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dc.contributor.authorBørset, Magne
dc.contributor.authorSundan, Anders
dc.contributor.authorWaage, Anders
dc.contributor.authorStandal, Therese
dc.date.accessioned2020-08-25T07:38:52Z
dc.date.available2020-08-25T07:38:52Z
dc.date.created2020-01-08T12:56:18Z
dc.date.issued2019
dc.identifier.citationBlood reviews. 2019, 00:100646 1-9.en_US
dc.identifier.issn0268-960X
dc.identifier.urihttps://hdl.handle.net/11250/2673774
dc.description.abstractThe question of how myeloma cells cause destruction of skeletal tissue has interested scientists for many years, and knowledge in this field has developed in parallel with the understanding of physiological bone remodeling. The identification of bioactive proteins of the cytokine class during the last decades of the previous century and mapping of their role in the regulation of anabolic and catabolic processes in bone, led to a sequence of hypotheses about how the same peptides also could be involved in myeloma-driven bone destruction. Although bone remodeling is now understood in detail, there is still no clear unified theory of how myeloma cells degrade bone. The reason for this could be that there is no single mechanism that is active in every patient. The common trait is possibly that myeloma cells benefit from bone destruction per se, and the strategy they use to accomplish this vary between patients.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleWhy do myeloma patients have bone disease? A historical perspective.en_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-9en_US
dc.source.volume00:100646en_US
dc.source.journalBlood reviewsen_US
dc.identifier.doi10.1016/j.blre.2019.100646
dc.identifier.cristin1768527
dc.description.localcode© 2019 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/).Ten_US
cristin.unitcode1920,14,0,0
cristin.unitcode194,65,15,0
cristin.unitcode1920,15,0,0
cristin.unitnameLaboratoriemedisinsk klinikk
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.unitnameMedisinsk klinikk
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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