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September 16, 2024

Figure S6 from Fibronectin contributes to a BRAF inhibitor-driven invasive phenotype in thyroid cancer through EGR1, which can be blocked by inhibition of ERK1/2.

Hannah M. Hicks Nikita Pozdeyev Sharon B. Sams Umarani Pugazhenthi Elise S. Bales Marie‐Claude Hofmann Logan R. McKenna Rebecca E. Schweppe

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Abstract

Figure S6. The ERK1/2 inhibitors SCH772984 and Ulixertinib have similar effects on cell viability in vitro.

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Cite This Study

Hicks et al. (2024) studied this question.

synapsesocial.com/papers/68e586b5b6db643587522cb1 https://doi.org/10.1158/1541-7786.27034867.v1

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Figure S2 from Fibronectin contributes to a BRAF inhibitor-driven invasive phenotype in thyroid cancer through EGR1, which can be blocked by inhibition of ERK1/2.2024
2Figure S4 from Fibronectin contributes to a BRAF inhibitor-driven invasive phenotype in thyroid cancer through EGR1, which can be blocked by inhibition of ERK1/2.2024
3Figure S8 from Fibronectin contributes to a BRAF inhibitor-driven invasive phenotype in thyroid cancer through EGR1, which can be blocked by inhibition of ERK1/2.2024
4Figure S7 from Fibronectin contributes to a BRAF inhibitor-driven invasive phenotype in thyroid cancer through EGR1, which can be blocked by inhibition of ERK1/2.2024
5Figure S1 from Fibronectin contributes to a BRAF inhibitor-driven invasive phenotype in thyroid cancer through EGR1, which can be blocked by inhibition of ERK1/2.2024

More related papers

Figure S3 from Fibronectin contributes to a BRAF inhibitor-driven invasive phenotype in thyroid cancer through EGR1, which can be blocked by inhibition of ERK1/2.2024
Figure S5 from Fibronectin contributes to a BRAF inhibitor-driven invasive phenotype in thyroid cancer through EGR1, which can be blocked by inhibition of ERK1/2.2024
Table S1 from Fibronectin contributes to a BRAF inhibitor-driven invasive phenotype in thyroid cancer through EGR1, which can be blocked by inhibition of ERK1/2.2024