<p>Cells were exposed to 42°C for the indicated amount of time. Apoptotic cells were measured by flow cytometry immediately after hyperthermia. <b>A:</b> Images showing flow cytometric analysis of apoptosis. <b>B:</b> The histogram shows the result from A (%). *P<0.05 compared to control. Each date point is the mean of three independent experiments.</p
Surviving fraction as function of radiation dose at different temperatures. Cells exposed for 1 hour...
<p>A) Control, B) NTEG, C) HTEG (room temperature vs. control group: p = 0.006; high temperature vs....
Mild hyperthermia is known to enhance apoptosis in a range of normal and neoplastic cell populations...
<p>Cells were exposed to 37°C and 42°C for the indicated amount of time. Apoptotic cells were measur...
<p>Phalloidin stained actin filaments (red) and DAPI stained nucleus (blue) of MLO-Y4 cells heat-tre...
<p>Flow cytometry analysis of Annexin-FITC/PI uptake to evaluate the percentage of cells in early an...
<p><b><i>A</i></b>.Whole cell extracts were prepared at indicated periods after 42.5°C hyperthermia ...
<p>Representative histograms (from four independent experiments), before the heat treatment (d 0) an...
<p>786-O-shKu80 and 786-O-scramble cells were subjected to 42°C for the indicated amount of time. Su...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
<p><b><i>A</i></b>. Phase contrast photographs of PC-10 cells, two days after treatment with HDACIs ...
DNA damage (tail intensity analyzed by Comet assay) in A549 cells (A). Apoptosis (B) and necrosis (C...
<p>Cells cultured at 37°C and cells cultured similarly at 37°C but exposed once a day for 15 min to ...
There is now abundant evidence that apoptosis, the cell death mechanism responsible for physiologial...
Surviving fraction as function of radiation dose at different temperatures. Cells exposed for 1 hour...
<p>A) Control, B) NTEG, C) HTEG (room temperature vs. control group: p = 0.006; high temperature vs....
Mild hyperthermia is known to enhance apoptosis in a range of normal and neoplastic cell populations...
<p>Cells were exposed to 37°C and 42°C for the indicated amount of time. Apoptotic cells were measur...
<p>Phalloidin stained actin filaments (red) and DAPI stained nucleus (blue) of MLO-Y4 cells heat-tre...
<p>Flow cytometry analysis of Annexin-FITC/PI uptake to evaluate the percentage of cells in early an...
<p><b><i>A</i></b>.Whole cell extracts were prepared at indicated periods after 42.5°C hyperthermia ...
<p>Representative histograms (from four independent experiments), before the heat treatment (d 0) an...
<p>786-O-shKu80 and 786-O-scramble cells were subjected to 42°C for the indicated amount of time. Su...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
<p><b><i>A</i></b>. Phase contrast photographs of PC-10 cells, two days after treatment with HDACIs ...
DNA damage (tail intensity analyzed by Comet assay) in A549 cells (A). Apoptosis (B) and necrosis (C...
<p>Cells cultured at 37°C and cells cultured similarly at 37°C but exposed once a day for 15 min to ...
There is now abundant evidence that apoptosis, the cell death mechanism responsible for physiologial...
Surviving fraction as function of radiation dose at different temperatures. Cells exposed for 1 hour...
<p>A) Control, B) NTEG, C) HTEG (room temperature vs. control group: p = 0.006; high temperature vs....
Mild hyperthermia is known to enhance apoptosis in a range of normal and neoplastic cell populations...