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Presenilin 1 Regulates Membrane Homeostatic Pathways that are Dysregulated in Alzheimer’s Disease

Mutations in the PSEN1 gene, encoding presenilin 1 (PS1), are the most common cause of familial Alzheimer’s disease(fAD). Since the first mutations in the PSEN1 gene were discovered more than 25 years ago, many postulated functions of PS1 have been investigated. The majority of earlier studies focus...

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Detalhes bibliográficos
Publicado no:J Alzheimers Dis
Main Authors: Deaton, Carol A., Johnson, Gail V.W.
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8056533/
https://ncbi.nlm.nih.gov/pubmed/32804090
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JAD-200598
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