<p>(A) mTNF-transfected Jurkat T cells were untreated or treated with TNFα antagonists or rituximab, at 100 nM and cultured for 24 hours. The stimulated cells were stained with FITC-conjugated Annexin V and PI and were then analyzed by flow cytometry. Ten thousand cells were measured and plotted. The proportion of cells residing in each quadrant is expressed as a percentage. (B) The proportions of Annexin V-positive cells in each sample after stimulation are indicated as solid columns.</p
<p>(A) Subconfluent 2774 ovarian cancer cells were maintained for 5 days in complete culture medium ...
<p>(A) DU145 cells were treated with vehicle, PMS1077 or PMS601 as the indicated concentration (0–80...
<p>Kupffer cells and HMNCs co-culture system was established as above. After co-culture for 20h, cel...
<p><i>A</i>, Confocal microscopy analysis of <i>in situ</i> cell death experiments. Slices from fres...
Cells were pretreated with DEX for 6 h before exposure to TNF-α for 24 h. (A) Representative images ...
<p>(A) Nuclear changes in the cells were detected by staining the cells with Hoechst 33258, a DNA-bi...
<p>(A) LY8 cells transfected with control siRNA and MTDH siRNA were either untreated or treated with...
<p>(A) Cells were untreated or treated with TNF-α (10 ng/ml) for the indicated time intervals. Phosp...
<p>(A) EMT6 cells were stably transfected with pU6m3 (control), siTR1, or siTrx1 vectors, and expres...
<p>Apoptosis was detected by flow cytometric analysis using the Annexin V-PE/7-AAD Apoptosis Detecti...
<p>Flow cytometry analysis using Annexin V and 7-AAD was used to evaluate the apoptosis in OVCA 429 ...
<p>Apoptosis was detected by flow cytometric analysis using the Annexin V-PE/7-AAD Apoptosis Detecti...
<p>Apoptosis was detected by flow cytometric analysis using the Annexin V-PE/7-AAD Apoptosis Detecti...
<p>Ba/F3-mock growing with IL-3, Ba/F3-BCR-JAK2 and Ba/F3-TEL-JAK2 cells (10<sup>5</sup>/ml) were gr...
<p>Untreated cells (A); cilengitide treated cells (B); RGDechi-hCit treated cells (C). Upper left qu...
<p>(A) Subconfluent 2774 ovarian cancer cells were maintained for 5 days in complete culture medium ...
<p>(A) DU145 cells were treated with vehicle, PMS1077 or PMS601 as the indicated concentration (0–80...
<p>Kupffer cells and HMNCs co-culture system was established as above. After co-culture for 20h, cel...
<p><i>A</i>, Confocal microscopy analysis of <i>in situ</i> cell death experiments. Slices from fres...
Cells were pretreated with DEX for 6 h before exposure to TNF-α for 24 h. (A) Representative images ...
<p>(A) Nuclear changes in the cells were detected by staining the cells with Hoechst 33258, a DNA-bi...
<p>(A) LY8 cells transfected with control siRNA and MTDH siRNA were either untreated or treated with...
<p>(A) Cells were untreated or treated with TNF-α (10 ng/ml) for the indicated time intervals. Phosp...
<p>(A) EMT6 cells were stably transfected with pU6m3 (control), siTR1, or siTrx1 vectors, and expres...
<p>Apoptosis was detected by flow cytometric analysis using the Annexin V-PE/7-AAD Apoptosis Detecti...
<p>Flow cytometry analysis using Annexin V and 7-AAD was used to evaluate the apoptosis in OVCA 429 ...
<p>Apoptosis was detected by flow cytometric analysis using the Annexin V-PE/7-AAD Apoptosis Detecti...
<p>Apoptosis was detected by flow cytometric analysis using the Annexin V-PE/7-AAD Apoptosis Detecti...
<p>Ba/F3-mock growing with IL-3, Ba/F3-BCR-JAK2 and Ba/F3-TEL-JAK2 cells (10<sup>5</sup>/ml) were gr...
<p>Untreated cells (A); cilengitide treated cells (B); RGDechi-hCit treated cells (C). Upper left qu...
<p>(A) Subconfluent 2774 ovarian cancer cells were maintained for 5 days in complete culture medium ...
<p>(A) DU145 cells were treated with vehicle, PMS1077 or PMS601 as the indicated concentration (0–80...
<p>Kupffer cells and HMNCs co-culture system was established as above. After co-culture for 20h, cel...