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dc.date.accessioned2023-03-11T17:40:13Z
dc.date.available2023-03-11T17:40:13Z
dc.date.created2022-09-28T17:52:51Z
dc.date.issued2022
dc.identifier.citationSamara, Athina Spildrejorde, Mari Sharma, Ankush Falck, Martin Leithaug, Magnus Modafferi, Stefania Bjørnstad, Pål Marius Ganesh, Acharya Gervin, Kristina Lyle, Robert Eskeland, Ragnhild . A multi-omics approach to visualize early neuronal differentiation from hESCs in 4D. iScience. 2022, 25(11)
dc.identifier.urihttp://hdl.handle.net/10852/101289
dc.description.abstractNeuronal differentiation of pluripotent stem cells is an established method to study physiology, disease, and medication safety. However, the sequence of events in human neuronal differentiation and the ability of in vitro models to recapitulate early brain development are poorly understood. We developed a protocol optimized for the study of early human brain development and neuropharmacological applications. We comprehensively characterized gene expression and epigenetic profiles at four timepoints, because the cells differentiate from embryonic stem cells towards a heterogeneous population of progenitors, immature and mature neurons bearing telencephalic signatures. A multi-omics roadmap of neuronal differentiation, combined with searchable interactive gene analysis tools, allows for extensive exploration of early neuronal development and the effect of medications.
dc.languageEN
dc.publisherCell Press
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleA multi-omics approach to visualize early neuronal differentiation from hESCs in 4D
dc.title.alternativeENEngelskEnglishA multi-omics approach to visualize early neuronal differentiation from hESCs in 4D
dc.typeJournal article
dc.creator.authorSamara, Athina
dc.creator.authorSpildrejorde, Mari
dc.creator.authorSharma, Ankush
dc.creator.authorFalck, Martin
dc.creator.authorLeithaug, Magnus
dc.creator.authorModafferi, Stefania
dc.creator.authorBjørnstad, Pål Marius
dc.creator.authorGanesh, Acharya
dc.creator.authorGervin, Kristina
dc.creator.authorLyle, Robert
dc.creator.authorEskeland, Ragnhild
cristin.unitcode185,53,0,0
cristin.unitnameInstitutt for klinisk medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2056570
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=iScience&rft.volume=25&rft.spage=&rft.date=2022
dc.identifier.jtitleiScience
dc.identifier.volume25
dc.identifier.issue11
dc.identifier.pagecount33
dc.identifier.doihttps://doi.org/10.1016/j.isci.2022.105279
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2589-0042
dc.type.versionPublishedVersion
cristin.articleid105279
dc.relation.projectNFR/287953
dc.relation.projectNFR/241117
dc.relation.projectSIGMA2/NN9632K
dc.relation.projectNFR/262484


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