VX680

ABL proto-oncogene 1, non-receptor tyrosine kinase ; Homo sapiens







13 Article(s)
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1 22772060 MK-0457, an Aurora kinase and BCR-ABL inhibitor, is active in patients with BCR-ABL T315I leukemia. 2013 Jan 3
2 23495751 Comparing immobilized kinase inhibitors and covalent ATP probes for proteomic profiling of kinase expression and drug selectivity. 2013 Apr 5 1
3 23556431 Activity of histone deacetylase inhibitors and an Aurora kinase inhibitor in BCR-ABL-expressing leukemia cells: Combination of HDAC and Aurora inhibitors in BCR-ABL-expressing cells. 2013 Apr 4 4
4 22521726 Gadd45a transcriptional induction elicited by the Aurora kinase inhibitor MK-0457 in Bcr-Abl-expressing cells is driven by Oct-1 transcription factor. 2012 Aug 1
5 19874801 Targets and effectors of the cellular response to aurora kinase inhibitor MK-0457 (VX-680) in imatinib sensitive and resistant chronic myelogenous leukemia. 2010 Mar 1 3
6 20388735 Activity of the Aurora kinase inhibitor VX-680 against Bcr/Abl-positive acute lymphoblastic leukemias. 2010 May 2
7 20563869 Efficacy of MK-0457 and in combination with vorinostat against Philadelphia chromosome positive acute lymphoblastic leukemia cells. 2010 Nov 3
8 19338751 Mechanism of MK-0457 efficacy against BCR-ABL positive leukemia cells. 2009 Mar 20 2
9 19549414 [Research progress on aurora kinase inhibitor MK-0457 in therapy for some hematological malignancies -- review]. 2009 Jun 2
10 18829489 Cotreatment with vorinostat enhances activity of MK-0457 (VX-680) against acute and chronic myelogenous leukemia cells. 2008 Oct 1 2
11 16990603 MK-0457, a novel kinase inhibitor, is active in patients with chronic myeloid leukemia or acute lymphocytic leukemia with the T315I BCR-ABL mutation. 2007 Jan 15 1
12 17710227 Sequential ABL kinase inhibitor therapy selects for compound drug-resistant BCR-ABL mutations with altered oncogenic potency. 2007 Sep 1
13 16046538 Inhibition of drug-resistant mutants of ABL, KIT, and EGF receptor kinases. 2005 Aug 2 1