A presenilin-independent aspartyl protease prefers the gamma-42 site cleavage-Reference-Cited by-同舟云学术

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A presenilin-independent aspartyl protease prefers the gamma-42 site cleavage

Published:2006-01 Issue:1 Volume:96 Page:118-125
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J Neurochem

Author:

Lai Ming-Tain,Crouthamel Ming-Chih,DiMuzio Jillian,Pietrak Beth Lynn,Donoviel Dorit B.,Bernstein Alan,Gardell Stephen J.,Li Yue-Ming,Hazuda Daria

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-4159.2005.03528.x/fullpdf

Reference40 articles.

1. Endogenous β-amyloid production in presenilin-deficient embryonic mouse fibroblasts

2. Characterization of New Polyclonal Antibodies Specific for 40 and 42 Amino Acid-Long Amyloid β Peptides: Their Use to Examine the Cell Biology of Presenilins and the Immunohistochemistry of Sporadic Alzheimer’s Disease and Cerebral Amyloid Angiopathy Cases

3. Inhibition of Receptor-mediated Endocytosis Demonstrates Generation of Amyloid β-Protein at the Cell Surface

4. Novel β-Secretase Cleavage of β-Amyloid Precursor Protein in the Endoplasmic Reticulum/Intermediate Compartment of NT2N Cells

5. γ-Secretase Exists on the Plasma Membrane as an Intact Complex That Accepts Substrates and Effects Intramembrane Cleavage*

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1. Are N- and C-terminally truncated Aβ species key pathological triggers in Alzheimer's disease?;Journal of Biological Chemistry;2018-10

2. Evidence For and Against a Pathogenic Role of Reduced γ-Secretase Activity in Familial Alzheimer’s Disease;Journal of Alzheimer's Disease;2016-05-23

3. p53, a Pivotal Effector of a Functional Cross-Talk Linking Presenilins and Pen-2;Neurodegenerative Diseases;2012

4. Advances in the identification of γ-secretase inhibitors for the treatment of Alzheimer's disease;Expert Opinion on Drug Discovery;2011-12-14

5. Interacting with γSecretase for Treating Alzheimer's Disease: From Inhibition to Modulation;Current Medicinal Chemistry;2011-12-01

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