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Characteristics and outcomes of patients with chronic myeloid leukemia and T315I mutation following failure of imatinib mesylate therapy
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Characterization of AMN107, a selective inhibitor of native and mutant Bcr-abl
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A phase i dose escalation study of KW-2449, an oral multikinase inhibitor against FLT3, Abl, FGFR1, and Aurora in patients with relapsed/refractory AML, treatment resistant/intolerant CML, ALL, and MDS [abstract]
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Cortes J, Roboz GJ, Kantarjian H, et al. A phase I dose escalation study of KW-2449, an oral multikinase inhibitor against FLT3, Abl, FGFR1, and Aurora in patients with relapsed/refractory AML, treatment resistant/intolerant CML, ALL, and MDS [abstract]. Blood 2007; 110:909.
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Simultaneous targeting of Aurora kinases and Bcr-Abl kinase by the small molecule inhibitor PHA-739358 is effective against imatinib-resistant BCR-ABL mutations including T315I
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