Presenilin Proteins Undergo Heterogeneous Endoproteolysis between Thr291and Ala299and Occur as Stable N- and C-Terminal Fragments in Normal and Alzheimer Brain Tissue

Presenilin Proteins Undergo Heterogeneous Endoproteolysis between Thr291and Ala299and Occur as Stable N- and C-Terminal Fragments in Normal and Alzheimer Brain Tissue

Humans inheriting missense mutations in thepresenilin(PS)1 and -2 genes undergo progressive cerebral deposition of the amyloid β-protein at an early age and develop a clinically and pathologically severe form of familial Alzheimer's disease (FAD). Because PS1 mutations cause the most aggressive...

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Bibliographic Details
Main Authors: Marcia B. Podlisny, Martin Citron, Patricia Amarante, Robin Sherrington, Weiming Xia, Jimin Zhang, Thekla Diehl, George Levesque, Paul Fraser, Christian Haass, Edward H.M. Koo, Peter Seubert, Peter St. George-Hyslop, David B. Teplow, Dennis J. Selkoe
Format: Article
Language:English
Published: Elsevier 1997-01-01
Series:Neurobiology of Disease
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996197901297

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