Reprogramming fate of central memory CD8+T cells by targetig the transcriptional coregulator Tle3

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细胞重编程

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数据链接：

https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE213041 数据链接链接失效反馈

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This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

创建时间：

2024-02-06

Effect of SAICAR accumulation on global transcription

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代谢途径

We investigated the effects of SAICAR accumulation on transcriptional regulation of purine biosynthesis and other metabolic pathways. These data were compared to those obtained in the ade16ade17 vs WT

NIAID Data Ecosystem70

Supplementary Table S8 from Transposable Elements Are Co-opted as Oncogenic Regulatory Elements by Lineage-Specific Transcription Factors in Prostate Cancer

癌症基因组数据

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Top 5% transcription factor cistromes enriched at intestine transposable elements

NIAID Data Ecosystem20

Additional file 20 of Enhancer looping protein LDB1 modulates MYB expression in T-ALL cell lines in vitro by cooperating with master transcription factors

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CUT&Tag表观基因组分析

Supplementary Material 21. Supplementary Table 9. The peaks identified by CUT&Tag analysis of LDB1 in 6T-CEM cells

NIAID Data Ecosystem00

OBF1 and Oct factors control the germinal center transcriptional program [Mouse]. OBF1 and Oct factors control the germinal center transcriptional program [Mouse]

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生发中心

OBF1 is a specific coactivator of the POU family transcription factors OCT1 and OCT2. OBF1 and OCT2 are B cell-specific and indispensable for germinal center (GC) formation, but their mechanism of act

NIAID Data Ecosystem60

Enhancer looping protein LDB1 affects T-ALL cell proliferation by cooperating with master transcription factors [RNA-Seq]. Enhancer looping protein LDB1 affects T-ALL cell proliferation by cooperating with master transcription factors [RNA-Seq]

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差异表达RNA分析

LIM domain-binding protein 1 (LDB1) is a highly conserved and widely expressed chromatin looping protein that connects enhancer-promoter genes through LIM and LIM homologous domains in various cell ty

NIAID Data Ecosystem00

Reprogramming fate of central memory CD8+T cells by targetig the transcriptional coregulator Tle3

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