ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/067/SRR11538467/SRR11538467_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/068/SRR11538468/SRR11538468_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/067/SRR11538467/SRR11538467_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR115/068/SRR11538468/SRR11538468_1.fastq.gzprimaryOK200GenomicsState Key Laboratory of Medical Genomics and Shanghai Institute of Hematology, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicinehttps://www.ebi.ac.uk/ena/browser/view/PRJNA624645Homo sapiensWe performed RNA sequencing to identify differentially expressed genes and associated functional pathways. Overall design: RNA sequencing was performed in NB4 cells infected with the CRNDE shRNA (sh-CRNDE) or the non-targeting control shRNA (sh-Control). NB4 cells were harvested at day three post-infection, and total RNA was extracted.xref:PubMed:33298855ENAfalseGene expression analysis after shRNA-mediated knockdown of lncRNA CRNDE in the APL cell line NB4Gene expression analysis after shRNA-mediated knockdown of lncRNA CRNDE in the APL cell line NB42025-09-242023-04-05PRJNA624645GSE148489960633298855