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早期人类造血的分子和功能特征。

Molecular and functional characterization of early human hematopoiesis.

机构信息

Campbell Family Institute for Cancer Research/Ontario Cancer Institute, Princess Margaret Hospital, University Health Network, Toronto, Ontario, Canada.

出版信息

Ann N Y Acad Sci. 2012 Aug;1266:68-71. doi: 10.1111/j.1749-6632.2012.06577.x.

DOI:10.1111/j.1749-6632.2012.06577.x
PMID:22901258
Abstract

Through improvements in xenograft assay methods and in the identification of novel cell surface markers, significant progress has been made in our understanding of the human hematopoietic stem and progenitor hierarchy. The isolation of clonally pure populations of stem cells and early progenitors opens the way to carry out gene expression profiling studies to uncover the molecular regulators of each developmental step and to gain insight into the process of lineage commitment in human hematopoiesis.

摘要

通过改进异种移植检测方法和鉴定新的细胞表面标记物,我们对人类造血干/祖细胞的层次结构有了更深入的了解。克隆纯的干细胞和早期祖细胞的分离为进行基因表达谱研究开辟了道路,以揭示每个发育步骤的分子调控因子,并深入了解人类造血谱系分化的过程。

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Molecular and functional characterization of early human hematopoiesis.早期人类造血的分子和功能特征。
Ann N Y Acad Sci. 2012 Aug;1266:68-71. doi: 10.1111/j.1749-6632.2012.06577.x.
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Chromatin modifications in hematopoietic multipotent and committed progenitors are independent of gene subnuclear positioning relative to repressive compartments.造血多能祖细胞和定向祖细胞中的染色质修饰与基因相对于抑制性区室的亚核定位无关。
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Human B-1 and B-2 B Cells Develop from Lin-CD34+CD38lo Stem Cells.
人类B-1和B-2 B细胞由Lin-CD34+CD38lo干细胞发育而来。
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Outlier analysis of functional genomic profiles enriches for oncology targets and enables precision medicine.功能基因组图谱的异常值分析丰富了肿瘤学靶点,并推动了精准医学的发展。
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