<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/GSE346nnn/GSE346333/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</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=GSE346333</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Single-cell transcriptomic analysis of B-cell-dependent gastric cellular responses during chronic Helicobacter felis infection</name><description>Chronic Helicobacter infection induces gastric inflammation and metaplastic changes through interactions among epithelial, stromal, and immune-cell populations. This study used single-cell RNA sequencing to determine how B-cell deficiency alters the gastric cellular microenvironment during chronic Helicobacter felis infection. Total gastric cell suspensions were prepared from lesser-curvature tissue containing the fundus and corpus of uninfected wild-type, H. felis-infected wild-type, and H. felis-infected JH-deficient mice. The dataset contains epithelial, stromal, and immune-cell populations and enables analysis of genotype- and infection-dependent differences in cellular composition, transcriptional programs, and intercellular communication.</description><dates><publication>2026/09/21</publication></dates><accession>GSE346333</accession><cross_references><GSM>GSM10032094</GSM><GSM>GSM10032095</GSM><GSM>GSM10032092</GSM><GSM>GSM10032093</GSM><GSM>GSM10032091</GSM><GPL>24247</GPL><GSE>346333</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>