<p>HUVEC migration was examined with a phase-contrast microscopy (×40) at the indicated time points (0h, 6h, 10h)(A). The wounding width was quantified, and bars represent the migration index of each treatment. The assay showed a significant increase of the distance moved by HUVECs treated with human serum that was cultured with H<sub>2</sub>O<sub>2</sub>-damaged ARPE-19 cells, when compared to HUVECs treated with the serum that was cultured with control ARPE-19 cells (P < 0.05) (B). The data were expressed as mean ± SD from results done with three independent biological samples, each analyzed with triplicates.</p
<p>(A) After HUVEC were incubated with 20 nM irisin, 5 μg/ml mitomycin C (MMC), or 20 nM irisin with...
<p>Cell migration was measured by wound-healing migration assay. HUVECs were treated with different ...
<p>At 1×10<sup>4</sup> cells/well were seeded in the the upper chamber in the serum-free media. The ...
<p>(A) ARPE 19 was cultivated with a wound healing culture insert and serum-starved for 48 h. After ...
<p>(A) HUVEC cells, grown to 100% confluence, were scratched to create a wound and then washed with ...
<p>(A) Scratch wound migration assay <i>in vitro</i>. After transfection with miR-21 mimics, miR-21 ...
<p>HUVEC and RPE cell migration was significantly inhibited after exposure to temsirolimus in a dose...
<p>SW-480 cells in 24-well plates were wounded by scratching with a pipette tip and the cells were i...
<p>HUVEC cells were cultured in 6-well plates overnight, creating a straight scratch on each conflue...
HUVECs were transfected with striatin siRNA1, 2, 3 or scrambled siRNA for 24h. Then cells were scrap...
<p><b>A.</b> Effect of AsA treatment on the migratory potential of HUVEC was analyzed through wound ...
<p>HUVEC migration was detected using a scratch wound assay. The cell monolayer was scraped with a s...
<p>ARPE-19 cells were transfected with LGR4 specific siRNA or a scrambled negative control (NC). Tra...
<p>The transwell assay was performed by using a 24-well chamber as the outer chambers and polycarbon...
<p>(A) HUVEC were incubated with PAPep(1, 10, 50 µM) or PAPS(50 µM) for 18 h, then stimulated with T...
<p>(A) After HUVEC were incubated with 20 nM irisin, 5 μg/ml mitomycin C (MMC), or 20 nM irisin with...
<p>Cell migration was measured by wound-healing migration assay. HUVECs were treated with different ...
<p>At 1×10<sup>4</sup> cells/well were seeded in the the upper chamber in the serum-free media. The ...
<p>(A) ARPE 19 was cultivated with a wound healing culture insert and serum-starved for 48 h. After ...
<p>(A) HUVEC cells, grown to 100% confluence, were scratched to create a wound and then washed with ...
<p>(A) Scratch wound migration assay <i>in vitro</i>. After transfection with miR-21 mimics, miR-21 ...
<p>HUVEC and RPE cell migration was significantly inhibited after exposure to temsirolimus in a dose...
<p>SW-480 cells in 24-well plates were wounded by scratching with a pipette tip and the cells were i...
<p>HUVEC cells were cultured in 6-well plates overnight, creating a straight scratch on each conflue...
HUVECs were transfected with striatin siRNA1, 2, 3 or scrambled siRNA for 24h. Then cells were scrap...
<p><b>A.</b> Effect of AsA treatment on the migratory potential of HUVEC was analyzed through wound ...
<p>HUVEC migration was detected using a scratch wound assay. The cell monolayer was scraped with a s...
<p>ARPE-19 cells were transfected with LGR4 specific siRNA or a scrambled negative control (NC). Tra...
<p>The transwell assay was performed by using a 24-well chamber as the outer chambers and polycarbon...
<p>(A) HUVEC were incubated with PAPep(1, 10, 50 µM) or PAPS(50 µM) for 18 h, then stimulated with T...
<p>(A) After HUVEC were incubated with 20 nM irisin, 5 μg/ml mitomycin C (MMC), or 20 nM irisin with...
<p>Cell migration was measured by wound-healing migration assay. HUVECs were treated with different ...
<p>At 1×10<sup>4</sup> cells/well were seeded in the the upper chamber in the serum-free media. The ...