<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/009/SRR9674449/SRR9674449.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/008/SRR9674448/SRR9674448.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/000/SRR9674440/SRR9674440.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/006/SRR9674446/SRR9674446.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/001/SRR9674441/SRR9674441.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/005/SRR9674445/SRR9674445.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/004/SRR9674444/SRR9674444.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/002/SRR9674442/SRR9674442.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/009/SRR9674439/SRR9674439.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/007/SRR9674447/SRR9674447.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/000/SRR9674450/SRR9674450.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR967/003/SRR9674443/SRR9674443.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Le Romancer, Cancer Cell Plasticity, Cancer Research Center of Lyon</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA554259</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>Using a genome-wide analysis, we demonstrated that PRMT1 is selectively required for progesterone-regulated expression of PR target genes, implicated in cell proliferation and migration. Overall design: We examined whether PRMT1 is required for progesterone-induced expression of genes, by depleting PRMT1 in T47D breast cancer cells, using siRNA. We examined gene expression changes at 6 hours progesterone (R5020) treatment compared with ethanol treatment as a control. siRNA for a nonspecific sequence (siCT) followed by 6h of R5020 treatment was performed as control.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>PRMT1 differentially regulates gene expression in T47D-breast cancer cells</name><description>PRMT1 differentially regulates gene expression in T47D-breast cancer cells</description><dates><last_updated>2025-09-24</last_updated><first_public>2020-06-14</first_public></dates><accession>PRJNA554259</accession><cross_references><GEO>GSE134194</GEO><taxon>9606</taxon></cross_references></HashMap>