<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/GSE335nnn/GSE335367/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Homo sapiens</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE335367</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>hLMR1, a hepatocyte-specific long noncoding RNA that represses amino acid catabolism through pre-mRNA interaction in human liver [ChIRP-seq]</name><description>To investigate the molecular mechanisms underlying hLMR1-mediated gene regulation, Chromatin Isolation by RNA Purification followed by RNA sequencing (ChIRP-RNA-seq) was performed using human liver tissues. Endogenous hLMR1-associated RNA molecules were isolated using biotinylated antisense oligonucleotide probes targeting hLMR1 and subsequently characterized by high-throughput sequencing. This approach was used to identify RNA transcripts physically associated with hLMR1 and to gain insight into the molecular pathways regulated by this human liver-enriched long non-coding RNA.</description><dates><publication>2026/06/30</publication></dates><accession>GSE335367</accession><cross_references><GSM>GSM9812589</GSM><GSM>GSM9812588</GSM><GSM>GSM9812587</GSM><GSM>GSM9812590</GSM><GPL>24676</GPL><GSE>335367</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>