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Essential control of early B-cell development by Mef2 transcription factors

ChEBI2015-12-14 更新2026-07-12 收录

B细胞发育

转录因子功能研究

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-73563 数据链接链接失效反馈

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资源简介：

Essential control of early B-cell development by Mef2 transcription factors

应用场景：

创建时间：

2015-12-14

胰腺基因表达

转录因子功能研究

RNA sequencing was used to identify gene expression changes in pancreatic acinar cells with ectopic expression of the homeodomain transcription factor Prox1 Overall design: The pancreas P7 control mic

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Induction of extracellular adenosine salvage and metabolic quiescence regulate the transitional to follicular B cell checkpoint in humans.

免疫代谢

B细胞发育

Transcriptional profiling of transitional and follicular B cells showed that metabolic quiescence was acquired at the follicular B cell stage in both humans and mice, characterized by an orchestrated

NIAID Data Ecosystem10

Expression data from TFIIA-non-cleavable mouse fetal liver hematopoietic stem cells

造血干细胞基因表达

转录因子功能研究

Expression data from TFIIA-non-cleavable mouse fetal liver hematopoietic stem cells

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Investigate the effect of gain of HAND2 on chromatin accessibility.

染色质可及性分析

转录因子功能研究

The overexpression of HAND2 in IMR32 cells results in a increase of chromation accessibility at the HAND2 and MYCN common binding sites. Overall design: In the HAND2 stably transfected IMR32 cells (IM

NIAID Data Ecosystem20

wt/myb77-Functional characterization of AtMYB77 transcription factor.

拟南芥分子生物学

转录因子功能研究

wt/myb77-Functional characterization of AtMYB77 transcription factor.

ChEBI2010-05-25 更新00