<p>Phosphorylation levels of JNK, ERK, and p38 MAPk following treatment with the inhibitor SP600125 (20 or 35 µM) or the control DMSO and 10 minutes of cyclic stretch at a rate of 0.25 Hz to a peak magnitude of 37% ΔSA normalized to stretched DMSO controls. Phosphorylation levels of all MAPks significantly increased above unstretched levels in DMSO treated wells. Both concentrations of SP600125 eliminated significant increases in JNK above unstretched levels. Stretch with a treatment of 35 µM of SP600125 resulted in significantly increased ERK phosphorylation compared to DMSO treated stretched wells. Significance is defined as p<0.05, and is depicted with (—) compared to unstretched, and (δ, lower) (*, higher) compared to DMSO treated. Repr...
<p>HUVECs were stimulated with S100A8 (2.0 µg/mL) (<b>A</b>), S100A9 (2.0 µg/mL) (<b>B</b>) and S100...
<p>Both L-165041(L-165) and doxorubicin (Dox) 0.1 µM activate MAPKs and Akt. If cells are pre-treate...
<p>SW1116/HCPT cells exposed to DMSO and SP600125 at concentrations 20 µM for 24 and 48 hours, with ...
<p>Phosphorylation levels of JNK, ERK, and p38 MAPk following treatment with the inhibitor U0126 (10...
<p>Phosphorylation levels of JNK, ERK, and p38 MAPk following 10, 30, and 60 minutes of cyclic stret...
<p>THSF cells were pretreated with ERK inhibitor (PD98059, 30 µM), p38 inhibitor (SB203580, 10 µM) o...
<p>Cells were pretreated with 800 µM SB203580 for 1 h, mock-irradiated or irradiated with 10 J/cm<su...
<p>Samples were obtained from the cortex. A JNK in vitro kinase assay showed a significant increase ...
<p>(A) The proteins ERK, p-ERK, p38, p-p38, JNK and p-JNK were determined using western blotting wit...
<p>H9c2 cells were treated with a JNK inhibitor, SP600125, followed by OGD-Rep. (A) Cell lysates wer...
<p>(Left) representative pictures of phospho-Ser63-c-Jun antibody signal in the nucleus upon pathway...
<p><b>A.</b> Phosphorylation of MAPK following exposure to S100A8/9. Freshly isolated neutrophils wi...
<p>SGC-7901 cells were treated with the indicated β,β-dimethylacrylshikonin concentration or the ind...
<p>No increases in MAPk phosphorylation were observed in either cell population when stretched to 12...
<p>(A):effects of exposure to 0,25 µM doxorubicin on MAPK activation by western blot using antibodie...
<p>HUVECs were stimulated with S100A8 (2.0 µg/mL) (<b>A</b>), S100A9 (2.0 µg/mL) (<b>B</b>) and S100...
<p>Both L-165041(L-165) and doxorubicin (Dox) 0.1 µM activate MAPKs and Akt. If cells are pre-treate...
<p>SW1116/HCPT cells exposed to DMSO and SP600125 at concentrations 20 µM for 24 and 48 hours, with ...
<p>Phosphorylation levels of JNK, ERK, and p38 MAPk following treatment with the inhibitor U0126 (10...
<p>Phosphorylation levels of JNK, ERK, and p38 MAPk following 10, 30, and 60 minutes of cyclic stret...
<p>THSF cells were pretreated with ERK inhibitor (PD98059, 30 µM), p38 inhibitor (SB203580, 10 µM) o...
<p>Cells were pretreated with 800 µM SB203580 for 1 h, mock-irradiated or irradiated with 10 J/cm<su...
<p>Samples were obtained from the cortex. A JNK in vitro kinase assay showed a significant increase ...
<p>(A) The proteins ERK, p-ERK, p38, p-p38, JNK and p-JNK were determined using western blotting wit...
<p>H9c2 cells were treated with a JNK inhibitor, SP600125, followed by OGD-Rep. (A) Cell lysates wer...
<p>(Left) representative pictures of phospho-Ser63-c-Jun antibody signal in the nucleus upon pathway...
<p><b>A.</b> Phosphorylation of MAPK following exposure to S100A8/9. Freshly isolated neutrophils wi...
<p>SGC-7901 cells were treated with the indicated β,β-dimethylacrylshikonin concentration or the ind...
<p>No increases in MAPk phosphorylation were observed in either cell population when stretched to 12...
<p>(A):effects of exposure to 0,25 µM doxorubicin on MAPK activation by western blot using antibodie...
<p>HUVECs were stimulated with S100A8 (2.0 µg/mL) (<b>A</b>), S100A9 (2.0 µg/mL) (<b>B</b>) and S100...
<p>Both L-165041(L-165) and doxorubicin (Dox) 0.1 µM activate MAPKs and Akt. If cells are pre-treate...
<p>SW1116/HCPT cells exposed to DMSO and SP600125 at concentrations 20 µM for 24 and 48 hours, with ...