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Loss of 5hmC identifies a new type of aberrant DNA hypermethylation in glioma

dc.contributor.authorFernández Fernández, Agustín 
dc.contributor.authorFernández Bayón, Gustavo 
dc.contributor.authorSierra Zapico, Marta Isabel 
dc.contributor.authorGonzález Urdinguio, Rocío 
dc.contributor.authorMangas Alonso, Cristina María 
dc.contributor.authorFerrero Rodríguez, Cecilia 
dc.contributor.authorRodrigo Sáez, Luis Ricardo 
dc.contributor.authorAstudillo González, María Aurora 
dc.contributor.authorCueto Díaz, Sergio 
dc.contributor.authorRodríguez González, Pablo
dc.contributor.authorGarcía Alonso, José Ignacio 
dc.contributor.authorFernández Fraga, Mario 
dc.date.accessioned2019-01-30T07:57:44Z
dc.date.available2019-01-30T07:57:44Z
dc.date.issued2018
dc.identifier.citationHuman Molecular Genetics, 27(17), p. 3046-3059 (2018); doi:10.1093/hmg/ddy214
dc.identifier.issn0964-6906
dc.identifier.issn1460-2083
dc.identifier.urihttp://hdl.handle.net/10651/49843
dc.description.sponsorshipThis work has been financially supported by: the Plan Nacional de IþDþI 2013–2016/FEDER (PI15/00892 to M.F.F. and A.F.F.; RTC2015-3393-1 to A.F.F.); the ISCIII-Subdirección General de Evaluación y Fomento de la Investigación, and the Plan Nacional de IþDþI 2008–2011/FEDER (CP11/00131 to A.F.F.); IUOPA (to G.F.B. and M.S); the Fundación Científica de la AECC (to R.G.U.); the Fundación Ramón Areces (to M.F.F); FICYT (to E.G.T., M.G.G. and A.C.); and the Asturias Regional Government (GRUPIN14-052 to M.F.F.). Work in P.M. laboratory is supported by the European Research Council (CoG-2014-646903), the Spanish Ministry of Economy-Competitiveness (SAF-SAF2013-43065), the Obra Social La Caixa-Fundació Josep Carreras, and the Generalitat de Catalunya. P.M. is an investigator in the Spanish Cell Therapy cooperative network (TERCEL). The IUOPA is supported by the Obra Social Cajastur-Liberbank, Spain.
dc.description.statementofresponsibilityFernandez, A.F., Bayón, G.F., Sierra, M.I., Urdinguio, R.G., Toraño, E.G., García, M.G., Carella, A., López, V., Santamarina, P., Pérez, R.F., Belmonte, T., Tejedor, J.R., Cobo, I., Menendez, P., Mangas, C., Ferrero, C., Rodrigo, L., Astudillo, A., Ortea, I., Díaz, S.C., Rodríguez-Gonzalez, P., Alonso, J.I.G., Mollejo, M., Meléndez, B., Domínguez, G., Bonilla, F., Fraga, M.F.
dc.language.isoeng
dc.relation.ispartofHuman Molecular Genetics, 27
dc.rights© The Author(s) 2018. Published by Oxford University Press.
dc.rightsThis is a pre-copyedited, author-produced version of an article accepted for publication in Human Molecular Genetics following peer review. The version of record Fernández Fernández et al. (2018) "Loss of 5hmC identifies a new type of aberrant DNA hypermethylation in glioma" is available online at: http://dx.doi.org/10.1093/hmg/ddy214
dc.rightsCC Reconocimiento - No comercial - Sin obras derivadas 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceWOS:000444202300008
dc.titleLoss of 5hmC identifies a new type of aberrant DNA hypermethylation in glioma
dc.typejournal article
dc.identifier.doi10.1093/hmg/ddy214
dc.relation.projectIDPI15/00892
dc.relation.projectIDGRUPIN14-052
dc.relation.projectIDMINECO/SAF-SAF2013-43065
dc.relation.publisherversionhttp://dx.doi.org/10.1093/hmg/ddy214
dc.rights.accessRightsopen access
dc.type.hasVersionAM


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