<p>A) Cell proliferation. Cells were counted every 24 hrs during treatment with 5-AZA. B) Cell viability was measured with MTT test. **, p<0,01; ***, p<0,005 (Mann-Whitney U-Test). <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0042704#s3" target="_blank">Results</a> are representative of 3 independent experiments.</p
<p>HT-29 cells were incubated for 24 hours with different concentrations of C3G (12.5 to 50 µM), 5-A...
<p>Cytotoxicity of camptothecin against MPC 4/30/PRR cells was tested in the presence or absence of ...
<p>Clonogenic survival of CNE2 and SUNE1 cells irradiated with a single-dose of 0, 2, 4, 6, 8 Gy aft...
<p>A) Densitometric analysis of the effect of 5-Aza for each cell line showing relative expression o...
<p>A. TAM-Wd and MCF-7 cell concentration response to E2 challenge (1×10<sup>−12</sup> M to 1×10<sup...
<p>Cell viability and proliferation capacity of the cervical cancer cell lines SiHa(A) and HeLa(B) a...
<p>As the drug concentration increased, the growth inhibition ratio for CNE2 and SUNE1 cells increas...
<p>A, Cell viability was determined after 72 h incubation by MTT assay. Results were normalized to t...
<p>The percentage of proliferation index +/− the SD has been reported in the y axis. The mean ± SD o...
<p>A) BP analysis of <i>UTF1</i> methylation status in cancer cell lines derived from the anogenital...
<p>Cells were treated with increasing concentrations of compounds for 48 hours; cell proliferation a...
<p>(A) CNE2 and SUNE1 cells were treated with 1 μmol/L 5-azaC and/or irradiated (IR) at 6 Gy. The ra...
MCF-7 cells were cultured in 96-well plates as above in Fig 3 and then treated with 5-ALA (A, 0.5 mM...
<p>Trypan blue dye exclusion viability assay in BPCs treated with 5Aza and TSA <b>(A)</b>. Prolifera...
<p>Cell viability was measured by MTT assay. Values represent the means ± SD of three independent ex...
<p>HT-29 cells were incubated for 24 hours with different concentrations of C3G (12.5 to 50 µM), 5-A...
<p>Cytotoxicity of camptothecin against MPC 4/30/PRR cells was tested in the presence or absence of ...
<p>Clonogenic survival of CNE2 and SUNE1 cells irradiated with a single-dose of 0, 2, 4, 6, 8 Gy aft...
<p>A) Densitometric analysis of the effect of 5-Aza for each cell line showing relative expression o...
<p>A. TAM-Wd and MCF-7 cell concentration response to E2 challenge (1×10<sup>−12</sup> M to 1×10<sup...
<p>Cell viability and proliferation capacity of the cervical cancer cell lines SiHa(A) and HeLa(B) a...
<p>As the drug concentration increased, the growth inhibition ratio for CNE2 and SUNE1 cells increas...
<p>A, Cell viability was determined after 72 h incubation by MTT assay. Results were normalized to t...
<p>The percentage of proliferation index +/− the SD has been reported in the y axis. The mean ± SD o...
<p>A) BP analysis of <i>UTF1</i> methylation status in cancer cell lines derived from the anogenital...
<p>Cells were treated with increasing concentrations of compounds for 48 hours; cell proliferation a...
<p>(A) CNE2 and SUNE1 cells were treated with 1 μmol/L 5-azaC and/or irradiated (IR) at 6 Gy. The ra...
MCF-7 cells were cultured in 96-well plates as above in Fig 3 and then treated with 5-ALA (A, 0.5 mM...
<p>Trypan blue dye exclusion viability assay in BPCs treated with 5Aza and TSA <b>(A)</b>. Prolifera...
<p>Cell viability was measured by MTT assay. Values represent the means ± SD of three independent ex...
<p>HT-29 cells were incubated for 24 hours with different concentrations of C3G (12.5 to 50 µM), 5-A...
<p>Cytotoxicity of camptothecin against MPC 4/30/PRR cells was tested in the presence or absence of ...
<p>Clonogenic survival of CNE2 and SUNE1 cells irradiated with a single-dose of 0, 2, 4, 6, 8 Gy aft...