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Accelerated leukemogenesis by truncated CBFb-SMMHC defective in high-affinity binding with RUNX1

ChEBI2011-03-29 更新2026-07-21 收录

白血病发病机制

蛋白质相互作用缺陷

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-21155 数据链接链接失效反馈

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资源简介：

Accelerated leukemogenesis by truncated CBFb-SMMHC defective in high-affinity binding with RUNX1

应用场景：

创建时间：

2011-03-29

白血病发病机制

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造血干细胞表观遗传学

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Aging is associated with functional decline of hematopoietic stem cells (HSC) as well as an increased risk of myeloid malignancies. We performed an integrative characterization of epigenomic and trans

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白血病发病机制

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Investigating Bcor target genes in BcorΔE9-10KrasG12D leukaemia with a custom CRISPR dropout screen BcorΔE9-10KrasG12D cell line was transduced with a custom CRISPR library and a dropout screen was pe

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Accelerated leukemogenesis by truncated CBFb-SMMHC defective in high-affinity binding with RUNX1

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