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Effects of Mediator subunit gene-deletions under conditions that repress ribosome synthesis

ChEBI2008-06-01 更新2026-07-21 收录

基因功能缺失分析

核糖体合成调控

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-11397 数据链接链接失效反馈

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资源简介：

Effects of Mediator subunit gene-deletions under conditions that repress ribosome synthesis

应用场景：

创建时间：

2008-06-01

基因功能缺失分析

癌细胞转录组

investigate the gene expression change between UBE2S konck down A375 cells mediated by Lentivirus and control A375 cells. Overall design: In the study, melanoma A375 cell line was selected and transfe

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Transcriptome profiling of NGLY1 deficient K562 cells. Transcriptome profiling of NGLY1 deficient K562 cells

基因功能缺失分析

疾病转录组学

The data includes a transcriptome analysis of K562 cell lines in which the gene N-glycanase 1 (NGLY1) was mutated in exon 1 and/or exon 3 to include loss of function mutations as described in Mueller

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Verticillium dahliae strain:XS11 Raw sequence reads. Verticillium dahliae strain:XS11

植物病原菌转录组

基因功能缺失分析

Transcriptomic analysis between wild type and gene deletion mutants.

NIAID Data Ecosystem30

EZH2 KO RNA-seq in HSC-5 cells. EZH2 KO RNA-seq in HSC-5 cells

基因功能缺失分析

转录组差异

CRISPR was used to deplete EZH2 in HSC-5 cells. RNA-seq was then carried out to identify changes in the transcriptome following EZH2 loss in these cells. Critically, we identified TP63 to be downregul

NIAID Data Ecosystem60

Transcriptomic profiling of wild-type C2C12 cells and C2C12 cells with Myod1 gene knockout by RNA-sequencing. Transcriptomic profiling of wild-type C2C12 cells and C2C12 cells with Myod1 gene knockout by RNA-sequencing

肌肉分化转录组学

基因功能缺失分析

C2C12 is a myoblast cell line usually used for study of muscle differentiation. Myod1 is a pro-differentiation factor for myogenesis. We found that CRISPR/Cas9-mediated Myod1 gene knockout in C2C12 ce

NIAID Data Ecosystem30

Effects of Mediator subunit gene-deletions under conditions that repress ribosome synthesis

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