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Re-specification of myeloid precursors from human pluripotent cells into engraftable multi-lineage progenitors

ChEBI2013-11-01 更新2026-07-21 收录

干细胞重编程

造血祖细胞工程

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-49938 数据链接链接失效反馈

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资源简介：

Re-specification of myeloid precursors from human pluripotent cells into engraftable multi-lineage progenitors

应用场景：

创建时间：

2013-11-01

干细胞重编程

染色体不稳定性

The discovery that somatic cells are reprogrammable to pluripotency by ectopic expression of a small subset of transcription factors has created great potential for the development of broadly applicab

NIAID Data Ecosystem90

Analysis of Differential Proteomes of Induced Pluripotent Stem Cells by Protein-Based Reprogramming of Fibroblasts

干细胞重编程

蛋白质组学比较分析

The recent generation of induced pluripotent stem (iPS) cells represents a novel opportunity to complement embryonic stem (ES) cell-based approaches. iPS cells can be generated by viral transduction o

Figshare2016-02-23 更新50

Establish a rapid and efficient chemical reprogramming platform (RNA-Seq II)

干细胞重编程

表观基因组图谱

Chemically reprogramming somatic cells to iPSCs is time-consuming and low-efficiency. Here, we discribe a rapid chemical reprogramming condition enabling generating iPSCs from MEFs in 12 days. To furt

NIAID Data Ecosystem40

Reprogramming of mouse somatic cells into pluripotent stem cells using a combination of small molecules

干细胞重编程

化学生物学

Somatic cells can be reprogrammed to generate induced pluripotent stem cells (iPSCs) by overexpression of four transcription factors, Oct4, Klf4, Sox2, and c-Myc. Bmi1 is responsible for conversion o

NIAID Data Ecosystem60

Epigenetic and transcriptional aberrations in human pluripotent stem cells reflect differences in reprogramming mechanisms [SNP array]

干细胞重编程

神经细胞表观遗传学

Human pluripotent stem cells hold great potential for regenerative medicine, but available cell types have important limitations. While embryonic stem cells derived from fertilized embryos (IVF-ESCs)

NIAID Data Ecosystem40

Re-specification of myeloid precursors from human pluripotent cells into engraftable multi-lineage progenitors

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