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Dissection of two routes to naive pluripotency using different kinase inhibitors

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dc.contributor.authorMartinez-Val, A
dc.contributor.authorLynch, CJ
dc.contributor.authorCalvo, I
dc.contributor.authorXiménez-Embún, P
dc.contributor.authorGarcia, F
dc.contributor.authorZarzuela, E
dc.contributor.authorSerrano, M
dc.contributor.authorMunoz, J
dc.date.accessioned2026-02-25T13:56:55Z
dc.date.available2026-02-25T13:56:55Z
dc.date.issued2021-03-25
dc.description.peerreviewedSí
dc.description.tableofcontentsWe thank all members of the Proteomics Unit (CNIO), the Cellular Plasticity and Disease Group (IRB) and A. Efeyan (CNIO) for discussions. We thank O. Fernandez-Capetillo and M. Drosten for antibodies. We also thank the CNIO Experimental Therapeutics Programme for work on the CDK8/19i. I.C. is a recipient of predoctoral research contract from AGAUR. Work in the laboratory of M.S. was funded by the IRB and by the Spanish Ministry of Science co-funded by the European Regional Development Fund (ERDF) (SAF2017-82613-R), the European Research Council (ERC-2014-AdG/669622), and "laCaixa" Foundation. This work was supported by J.M. grant SAF2013-45504-R (MINECO). The CNIO Proteomics Unit belongs to ProteoRed, PRB3- ISCIII, supported by grant PT17/0019/0005. J.M. is supported by the Ramon y Cajal Programme (MINECO) RYC- 2012-10651. A.M.-V. is supported by BES-2014-070098 (MINECO).
dc.identifier.citationNat Commun. 2021 Mar 25;12(1):1863.
dc.identifier.journalNATURE COMMUNICATIONS
dc.identifier.urihttps://hdl.handle.net/20.500.12105/27272
dc.language.isoeng
dc.relation.isreferencedbyPubMed
dc.relation.publisherversion10.1038/s41467-021-22181-5
dc.repisalud.institucionCNIC
dc.rights.accessRightsopen access
dc.titleDissection of two routes to naive pluripotency using different kinase inhibitors
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication

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