<p>(A) Aspect of U2OS G1, R1, and YFP co-cultures in fluorescence microscopy. Cells were plated at a 1:1 ratio as indicated (R1:G1 or R1:YFP) and allowed to grow for 1, 3 or 6 days. (B) Cp3-IF apoptosis quantification. R1 cells behave as “winners” in R1:YFP cultures but as “losers” in the presence of G1 cells, indicating that R1 cells assume “winner” or “loser” status depending on the properties of their co-culture partners. *: p<0.001 by Student’s <i>t</i>-test.</p
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
<p><b>A</b>, H&E images (2X) and FISH images (100X) of i.c. xenografts derived from NS1. <i>Arrowhea...
<p>A) Crystal violet proliferation assay, in which absorbances were normalized to that of 10% FBS to...
<p>(A) Schematic representation of U2OS transwell cultures, Cells shared culture medium but were sep...
<p>(A) Cell counts showing YFP (“loser” cells) cells first expand, then decline, in the presence of ...
<p>(A) Quantification of apoptosis (Cp3 immunofluorescence) in U2OS cultures grown for 72 hours unde...
<p>(<b>A</b>) Survival of WT, <i>Δyca1</i>, <i>Δdot1</i>, <i>Δset1</i>, <i>Δset1Δdot1</i> and <i>Δse...
<p>(<b>A</b>) Average normalized levels of free GFP-H3.1 relative to mock-infected cells at 4 or 7 h...
<p>U2OS cells were transfected with p16, p16-ACT, p14ARF, chARF, GFP, or no DNA (mock). 24 hours aft...
A) Phase contrast and fluorescence images of U251 cells in the form of a spheroid produced in a 150 ...
<p>(A) U2OS cells were transfected with p16, p16-ACT, p14ARF, chARF, or GFP control. After 48 hours,...
<p>Cell viability and proliferation analyzed by (a) ATP assay and (b) DNA quantification, respective...
<p>(A) Number of residual GFP-S was evaluated after cell mixture was treated with vehicle or 250 nm ...
<p>(<b>A</b>) Survival of WT, <i>Δdot1, Δyca1</i> and <i>Δdot1Δyca1</i> cells was determined by clon...
<p>(A) U2OS cells were transfected with the indicated siRNAs and treated with 10Gy IR. The cells wer...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
<p><b>A</b>, H&E images (2X) and FISH images (100X) of i.c. xenografts derived from NS1. <i>Arrowhea...
<p>A) Crystal violet proliferation assay, in which absorbances were normalized to that of 10% FBS to...
<p>(A) Schematic representation of U2OS transwell cultures, Cells shared culture medium but were sep...
<p>(A) Cell counts showing YFP (“loser” cells) cells first expand, then decline, in the presence of ...
<p>(A) Quantification of apoptosis (Cp3 immunofluorescence) in U2OS cultures grown for 72 hours unde...
<p>(<b>A</b>) Survival of WT, <i>Δyca1</i>, <i>Δdot1</i>, <i>Δset1</i>, <i>Δset1Δdot1</i> and <i>Δse...
<p>(<b>A</b>) Average normalized levels of free GFP-H3.1 relative to mock-infected cells at 4 or 7 h...
<p>U2OS cells were transfected with p16, p16-ACT, p14ARF, chARF, GFP, or no DNA (mock). 24 hours aft...
A) Phase contrast and fluorescence images of U251 cells in the form of a spheroid produced in a 150 ...
<p>(A) U2OS cells were transfected with p16, p16-ACT, p14ARF, chARF, or GFP control. After 48 hours,...
<p>Cell viability and proliferation analyzed by (a) ATP assay and (b) DNA quantification, respective...
<p>(A) Number of residual GFP-S was evaluated after cell mixture was treated with vehicle or 250 nm ...
<p>(<b>A</b>) Survival of WT, <i>Δdot1, Δyca1</i> and <i>Δdot1Δyca1</i> cells was determined by clon...
<p>(A) U2OS cells were transfected with the indicated siRNAs and treated with 10Gy IR. The cells wer...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
<p><b>A</b>, H&E images (2X) and FISH images (100X) of i.c. xenografts derived from NS1. <i>Arrowhea...
<p>A) Crystal violet proliferation assay, in which absorbances were normalized to that of 10% FBS to...