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ZRF1 knockdown with shRNA in SK-N-BE(2) cells
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Role for the Transcriptional Activator ZRF1 in Breast Cancer Progression and Endocrine Resistance
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Transcription factor activating protein 2 beta (TFAP2B) mediates noradrenergic neuronal differentiation in neuroblastoma
Combined epigenetic and differentiation-based treatment inhibits neuroblastoma tumor growth and links HIF2α to tumor suppression
Combined epigenetic and differentiation-based treatment inhibits neuroblastoma tumor growth and links HIF2α to tumor suppression [array]
Combined epigenetic and differentiation-based treatment inhibits neuroblastoma tumor growth and links HIF2α to tumor suppression [RNA-Seq]
The transcriptional repressor SNAI2 impairs neuroblastoma differentiation and inhibits response to retinoic acid therapy
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FOXP1 inhibits cell growth and attenuates tumorigenicity of neuroblastoma
GRHL1 acts as a tumor suppressor in neuroblastoma and is negatively regulated by MYCN and HDAC3
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Enforced Grainyhead-like 1 expression effect on BE(2)-C neuroblastoma cell line: time course
PubMed Similar studies GEO Profiles Analyze DataSet
Gene expression profiling in neuroblastoma cells upon CHAF1A silencing
Chromatin assembly factor 1A deficiency effect on IMR32 neuroblastoma cells: time course
ZNF281 inhibits neuronal differentiation
The effect of knock-down of neuroblastoma associated lncRNA on transcriptome
Genome-wide mRNA expression analyses revealed dysregulation of genes important for sympathetic neuron development in isl1 cko and hypomorphic mutant embryos.
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Genome-wide chromatin-immunoprecipitation studies of sympathetic neurons reveals critical direct targets of ISL1 and suggests potential co-factor families for ISL1 action in sympathetic neurons
ChIP-seq-based analysis of differential K27me3 coverage in neuroblastoma cell lines treated with epigenetic drugs
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Global transcriptome analysis in the MYCN-amplified neuroblastoma cell line IMR5-75 upon inducible MYCN-knockdown
DNA methylation analysis of neuroblastoma cell lines treated with epigenetic drugs
ChIP-seq-based analysis of i) K27me3 promoter coverage and ii) enhancer elements in neuroblastoma cell lines
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