<p>HepG2 cells were treated in different sub-fractions and concentrations for 24 h, and then cell were stained with Hoechst/PI as mentioned in the ‘<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0058004#s2" target="_blank">Materials and Methods</a>’ section. (A–C) Cells were absence of any treatment; (D–F) Cells were exposure to 6.25 µg/ml sch of FRP; (G–I) Cells were exposure to 50 µg/ml sch of PSP; (J–L) Cells were exposure to 50 µg/ml sch of FRP; magnification:×200.</p
<p>A. Hepatic cell in SC group. B. Hepatic cell in 12 weeks in HSHF group. C. Hepatic cell in 24 wee...
The percentage of viable and necrotic cells was measured by high-content analysis at specific time i...
Apoptosis or programmed cell death is a standard physiological mechanism. It is essential to control...
<p>(A) HepG2 cells were treated with various concentrations of EF25-(GSH)<sub>2</sub> for 24 h and 4...
<p>(A) HepG2 cells were treated with medium alone and 12.5 µg/mL CF, HF, or BF, then stained with Ho...
<p>A(a)-(c). The morphology changes of HepG2 cells treated with gradient H-EtOAc fraction for 24 h u...
<p>(a) HepG-2 cells without Compound 1 treatment were used as control and (b, c) HepG-2 cells treate...
<p>(A) LX-2 cells were cultured with mock control, conditioned media from HepG2 (HepG2-CM), or condi...
<p>A) TUNEL staining for apoptosis in HeLa cells after treatment for 48 h in control, FP and HF grou...
<p>(A) Cells were treated with indicated concentrations of RY10-4 for 24 h, and the nuclei were stai...
<p>HepG2 cells were stained with 1 μM of Hoechst 33342. Cells were treated with siRNA for 24 h and f...
<div><p>HepG2 cells were exposed to vehicle (DMSO, control), lithocholic (LCA, <b>A, C, E & F</b>), ...
<p>A, apoptosis analysis in HepG2 cells was assessed by Annexin V/PI double staining. After cells we...
<p>HepG2 cells were treated with 0.6 mM H<sub>2</sub>O<sub>2</sub> for 8 h. (A) The percentage of ap...
<p>HepG2-NS5A (<i>A</i>) and HepG2 control (<i>B</i>) cells were treated with 0–10 μM MG132 for 48 h...
<p>A. Hepatic cell in SC group. B. Hepatic cell in 12 weeks in HSHF group. C. Hepatic cell in 24 wee...
The percentage of viable and necrotic cells was measured by high-content analysis at specific time i...
Apoptosis or programmed cell death is a standard physiological mechanism. It is essential to control...
<p>(A) HepG2 cells were treated with various concentrations of EF25-(GSH)<sub>2</sub> for 24 h and 4...
<p>(A) HepG2 cells were treated with medium alone and 12.5 µg/mL CF, HF, or BF, then stained with Ho...
<p>A(a)-(c). The morphology changes of HepG2 cells treated with gradient H-EtOAc fraction for 24 h u...
<p>(a) HepG-2 cells without Compound 1 treatment were used as control and (b, c) HepG-2 cells treate...
<p>(A) LX-2 cells were cultured with mock control, conditioned media from HepG2 (HepG2-CM), or condi...
<p>A) TUNEL staining for apoptosis in HeLa cells after treatment for 48 h in control, FP and HF grou...
<p>(A) Cells were treated with indicated concentrations of RY10-4 for 24 h, and the nuclei were stai...
<p>HepG2 cells were stained with 1 μM of Hoechst 33342. Cells were treated with siRNA for 24 h and f...
<div><p>HepG2 cells were exposed to vehicle (DMSO, control), lithocholic (LCA, <b>A, C, E & F</b>), ...
<p>A, apoptosis analysis in HepG2 cells was assessed by Annexin V/PI double staining. After cells we...
<p>HepG2 cells were treated with 0.6 mM H<sub>2</sub>O<sub>2</sub> for 8 h. (A) The percentage of ap...
<p>HepG2-NS5A (<i>A</i>) and HepG2 control (<i>B</i>) cells were treated with 0–10 μM MG132 for 48 h...
<p>A. Hepatic cell in SC group. B. Hepatic cell in 12 weeks in HSHF group. C. Hepatic cell in 24 wee...
The percentage of viable and necrotic cells was measured by high-content analysis at specific time i...
Apoptosis or programmed cell death is a standard physiological mechanism. It is essential to control...