Transcriptome sequencing reveals a profile that corresponds to genomic variants in Waldenström macroglobulinemia

Whole-genome sequencing has identified highly prevalent somatic mutations including MYD88, CXCR4, and ARID1A in Waldenström macroglobulinemia (WM). The impact of these and other somatic mutations on transcriptional regulation in WM remains to be clarified. We performed next-generation transcriptiona...

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Udgivet i:Blood
Main Authors: Hunter, Zachary R., Xu, Lian, Yang, Guang, Tsakmaklis, Nicholas, Vos, Josephine M., Liu, Xia, Chen, Jie, Manning, Robert J., Chen, Jiaji G., Brodsky, Philip, Patterson, Christopher J., Gustine, Joshua, Dubeau, Toni, Castillo, Jorge J., Anderson, Kenneth C., Munshi, Nikhil M., Treon, Steven P.
Format: Artigo
Sprog:Inglês
Udgivet: American Society of Hematology 2016
Fag:
Lymphoid Neoplasia
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4982454/
https://ncbi.nlm.nih.gov/pubmed/27301862
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2016-03-708263
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