<p>SUM159 cells (<b>A</b>) and MDA-MB-231 cells (<b>B</b>) were incubated with vehicle control or CDDO-Im (10, 100 or 200 nM) for 24 h. The cells were stained with annexin V and propidium iodide (PI), and apoptotic cell death was determined by flow cytometry. Three separate experiments were conducted for each cell line, and representative results are shown. Averages of the three separate experiments are shown in the graph (*p<0.05, **p<0.01).</p
<p>T47D, MDA-MB-231, MCF-7 and Hs518bst cells were transfected with the pre-miR control , <i>miR-101...
<p><b>Apoptotic assay was examined in MCF-7 cells treated with 100 μg/mL DESs for 48 h.</b> Cells we...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
<p>(<b>A</b>) The structure of 1-[2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oyl]-imidazole (CDDO-Im)....
<p>Cells were exposed to CdCl<sub>2</sub> (5 and 10 μM) for 24 h in the absence or presence of NAC (...
<p>(A) MCF-7, MDA-MB-231 cells were stained with Annexin V/PI and subjected to flow cytometric analy...
<p>Cells were treated with the indicated concentrations of PD for 48 h, stained with Muse Annexin V ...
<p>(A) Cells treated with vehicle and CDRI-85/287 were analyzed by flow cytometry of annexin-V/PI st...
<p>The cytotoxicity is confirmed as apoptosis through flow cytometry. A, effect of MSM on triple-neg...
<p>In Vitro Drug Induced Apoptosis in Triple Negative Breast Cancer Patients.</p
<p><b>A.</b> Detection of apoptosis by the annexin V-fluorescein isothiocyanate (FITC)/porpidium iod...
<p>Viability of MDA-MB-231 cells was assessed by MTT assay after treatment with IMD-0354 for 24 h (A...
<p>A. Cells were treated with TCS at the indicated concentrations for 24 h. Cells were harvested and...
<p>(A) Cell cycle distribution was analyzed by flow cytometry 72 h after transfection. Bars are show...
<p><b>A:</b> TMI-1 induces cell cycle arrest in the G0/G1 phase. SUM149 cells were treated for 48 h ...
<p>T47D, MDA-MB-231, MCF-7 and Hs518bst cells were transfected with the pre-miR control , <i>miR-101...
<p><b>Apoptotic assay was examined in MCF-7 cells treated with 100 μg/mL DESs for 48 h.</b> Cells we...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
<p>(<b>A</b>) The structure of 1-[2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oyl]-imidazole (CDDO-Im)....
<p>Cells were exposed to CdCl<sub>2</sub> (5 and 10 μM) for 24 h in the absence or presence of NAC (...
<p>(A) MCF-7, MDA-MB-231 cells were stained with Annexin V/PI and subjected to flow cytometric analy...
<p>Cells were treated with the indicated concentrations of PD for 48 h, stained with Muse Annexin V ...
<p>(A) Cells treated with vehicle and CDRI-85/287 were analyzed by flow cytometry of annexin-V/PI st...
<p>The cytotoxicity is confirmed as apoptosis through flow cytometry. A, effect of MSM on triple-neg...
<p>In Vitro Drug Induced Apoptosis in Triple Negative Breast Cancer Patients.</p
<p><b>A.</b> Detection of apoptosis by the annexin V-fluorescein isothiocyanate (FITC)/porpidium iod...
<p>Viability of MDA-MB-231 cells was assessed by MTT assay after treatment with IMD-0354 for 24 h (A...
<p>A. Cells were treated with TCS at the indicated concentrations for 24 h. Cells were harvested and...
<p>(A) Cell cycle distribution was analyzed by flow cytometry 72 h after transfection. Bars are show...
<p><b>A:</b> TMI-1 induces cell cycle arrest in the G0/G1 phase. SUM149 cells were treated for 48 h ...
<p>T47D, MDA-MB-231, MCF-7 and Hs518bst cells were transfected with the pre-miR control , <i>miR-101...
<p><b>Apoptotic assay was examined in MCF-7 cells treated with 100 μg/mL DESs for 48 h.</b> Cells we...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...