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dc.creatorRoman-Gomez, J. (José)
dc.creatorJimenez-Velasco, A. (A.)
dc.creatorAguirre-Ena, X. (Xabier)
dc.creatorCastillejo, J.A. (J.A.)
dc.creatorNavarro, G. (Germán)
dc.creatorSan-Jose-Eneriz, E. (Edurne)
dc.creatorGarate, L. (Leire)
dc.creatorCordeu, L. (Lucía)
dc.creatorCervantes, F. (F.)
dc.creatorProsper-Cardoso, F. (Felipe)
dc.creatorHeiniger, A. (A.)
dc.creatorTorres, A. (Antonio)
dc.date.accessioned2011-04-13T14:01:18Z-
dc.date.available2011-04-13T14:01:18Z-
dc.date.issued2007-
dc.identifier.citationRomán-Gómez, J., Jiménez-Velasco, A., Agirre, X., Castillejo, J. A. et al. Leukemia Research 2007; 31 (11): 1521-1528es_ES
dc.identifier.issn0145-2126-
dc.identifier.urihttps://hdl.handle.net/10171/17700-
dc.description.abstractRepetitive elements are heavily methylated in normal tissues, but hypomethylated in malignant tissues, driving the global genomic hypomethylation found in cancer. This hypomethylation results in chromosomal instability, a well-characterized feature of the advanced phases of chronic myeloid leukemia (CML). We investigated methylation changes of DNA repetitive elements (LINE1, Alu, Satellite-alpha and Satellite-2) during the progression of CML from chronic phase (CP) to blast crisis (BC). CP-CML samples were significantly more hypomethylated for all repetitive sequences compared with normal samples. Furthermore, a more profound level of hypomethylation was observed among BC samples compared with CP samples. Our data suggest that repetitive DNA hypomethylation are closely associated with CML progression.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/closedAccess-
dc.subjectLINE1es_ES
dc.subjectAlues_ES
dc.subjectSatellite-alphaes_ES
dc.subjectSatellite-2es_ES
dc.subjectHypomethylationes_ES
dc.subjectCMLes_ES
dc.titleRepetitive DNA hypomethylation in the advanced phase of chronic myeloid leukemiaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttp://www.sciencedirect.com/science/journal/01452126es_ES

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