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Gain-of-function enhancement of InsP(3) receptor modal gating by familial Alzheimer’s disease-linked presenilin mutants in human cells and mouse neurons

Familial Alzheimer’s disease (FAD) is caused by mutations in amyloid precursor protein or presenilins (PS1, PS2). Many FAD-linked PS mutations affect intracellular calcium (Ca(2+)) homeostasis by mechanisms proximal to and independent of amyloid production, although the molecular details are controv...

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Bibliografski detalji
Glavni autori: Cheung, King-Ho, Mei, Lijuan, Daniel Mak, Don-On, Hayashi, Ikuo, Iwatsubo, Takeshi, Kang, David E., Foskett, J. Kevin
Format: Artigo
Jezik:Inglês
Izdano: 2010
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2898196/
https://ncbi.nlm.nih.gov/pubmed/20332427
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/scisignal.2000818
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