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dc.contributor.authorHolien, Toril
dc.contributor.authorSundan, Anders
dc.date.accessioned2017-12-12T09:12:30Z
dc.date.available2017-12-12T09:12:30Z
dc.date.created2014-12-30T17:25:04Z
dc.date.issued2014
dc.identifier.citationCytokine & growth factor reviews. 2014, 25 (3), 343-350.nb_NO
dc.identifier.issn1359-6101
dc.identifier.urihttp://hdl.handle.net/11250/2470556
dc.description.abstractMultiple myeloma is characterized by slowly growing clones of malignant plasma cells in the bone marrow. The malignant state is frequently accompanied by osteolytic bone disease due to a disturbed balance between osteoblasts and osteoclasts. Bone morphogenetic proteins (BMPs) are present in the bone marrow and are important for several aspects of myeloma pathogenesis including growth and survival of tumor cells, bone homeostasis, and anemia. Among cancer cells, myeloma cells are particularly sensitive to growth inhibition and apoptosis induced by BMPs and therefore represent good models to study BMP receptor usage and signaling. Our review highlights and discusses the current knowledge on BMP signaling in myeloma.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.titleThe role of bone morphogenetic proteins in myeloma cell survivalnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionsubmittedVersionnb_NO
dc.source.pagenumber343-350nb_NO
dc.source.volume25nb_NO
dc.source.journalCytokine & growth factor reviewsnb_NO
dc.source.issue3nb_NO
dc.identifier.doi10.1016/j.cytogfr.2014.04.009
dc.identifier.cristin1189328
dc.relation.projectNorges forskningsråd: 223255nb_NO
dc.description.localcode© 2014 The authors. This document is the Author's version of a submitted work that was subsequently accepted for publication after peer review. To access the final edited and published work see http://dx.doi.org/10.1016/j.cytogfr.2014.04.009nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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