Figure S2. Dose-response curves of selected kinase inhibitors in parental and BRAFi-resistant IGR37 and 501Mel cells. Response to 3-fold serial dilutions of each kinase inhibitor was assessed 72âh after treatment by measuring cell viability in IGR37 (A) and 501Mel (B) cells. The values depicted in the different graphs indicate the half-maximal inhibitory concentrations (IC50) of inhibitors for which IC50 values could be determined (as explained in Methods). Values represent the mean of at least three biological replicates; one representative curve of at least 3 biological replicates is depicted. _XP: cells resistant to Vemurafenib (red), _GP: cells resistant to Dabrafenib (green). (PDF 304 kb
Figure S6: (A) Percentage of sub-G1 population identified using propidium iodide staining and quanti...
A375 growth data. Single-treatment of 10 μM PPL-008C and PPL-008CSS significantly attenuated A375 ce...
During the last two decades, kinase inhibitors have become the major drug class for targeted cancer ...
Figure S1. Dose-response curves of selected kinase inhibitors in parental and BRAFi-resistant A375 c...
Figure 6. Dose-response curves of selected kinase inhibitors in the presence or absence of BRAF inhi...
Table S1. Kinase inhibitor library screening. A commercial kinase inhibitor library of 274 compounds...
Figure S3. BRAF inhibitors in combination with selected kinase inhibitors synergistically inhibit pr...
Figure S5. Chou-Talalay analysis: A combination of Wee1 and Chk inhibitors synergistically inhibits ...
Figure S4. Western blot analysis for selected drug treatments and apoptosis assays in healthy and me...
Figure S2: (A) Hs578T cells were exposed to different concentrations of MEK1/2 inhibitor (AZD6244) a...
The effect of vemurafenib and PLX8394 on the BRAF V600E melanoma cell line LM-MEL-64 and the BRAF wt...
The effect of BRAF inhibitors vemurafenib and PLX8394 on BRAF wt / KRAS G13D cell line HCT 116. Cell...
Figure S1. Dose–response curves for sorafenib without or with the indicated selumetinib concentratio...
Viability analysis of U-87 MG cells. Cells were treated with variable concentrations of D11 for the ...
(A/B) Ba/F3 vector cells and cells transformed with pBABE Bcr-Abl were exposed to the indicated inhi...
Figure S6: (A) Percentage of sub-G1 population identified using propidium iodide staining and quanti...
A375 growth data. Single-treatment of 10 μM PPL-008C and PPL-008CSS significantly attenuated A375 ce...
During the last two decades, kinase inhibitors have become the major drug class for targeted cancer ...
Figure S1. Dose-response curves of selected kinase inhibitors in parental and BRAFi-resistant A375 c...
Figure 6. Dose-response curves of selected kinase inhibitors in the presence or absence of BRAF inhi...
Table S1. Kinase inhibitor library screening. A commercial kinase inhibitor library of 274 compounds...
Figure S3. BRAF inhibitors in combination with selected kinase inhibitors synergistically inhibit pr...
Figure S5. Chou-Talalay analysis: A combination of Wee1 and Chk inhibitors synergistically inhibits ...
Figure S4. Western blot analysis for selected drug treatments and apoptosis assays in healthy and me...
Figure S2: (A) Hs578T cells were exposed to different concentrations of MEK1/2 inhibitor (AZD6244) a...
The effect of vemurafenib and PLX8394 on the BRAF V600E melanoma cell line LM-MEL-64 and the BRAF wt...
The effect of BRAF inhibitors vemurafenib and PLX8394 on BRAF wt / KRAS G13D cell line HCT 116. Cell...
Figure S1. Dose–response curves for sorafenib without or with the indicated selumetinib concentratio...
Viability analysis of U-87 MG cells. Cells were treated with variable concentrations of D11 for the ...
(A/B) Ba/F3 vector cells and cells transformed with pBABE Bcr-Abl were exposed to the indicated inhi...
Figure S6: (A) Percentage of sub-G1 population identified using propidium iodide staining and quanti...
A375 growth data. Single-treatment of 10 μM PPL-008C and PPL-008CSS significantly attenuated A375 ce...
During the last two decades, kinase inhibitors have become the major drug class for targeted cancer ...