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A Regulatory Pathway Involving Notch1/β-Catenin/Isl1 Determines Cardiac Progenitor Cell Fate

ChEBI2009-05-13 更新2026-07-21 收录

发育调控

细胞命运决定

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-15232 数据链接链接失效反馈

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资源简介：

A Regulatory Pathway Involving Notch1/β-Catenin/Isl1 Determines Cardiac Progenitor Cell Fate

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创建时间：

2009-05-13

细胞信号传导

细胞命运决定

In the epithelial follicle stem cells (FSCs) of the Drosophila ovary, Epidermal Growth Factor Receptor (EGFR) signaling promotes self-renewal, whereas Notch signaling promotes differentiation of the p

DataONE2020-06-24 更新50

Notch and TLR signaling coordinate monocyte cell fate and inflammation

细胞命运决定

Notch/TLR信号通路

We studied the role of Notch2 signaling in Ly6Chi monocyte cell fate during TLR7-induced acute inflammation. To characterize the gene expression changes involved in monocyte differentiation, we subjec

NIAID Data Ecosystem40

An integrated global regulatory network of hematopoietic precursor cell self-renewal and differentiation. Mus musculus

造血干细胞调控

细胞命运决定

The mammalian blood system is a hierarchically structured tissue. Hematopoietic stem cells (HSC) reside at the top of this hierarchy and the HSC-derived progenitor cells (HPC) have capacities for both

NIAID Data Ecosystem30

Cul5 regulates CD4+ T cell fate choice and allergic inflammation [RNA-seq]

细胞命运决定

炎症机制

Antigen encounter directs CD4+ T cells to differentiate into T-helper or -regulatory cells. This process focuses the immune response on the invading pathogen and limits tissue damage. Mechanisms that

NIAID Data Ecosystem50

Spatiotemporal dynamics of Bach2 orchestrates B cell responses and fate decision

细胞命运决定

免疫转录调控

The molecular circuits that direct early T-dependent B cell responses and alternative cell-fate decisions remain poorly understood. Here, we show that either B cell receptor (BCR) or CD40 signals prom

NIAID Data Ecosystem30

A Regulatory Pathway Involving Notch1/β-Catenin/Isl1 Determines Cardiac Progenitor Cell Fate

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