Figure S1. Dose–response curves for sorafenib without or with the indicated selumetinib concentrations. Viability was measured by SRB assay after 10 days drug exposure and normalized to untreated controls (mean values +/− SEM). The respective combination indices (CI) were calculated by CompuSyn Software and are shown in Fig. 1c. (EPS 4764 kb
BACKGROUND: Currently, there are no available targeted therapy options for non-V600 BRAF mutated tum...
Figure S2: (A) Hs578T cells were exposed to different concentrations of MEK1/2 inhibitor (AZD6244) a...
Figure S1. Genome-wide synthetic lethal screens with RAS1(V19) and RAS2(V19) identify overlapping se...
Figure S2. Analysis of cell cycle after treatment with selumetinib or sorafenib and combination. Cel...
Figure S1. Dose-response curves of selected kinase inhibitors in parental and BRAFi-resistant A375 c...
Figure S2. Dose-response curves of selected kinase inhibitors in parental and BRAFi-resistant IGR37 ...
Supplementary Methods. Figure S1. RAF inhibition induces BRAF/CRAF heterodimerization in KRAS-mut co...
(A/B) Ba/F3 vector cells and cells transformed with pBABE Bcr-Abl were exposed to the indicated inhi...
The effect of BRAF inhibitors vemurafenib and PLX8394 on BRAF wt / KRAS G13D cell line HCT 116. Cell...
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...
The effect of vemurafenib and PLX8394 on the BRAF V600E melanoma cell line LM-MEL-64 and the BRAF wt...
Anti-GAB2 IP of Imatinib vs DMSO treated cells. Experiment 1 and 2 are averages of two replicates ea...
Figure S3. BRAF inhibitors in combination with selected kinase inhibitors synergistically inhibit pr...
Abstract Background Currently, there are no available targeted therapy options for non-V600 BRAF mut...
BACKGROUND: Currently, there are no available targeted therapy options for non-V600 BRAF mutated tum...
Figure S2: (A) Hs578T cells were exposed to different concentrations of MEK1/2 inhibitor (AZD6244) a...
Figure S1. Genome-wide synthetic lethal screens with RAS1(V19) and RAS2(V19) identify overlapping se...
Figure S2. Analysis of cell cycle after treatment with selumetinib or sorafenib and combination. Cel...
Figure S1. Dose-response curves of selected kinase inhibitors in parental and BRAFi-resistant A375 c...
Figure S2. Dose-response curves of selected kinase inhibitors in parental and BRAFi-resistant IGR37 ...
Supplementary Methods. Figure S1. RAF inhibition induces BRAF/CRAF heterodimerization in KRAS-mut co...
(A/B) Ba/F3 vector cells and cells transformed with pBABE Bcr-Abl were exposed to the indicated inhi...
The effect of BRAF inhibitors vemurafenib and PLX8394 on BRAF wt / KRAS G13D cell line HCT 116. Cell...
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...
The effect of vemurafenib and PLX8394 on the BRAF V600E melanoma cell line LM-MEL-64 and the BRAF wt...
Anti-GAB2 IP of Imatinib vs DMSO treated cells. Experiment 1 and 2 are averages of two replicates ea...
Figure S3. BRAF inhibitors in combination with selected kinase inhibitors synergistically inhibit pr...
Abstract Background Currently, there are no available targeted therapy options for non-V600 BRAF mut...
BACKGROUND: Currently, there are no available targeted therapy options for non-V600 BRAF mutated tum...
Figure S2: (A) Hs578T cells were exposed to different concentrations of MEK1/2 inhibitor (AZD6244) a...
Figure S1. Genome-wide synthetic lethal screens with RAS1(V19) and RAS2(V19) identify overlapping se...