<p>(A) Immunoblotting analyses after incubation of HepG2 cells in the absence or presence of 5.5 mM of glucose and absence or presence of 30 µM of LY294002 for the indicated times. (B) HepG2 cells treated or not treated with various concentrations of glucose for 0.5 h were subjected to immunoblotting. (C) Immunoblotting analyses of HepG2 cells treated or not treated with 5.5 mM of glucose, 5.5 mM of galactose, or 5.5 mM of fructose for 0.5 h. (D) Immunoblotting analyses of HepG2 cells treated or not treated with 5.5 mM of glucose, 5.5 mM of 2-DG, or 5.5 mM of glucose plus 5.5 mM of 2-DG for 0.5 h.</p
HeLa cells treated as indicated were serum starved for 6 h and stimulated with 100 nM insulin. (Top)...
<p>A: Representative Western blots of Akt, pAkt, FoxO3a, pFoxO3a, Bim and Bcl-xL in CMECs incubation...
<p>InR1G cells were exposed to regular (11.1 mM, white) or high (25 mM, black) glucose levels for 12...
<p>(A) Immunoblotting analyses of HepG2 cells in the absence or presence of 5.5 mM of glucose <u>in ...
<p>(A)(B)(D) HepG2 cells were cultured in either glucose-containing medium or glucose-deprived mediu...
<p>NG: normal glucose condition (5.5 mmol/L); HG: high glucose condition (28 mmol/L); A: ALA; LY: LY...
<p>(A) siRNA-treated HepG2 cells were subjected to reverse-transcriptase PCR (RT-PCR) to confirm NOX...
<p>Western blots of extracts from HepG2 cells incubated for 6 hr in media having either 0 mM or 5 mM...
Glucose is the most efficient energy source, and various cancer cells depend on glycolysis for energ...
<div><p>Glucose is the most efficient energy source, and various cancer cells depend on glycolysis f...
<p>HepG2 cells were treated with 50 μM of PI3K ((LY294002), p38 (SB202190) or JNK (SP600125) inhibit...
<p>(A) HepG2 cells were pretreated with GH or 30 min or 4 hours and harvested after insulin stimulat...
<p>(<b>A-C</b>) HepG2 cells were treated in parallel for 24 hr in medium with 25 mM, 5 mM or 0 mM gl...
<p>The figure shows a Western blot of a representative experiment (top) and densitometric analyses f...
<p>(A) HepG2 cells transfected with myc-TBC1D3 or empty vector were serum-starved, and stimulated wi...
HeLa cells treated as indicated were serum starved for 6 h and stimulated with 100 nM insulin. (Top)...
<p>A: Representative Western blots of Akt, pAkt, FoxO3a, pFoxO3a, Bim and Bcl-xL in CMECs incubation...
<p>InR1G cells were exposed to regular (11.1 mM, white) or high (25 mM, black) glucose levels for 12...
<p>(A) Immunoblotting analyses of HepG2 cells in the absence or presence of 5.5 mM of glucose <u>in ...
<p>(A)(B)(D) HepG2 cells were cultured in either glucose-containing medium or glucose-deprived mediu...
<p>NG: normal glucose condition (5.5 mmol/L); HG: high glucose condition (28 mmol/L); A: ALA; LY: LY...
<p>(A) siRNA-treated HepG2 cells were subjected to reverse-transcriptase PCR (RT-PCR) to confirm NOX...
<p>Western blots of extracts from HepG2 cells incubated for 6 hr in media having either 0 mM or 5 mM...
Glucose is the most efficient energy source, and various cancer cells depend on glycolysis for energ...
<div><p>Glucose is the most efficient energy source, and various cancer cells depend on glycolysis f...
<p>HepG2 cells were treated with 50 μM of PI3K ((LY294002), p38 (SB202190) or JNK (SP600125) inhibit...
<p>(A) HepG2 cells were pretreated with GH or 30 min or 4 hours and harvested after insulin stimulat...
<p>(<b>A-C</b>) HepG2 cells were treated in parallel for 24 hr in medium with 25 mM, 5 mM or 0 mM gl...
<p>The figure shows a Western blot of a representative experiment (top) and densitometric analyses f...
<p>(A) HepG2 cells transfected with myc-TBC1D3 or empty vector were serum-starved, and stimulated wi...
HeLa cells treated as indicated were serum starved for 6 h and stimulated with 100 nM insulin. (Top)...
<p>A: Representative Western blots of Akt, pAkt, FoxO3a, pFoxO3a, Bim and Bcl-xL in CMECs incubation...
<p>InR1G cells were exposed to regular (11.1 mM, white) or high (25 mM, black) glucose levels for 12...