<p>Confluent cell cultures were wounded post-treatment and migration distances were measured at 8 hours. The experiment was carried out in canine smooth muscle cells untreated or treated with 10 μg/ml of PLG, 1 μg/ml of rDiACT/rDiFBAL, 1 μg/ml of rDiACT/rDiFBAL + 10 μg/ml of PLG or with 1 μg/ml of rDiACT/rDiFBAL + 10 μg/ml of PLG + 50 mM of the εACA. The results were expressed as percentage of the migration ability of the negative control cells (100%). Data are shown as representative images or means ± SD from three independent experiments. The asterisk (*) designates significant (p<0.05) differences between rDiACT or rDiFBAL + PLG treatment and control groups.</p
(a) Representative photomicrographs of PC-3M-1E8 cells and PC-3M-2B4 cells are presented at 200 × ma...
<p>For the wound-healing assay, photographs at 0 (A, C, E, G, and I) and 24 hours (B, D, F, H, and J...
<p>(A) Representative 10x images of wounding at 12h are shown. (B) Graphs of wound closure percentag...
<p>Confluent cell cultures were wounded post-treatment and migration distances were measured at 8 ho...
<p>(A and B) To measure cell migration activity, A549 (left panels) and Panc-1 (right panels) cells ...
<p>MGC803 cells transfected with LGR5 and mock-transfected cells were compared. <b>A</b>. The cell w...
<p><b>(A)</b> The wound-healing migration of stable transfectants was recorded with an optical micro...
<p>Width of invaded space by RM1 cells cultured with PACM, ACM and control media in the “wound heali...
<p>Quantification of migration of CMT-W1 (A), CMT-W2 (B) CMT-W1M (C) cell lines are presented as per...
<p>(A) BHP10-3 and TPC1 cells were plated in 12-well plates, grown to confluency, and the monolayer ...
BACKGROUND: Cell migration is a vital process for growth and repair. In vitro migration assays, util...
<p>A) Wound healing assay images at the indicated time points. B) Wound width distance at the indica...
(A) NCCIT scramble control and NCCIT Np9 KD clones 8 and 9 were used for the migration assay. A tota...
<p><b>A</b>- Panc-1, Aspc-1 and HPDE cells were plated and allowed to grow as a monolayer after whic...
<p>(a) A scratch wound assay was used to detect cell migration of BALB/c 3T3 cells from different ex...
(a) Representative photomicrographs of PC-3M-1E8 cells and PC-3M-2B4 cells are presented at 200 × ma...
<p>For the wound-healing assay, photographs at 0 (A, C, E, G, and I) and 24 hours (B, D, F, H, and J...
<p>(A) Representative 10x images of wounding at 12h are shown. (B) Graphs of wound closure percentag...
<p>Confluent cell cultures were wounded post-treatment and migration distances were measured at 8 ho...
<p>(A and B) To measure cell migration activity, A549 (left panels) and Panc-1 (right panels) cells ...
<p>MGC803 cells transfected with LGR5 and mock-transfected cells were compared. <b>A</b>. The cell w...
<p><b>(A)</b> The wound-healing migration of stable transfectants was recorded with an optical micro...
<p>Width of invaded space by RM1 cells cultured with PACM, ACM and control media in the “wound heali...
<p>Quantification of migration of CMT-W1 (A), CMT-W2 (B) CMT-W1M (C) cell lines are presented as per...
<p>(A) BHP10-3 and TPC1 cells were plated in 12-well plates, grown to confluency, and the monolayer ...
BACKGROUND: Cell migration is a vital process for growth and repair. In vitro migration assays, util...
<p>A) Wound healing assay images at the indicated time points. B) Wound width distance at the indica...
(A) NCCIT scramble control and NCCIT Np9 KD clones 8 and 9 were used for the migration assay. A tota...
<p><b>A</b>- Panc-1, Aspc-1 and HPDE cells were plated and allowed to grow as a monolayer after whic...
<p>(a) A scratch wound assay was used to detect cell migration of BALB/c 3T3 cells from different ex...
(a) Representative photomicrographs of PC-3M-1E8 cells and PC-3M-2B4 cells are presented at 200 × ma...
<p>For the wound-healing assay, photographs at 0 (A, C, E, G, and I) and 24 hours (B, D, F, H, and J...
<p>(A) Representative 10x images of wounding at 12h are shown. (B) Graphs of wound closure percentag...