<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/GSE319nnn/GSE319472/</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=GSE319472</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>scRNAseq analysis of human bronchial epithelial cell air liquid interface cultures infected with the A/Perth/16/2009 H3N2 with and without PA-X</name><description>The goal of this analysis was to examine the impact of PA-X activity during infection in a model of the human airway epithelium, using primary airway cells from two different donors. We profiled the effects of infection and PA-X activity in various airway epithelial cell types. Donor H1: Male, 21, Caucasian, no health issues noted. Donor H2: Male, 55, Caucasian, no health issues noted.</description><dates><publication>2026/02/27</publication></dates><accession>GSE319472</accession><cross_references><GSM>GSM9518371</GSM><GSM>GSM9518370</GSM><GSM>GSM9518373</GSM><GSM>GSM9518372</GSM><GSM>GSM9518375</GSM><GSM>GSM9518374</GSM><GSM>GSM9518377</GSM><GSM>GSM9518376</GSM><GSM>GSM9518368</GSM><GSM>GSM9518367</GSM><GSM>GSM9518378</GSM><GSM>GSM9518369</GSM><GPL>34284</GPL><GSE>319472</GSE><taxon>Homo sapiens</taxon><PMID>[41659510]</PMID></cross_references></HashMap>