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LIN28B Regulates Transcription and Potentiates MYCN-induced Neuroblastoma in a let-7-independent Manner [ChIP-seq]
PubMed Full text in PMC Similar studies SRA Run Selector
LIN28B Regulates Transcription and Potentiates MYCN-induced Neuroblastoma in a let-7-independent Manner
PubMed Full text in PMC Similar studies
LIN28B Regulates Transcription and Potentiates MYCN-induced Neuroblastoma in a let-7-independent Manner [RNA-seq]
PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector
Integrated bioinformatic and wet-lab approach to identify potential oncogenic networks in neuroblastoma
PubMed Full text in PMC Similar studies Analyze with GEO2R
Multiple mechanisms disrupt let-7 miRNA biogenesis and function in neuroblastoma
Multiple mechanisms disrupt let-7 miRNA biogenesis and function in neuroblastoma [shortRNA]
Multiple mechanisms disrupt let-7 miRNA biogenesis and function in neuroblastoma [longRNA]
Multiple mechanisms disrupt let-7 miRNA biogenesis and function in neuroblastoma [Let7Targets]
Effects of MYCN knockdwon on miRNA expression in neuroblastoma cells
Genome-wide mapping of MYCN binding in neuroblastoma cells
LMO1 Synergizes with MYCN to Promotes Neuroblastoma Initiation and Metastasis
Differential gene expression in neuroblastoma cells after transfection with control siRNA, MYCN siRNA or TFAP4 siRNA.
ASCL1 is a MYCN- and LMO1-dependent member of the adrenergic neuroblastoma core regulatory circuitry
RNA-seq analysis after knockdown of ASCL1 gene in Kelly cells
Gene expression profile of human neuroblastoma cell line SHSY-5Y after LMO1 knockdown
ASCL1 is directly activated by the LMO1 and MYCN oncogenes and is a master regulator of the differentiation program in neuroblastoma
RNA-seq analysis after LMO1 or MYCN knockdown in Kelly cells
An ALYREF-MYCN coactivator complex drives neuroblastoma tumorigenesis through effects on USP3 and MYCN stability
RACS: Rapid Analysis of ChIP-Seq data for contig based genomes
A multi-omics approach reveals enrichment in metabolites involved in the regulation of the glutathione pathway in LIN28B-dependent cancer cells.
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