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24. The Potent ALK Inhibitor Brigatinib (AP26113) Overcomes Mechanisms of Resistance to First- and Second-Generation ALK Inhibitors in Preclinical Models. Zhang S; Anjum R; Squillace R; Nadworny S; Zhou T; Keats J; Ning Y; Wardwell SD; Miller D; Song Y; Eichinger L; Moran L; Huang WS; Liu S; Zou D; Wang Y; Mohemmad Q; Jang HG; Ye E; Narasimhan N; Wang F; Miret J; Zhu X; Clackson T; Dalgarno D; Shakespeare WC; Rivera VM Clin Cancer Res; 2016 Nov; 22(22):5527-5538. PubMed ID: 27780853 [TBL] [Abstract][Full Text] [Related]
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28. The growth inhibitory effect of 17-DMAG on ALK and MYCN double-positive neuroblastoma cell line. Yi B; Yang J; Wang L Tumour Biol; 2014 Apr; 35(4):3229-35. PubMed ID: 24293393 [TBL] [Abstract][Full Text] [Related]
29. Brigatinib, an anaplastic lymphoma kinase inhibitor, abrogates activity and growth in ALK-positive neuroblastoma cells, Drosophila and mice. Siaw JT; Wan H; Pfeifer K; Rivera VM; Guan J; Palmer RH; Hallberg B Oncotarget; 2016 May; 7(20):29011-22. PubMed ID: 27049722 [TBL] [Abstract][Full Text] [Related]
30. Induction of anaplastic lymphoma kinase (ALK) as a novel mechanism of EGFR inhibitor resistance in head and neck squamous cell carcinoma patient-derived models. Ouyang X; Barling A; Lesch A; Tyner JW; Choonoo G; Zheng C; Jeng S; West TM; Clayburgh D; Courtneidge SA; McWeeney SK; Kulesz-Martin M Cancer Biol Ther; 2018; 19(10):921-933. PubMed ID: 29856687 [TBL] [Abstract][Full Text] [Related]
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32. Activated ALK Cooperates with N-Myc via Wnt/β-Catenin Signaling to Induce Neuroendocrine Prostate Cancer. Unno K; Chalmers ZR; Pamarthy S; Vatapalli R; Rodriguez Y; Lysy B; Mok H; Sagar V; Han H; Yoo YA; Ku SY; Beltran H; Zhao Y; Abdulkadir SA Cancer Res; 2021 Apr; 81(8):2157-2170. PubMed ID: 33637566 [TBL] [Abstract][Full Text] [Related]
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34. Constitutive activation of Pim1 kinase is a therapeutic target for adult T-cell leukemia. Bellon M; Lu L; Nicot C Blood; 2016 May; 127(20):2439-50. PubMed ID: 26813676 [TBL] [Abstract][Full Text] [Related]
35. Role of anaplastic lymphoma kinase inhibition in the treatment of non-small-cell lung cancer. Croegaert K; Kolesar JM Am J Health Syst Pharm; 2015 Sep; 72(17):1456-62. PubMed ID: 26294238 [TBL] [Abstract][Full Text] [Related]
36. CEP-28122, a highly potent and selective orally active inhibitor of anaplastic lymphoma kinase with antitumor activity in experimental models of human cancers. Cheng M; Quail MR; Gingrich DE; Ott GR; Lu L; Wan W; Albom MS; Angeles TS; Aimone LD; Cristofani F; Machiorlatti R; Abele C; Ator MA; Dorsey BD; Inghirami G; Ruggeri BA Mol Cancer Ther; 2012 Mar; 11(3):670-9. PubMed ID: 22203728 [TBL] [Abstract][Full Text] [Related]
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