Microarray analysis of 1-month-old, 3-month-old, 6-month-old, and 9-month-old digenic APP/PS1 mice on a C57Bl/6 J background were employed, which express a chimeric mouse/human APP bearing the Swedish mutation (K595N/M596L) and the PS1 protein with a deletion on exon 9, recognized as a routinely used mouse model of familial AD for investigating AD-associated pathogenesis [19], together with matched wild-type (WT) controls. The gene discussed is APP; the disease is Alzheimer disease.