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dc.contributor.authorMenegatti, S
dc.contributor.authorde Kruijf, M
dc.contributor.authorGarcia-Alegria, E
dc.contributor.authorLacaud, Georges
dc.contributor.authorKouskoff, V
dc.date.accessioned2019-10-04T09:48:30Z
dc.date.available2019-10-04T09:48:30Z
dc.date.issued2019en
dc.identifier.citationMenegatti S, de Kruijf M, Garcia-Alegria E, Lacaud G, Kouskoff V. Transcriptional control of blood cell emergence. FEBS Lett. 2019 Aug 21.en
dc.identifier.pmid31432499en
dc.identifier.doi10.1002/1873-3468.13585en
dc.identifier.urihttp://hdl.handle.net/10541/622149
dc.description.abstractThe haematopoietic system is established during embryonic life through a series of developmental steps that culminates with the generation of haematopoietic stem cells. Characterisation of the transcriptional network that regulates blood cell emergence has led to the identification of transcription factors essential for this process. Among the many factors wired within this complex regulatory network, ETV2, SCL and RUNX1 are the central components. All three factors are absolutely required for blood cell generation, each one controlling a precise step of specification from the mesoderm germ layer to fully functional blood progenitors. Insight into the transcriptional control of blood cell emergence has been used for devising protocols to generate blood cells de novo, either through reprogramming of somatic cells or through forward programming of pluripotent stem cells. Interestingly, the physiological process of blood cell generation and its laboratory-engineered counterpart have very little in common.en
dc.language.isoenen
dc.relation.urlhttps://dx.doi.org/10.1002/1873-3468.13585en
dc.titleTranscriptional control of blood cell emergenceen
dc.typeArticleen
dc.contributor.departmentDevelopmental Haematopoiesis Group, Faculty of Biology, Medicine and Health, the University of Manchester, UKen
dc.identifier.journalFEBS Lettersen
dc.description.noteen]
refterms.dateFOA2019-10-08T20:21:53Z


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