 18h after wounding. Scale bar = 100μm. B: Quantification of the percent wound closure at 18 h (Mean and standard error are shown; ***p(C-E) Data from representative IncuCyte wound scratch assays are shown. Using the IncuCyte live imaging system, the rate of wound closure was compared pairwise for vector control MCF10A cells (black circles) and 3XF-VRK1 overexpressing MCF10A cells (gray triangles) (C), or for vector control MDA-MB-231 cells (black circles) vs. 3XF-VRK1- overexpressin...
<p>A, B. Immunoblot analysis of cell lysates from A549 cell clones (A) or NCI-H441 cell clones (B) t...
<p>A) HEK-293 cells depleted of DEPDC7 and control cells were cultured for 24 hrs. The cell monolaye...
(A) NCCIT scramble control and NCCIT Np9 KD clones 8 and 9 were used for the migration assay. A tota...
(A) Generation of MCF10A derivatives: MCF10A cells were transduced to stably overexpress 3XF-VRK1 or...
(A) To assess the rate of cell spreading, the areas of individual vector control (blue circles) and ...
(A and B) Immunofluorescence analysis of E-Cadherin (A) and vimentin (B) in control and 3XF-VRK1-ove...
(A) Representative brightfield images of 3D acini formed by control, 3XF-VRK1- overexpressing cells ...
<p>Endogenous CRK is silenced in all conditions by siRNA. B- Measurement of wound surface area 24 ho...
Background: Cell migration is a complex phenomenon that requires the coordination of numerous cellul...
<p>A) (Left panel) U2OS or MCF-7 cells were transfected with siRNA directed to PAK4 or Cdc42 as indi...
<p>Cell wounds were generated for glycosylated and unglycosylated Kv3.1, and then images were captur...
<p>(A). Flow cytometry profile of WS1 cell cycle in non-synchronized (left) and serum starved cells ...
<p>Following transfection with control pre-miR or pre-miR-21, cells were plated on Radius Migration ...
<p>A) The fields of view at 0 h (red) and at 18 h (green) after scratch were overlaid to visualize t...
<p>A) Scratch wound assay showed a moderate but significant increase in migration of p115RhoGEF-depl...
<p>A, B. Immunoblot analysis of cell lysates from A549 cell clones (A) or NCI-H441 cell clones (B) t...
<p>A) HEK-293 cells depleted of DEPDC7 and control cells were cultured for 24 hrs. The cell monolaye...
(A) NCCIT scramble control and NCCIT Np9 KD clones 8 and 9 were used for the migration assay. A tota...
(A) Generation of MCF10A derivatives: MCF10A cells were transduced to stably overexpress 3XF-VRK1 or...
(A) To assess the rate of cell spreading, the areas of individual vector control (blue circles) and ...
(A and B) Immunofluorescence analysis of E-Cadherin (A) and vimentin (B) in control and 3XF-VRK1-ove...
(A) Representative brightfield images of 3D acini formed by control, 3XF-VRK1- overexpressing cells ...
<p>Endogenous CRK is silenced in all conditions by siRNA. B- Measurement of wound surface area 24 ho...
Background: Cell migration is a complex phenomenon that requires the coordination of numerous cellul...
<p>A) (Left panel) U2OS or MCF-7 cells were transfected with siRNA directed to PAK4 or Cdc42 as indi...
<p>Cell wounds were generated for glycosylated and unglycosylated Kv3.1, and then images were captur...
<p>(A). Flow cytometry profile of WS1 cell cycle in non-synchronized (left) and serum starved cells ...
<p>Following transfection with control pre-miR or pre-miR-21, cells were plated on Radius Migration ...
<p>A) The fields of view at 0 h (red) and at 18 h (green) after scratch were overlaid to visualize t...
<p>A) Scratch wound assay showed a moderate but significant increase in migration of p115RhoGEF-depl...
<p>A, B. Immunoblot analysis of cell lysates from A549 cell clones (A) or NCI-H441 cell clones (B) t...
<p>A) HEK-293 cells depleted of DEPDC7 and control cells were cultured for 24 hrs. The cell monolaye...
(A) NCCIT scramble control and NCCIT Np9 KD clones 8 and 9 were used for the migration assay. A tota...