Ontology highlight
ABSTRACT: Background
Preclinical Alzheimer's disease (AD) research strongly depends on transgenic mouse models that display major symptoms of the disease. Although several AD mouse models have been developed representing relevant pathologies, only a fraction of available mouse models, like the Tg4-42 mouse model, display hippocampal atrophy caused by the death of neurons as the key feature of AD. The Tg4-42 mouse model is therefore very valuable for use in preclinical research. Furthermore, metabolic biomarkers which have the potential to detect biochemical changes, are crucial to gain deeper insights into the pathways, the underlying pathological mechanisms and disease progression.Objective
We thus performed an in-depth characterization of Tg4-42 mice by using an integrated approach
SUBMITTER: Hinteregger B
PROVIDER: S-EPMC8150512 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature