Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/94960
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dc.contributor.authorSoverini, S.-
dc.contributor.authorBranford, S.-
dc.contributor.authorNicolini, F.E.-
dc.contributor.authorTalpaz, M.-
dc.contributor.authorDeininger, M.W.N.-
dc.contributor.authorMartinelli, G.-
dc.contributor.authorMüller, M.C.-
dc.contributor.authorRadich, J.P.-
dc.contributor.authorShah, N.P.-
dc.date.issued2014-
dc.identifier.citationLeukemia Research, 2014; 38(1):10-20-
dc.identifier.issn0145-2126-
dc.identifier.issn1873-5835-
dc.identifier.urihttp://hdl.handle.net/2440/94960-
dc.description.abstractPatients with chronic myeloid leukemia develop resistance to both first-generation and second-generation tyrosine kinase inhibitors (TKIs) as a result of mutations in the kinase domain (KD) of BCR-ABL1. A wide range of BCR-ABL1 KD mutations that confer resistance to TKIs have been identified, and the T315I mutant has proven particularly difficult to target. This review summarizes the prevalence, impact, and prognostic implications of BCR-ABL1 KD mutations in patients with chronic myeloid leukemia who are treated with current TKIs and provides an overview of recent treatment guidelines and future trends for the detection of mutations.-
dc.description.statementofresponsibilitySimona Soverini, Susan Branford, Franck E. Nicolini, Moshe Talpaz, Michael W.N. Deininger, Giovanni Martinelli, Martin C. Müller, Jerald P. Radich, Neil P. Shah-
dc.language.isoen-
dc.publisherElsevier-
dc.rights© 2013 The Authors. Published by Elsevier Ltd. Open access CC BY-NC-SA 3.0-
dc.source.urihttp://dx.doi.org/10.1016/j.leukres.2013.09.011-
dc.subjectBCR-ABL1; Kinase domain; Tyrosine kinase inhibitors; Philadelphia chromosome; Chronic myeloid leukemia; Resistance; Mutations-
dc.titleImplications of BCR-ABL1 kinase domain-mediated resistance in chronic myeloid leukemia-
dc.typeJournal article-
dc.identifier.doi10.1016/j.leukres.2013.09.011-
pubs.publication-statusPublished-
dc.identifier.orcidBranford, S. [0000-0002-1964-3626] [0000-0002-5095-7981]-
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