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dc.contributor.authorAyllon, Verónica
dc.contributor.authorVogel González, Marina
dc.contributor.authorGonzález-Pozas, Federico
dc.contributor.authorDomingo Reinés, Joan
dc.contributor.authorMontes, Rosa
dc.contributor.authorMorales Cacho, Lucía
dc.contributor.authorRamos Mejía, Verónica 
dc.date.accessioned2025-01-20T10:51:31Z
dc.date.available2025-01-20T10:51:31Z
dc.date.issued2017-03-19
dc.identifier.urihttps://hdl.handle.net/10481/99691
dc.description.abstractPediatric Acute Megakaryoblastic Leukemia not associated to Down Syndrome (non-DS AMKL) is a rare disease with a dismal prognosis. Around 15% of patients carry the chromosomal translocation t(1;22) that originates the fusion oncogene RBM15-MKL1, which is linked to an earlier disease onset (median of 6months of age) and arises in utero. Here we report the generation of two hPSC cell lines constitutively expressing the oncogene RBM15-MKL1, resulting in an increased expression of known RBM15-MKL1 gene targets. These cell lines represent new disease models of pediatric AMKL to study the impact of the RBM15-MKL1 oncogene on human embryonic hematopoietic development.es_ES
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleNew hPSC-based human models to study pediatric Acute Megakaryoblastic Leukemia harboring the fusion oncogene RBM15-MKL1es_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1016/j.scr.2016.12.019


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internacional