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dc.contributor.authorCliff I. Oduor, Yasin Kaymaz, Kiprotich Chelimo, Juliana A. Otieno, John Michael Ong’echa, Ann M. Moormann & Jeffrey A. Bailey
dc.date.accessioned2022-01-29T08:33:15Z
dc.date.available2022-01-29T08:33:15Z
dc.date.issued2017
dc.identifier.urihttps://repository.maseno.ac.ke/handle/123456789/4748
dc.descriptionhttps://link.springer.com/content/pdf/10.1186/s12885-017-3711-9.pdfen_US
dc.description.abstractBurkitt lymphoma (BL) is characterized by overexpression of the c-myc oncogene, which in the vast majority of cases is a consequence of an IGH/MYC translocation. While myc is the seminal event, BL is a complex amalgam of genetic and epigenetic changes causing dysregulation of both coding and non-coding transcripts. Emerging evidence suggest that abnormal modulation of mRNA transcription via miRNAs might be a significant factor in lymphomagenesis. However, the alterations in these miRNAs and their correlations to their putative mRNA targets have not been extensively studied relative to normal germinal center (GC) B cells.en_US
dc.publisherSpringeren_US
dc.subjectEndemic Burkitt lymphoma, miRNA, mRNA, RNA sequencing, Lymphomagenesisen_US
dc.titleIntegrative microRNA and mRNA deep-sequencing expression profiling in endemic Burkitt lymphomaen_US
dc.typeArticleen_US


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