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Comparison of the efficiencies of two TR-FRET methods to detect in vitro natural and synthesized inhibitors of the Raf/MEK/ERK signaling pathway

机译：两种TR-FRET方法检测RAF / MEK / ERK信号通路体外自然和合成抑制剂的效率比较

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1. Comparison of the efficiencies of two TR-FRET methods to detect in vitro natural and synthesized inhibitors of the Raf/MEK/ERK signaling pathway [J] . Fabienne Saab, Sylvain Routier, Jean-Yves Mérour, International Journal of High Throughput Screening . 2010,第5期

机译：比较两种TR-FRET方法检测Raf / MEK / ERK信号传导途径的体外天然和合成抑制剂的效率
2. Dequalinium induces cytotoxicity in human leukemia NB4 cells by downregulation of Raf/MEK/ERK and PI3K/Akt signaling pathways and potentiation of specific inhibitors of these pathways [J] . Garc铆a-P茅rezA.I., García-PérezA.I., GaleanoE., Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis . 2014,第7期

机译：地夸林通过下调Raf / MEK / ERK和PI3K / Akt信号通路并增强这些通路的特定抑制剂来诱导人白血病NB4细胞的细胞毒性
3. Peptide V3 Inhibits the Growth of Human Hepatocellular Carcinoma by Inhibiting the Ras/Raf/MEK/ERK Signaling Pathway [J] . Dongdong Wu, Mengling Li, Yingran Gao, Journal of Cancer . 2019,第7期

机译：V3肽通过抑制Ras / Raf / MEK / ERK信号通路抑制人类肝细胞癌的生长
4. INHIBITORS OF THE RAS/ERK SIGNALING PATHWAY INCORPORATING THE FXF MOTIF FOR FHE DEVELOPMENT OF ANTICANCER DRUGS [C] . Theodore Skarlas, EugeniaJPanou-Pomonis, Dimitrios Krikorian the European Peptide Symposium . 2007

机译：RAS / ERK信号传导途径的抑制剂包括FXF基序用于抗癌药物的发育
5. Silibinin Inhibits Glioblastoma Cell Proliferation via AKT/S6/4EBP1 and STAT3 Signaling Pathways In Vitro. [D] . Us, Ilkay. 2014

机译：水飞蓟宾通过AKT / S6 / 4EBP1和STAT3信号通路体外抑制胶质母细胞瘤细胞增殖。
6. Peptide V3 Inhibits the Growth of Human Hepatocellular Carcinoma by Inhibiting the Ras/Raf/MEK/ERK Signaling Pathway [O] . Dongdong Wu, Mengling Li, Yingran Gao, 2019

机译：V3肽通过抑制Ras / Raf / MEK / ERK信号通路抑制人类肝癌的生长
7. Development of Dual-Pathway Inhibitors of Raf/MEK/ERK and PI3K/Akt Signaling Pathways. [O] . Fraser Sasha 2011

机译：Raf / MEK / ERK和PI3K / Akt信号通路双通路抑制剂的开发。

Comparison of the efficiencies of two TR-FRET methods to detect in vitro natural and synthesized inhibitors of the Raf/MEK/ERK signaling pathway

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