<p>(A) Immunoblotting analyses of HepG2 cells in the absence or presence of 5.5 mM of glucose <u>in the</u> and absence or presence of 20 µM of PP2 for the indicated times. (B) Addition of H<sub>2</sub>O<sub>2</sub> to the culture medium containing 5.5 mM glucosein the absence or presence of 20 µM of PP2 for 0.5 h, followed by immunoblotting. (C) HepG2 cells were cultured in medium containing or not containing (glucose-deprived) 5.5 mM of glucose in the absence or presence of 30 µM of LY204002 or 20 µM of PP2 for 0.5 h. The cells were stained with 5 µM of BES-H<sub>2</sub>O<sub>2</sub>. ROS production was measured using flow cytometry. (D) siRNA-treated HepG2 cells were subjected to immunoblotting analyses using OSSA antibody. (E) Immunoblo...
<p>A. BsB8 cells were incubated with 24 mM N-acetylcysteine (NAC), 1 mM pyruvate, or were untreated ...
The effect of SRPK2 knockout on the phosphorylation of core protein in HepG2 and HepG2(K2KO) cell li...
<p>(A-D) RAW264.7 cells were pretreated with 1 μM SRT1720 for 6h and then cultured in 30 mM D-glucos...
<p>(A)(B)(D) HepG2 cells were cultured in either glucose-containing medium or glucose-deprived mediu...
<p>(A) Immunoblotting analyses after incubation of HepG2 cells in the absence or presence of 5.5 mM ...
<p>(A) siRNA-treated HepG2 cells were subjected to reverse-transcriptase PCR (RT-PCR) to confirm NOX...
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>A, Effect of siRNA depletion of c-Src on ghrelin-induced Akt phosphorylation. HEK-GHSR1a cells tr...
<p>(<b>A</b>) High glucose did not affect the stability of <i>Adar2</i> mRNA transcripts. INS-1 cell...
Aims/Introduction: Src, a non-receptor tyrosine kinase, regulates a wide range of cellular functions...
<p>HepG2 cells were cultured in high (20 mM) glucose or in growth media containing 5.5 mM glucose fo...
<p>(A) HepG2 cells transfected with myc-TBC1D3 or empty vector were serum-starved, and stimulated wi...
<p>3T3-L1 preadipocytes with stable knockdown of SRA (shSRA) or with shControl infection were induce...
<p>(A-E) HepG2 cells were reverse-transfected with the scRNA (100 nM), AntimiR-96 (100 nM) and/or mi...
<p>A. BsB8 cells were incubated with 24 mM N-acetylcysteine (NAC), 1 mM pyruvate, or were untreated ...
The effect of SRPK2 knockout on the phosphorylation of core protein in HepG2 and HepG2(K2KO) cell li...
<p>(A-D) RAW264.7 cells were pretreated with 1 μM SRT1720 for 6h and then cultured in 30 mM D-glucos...
<p>(A)(B)(D) HepG2 cells were cultured in either glucose-containing medium or glucose-deprived mediu...
<p>(A) Immunoblotting analyses after incubation of HepG2 cells in the absence or presence of 5.5 mM ...
<p>(A) siRNA-treated HepG2 cells were subjected to reverse-transcriptase PCR (RT-PCR) to confirm NOX...
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>A, Effect of siRNA depletion of c-Src on ghrelin-induced Akt phosphorylation. HEK-GHSR1a cells tr...
<p>(<b>A</b>) High glucose did not affect the stability of <i>Adar2</i> mRNA transcripts. INS-1 cell...
Aims/Introduction: Src, a non-receptor tyrosine kinase, regulates a wide range of cellular functions...
<p>HepG2 cells were cultured in high (20 mM) glucose or in growth media containing 5.5 mM glucose fo...
<p>(A) HepG2 cells transfected with myc-TBC1D3 or empty vector were serum-starved, and stimulated wi...
<p>3T3-L1 preadipocytes with stable knockdown of SRA (shSRA) or with shControl infection were induce...
<p>(A-E) HepG2 cells were reverse-transfected with the scRNA (100 nM), AntimiR-96 (100 nM) and/or mi...
<p>A. BsB8 cells were incubated with 24 mM N-acetylcysteine (NAC), 1 mM pyruvate, or were untreated ...
The effect of SRPK2 knockout on the phosphorylation of core protein in HepG2 and HepG2(K2KO) cell li...
<p>(A-D) RAW264.7 cells were pretreated with 1 μM SRT1720 for 6h and then cultured in 30 mM D-glucos...