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dc.creatorSan-Jose-Eneriz, E. (Edurne)
dc.creatorRoman-Gomez, J. (José)
dc.creatorJimenez-Velasco, A. (A.)
dc.creatorGarate, L. (Leire)
dc.creatorMartin, V. (Vanesa)
dc.creatorCordeu, L. (Lucía)
dc.creatorVilas, A. (Amaia)
dc.creatorRodriguez-Otero, P. (Paula)
dc.creatorCalasanz-Abinzano, M.J. (Maria Jose)
dc.creatorProsper-Cardoso, F. (Felipe)
dc.creatorAguirre-Ena, X. (Xabier)
dc.date.accessioned2011-05-23T13:52:06Z-
dc.date.available2011-05-23T13:52:06Z-
dc.date.issued2009-
dc.identifier.citationSan Jose-Eneriz, E.; Roman-Gomez, J., Jimenez-Velasco, A., Garate, L. et al. MicroRNA expression profiling in Imatinib-resistant Chronic Myeloid Leukemia patients without clinically significant ABL1-mutations. Mol. cancer 2009, 8: 69es_ES
dc.identifier.issn1476-4598-
dc.identifier.urihttps://hdl.handle.net/10171/18133-
dc.description.abstractThe development of Imatinib Mesylate (IM), the first specific inhibitor of BCR-ABL1, has had a major impact in patients with Chronic Myeloid Leukemia (CML), establishing IM as the standard therapy for CML. Despite the clinical success obtained with the use of IM, primary resistance to IM and molecular evidence of persistent disease has been observed in 20-25% of IM treated patients. The existence of second generation TK inhibitors, which are effective in patients with IM resistance, makes identification of predictors of resistance to IM an important goal in CML. In this study, we have identified a group of 19 miRNAs that may predict clinical resistance to IM in patients with newly diagnosed CML.es_ES
dc.language.isoenges_ES
dc.publisherBioMed Centrales_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectMaterias Investigacion::Ciencias de la Salud::Oncologíaes_ES
dc.titleMicroRNA expression profiling in Imatinib-resistant Chronic Myeloid Leukemia patients without clinically significant ABL1-mutationses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doihttp://dx.doi.org/10.1186/1476-4598-8-69es_ES

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