<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/GSE315nnn/GSE315683/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></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=GSE315683</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptional and proteome profiling of human bronchial epithelial cell BEAS-2B exposed to e-cigarette aerosol condensate</name><description>We performed RNA-sequencing to evaluate the effect of acute exposure to e-cigarette aerosol condensate on lung bronchial epithelial cells by comparing the effects of carrier liquid consisting solely of propylene glycol and vegetable glycerine with e-cigarette containing nicotine and flavor. Overall design BEAS-2B cells were exposed to e-cigarette aerosol condensate generated from carrier liquid (propylene glycol and vegetable glycerine) and from e-cigarette containing 18mg/ml nicotine and Virginia tobacco flavor for 24h. Untreated cells were used as control.</description><dates><publication>2026/04/01</publication></dates><accession>GSE315683</accession><cross_references><GSM>GSM9435173</GSM><GSM>GSM9435172</GSM><GSM>GSM9435171</GSM><GSM>GSM9435170</GSM><GSM>GSM9435169</GSM><GSM>GSM9435168</GSM><GSM>GSM9435167</GSM><GSM>GSM9435166</GSM><GSM>GSM9435174</GSM><GPL>24676</GPL><GSE>315683</GSE><taxon>Homo sapiens</taxon><PMID>[41892316]</PMID></cross_references></HashMap>