<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE322nnn/GSE322523/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE322523</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Mouse heart RNA-seq in isoproterenol (ISO) injury model with or without polystyrene nanoplastics co-exposure</name><description>Male C57BL/6 mice were assigned to three groups (n=6 per group): ISO, ISO+100 nm polystyrene nanoplastics (PS), and ISO+1 µm PS. Hearts were collected at the study endpoint and profiled by bulk mRNA-seq to identify transcriptional signatures associated with PS size in the setting of ISO-induced myocardial injury. Libraries were prepared and sequenced in two batches (Batch 1 by Novogene; Batch 2 by Majorbio Bio-Pharm Technology).</description><dates><publication>2026/03/28</publication></dates><accession>GSE322523</accession><cross_references><GSM>GSM9553615</GSM><GSM>GSM9553614</GSM><GSM>GSM9553625</GSM><GSM>GSM9553624</GSM><GSM>GSM9553613</GSM><GSM>GSM9553612</GSM><GSM>GSM9553623</GSM><GSM>GSM9553611</GSM><GSM>GSM9553622</GSM><GSM>GSM9553610</GSM><GSM>GSM9553621</GSM><GSM>GSM9553620</GSM><GSM>GSM9553609</GSM><GSM>GSM9553608</GSM><GSM>GSM9553619</GSM><GSM>GSM9553618</GSM><GSM>GSM9553617</GSM><GSM>GSM9553616</GSM><GPL>24247</GPL><GSE>322523</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>