<p>HUVEC were treated during 24 h in medium without serum, in the presence of EBM2 alone or EBM2 with different concentrations of netrin-4. (A)Pictures were taken at 0 h and 24 h after insert removing. (B) Results are expressed as percentage of wound closure (percentage closure) (mean ± SD). (C) Netrin-4 affects HUVEC migration in a transwell assay. HUVEC cells were allowed to migrate for 24 h at 37°C in a 5% CO<sub>2</sub> humidified incubator. After 24 h, the cells that migrated across the membrane were stained with DAPI and the fluorescence intensity was measured. (D)The % invasion is compared to the fluorescence intensity of migrated cells in the absence of netrin-4 (** <i>p</i> < 0.01). Each experiment was performed three times and a r...
<p>HUVEC cells were cultured in 6-well plates overnight, creating a straight scratch on each conflue...
<p>(A) Scratch wound migration assay <i>in vitro</i>. After transfection with miR-21 mimics, miR-21 ...
<p>(A) Huh7 cells were treated with NCTD (0, 2.5, 5, 10 and 20 µM) for 24 h before being subjected t...
<p>BMDMs were incubated with either vehicle, 3 nM or 30 nM netrin-1 for 45 min at 37°C, 5% CO<sub>2<...
<p>Tube formation was assessed in tubulogenesis assay in vitro model, HUVECs were serum-starved with...
<p>(A) After HUVEC were incubated with 20 nM irisin, 5 μg/ml mitomycin C (MMC), or 20 nM irisin with...
<p>(A,B) Addition of 100 ng/ml netrin-1 to the bottom compartment (NB) of the transfilter microchemo...
<p>(A) Cultured HUVECs were serum-starved for 24 h followed by 72 h culture in serum free media with...
<p>(A) An <i>in </i><i>vitro</i> wound-healing assay indicates that FABP4 at 60 ng/ml induced HCASMC...
<p>(A) Wound healing assay, panc-1 cells grown at 80% confluency. The monolayers were incised with a...
<p>(A) and (C) HUVEC were pretreated with the ERK inhibitor U0126 (10 μM) for 30 min and cultured wi...
<p>Cell migration was measured by wound-healing migration assay. HUVECs were treated with different ...
<p>(<b>A</b>) After 24 hours serum starvation, a wound was created with a plastic tip on plates cont...
<p>(A) HCT116 cells were allowed to migrate transwell chambers for 24 h in the presence or absence o...
<p>(a, b) NSK-01105 inhibited HUVECs migration by wound-healing assay. Cells were starved to inactiv...
<p>HUVEC cells were cultured in 6-well plates overnight, creating a straight scratch on each conflue...
<p>(A) Scratch wound migration assay <i>in vitro</i>. After transfection with miR-21 mimics, miR-21 ...
<p>(A) Huh7 cells were treated with NCTD (0, 2.5, 5, 10 and 20 µM) for 24 h before being subjected t...
<p>BMDMs were incubated with either vehicle, 3 nM or 30 nM netrin-1 for 45 min at 37°C, 5% CO<sub>2<...
<p>Tube formation was assessed in tubulogenesis assay in vitro model, HUVECs were serum-starved with...
<p>(A) After HUVEC were incubated with 20 nM irisin, 5 μg/ml mitomycin C (MMC), or 20 nM irisin with...
<p>(A,B) Addition of 100 ng/ml netrin-1 to the bottom compartment (NB) of the transfilter microchemo...
<p>(A) Cultured HUVECs were serum-starved for 24 h followed by 72 h culture in serum free media with...
<p>(A) An <i>in </i><i>vitro</i> wound-healing assay indicates that FABP4 at 60 ng/ml induced HCASMC...
<p>(A) Wound healing assay, panc-1 cells grown at 80% confluency. The monolayers were incised with a...
<p>(A) and (C) HUVEC were pretreated with the ERK inhibitor U0126 (10 μM) for 30 min and cultured wi...
<p>Cell migration was measured by wound-healing migration assay. HUVECs were treated with different ...
<p>(<b>A</b>) After 24 hours serum starvation, a wound was created with a plastic tip on plates cont...
<p>(A) HCT116 cells were allowed to migrate transwell chambers for 24 h in the presence or absence o...
<p>(a, b) NSK-01105 inhibited HUVECs migration by wound-healing assay. Cells were starved to inactiv...
<p>HUVEC cells were cultured in 6-well plates overnight, creating a straight scratch on each conflue...
<p>(A) Scratch wound migration assay <i>in vitro</i>. After transfection with miR-21 mimics, miR-21 ...
<p>(A) Huh7 cells were treated with NCTD (0, 2.5, 5, 10 and 20 µM) for 24 h before being subjected t...