<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Department of Medical Genetics, Aging Research Center (CESI), G. d’Annunzio University Foundation Chieti</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA150875</full_dataset_link><scientific_name>Mus musculus</scientific_name><long_description>In this study, using a microarray approach, we investigated the age-dependent changes in the gene expression profile of hippocampi obtained from young and old 3xTg-AD and WT control mice, in order to identify the molecular mechanisms involved in the development of AD and assess the role of aging in the development of the disease. A global gene expression profile in the hippocampi obtained from 3xTgAD (expressing mutant human APP, PS1, and tau) and WT mice at 3 and 12 months of age was studied by employing a Mouse OneArray Whole Genome DNA microarray. Data were analyzed with the Ingenuity Pathways Analysis (IPA) in order to achieve a classification of the results on the basis of their biological functions and disclose functional networks and/or pathways. Overall design: In this study we performed gene expression profiles for a total of 9 experiments. Hippocampi were collected from 2 3xTG and 2 WT mice at 3 months of age and from 2 3xTG and 2 WT mice at 12 months of age. Three MicroArray experiments were performed for each condition (WT 12 moa versus WT 3 moa 3xTG 3 moa versus WT 3 moa 3xTG 12 moa versus WT 12moa). On the total of 9 experiments 6 were biological replicates and 3 were technical replicates.</long_description><tag>xref:PubMed:24525730</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Mus musculus</name><description>Age-dependent changes in the gene expression profile of mice over-expressing mutant APP, PS1 and phosphorilated tau</description><dates><last_updated>2025-09-24</last_updated><first_public>2014-02-11</first_public></dates><accession>PRJNA150875</accession><cross_references><GEO>GSE35210</GEO><taxon>10090</taxon><PubMed>24525730</PubMed></cross_references></HashMap>