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Master Transcription Factors and Mediator Establish Super-Enhancers at Key Cell Identity Genes

ChEBI2013-01-02 更新2026-07-21 收录

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https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-42474 数据链接链接失效反馈

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Master Transcription Factors and Mediator Establish Super-Enhancers at Key Cell Identity Genes

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创建时间：

2013-01-02

DNA甲基化

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Correlation between the densities of DMPs around transcription start and end sites.

Figshare2016-03-11 更新50

Cut & Run mapping the alteration of H4K20me1 and transcription activity in cultured MuSC upon Suv420h1 depletion.

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H4K20me1/2/3 is dynamically regulated during cell cycle to maintain the genomic stability. Here, we found that depletion of H4K20 di-methyltransferase Suv420h1 in mouse adult MuSCs leads to strong acc

NIAID Data Ecosystem30

Microscopy data (2/2): interaction of the gene iscub with RNA polymerase II clusters in inhibitor-treated zebrafish embryos

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Microscopy image data containing fluorescently labeled gene loci, recruited RNA polymerase II, and elongating RNA polymerase II. This data set is for the gene iscub and is obtained from fixed

Zenodo2022-12-14 更新00

Interconversion between active and inactive TATA-binding protein transcription complexes in the mouse genome.

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表观遗传

The conserved core domain of the TATA binding protein (TBP) interacts with multiple partners forming the complexes required for transcription by RNA Polymerases I, II and III. We use genetically modif

NIAID Data Ecosystem50

Actin R256 mono-methylation is a conserved post-translational modification involved in transcription

肌动蛋白甲基化修饰

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Nuclear actin has been elusive due to the lack of molecular mechanisms. From actin-containing chromatin remodeling complexes, we discovered an arginine mono-methylation mark on evolutionarily conserve

Alliance of Genome Resources10

Master Transcription Factors and Mediator Establish Super-Enhancers at Key Cell Identity Genes

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