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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15370
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dc.contributor.authorChowdhury, Rajdeep-
dc.contributor.authorChowdhury, Shibasish-
dc.contributor.authorMukherjee, Sudeshna-
dc.date.accessioned2024-08-23T04:26:18Z-
dc.date.available2024-08-23T04:26:18Z-
dc.date.issued2021-10-
dc.identifier.urihttps://link.springer.com/article/10.1007/s12672-021-00441-6-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15370-
dc.description.abstractRecurrence after cisplatin therapy is one of the major hindrances in the management of cancer. This necessitates a deeper understanding of the molecular signatures marking the acquisition of resistance. We therefore modeled the response of osteosarcoma (OS) cells to the first-line chemotherapeutic drug cisplatin. A small population of nondividing cells survived acute cisplatin shock (persisters; OS-P). These cells regained proliferative potential over time re-instating the population again (extended persisters; OS-EP).en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.subjectBiologyen_US
dc.subjectGenomesen_US
dc.subjectRNAs (lncRNAs)en_US
dc.titleA genome wide expression profile of non-coding RNAs in human osteosarcoma cells as they acquire resistance to cisplatinen_US
dc.typeArticleen_US
Appears in Collections:Department of Biological Sciences

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