<p><b>A)</b> HPDE cells were treated with 50 μM tBHQ or 10 ng/mL TGF-β1, or were left untreated for 24h. Then, cells were analysed by microscopy (at 200x magnification) and photographs were taken. <b>B)</b> Confluently grown HPDE cells in a two-chamber insert were treated with 50 μM tBHQ or 10 ng/mL TGF-β1, either alone or in combination, or were left untreated. Then, the insert was removed (t = 0h) and selected areas were analysed by microscopy (at 100x magnification) and photographed at the indicated periods. *marks the intitial wound edges.</p
<p>(A) Huh7 cells were treated with NCTD (0, 2.5, 5, 10 and 20 µM) for 24 h before being subjected t...
For more than a century, a role for wound healing in the outgrowth of tumours has been implied based...
<p>SV40T immortalised MEFS infected with pTRH1-NF-κB-GFP were treated with HPSE (10 µg/mL) or LPS (1...
<p>(a) NHU cells were differentiated with or without TZ/PD or ABS/Ca<sup>2+</sup> in the presence or...
<p>(<b>A</b>) Boyden chamber migration and invasion assay. Cells were treated with TGFβ for the indi...
<p>(A) hPTECs were seeded at passage 1 at low (25 000 cells/cm<sup>2</sup>) or high density (75 000 ...
<p><b>A</b>- Panc-1, Aspc-1 and HPDE cells were plated and allowed to grow as a monolayer after whic...
<p>(A) ARPE 19 was cultivated with a wound healing culture insert and serum-starved for 48 h. After ...
SGC Open Notebook Project to Characterize the HMTase NSD3 Exp022 Objective: During epithelial to me...
<p>Morphometric analysis of serial sections was used to calculate the wound volume (a). Wound length...
<p>(A) TNFα enhanced cell migration in a wound healing assay. After mechanical wounding, confluent A...
<p>(a) N-cadherin was suppressed though shCDH2. Actin was used as the loading control. (b) RT-PCR (l...
The effects of recombinant human transforming growth factor β1 (rhTGF-β1) on wound healing were exam...
<p> Graphs of time-lapse data represent mean values of four independent experiments ± S.E.M. (p<0.00...
<p>(A) Representative images of migration assay showing the effect of IP-10, PF4 and collagen type I...
<p>(A) Huh7 cells were treated with NCTD (0, 2.5, 5, 10 and 20 µM) for 24 h before being subjected t...
For more than a century, a role for wound healing in the outgrowth of tumours has been implied based...
<p>SV40T immortalised MEFS infected with pTRH1-NF-κB-GFP were treated with HPSE (10 µg/mL) or LPS (1...
<p>(a) NHU cells were differentiated with or without TZ/PD or ABS/Ca<sup>2+</sup> in the presence or...
<p>(<b>A</b>) Boyden chamber migration and invasion assay. Cells were treated with TGFβ for the indi...
<p>(A) hPTECs were seeded at passage 1 at low (25 000 cells/cm<sup>2</sup>) or high density (75 000 ...
<p><b>A</b>- Panc-1, Aspc-1 and HPDE cells were plated and allowed to grow as a monolayer after whic...
<p>(A) ARPE 19 was cultivated with a wound healing culture insert and serum-starved for 48 h. After ...
SGC Open Notebook Project to Characterize the HMTase NSD3 Exp022 Objective: During epithelial to me...
<p>Morphometric analysis of serial sections was used to calculate the wound volume (a). Wound length...
<p>(A) TNFα enhanced cell migration in a wound healing assay. After mechanical wounding, confluent A...
<p>(a) N-cadherin was suppressed though shCDH2. Actin was used as the loading control. (b) RT-PCR (l...
The effects of recombinant human transforming growth factor β1 (rhTGF-β1) on wound healing were exam...
<p> Graphs of time-lapse data represent mean values of four independent experiments ± S.E.M. (p<0.00...
<p>(A) Representative images of migration assay showing the effect of IP-10, PF4 and collagen type I...
<p>(A) Huh7 cells were treated with NCTD (0, 2.5, 5, 10 and 20 µM) for 24 h before being subjected t...
For more than a century, a role for wound healing in the outgrowth of tumours has been implied based...
<p>SV40T immortalised MEFS infected with pTRH1-NF-κB-GFP were treated with HPSE (10 µg/mL) or LPS (1...