Приказ основних података о документу

dc.creatorMilošević, Emilija
dc.creatorJasnić, Jovana
dc.creatorNovković, Mirjana
dc.creatorCenni, V.
dc.creatorBavelloni, A.
dc.creatorKojić, Snežana
dc.date.accessioned2023-06-27T11:23:02Z
dc.date.available2023-06-27T11:23:02Z
dc.date.issued2023
dc.identifier.urihttps://febs.onlinelibrary.wiley.com/doi/10.1002/1878-0261.13471
dc.identifier.urihttps://imagine.imgge.bg.ac.rs/handle/123456789/1911
dc.description.abstractIntroduction: Rhabdomyosarcoma (RMS) is the most common soft tissue malignancy in children and adolescents. Respecting the age of the patients and the tumor aggressiveness, investigation of the molecular mechanisms of RMS tumorigenesis is essential, most notably due to the possible identification of novel therapeutic targets. To contribute to a better understanding of the molecular pathology of RMS, we investigated ANKRD1 (ankyrin repeat domain 1) gene, considered a potential RMS diagnostic marker. The changes in its expression are related to carcinogenesis and resistance to chemotherapy in several types of tumors.sr
dc.language.isoensr
dc.publisherWileysr
dc.rightsopenAccesssr
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceMolecular oncologysr
dc.subjectRhabdomyosarcoma
dc.subjectANKRD1
dc.subjectCajal bodies
dc.subjectProteasomal degradation
dc.titleExpression profiling of ANKRD1 in rhabdomyosarcoma cell linessr
dc.typeconferenceObjectsr
dc.rights.licenseBYsr
dc.citation.epage197
dc.citation.spage196
dc.citation.volume17
dc.citation.volumeSupplement 1
dc.description.otherEACR 2023: Innovative Cancer Science, 12-15 June 2023, Torino, Italysr
dc.identifier.doidoi.org/10.1002/1878-0261.13471
dc.identifier.fulltexthttps://imagine.imgge.bg.ac.rs/bitstream/id/261174/bitstream_261174.pdf
dc.type.versionpublishedVersionsr


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Приказ основних података о документу