scholarly journals A dinucleotide deletion in amyloid precursor protein (APP) mRNA associated with sporadic Alzheimer's disease results in efficient secretion of truncated APP isoforms from neuroblastoma cell cultures

2001 ◽  
Vol 76 (5) ◽  
pp. 1308-1314 ◽  
Author(s):  
Martin Hersberger ◽  
Juan Santiago-Garcia ◽  
Susannah Patarroyo-White ◽  
Jimmy Yan ◽  
Xiao Xu
2012 ◽  
Vol 47 (1) ◽  
pp. 425-434 ◽  
Author(s):  
Ryszard Pluta ◽  
Wanda Furmaga-Jabłońska ◽  
Ryszard Maciejewski ◽  
Marzena Ułamek-Kozioł ◽  
Mirosław Jabłoński

2003 ◽  
Vol 70 ◽  
pp. 213-220 ◽  
Author(s):  
Gerald Koelsch ◽  
Robert T. Turner ◽  
Lin Hong ◽  
Arun K. Ghosh ◽  
Jordan Tang

Mempasin 2, a ϐ-secretase, is the membrane-anchored aspartic protease that initiates the cleavage of amyloid precursor protein leading to the production of ϐ-amyloid and the onset of Alzheimer's disease. Thus memapsin 2 is a major therapeutic target for the development of inhibitor drugs for the disease. Many biochemical tools, such as the specificity and crystal structure, have been established and have led to the design of potent and relatively small transition-state inhibitors. Although developing a clinically viable mempasin 2 inhibitor remains challenging, progress to date renders hope that memapsin 2 inhibitors may ultimately be useful for therapeutic reduction of ϐ-amyloid.


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