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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Detalhes bibliográficos
Publicado no: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.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2016
Assuntos:
Lymphoid Neoplasia
Acesso em linha: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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