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Amyloid precursor protein processing in human neurons with an allelic series of the PSEN1 intron 4 deletion mutation and total presenilin-1 knockout
Mutations in presenilin-1 (PSEN1), encoding the catalytic subunit of the amyloid precursor protein-processing enzyme γ-secretase, cause familial Alzheimer’s disease. However, the mechanism of disease is yet to be fully understood and it remains contentious whether mutations exert their effects predo...
Autores principales: | Arber, Charles, Villegas-Llerena, Claudio, Toombs, Jamie, Pocock, Jennifer M, Ryan, Natalie S, Fox, Nick C, Zetterberg, Henrik, Hardy, John, Wray, Selina |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7212081/ https://www.ncbi.nlm.nih.gov/pubmed/32395715 http://dx.doi.org/10.1093/braincomms/fcz024 |
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