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Image Search Results
Journal: Oncogene
Article Title: LMTK3 is essential for oncogenic KIT expression in KIT -mutant GIST and melanoma
doi: 10.1038/s41388-018-0508-5
Figure Lengend Snippet: A. Venn diagram of hits from RAPID tyrosine kinase siRNA screens performed in KIT -mutant GIST430 (ex11), GIST-T1, and MaMel cell lines. B. Viability 96 hours post-transfection with non-targeting (NT), LMTK3 , and KIT siRNA. C. Viability of KIT -mutant GIST cell lines was measured 96 hours post-transfection with indicated siRNAs. D. Viability of KIT-independent GIST and melanoma cells measured 96 hours post-transfection with indicated siRNA. E-F. Viability of GIST430 (ex11) and GIST430-LMTK3 myc cells 96 hours post-transfection with shown siRNA. The p values of one-way ANOVA for each cell line to NT siRNA are indicated by asterisks: *, p<0.05; **, p<0.005; ***, p<0.001; ****, p<0.0001. (N>3).
Article Snippet: LMTK3 silencing does not affect the cell viability of the
Techniques: Mutagenesis, Transfection
Journal: Oncogene
Article Title: LMTK3 is essential for oncogenic KIT expression in KIT -mutant GIST and melanoma
doi: 10.1038/s41388-018-0508-5
Figure Lengend Snippet: A. Activity of caspases 3 and 7 96 hours post-transfection with NT or LMTK3 siRNA in KIT -mutant cells. (N=5) B. Immunoblot showing cleavage (lower arrowhead, 90kDa) of full-length PARP (upper arrowhead, 110kDa), 72 hours post-siRNA transfection. C. Activity of caspases 3 and 7 96 hours post-transfection with NT, LMTK3 CDS or 3’UTR siRNA in GIST430 (ex11) or GIST430-LMTK3 myc cells. (N=3) The p values of t test for each cell line are indicated by asterisks: **, p<0.005; ***, p<0.001; ****, p<0.0001.
Article Snippet: LMTK3 silencing does not affect the cell viability of the
Techniques: Activity Assay, Transfection, Mutagenesis, Western Blot
Journal: Oncogene
Article Title: LMTK3 is essential for oncogenic KIT expression in KIT -mutant GIST and melanoma
doi: 10.1038/s41388-018-0508-5
Figure Lengend Snippet: Immunoblotting of imatinib-sensitive GIST and melanoma cell lines ( A ) or imatinib-resistant GIST cell lines ( B ) 72 hrs post-transfection with NT or LMTK3 siRNA. C-D. Quantification of phospho-KIT (Y721) and total KIT protein from immunoblots, normalized to β-tubulin. (N=3) E. Immunoblot and quantification of GIST430-LMTK3 myc stable cells 72 hrs post-transfection with NT, LMTK3 CDS, or LMTK3 3’UTR siRNA, (N=4). Bars show average protein relative to NT siRNA. The p values of t tests for each cell line compared to NT indicated by asterisks: **, p<0.005; ***, p<0.001; ****, p<0.0001.
Article Snippet: LMTK3 silencing does not affect the cell viability of the
Techniques: Western Blot, Transfection
Journal: Oncogene
Article Title: LMTK3 is essential for oncogenic KIT expression in KIT -mutant GIST and melanoma
doi: 10.1038/s41388-018-0508-5
Figure Lengend Snippet: A. LMTK3 and KIT transcript abundance relative to NT siRNA at 72 hours post-transfection with LMTK3 3’UTR siRNA in GIST430 (ex 11). B. KIT protein abundance after inhibition of translation with cycloheximide in GIST430 (ex 11) 48 hrs post-siRNA transfection. Protein half-life calculated by one-phase decay. C. Gel showing immunoprecipitated S 35 -KIT and quantification relative to NT (N=4). GIST430 (ex 11) cells labeled 48 hrs post- siRNA transfection. The p values of one-way ANOVA indicated by asterisks: *, p<0.05; ***, p<0.001.
Article Snippet: LMTK3 silencing does not affect the cell viability of the
Techniques: Transfection, Quantitative Proteomics, Inhibition, Immunoprecipitation, Labeling