Presenilin mutations associated with fronto-temporal dementia
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference26 articles.
1. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
2. Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
3. A Presenilin 1 Mutation Associated with Familial Frontotemporal Dementia Inhibits γ-Secretase Cleavage of APP and Notch
4. Familial Frontotemporal Dementia Associated with a Novel Presenilin-1 Mutation
5. Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation
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2. Presenilin: A Multi-Functional Molecule in the Pathogenesis of Alzheimer’s Disease and Other Neurodegenerative Diseases;International Journal of Molecular Sciences;2024-02-01
3. Presenilin-dependent regulation of tau pathology via the autophagy/proteasome pathway;2023-12-23
4. Loss of presenilin function enhances tau phosphorylation and aggregation in mice;Acta Neuropathologica Communications;2021-09-30
5. Systematic Review: Genetic, Neuroimaging, and Fluids Biomarkers for Frontotemporal Dementia Across Latin America Countries;Frontiers in Neurology;2021-06-24
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