<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/GSE262nnn/GSE262820/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Drosophila melanogaster</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=GSE262820</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>A nuclear role of tau in control DNA damage repair</name><description>Neuronal protein tau has been implicated in the pathogenesis of Alzheimer's disease and related disorders termed as tauopathies. The tau proteins has been shown to primarily play a cytosolic role in the maintenence of actin and microtubules cytoskeleton but emerging evidence suggests a nuclear role of tau. In this study, we investigated a nuclear role of tau by doing scRNA-seq on the tau knock out Drosophila brains and subsequent in-vivo experiments to validate the findings. The results show tau protein to be a key modular of important nuclear signaling process such as DNA damage repair.</description><dates><publication>2026/03/31</publication></dates><accession>GSE262820</accession><cross_references><GSM>GSM8179944</GSM><GSM>GSM8179943</GSM><GSM>GSM8179945</GSM><GPL>25244</GPL><GSE>262820</GSE><taxon>Drosophila melanogaster</taxon></cross_references></HashMap>