Effect of Tup1, Xbp1, Isw2, and Sds3 on H3K23ac in stationary phase.

Alliance of Genome Resources2026-08-01 收录

组蛋白乙酰化修饰调控

基因敲除表观遗传学

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https://www.yeastgenome.org/dataset/GSE210928 数据链接链接失效反馈

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To investigate the effect of Tup1, Xbp1, Isw2, and Sds3 on H3K23acc we generated knockout strains and measured H3K23ac levels during stationary phase.

Histone methylation profiles of H3K4me3, H3K27me3, H3K9me3, and H3R8me2a in WT and mdig/mina53 KO BEAS-2B cells

组蛋白甲基化分析

基因敲除表观遗传学

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H3K4 trimethylation ChIP - ctk1 deletion. Saccharomyces cerevisiae

组蛋白修饰ChIP-seq

基因敲除表观遗传学

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NIAID Data Ecosystem30

Epigenome analysis of NNMT KO versus WT cells. Epigenome analysis of NNMT KO versus WT cells

DNA甲基化分析

基因敲除表观遗传学

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Whole genome bisulfite sequencing of Ing1/Gadd45a double knockout and wildtype mouse embryonic fibroblasts. Mus musculus

差异甲基化分析

基因敲除表观遗传学

ING1b and GADD45a are nuclear proteins involved in the regulation of cell growth, apoptosis and DNA repair. We previously found that ING1b is essential to target GADD45a-mediated active DNA-demethylat

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ATAC-seq for E14 cells knockdown with siRNA or shRNA. ATAC-seq for E14 cells knockdown with siRNA or shRNA

染色质可及性分析

基因敲除表观遗传学

ATAC-seq was performed on cells E14 cells knockdown with siRNA or shRNA Overall design: Chormatin accssibility were evaluated for E14 cells with factors knocked down

NIAID Data Ecosystem30

Effect of Tup1, Xbp1, Isw2, and Sds3 on H3K23ac in stationary phase.

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