Early downstream targets of Notch signaling which contribute to multiciliate cell fate

ChEBI2012-03-01 更新2026-07-21 收录

Notch信号通路

毛细胞分化

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https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-32331 数据链接链接失效反馈

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Early downstream targets of Notch signaling which contribute to multiciliate cell fate

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2012-03-01

Table S1 from The Notch pathway in the annelid Platynereis : insights into chaetogenesis and neurogenesis processes

Notch信号通路

毛发生长

Notch is a key signalling pathway playing multiple and varied functions during development. Notch regulates the selection of cells with a neurogenic fate and maintains a pool of yet uncommitted precur

DataCite Commons2020-09-02 更新810

Notch ligand Dll4 impairs the recruitment of hemogenic cells into intra-aortic clusters and limits hematopoietic stem cell production

造血干细胞

Notch信号通路

Hematopoietic stem cells (HSCs) develop from the hemogenic endothelium in the embryonic aorta. In most vertebrates, hemogenic cells protrude into the aortic lumen forming clusters where the hematopoie

干细胞与再生医学数据中心2022-02-20 更新50

Gene expression data from T-cell progenitors developing in response to DLL4 stimulation in the plastic thymus. Mus musculus

T细胞发育

Notch信号通路

Since the first description of the involvement of Notch signaling in homeostasis especially of T cells, there is great effort in research to find new target genes of Notch that are involved in T cell

NIAID Data Ecosystem40

Expression data from in vitro decidualized human uterine fibroblast cells (HuF cells) with or without NOTCH1 silencing. Homo sapiens

蜕膜化机制研究

Notch信号通路

Decidualization is a critical process for embryo implatation during which uterine stromal fibroblasts are transformed into large, epithelioid-like decidual cell. NOTCH1 is recepotor of Notch signaling

NIAID Data Ecosystem90

Oncogenic Notch promotes long-range regulatory interactions within hyperconnected 3D cliques [Rec1_ChIP-seq]

癌症三维基因组学

Notch信号通路

Purpose: To investigate the impact of oncogenic Notch on the 3D genome organization of cancer cells. Methods: We generated cohesin HiChIP and 1D epigenomic data sets in two different Notch-dependent c

NIAID Data Ecosystem50

Early downstream targets of Notch signaling which contribute to multiciliate cell fate

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