<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/GSE328nnn/GSE328648/</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=GSE328648</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Investigation of gene expression in human brain samples</name><description>Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by a gradual decline in neuronal activity, which affects memory and thinking. As it progresses, it can interfere with daily life, and it can eventually lead to death. AD accounts for approximately 60-70% of dementia cases and is particularly prevalent in the elderly. However, the gene regulatory mechanism for AD development in human brain tissues is still unclear. To deepen our understanding of the molecular mechanims involved in this cognitive decline, we conducted RNA-sequencing (RNA-seq) on six brain tissues from both control (Ct) without dementia and AD patients to analyze differentially expressed genes (DEGs) between Ct and AD brains.</description><dates><publication>2026/09/09</publication></dates><accession>GSE328648</accession><cross_references><GSM>GSM9686617</GSM><GSM>GSM9686618</GSM><GSM>GSM9802734</GSM><GSM>GSM9686619</GSM><GSM>GSM9686620</GSM><GSM>GSM9686621</GSM><GSM>GSM9686622</GSM><GPL>34284</GPL><GSE>328648</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>