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YTHDF2 Suppresses the 2C-like State in Mouse Embryonic Stem Cells. YTHDF2 Suppresses the 2C-like State in Mouse Embryonic Stem Cells

NIAID Data Ecosystem2026-05-02 收录

胚胎干细胞干性调控

YTHDF2功能

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1128685 数据链接链接失效反馈

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资源简介：

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

应用场景：

创建时间：

2024-06-26

胚胎干细胞干性调控

翻译起始机制

Stemness is a defining feature in embryonic and cancer stem cells. How stemness is regulated at the mRNA translational initiation remains undefined. We carried out an RNAi screen for key translation i

NIAID Data Ecosystem80

eIF4A2 targets developmental potency and histone H3.3 transcripts for translational control of embryonic and cancer stemness [eCLIP-seq]

胚胎干细胞干性调控

翻译起始因子结合谱

NIAID Data Ecosystem40

Function of deubiquitinase USP21 in mouse embryonic stem cell [ChIP-Seq]. Mus musculus

胚胎干细胞干性调控

USP21去泛素化酶功能

Nanog is a master pluripotency factor of embryonic stem cells (ESCs). Stable expression of Nanog is required to maintain the stemness of ESCs, although Nanog is a short-lived protein and quickly degra

NIAID Data Ecosystem20

Comparative profiling of Tcl1 gene disruptants and Tcl1 stable transformants.. Mus musculus

胚胎干细胞干性调控

Tcl1基因功能

Tcl1 is one of embryonic stem cell specific transcripts identified by digital differential display analysis. Tcl1 is highly expressed during early embryogenesis and to some extent in embryonic stem ce

NIAID Data Ecosystem50

Genome-wide Analysis of Smad7-Mediated Transcription in Mouse Embryonic Stem Cells [RNA-Seq]. Genome-wide Analysis of Smad7-Mediated Transcription in Mouse Embryonic Stem Cells [RNA-Seq]

胚胎干细胞干性调控

Smad7转录因子功能

Smad7 has been identified as a negative regulator of the transforming growth factor TGF-β pathway by direct interaction with the TGF-β type I receptor (TβR-I). Although Smad7 has also been shown to pl

NIAID Data Ecosystem40

YTHDF2 Suppresses the 2C-like State in Mouse Embryonic Stem Cells. YTHDF2 Suppresses the 2C-like State in Mouse Embryonic Stem Cells

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