Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56bright subset
出版年份 2013 全文链接
标题
Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56bright subset
作者
关键词
-
出版物
BLOOD
Volume 121, Issue 14, Pages 2669-2677
出版商
American Society of Hematology
发表日期
2013-01-31
DOI
10.1182/blood-2012-09-453969
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。- Bilateral adrenal EBV-associated smooth muscle tumors in a child with a natural killer cell deficiency
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- Human Natural Killer Cell Maturation Defect Supports In Vivo CD56bright to CD56dim Lineage Development
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- Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature
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- Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency
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- Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
- (2011) Christopher N Hahn et al. NATURE GENETICS
- Autosomal dominant and sporadic monocytopenia with susceptibility to mycobacteria, fungi, papillomaviruses, and myelodysplasia
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- GATA-2 regulates granulocyte-macrophage progenitor cell function
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- Mouse fetal and embryonic liver cells differentiate human umbilical cord blood progenitors into CD56-negative natural killer cell precursors in the absence of interleukin-15
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- Bcl-xL is associated with the anti-apoptotic effect of IL-15 on the survival of CD56dim natural killer cells
- (2008) Xiaodong Zheng et al. MOLECULAR IMMUNOLOGY
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