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dc.contributor.authorEkici, Y.
dc.contributor.authorYilmaz, A.
dc.contributor.authorKucuksezer, U.C.
dc.contributor.authorGazioglu, S.B.
dc.contributor.authorYamalioglu, Z.D.
dc.contributor.authorGurol, A.O.
dc.contributor.authorLinn, T.
dc.contributor.authorTuncer, F.N.
dc.date.accessioned2021-12-21T08:40:29Z
dc.date.available2021-12-21T08:40:29Z
dc.date.issued2021
dc.identifier.issn13570560
dc.identifier.urihttps://doi.org/10.1007/s12032-021-01560-4
dc.identifier.urihttp://dspace.yeniyuzyil.edu.tr:8080/xmlui/handle/20.500.12629/1013
dc.description.abstractPancreatic ductal adenocarcinoma (PDAC) is among the most deadly cancers. Since most patients develop resistance to conventional treatments, new approaches are in urgency. Valproic acid (VPA) was shown to induce apoptosis and reduce proliferation in PANC-
dc.description.sponsorshipThis work was supported by the Scientific Research Projects Coordination Unit of Istanbul University. Project No.: 32763.
dc.language.isoEnglish
dc.publisherSpringer
dc.titleCombined evaluation of proliferation and apoptosis to calculate IC50 of VPA-induced PANC-1 cells and assessing its effect on the Wnt signaling pathway
dc.typeArticle
dc.relation.journalMedical Oncology
dc.identifier.issue9
dc.identifier.volume38
dc.identifier.doi10.1007/s12032-021-01560-4
dc.relation.issue9
dc.relation.volume38


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