<p>Morphology of control and treated cells is shown in E. Values are presented as mean ± SEM of three independent experiments. Statistical significance (P values) between the control and H<sub>2</sub>O<sub>2</sub>-treated group recovered either in i-Extract, (1 μg/ml for C6 and 0.4 μg/ml for IMR32), withaferin A (0.3 μg/ml for C6 and 0.2 μg/ml for IMR32), withanone (5 μg/ml for C6 and 2 μg/ml for IMR32) and WEX 1% supplemented medium for 24 h are shown. Statistical significance with P<0.05 was considered significant.</p
<p>Peptide concentration in μM. Cell viability was measured 24-hours after the addition of peptide. ...
<p>SK-N-SH cells were differentiated using 20 µM retinoic acid for 10 days and ddifferentiated media...
<p>(<b>A</b>) Dexamethasone (DEXA) treatment induces tumor cell death in glioma cell implanted brain...
<p>Morphology of control and treated C6 and IMR32 cells is shown in C. Immunostaining of control and...
<p>Whereas the level of GFAP expression decreased in cells stressed with H<sub>2</sub>O<sub>2</sub> ...
<p>Glioma and MRC-5 non-tumor cell viability. 1321N1, SF-767 and U118 human glioma cells and MRC-5 h...
<p>Quantitation of the protein levels as determined by three independent experiments is shown in C. ...
<p>Cells were incubated with vehicle (DMSO), TTD (0.1 µM) or AAP alone or in the presence of TTD (0....
<p>Cell viability and toxicity of various concentrations of glutamate was assayed by MTT and LDH ass...
<p>Cell death was measured using LDH release; it was significantly enhanced when cells were exposed ...
<p>Peptide concentration in μM. Cell viability was measured 24-hours after the addition of peptide. ...
<p>ARPE19 cells were treated with 6-15 µM 7KCh for 24 hr and the cell viability was measured by dete...
<p>Figure A to H showed the morphology of rat cardiomyocyte monolayer (×400). Control cells were not...
<p>Primary astrocytes (1×10<sup>5</sup> cells/ml), were activated with LPS (10 μg/ml) and simultaneo...
Increasing evidence shows that discrepancies exist among in vitro cytotoxicity methods resulting in ...
<p>Peptide concentration in μM. Cell viability was measured 24-hours after the addition of peptide. ...
<p>SK-N-SH cells were differentiated using 20 µM retinoic acid for 10 days and ddifferentiated media...
<p>(<b>A</b>) Dexamethasone (DEXA) treatment induces tumor cell death in glioma cell implanted brain...
<p>Morphology of control and treated C6 and IMR32 cells is shown in C. Immunostaining of control and...
<p>Whereas the level of GFAP expression decreased in cells stressed with H<sub>2</sub>O<sub>2</sub> ...
<p>Glioma and MRC-5 non-tumor cell viability. 1321N1, SF-767 and U118 human glioma cells and MRC-5 h...
<p>Quantitation of the protein levels as determined by three independent experiments is shown in C. ...
<p>Cells were incubated with vehicle (DMSO), TTD (0.1 µM) or AAP alone or in the presence of TTD (0....
<p>Cell viability and toxicity of various concentrations of glutamate was assayed by MTT and LDH ass...
<p>Cell death was measured using LDH release; it was significantly enhanced when cells were exposed ...
<p>Peptide concentration in μM. Cell viability was measured 24-hours after the addition of peptide. ...
<p>ARPE19 cells were treated with 6-15 µM 7KCh for 24 hr and the cell viability was measured by dete...
<p>Figure A to H showed the morphology of rat cardiomyocyte monolayer (×400). Control cells were not...
<p>Primary astrocytes (1×10<sup>5</sup> cells/ml), were activated with LPS (10 μg/ml) and simultaneo...
Increasing evidence shows that discrepancies exist among in vitro cytotoxicity methods resulting in ...
<p>Peptide concentration in μM. Cell viability was measured 24-hours after the addition of peptide. ...
<p>SK-N-SH cells were differentiated using 20 µM retinoic acid for 10 days and ddifferentiated media...
<p>(<b>A</b>) Dexamethasone (DEXA) treatment induces tumor cell death in glioma cell implanted brain...