ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR673/007/SRR6737177/SRR6737177.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR673/006/SRR6737176/SRR6737176.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR673/005/SRR6737175/SRR6737175.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR673/004/SRR6737174/SRR6737174.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR673/003/SRR6737173/SRR6737173.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR673/002/SRR6737172/SRR6737172.fastq.gzprimaryOK200GenomicsUniversity of Copenhagenhttps://www.ebi.ac.uk/ena/browser/view/PRJNA434284Mus musculusWe report maturity loss and dysfunction of primary mouse islets exposed to prolonged low Interleukin-1B exposure is associated with a decreassed expresion of key beta cell genes and a decreased H3K27ac mark Overall design: Examination of mRNA profile of primary mouse islets exposed or non-exposed to Interleukin-1B for 10 daysxref:PubMed:31362031ENAfalseBeta cell dysfunction and identity loss induced by low dose of Interleukin-1β is associated with changes in histone acetylation and gene expression [RNA-seq]Beta cell dysfunction and identity loss induced by low dose of Interleukin-1β is associated with changes in histone acetylation and gene expression [RNA-seq]2025-09-242019-08-07PRJNA434284GSE1106901009031362031