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Abrogation of stemness in osteosarcoma by the mithramycin analog EC-8042 is mediated by its ability to inhibit NOTCH-1 signaling

dc.contributor.authorEstupiñán Sánchez, Óscar Rafael
dc.contributor.authorRey, Verónica
dc.contributor.authorTornín, Juan
dc.contributor.authorMurillo, D.
dc.contributor.authorGallego, B.
dc.contributor.authorHuergo, C.
dc.contributor.authorBlanco Lorenzo, V.
dc.contributor.authorGonzález Meana, María Victoria 
dc.contributor.authorRodríguez, A.
dc.contributor.authorMoris, F.
dc.contributor.authorGonzález, J.
dc.contributor.authorAyllón, V.
dc.contributor.authorRamos Mejía, V.
dc.contributor.authorBigas, A.
dc.contributor.authorRodríguez, R.
dc.date.accessioned2023-06-26T09:03:09Z
dc.date.available2023-06-26T09:03:09Z
dc.date.issued2023
dc.identifier.citationBiomedicine and Pharmacotherapy, 162 (2023); doi:10.1016/j.biopha.2023.114627
dc.identifier.issn0753-3322
dc.identifier.urihttp://hdl.handle.net/10651/68549
dc.description.sponsorshipThis work was supported by the Agencia Estatal de Investigación (AEI) [MICINN/Fondo Europeo de Desarrollo Regional (FEDER) (grant PID2019–106666RB-I00 to R.R.) and ISCIII/FEDER (Consorcio CIBERONC - CB16/12/00390)] and the Plan de Ciencia Tecnología e Innovación del Principado de Asturias/FEDER [grant IDI/2021/000027 and Severo Ochoa predoctoral fellowships BP-17–108 to O.E., BP20–046 to B.G. and BP-21–084 to DM].
dc.language.isoeng
dc.relation.ispartofBiomedicine and Pharmacotherapy
dc.rights© 2023 The authors. Published by Elsevier Masson SAS
dc.rightsCC Reconocimiento 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScopus
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85151414289&doi=10.1016%2fj.biopha.2023.114627&partnerID=40&md5=4d4a70ab26e3ee400e8ff362e73a99f4
dc.titleAbrogation of stemness in osteosarcoma by the mithramycin analog EC-8042 is mediated by its ability to inhibit NOTCH-1 signaling
dc.typejournal article
dc.identifier.doi10.1016/j.biopha.2023.114627
dc.relation.projectIDMICINN/FEDER/PID2019–106666RB-I00
dc.relation.projectIDISCIII/FEDER/CB16/12/00390
dc.relation.projectIDFICYT/FEDER/IDI/2021/000027
dc.relation.projectIDSevero Ochoa/BP-17–108
dc.relation.projectIDSevero Ochoa/BP20–046
dc.relation.projectIDSevero Ochoa/BP-21–08
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.biopha.2023.114627
dc.rights.accessRightsopen access
dc.type.hasVersionVoR


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© 2023 The authors. Published by Elsevier Masson SAS
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