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pubmed-article:20673586pubmed:abstractTextThis report aims to more accurately define the frequency of the involvement of SRC Family Kinases (SFKs) in imatinib- and dasatinib-resistant CML patients. Clinical samples were analysed during in vivo treatment. We confirmed the high frequency of SFKs involvement in Tyrosine kinase inhibitor-resistant CML (52% of the cases) and even further in progressive disease and blast crises (60% of the cases). The SFKs deregulation is also observed in patients harboring BCR-ABL mutations. In T315I and F317L mutated patients, CML-resistance appears to be promoted by SFKs kinase protein reactivation once the BCR-ABL mutated clone has decreased on Omacetaxine.lld:pubmed
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pubmed-article:20673586pubmed:authorpubmed-author:MagaudJean-Pi...lld:pubmed
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pubmed-article:20673586pubmed:authorpubmed-author:SalesseStépha...lld:pubmed
pubmed-article:20673586pubmed:copyrightInfoCopyright © 2010 Elsevier Ltd. All rights reserved.lld:pubmed
pubmed-article:20673586pubmed:issnTypeElectroniclld:pubmed
pubmed-article:20673586pubmed:volume35lld:pubmed
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pubmed-article:20673586pubmed:year2011lld:pubmed
pubmed-article:20673586pubmed:articleTitleLongitudinal studies of SRC family kinases in imatinib- and dasatinib-resistant chronic myelogenous leukemia patients.lld:pubmed
pubmed-article:20673586pubmed:affiliationHospices Civils de Lyon, Centre Hospitalier Lyon Sud, Laboratory for Molecular Biology and UMR5239 CNRS, Pierre-Bénite, France. sandrine.hayette@chu-lyon.frlld:pubmed
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