MYD88L265P andCXCR4mutations in lymphoplasmacytic lymphoma identify cases with high disease activity
出版年份 2015 全文链接
标题
MYD88L265P andCXCR4mutations in lymphoplasmacytic lymphoma identify cases with high disease activity
作者
关键词
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出版物
BRITISH JOURNAL OF HAEMATOLOGY
Volume 169, Issue 6, Pages 795-803
出版商
Wiley
发表日期
2015-03-30
DOI
10.1111/bjh.13361
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Somatic mutations in MYD88 and CXCR4 are determinants of clinical presentation and overall survival in Waldenstrom macroglobulinemia
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- Mutations in TLR/MYD88 pathway identify a subset of young chronic lymphocytic leukemia patients with favorable outcome
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- The WHIM-like CXCR4S338X somatic mutation activates AKT and ERK and promotes resistance to ibrutinib and other agents used in the treatment of Waldenstrom’s Macroglobulinemia
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- A mutation in MYD88 (L265P) supports the survival of lymphoplasmacytic cells by activation of Bruton tyrosine kinase in Waldenstrom macroglobulinemia
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