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dc.contributor.authorIgarashi, Kei M
dc.contributor.authorIto, Hiroshi
dc.contributor.authorMoser, Edvard Ingjald
dc.contributor.authorMoser, May-Britt
dc.date.accessioned2017-12-14T09:55:08Z
dc.date.available2017-12-14T09:55:08Z
dc.date.created2014-06-16T23:02:16Z
dc.date.issued2014
dc.identifier.citationFEBS Letters. 2014, 588 (15), 2470-2476.nb_NO
dc.identifier.issn0014-5793
dc.identifier.urihttp://hdl.handle.net/11250/2471615
dc.description.abstractDecades of neuroscience research have shed lights on the hippocampus as a key structure for the formation of episodic memory. The hippocampus is divided into distinct subfields – CA1, CA2 and CA3. Whereas accumulating evidence points to cellular and synaptic heterogeneity within each subfield, this heterogeneity has not received much attention in computational and behavioural studies and subfields have until recently been considered functionally uniform. However, a couple of recent studies have demonstrated prominent functional differences along the proximodistal axis of the CA1 subfield. Here, we review anatomical and physiological differences that might give rise to heterogeneity along the proximodistal axis of CA1 as well as the functional implications of such heterogeneity. We suggest that such heterogeneity in CA1 operates dynamically in the sense that the CA1 network alternates, on a subsecond scale, between a state where the network is primarily responsive to functionally segregated direct inputs from entorhinal cortex and a state where cells predominantly are controlled by more integrated inputs from CA3.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleFunctional diversity along the transverse axis of hippocampal area CA1nb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber2470-2476nb_NO
dc.source.volume588nb_NO
dc.source.journalFEBS Lettersnb_NO
dc.source.issue15nb_NO
dc.identifier.doi10.1016/j.febslet.2014.06.004
dc.identifier.cristin1138395
dc.relation.projectNorges forskningsråd: 223262nb_NO
dc.relation.projectEU/268598nb_NO
dc.relation.projectAndre: Kavli Foundationnb_NO
dc.description.localcode© 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.This is the authors’ accepted and refereed manuscript to the article. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/nb_NO
cristin.unitcode194,65,60,0
cristin.unitnameKavliinstitutt for nevrovitenskap
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal