<p>HUVEC were treated with 2-APB and Co(III)hexaammine or transfected with a shRNA against <i>TRPM7</i> for 24 h. (A) The cells were wounded and migration was allowed for 10 h. Microphotographs show the result of a representative assay (20×magnification). (B) The wound area was calculated by ImageJ software and expressed using an arbitrary value scale to quantify the results. The values are expressed as the mean of 3 different experiments ± standard deviation. *p<0.05, **p<0.01. (C) NOS activity was measured by using the Griess method.</p
<p>(A) U87 cells were treated with artemether of 300 µmol/L, shRNA transfected or treated with both....
<p>Cell migration was measured by wound-healing migration assay. HUVECs were treated with different ...
<p>HUVEC and RPE cell migration was significantly inhibited after exposure to temsirolimus in a dose...
<p>A. Lack of effect of SKF-96365 on TRPM7 currents. Representative TRPM7 currents in activated T ce...
<p>(A) HUVEC were either cultured in complete growth medium (proliferating cells, P) or in starvatio...
<p>The cells were preincubated with TRPM7 siRNA or control siRNA for 48h, and then stimulated with H...
<p>The effects of artemether on the migration of U87 cells were assessed by wound healing assay. (A)...
<p>(A) Cell migration capability was determined with a wound healing assay. Photographs were taken i...
<p>HUVEC migration was examined with a phase-contrast microscopy (×40) at the indicated time points ...
<p>Wound healing assays were performed on PNT1A, LNCaP, PC3 and DU145 cells in the absence or the pr...
<p>(A) Representative immunoblots showing TRPM7 protein expression in HUVECs with or without HG (30 ...
<p>(A) Scratch wound migration assay <i>in vitro</i>. After transfection with miR-21 mimics, miR-21 ...
A) Comparison of direct and automated cell counting of U87 cells maintained 48 h in culture in the p...
<p>A) Three-dimensional (3D) invasion assay of TREx293-TRPM4 cells. TRPM4 expression was induced by ...
(A and B) The indicated cells grown in 12-well plates were left untreated, or subjected to lentivira...
<p>(A) U87 cells were treated with artemether of 300 µmol/L, shRNA transfected or treated with both....
<p>Cell migration was measured by wound-healing migration assay. HUVECs were treated with different ...
<p>HUVEC and RPE cell migration was significantly inhibited after exposure to temsirolimus in a dose...
<p>A. Lack of effect of SKF-96365 on TRPM7 currents. Representative TRPM7 currents in activated T ce...
<p>(A) HUVEC were either cultured in complete growth medium (proliferating cells, P) or in starvatio...
<p>The cells were preincubated with TRPM7 siRNA or control siRNA for 48h, and then stimulated with H...
<p>The effects of artemether on the migration of U87 cells were assessed by wound healing assay. (A)...
<p>(A) Cell migration capability was determined with a wound healing assay. Photographs were taken i...
<p>HUVEC migration was examined with a phase-contrast microscopy (×40) at the indicated time points ...
<p>Wound healing assays were performed on PNT1A, LNCaP, PC3 and DU145 cells in the absence or the pr...
<p>(A) Representative immunoblots showing TRPM7 protein expression in HUVECs with or without HG (30 ...
<p>(A) Scratch wound migration assay <i>in vitro</i>. After transfection with miR-21 mimics, miR-21 ...
A) Comparison of direct and automated cell counting of U87 cells maintained 48 h in culture in the p...
<p>A) Three-dimensional (3D) invasion assay of TREx293-TRPM4 cells. TRPM4 expression was induced by ...
(A and B) The indicated cells grown in 12-well plates were left untreated, or subjected to lentivira...
<p>(A) U87 cells were treated with artemether of 300 µmol/L, shRNA transfected or treated with both....
<p>Cell migration was measured by wound-healing migration assay. HUVECs were treated with different ...
<p>HUVEC and RPE cell migration was significantly inhibited after exposure to temsirolimus in a dose...