<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/GSE235nnn/GSE235890/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE235890</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Role of mitochondrial RNase P complex in the processing of primary RNA in human mitochondria</name><description>The human mitochondrial genome is transcribed into long polycistronic RNA that undergoes subsequent endonucleolytic processing. The role of the mitochondrial RNase P, a protein complex composed of RNA methyltransferase, ribonuclease and dehydrogenase, has been revealed in the processing of the primary mitochondrial RNA. Still, the contribution of catalytic activities of RNase P subunits in the processing of individual processing sites has not been fully described. This study aims to define the role of RNase P subunits in regulating the efficiency of the processing of the primary mitochondrial RNA.</description><dates><publication>2026/06/27</publication></dates><accession>GSE235890</accession><cross_references><GSM>GSM7511537</GSM><GSM>GSM7511538</GSM><GPL>24676</GPL><GSE>235890</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>