EMD 1214063 and EMD 1204831 Constitute a New Class of Potent and Highly Selective c-Met Inhibitors-Reference-Cited by-同舟云学术

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EMD 1214063 and EMD 1204831 Constitute a New Class of Potent and Highly Selective c-Met Inhibitors

Published:2013-04-03 Issue:11 Volume:19 Page:2941-2951
ISSN:1078-0432
Container-title:Clinical Cancer Research
language:en
Short-container-title:Clin Cancer Res

Author:

Bladt Friedhelm,Faden Bettina,Friese-Hamim Manja,Knuehl Christine,Wilm Claudia,Fittschen Claus,Grädler Ulrich,Meyring Michael,Dorsch Dieter,Jaehrling Frank,Pehl Ulrich,Stieber Frank,Schadt Oliver,Blaukat Andree

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

Cited by 116 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. E2F1-Associated Purine Synthesis Pathway Is a Major Component of the MET-DNA Damage Response Network;Cancer Research Communications;2024-07-01

2. Brief Report: Tepotinib as a Treatment Option in MET Exon 14 Skipping-Positive Lung Cancers—Investigating Discordance Between ArcherMET and the Oncomine Dx Target Test;JTO Clinical and Research Reports;2024-06

3. Kinase Inhibitors and Kinase-Targeted Cancer Therapies: Recent Advances and Future Perspectives;International Journal of Molecular Sciences;2024-05-17

4. Recording and classifying MET receptor mutations in cancers;eLife;2024-04-23

5. Case report: The effect of second-line vebreltinib treatment on a patient with advanced NSCLC harboring the MET exon 14 skipping mutation after tepotinib treatment;Frontiers in Oncology;2024-04-19

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