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Pancancer analysis of somatic mutations in repetitive regions reveals recurrent mutations in snRNA U2
dc.contributor.author | Bousquets Muñoz, Pablo | |
dc.contributor.author | Díaz Navarro, Ander | |
dc.contributor.author | Nadeu, F. | |
dc.contributor.author | Sánchez Pitiot, Ana | |
dc.contributor.author | López Tamargo, Sara | |
dc.contributor.author | Shuai, S. | |
dc.contributor.author | Balbín, M. | |
dc.contributor.author | Tubio, J. M. C. | |
dc.contributor.author | Beà, S. | |
dc.contributor.author | Martin Subero, J. I. | |
dc.contributor.author | Gutiérrez Fernández, Ana Yolanda | |
dc.contributor.author | Stein, L. D. | |
dc.contributor.author | Campo, E. | |
dc.contributor.author | Suárez Puente, Xosé Antón | |
dc.date.accessioned | 2022-10-25T11:10:31Z | |
dc.date.available | 2022-10-25T11:10:31Z | |
dc.date.issued | 2022 | |
dc.identifier.citation | NPJ Genomic Medicine, 7(1) (2022); doi:10.1038/s41525-022-00292-2 | |
dc.identifier.issn | 2056-7944 | |
dc.identifier.uri | http://hdl.handle.net/10651/65149 | |
dc.description.sponsorship | X.S.P. is supported by Ministerio de Ciencia e Innovación SAF2017-87811-R, PID2020-117185RB-I00, Fundación Asociación Española Contra el Cáncer (AECC) and CIBERONC. E.C. is supported by grants from Instituto de Salud Carlos III (PMP15/00007, CIBERONC); Ministerio de Economía y Competitividad (MINECO) SAF2015-64885-R y SAF2016-81860-REDT; S.B. from Fondo de Investigaciones Sanitarias, Instituto de Salud Carlos III (PI17/01061). S.L.T. is recipient of a Severo Ochoa fellowship from the Asturian Goverment (...) | |
dc.language.iso | eng | |
dc.relation.ispartof | Npj genomic medicine | |
dc.rights | © Los autores 2022 | |
dc.rights | CC Reconocimiento 4.0 Internacional | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Scopus | |
dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85126248789&doi=10.1038%2fs41525-022-00292-2&partnerID=40&md5=927ee2b4625d1c5d61a1288b3e3fa9f9 | |
dc.title | Pancancer analysis of somatic mutations in repetitive regions reveals recurrent mutations in snRNA U2 | |
dc.type | journal article | |
dc.identifier.doi | 10.1038/s41525-022-00292-2 | |
dc.relation.projectID | MICINN/SAF2017-87811-R | |
dc.relation.projectID | MICINN/PID2020-117185RB-I00 | |
dc.relation.projectID | ISCIII/PMP15/00007 | |
dc.relation.projectID | MINECO/SAF2015-64885-R | |
dc.relation.projectID | MINECO/SAF2016-81860-REDT | |
dc.relation.projectID | ISCIII/FIS/PI17/01061 | |
dc.relation.publisherversion | http://dx.doi.org/10.1038/s41525-022-00292-2 | |
dc.rights.accessRights | open access | |
dc.type.hasVersion | VoR |
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