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Impaired condensin complex and Aurora B kinase underlie mitotic and chromosomal defects in hyperdiploid B-cell ALL
dc.contributor.author | Molina, O. | |
dc.contributor.author | Vinyoles, M. | |
dc.contributor.author | Granada, I. | |
dc.contributor.author | Roca Ho, H. | |
dc.contributor.author | Gutiérrez Agüera, F. | |
dc.contributor.author | Valledor, L. | |
dc.contributor.author | López López, C. M. | |
dc.contributor.author | Rodríguez González, Pablo | |
dc.contributor.author | Trincado, J. L. | |
dc.contributor.author | Tirados Menéndez, Sofía | |
dc.date.accessioned | 2021-01-27T10:19:46Z | |
dc.date.available | 2021-01-27T10:19:46Z | |
dc.date.issued | 2020 | |
dc.identifier.citation | Blood, 136(3), p. 313-327 (2020); doi:10.1182/blood.2019002538 | |
dc.identifier.issn | 1528-0020 | |
dc.identifier.uri | http://hdl.handle.net/10651/57529 | |
dc.description.sponsorship | This work was supported by the European Research Council (CoG-2014-646903 [P.M.]), the Spanish Ministry of Economy and Competitiveness (SAF-2016-80481-R [P.M.]), the Asociación Española Contra el Cáncer (AECC-CI-2015), and the ISCIII (PI17/01028) (C.B.). This work was also supported by the Spanish Ministry of Economy and Competitiveness (SAF-2016-75286-R [R.R.]), the ISCIII/FEDER (Miguel Servet Program CPII16/00049 [R.R.], Sara Borrell Program CD16/00103 [S.T.M.], and PI16/00280), and Consorcio CIBERONC (CB16/12/00390) (...) | |
dc.description.statementofresponsibility | Molina, O., Vinyoles, M., Granada, I., Roca-Ho, H., Gutierrez-Agüera, F., Valledor, L., López-López, C.M., Rodríguez-González, P., Trincado, J.L., Menéndez, S.T., Pal, D., Ballerini, P., den Boer, M.L., Plensa, I., Mar Perez-Iribarne, M., Rodríguez-Perales, S., Calasanz, M.J., Ramírez-Orellana, M., Rodríguez, R., Camós, M., Calvo, M., Bueno, C., Menéndez, P. | |
dc.format.extent | p. 313-327 | |
dc.language.iso | eng | |
dc.relation.ispartof | Blood | |
dc.rights | © 2020 The American Society of Hematology | |
dc.source | Scopus | |
dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85088155117&doi=10.1182%2fblood.2019002538&partnerID=40&md5=38080dfcf1381ea91e0827a4a0e74721 | |
dc.title | Impaired condensin complex and Aurora B kinase underlie mitotic and chromosomal defects in hyperdiploid B-cell ALL | |
dc.type | journal article | |
dc.identifier.doi | 10.1182/blood.2019002538 | |
dc.relation.publisherversion | http://dx.doi.org/10.1182/blood.2019002538 |
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