首页/数据集/mRNA expression profiles of SK-N-AS neuroblastoma cells with induced ALK-wt, ALK-F1174L or ALK-R1275Q

mRNA expression profiles of SK-N-AS neuroblastoma cells with induced ALK-wt, ALK-F1174L or ALK-R1275Q

ChEBI2015-05-04 更新2026-07-21 收录

神经母细胞瘤基因表达

ALK突变分子机制

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-MTAB-3207 数据链接链接失效反馈

官方服务：

资源简介：

mRNA expression profiles of SK-N-AS neuroblastoma cells with induced ALK-wt, ALK-F1174L or ALK-R1275Q

应用场景：

创建时间：

2015-05-04

相关数据集

Downregulation of DDX5/DDX17 and REST

RNA解旋酶与转录因子基因调控

神经母细胞瘤基因表达

We aimed at analysing the effect of RNA helicases DDX5 and DDX17 and of the transcription factor REST on gene expression in the human SH-SY5Y neuroblastoma cell line (European Collection of Cell Cultu

NIAID Data Ecosystem50

The cooperation between MYCN and its cofactors WDR5 and G9a on gene transcription regulation [siWDR5]. The cooperation between MYCN and its cofactors WDR5 and G9a on gene transcription regulation [siWDR5]

转录调控机制

神经母细胞瘤基因表达

MYCN cooperates with WDR5 to activate canonical MYC targets and cooperates with G9a to repress neuronal differentiation genes. Overall design: IMR32 cells were transfected with control siRNA (siCtrl)

NIAID Data Ecosystem30

mRNA analysis in depolarized neuroblastoma cells. mRNA analysis in depolarized neuroblastoma cells

神经元活动依赖性转录

神经母细胞瘤基因表达

We profiled mRNA using RNA-seq in the depolarized neuroblastoma cells Overall design: There were two conditions including depolarized cells (4 samples) treated with KCl and sham-depolarized controls (

NIAID Data Ecosystem20

SH-SY5Y cells treated with Quercetin-3-glucoside then H2O2

氧化应激细胞保护机制

神经母细胞瘤基因表达

Flavonoids are polyphenolic compounds with potent anti-oxidant and free radical scavenging activities. Here, we examined the cytoprotective actions of Quercetin-3-glucoside (Q3G) against oxidative str

NIAID Data Ecosystem30

RNAseq in IMR-32 neuroblastoma cells. Homo sapiens

神经母细胞瘤基因表达

RNA测序分析

IMR-32 cells were subjected to lentiviral YRNA infection or nELAVL RNAi and/or UV stress followed by RNAseq analysis to monitor RNA level changes Overall design: RNA from IMR-32 cells was Trizol extra

NIAID Data Ecosystem20