<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/GSE301nnn/GSE301769/</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=GSE301769</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Dysregulated Proline Metabolism Contributes to Subretinal Fibrosis in Neovascular AMD: Therapeutic Potential of Prolyl-4-Hydroxylase Inhibition</name><description>Subretinal fibrosis is a key pathological feature of late-stage neovascular age-related macular degeneration (nAMD), often leading to irreversible vision loss. To investigate early molecular changes underlying subretinal fibrosis, we performed transcriptomic analysis on JR5558 mice, a spontaneous model of retinal neovascularisation, at 4 and 8 weeks of age. Age-matched C57BL/6J mice were used as controls. Bulk RNA sequencing was performed on whole retinas to identify differentially expressed genes and enriched biological pathways.</description><dates><publication>2026/08/10</publication></dates><accession>GSE301769</accession><cross_references><GSM>GSM9088914</GSM><GSM>GSM9088915</GSM><GSM>GSM9088904</GSM><GSM>GSM9088905</GSM><GSM>GSM9088906</GSM><GSM>GSM9088910</GSM><GSM>GSM9088911</GSM><GSM>GSM9088912</GSM><GSM>GSM9088913</GSM><GSM>GSM9088907</GSM><GSM>GSM9088908</GSM><GSM>GSM9088909</GSM><GPL>24247</GPL><GSE>301769</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>