<p>HUVEC were grown under 0.5% serum conditions and treated with or without VEGF (10 ng/mL) and various doses of AsA (5–20 µM) for 12 h as described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0022745#s4" target="_blank">Materials and Methods</a>. After 12 h, both adherent and non-adherent cells were collected and processed for determination of total cell number (<b>A</b>) and dead cells percentage (<b>B</b>) as mentioned in ‘<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0022745#s4" target="_blank">Materials and Methods</a>’. <b>C.</b> HUVEC with or without VEGF (10 ng/mL) in 0.5% serum media were placed in 24-well plates coated with Matrigel and treated with AsA at indicated doses. After...
<p>Antagonistic potency of anti-VEGF aptamers was measured by a capillary tube formation assay using...
<p>The tube formation assay was conducted essentially as described by Babaei and colleagues <a href=...
<p>(A) BEAS-2B cells were treated with DPI or catalase for 30 min, then with 5 µM arsenic for 24 h. ...
<p><b>A.</b> Effect of AsA treatment on the migratory potential of HUVEC was analyzed through wound ...
<p><b>A & B.</b> HUVEC (4×10<sup>4</sup> cells per well) were treated with DMSO or different doses o...
<p><b>A.</b> LN18 and U87-MG cells were treated with DMSO or AsA (20 µM) for 24 and 48 h. After each...
<p>HUVECs were cultured on fibrin matrices with the indicated treatments (VEGF: 20 ng/mL; 17K r-apo(...
<p>HUVECs were cultured on fibrin matrices with the indicated treatments (VEGF: 20 ng/mL; 17K r-apo(...
<p>HUVECs were cultured on fibrin matrices with the indicated treatments (VEGF: 20 ng/mL; 17K r-apo(...
<p>Serum-starved HUVECs were stimulated with VEGF (30 ng/mL) in the presence or absence of <b>1</b> ...
<p>(A) Representative RTCA profile of VEGF induced growth and survival. HUVECs were seeded in an E-P...
<p>1 × 10<sup>4</sup> of HUVECs treated with 0–1 μM TSA for 24 h were transferred in 150 μL of endot...
<p>QODG inhibited VEGF-induced tube formation of HUVECs. HUVECs were starved with ECGM containing 0....
<p>468GFP cells when co-cultured with HMVEC-dLy cells formed sparse and incomplete tube like structu...
<p><b>A. HUVEC</b>: ApoEdp has a significant effect on VEGF-induced HUVEC viability. Cells were trea...
<p>Antagonistic potency of anti-VEGF aptamers was measured by a capillary tube formation assay using...
<p>The tube formation assay was conducted essentially as described by Babaei and colleagues <a href=...
<p>(A) BEAS-2B cells were treated with DPI or catalase for 30 min, then with 5 µM arsenic for 24 h. ...
<p><b>A.</b> Effect of AsA treatment on the migratory potential of HUVEC was analyzed through wound ...
<p><b>A & B.</b> HUVEC (4×10<sup>4</sup> cells per well) were treated with DMSO or different doses o...
<p><b>A.</b> LN18 and U87-MG cells were treated with DMSO or AsA (20 µM) for 24 and 48 h. After each...
<p>HUVECs were cultured on fibrin matrices with the indicated treatments (VEGF: 20 ng/mL; 17K r-apo(...
<p>HUVECs were cultured on fibrin matrices with the indicated treatments (VEGF: 20 ng/mL; 17K r-apo(...
<p>HUVECs were cultured on fibrin matrices with the indicated treatments (VEGF: 20 ng/mL; 17K r-apo(...
<p>Serum-starved HUVECs were stimulated with VEGF (30 ng/mL) in the presence or absence of <b>1</b> ...
<p>(A) Representative RTCA profile of VEGF induced growth and survival. HUVECs were seeded in an E-P...
<p>1 × 10<sup>4</sup> of HUVECs treated with 0–1 μM TSA for 24 h were transferred in 150 μL of endot...
<p>QODG inhibited VEGF-induced tube formation of HUVECs. HUVECs were starved with ECGM containing 0....
<p>468GFP cells when co-cultured with HMVEC-dLy cells formed sparse and incomplete tube like structu...
<p><b>A. HUVEC</b>: ApoEdp has a significant effect on VEGF-induced HUVEC viability. Cells were trea...
<p>Antagonistic potency of anti-VEGF aptamers was measured by a capillary tube formation assay using...
<p>The tube formation assay was conducted essentially as described by Babaei and colleagues <a href=...
<p>(A) BEAS-2B cells were treated with DPI or catalase for 30 min, then with 5 µM arsenic for 24 h. ...