Separation of presenilin function in amyloid β-peptide generation and endoproteolysis of Notch

Most of the genetically inherited Alzheimer's disease cases are caused by mutations in the presenilin genes, PS1 and PS2. PS mutations result in the enhanced production of the highly amyloidogenic 42/43 amino acid variant of amyloid β-peptide (Aβ). We have introduced arbitrary mutations at posi...

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Hlavní autoři: Kulic, Luka, Walter, Jochen, Multhaup, Gerd, Teplow, David B., Baumeister, Ralf, Romig, Helmut, Capell, Anja, Steiner, Harald, Haass, Christian
Médium: Artigo
Jazyk:Inglês
Vydáno: The National Academy of Sciences 2000
Témata:
Biological Sciences
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC18533/
https://ncbi.nlm.nih.gov/pubmed/10811883
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