<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/GSE314nnn/GSE314869/</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=GSE314869</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Potential of an in vitro mouse testicular organ culture system as a platform for mechanism-based evaluation of testicular toxicity</name><description>This study examined testicular toxicity induced by methoxyacetic acid (MAA) using an in vitro mouse testicular organ culture system. Testis tissues were cultured for 4 weeks and then exposed to MAA (1–4 mM) for 24 hours. Higher MAA concentrations reduced germ-cell viability and spermatocyte populations, accompanied by increased apoptosis. RNA-seq analysis revealed early transcriptional perturbations at 1 mM and broad suppression of cell-cycle and meiotic pathways at 4 mM. These findings characterize dose-dependent molecular and cellular changes associated with MAA-induced testicular toxicity.</description><dates><publication>2026/05/12</publication></dates><accession>GSE314869</accession><cross_references><GSM>GSM9414772</GSM><GSM>GSM9414771</GSM><GSM>GSM9414770</GSM><GSM>GSM9414776</GSM><GSM>GSM9414765</GSM><GSM>GSM9414775</GSM><GSM>GSM9414764</GSM><GSM>GSM9414763</GSM><GSM>GSM9414773</GSM><GSM>GSM9414762</GSM><GSM>GSM9414769</GSM><GSM>GSM9414779</GSM><GSM>GSM9414768</GSM><GSM>GSM9414778</GSM><GSM>GSM9414767</GSM><GSM>GSM9414766</GSM><GSM>GSM9414777</GSM><GPL>34290</GPL><GSE>314869</GSE><taxon>Mus musculus</taxon><PMID>[41903202]</PMID></cross_references></HashMap>