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BRG1/SMARCA4 is essential for neuroblastoma cell viability through modulation of cell death and survival pathways

ChEBI2016-03-01 更新2026-07-12 收录

神经母细胞瘤分子机制

肿瘤细胞生存通路

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-74622 数据链接链接失效反馈

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资源简介：

BRG1/SMARCA4 is essential for neuroblastoma cell viability through modulation of cell death and survival pathways

应用场景：

创建时间：

2016-03-01

神经母细胞瘤分子机制

E2F信号通路

We report a previously unrecognized role of SAPCD2 in E2F signaling pathway in neuroblastoma. To explore SAPCD2-dependent gene regulation, RNA-seq analysis was conducted and the differently expressed

NIAID Data Ecosystem80

Hox-C9 activates the intrinsic pathway of apoptosis and is associated with spontaneous regression in neuroblastoma [tumor_genex_44k]

神经母细胞瘤分子机制

HOX基因功能

Single-color gene expression profiles from 649 neuroblastoma tumors were generated using 44K oligonucleotide microarrays. We aimed at determining the association of class I HOX gene expression pattern

NIAID Data Ecosystem50

Transcriptomic analysis of neuroblastoma cells in response to stable over-expression of circular RNA derived from CUX1 gene (circ-CUX1)

神经母细胞瘤分子机制

环状RNA功能研究

Circular RNAs (circRNAs), a subclass of noncoding RNAs characterized by covalently closed continuous loops, play emerging roles in tumorigenesis and aggressiveness. However, the functions and underlyi

NIAID Data Ecosystem40

TRPM7 maintains progenitor-like features of neuroblastoma cells

神经母细胞瘤分子机制

基因表达调控

Analysis of the effect of shRNA-mediated knockdown of TRPM7 on gene expression levels in SH-SY5Y and SH-EP2 human neuroblastoma cells. Results were used for the identification of neural-crest-associat

NIAID Data Ecosystem70

The Risk-Associated Long Noncoding RNA NBAT-1 Controls Neuroblastoma Progression by Regulating Cell Proliferation and Neuronal Differentiation.. Neuroblastoma transcriptome sequencing.

神经母细胞瘤分子机制

非编码RNA功能

Neuroblastoma is one of the most common extracranial solid tumors in children. By sequencing transcriptomes of low- and high-risk neuroblastomas, we have identified differentially expressed annotated

NIAID Data Ecosystem50

BRG1/SMARCA4 is essential for neuroblastoma cell viability through modulation of cell death and survival pathways

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