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April 2008 (v1)Journal articleUploaded on: December 4, 2022
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February 2012 (v1)Journal article
Proteases regulate numerous physiological functions in all living organisms. Because of their contribution to βAPP processing, α-, β- and γ-secretases have focused particular attention of researchers in the field of Alzheimer's disease (AD) during the past 20 years. Whereas the β-secretase BACE1 and the heterotetrameric presenilin-dependent γ-...
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February 1, 2012 (v1)Journal article
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February 25, 2020 (v1)Journal article
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November 2018 (v1)Journal article
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January 1, 2010 (v1)Journal article
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October 5, 2018 (v1)Journal article
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April 1994 (v1)Journal article
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May 11, 2018 (v1)Journal article
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January 15, 2019 (v1)Journal article
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April 1, 2008 (v1)Journal article
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May 2009 (v1)Journal article
Sporadic inclusion-body myositis (s-IBM) is the only muscle disease in which accumulation of amyloid-beta (Abeta) in abnormal muscle fibers appears to play a key pathogenic role. Increased amyloid-beta precursor protein (AbetaPP) and Abeta accumulation have been reported to be upstream steps in the development of the s-IBM pathologic phenotype,...
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July 1995 (v1)Journal article
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April 1999 (v1)Journal article
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August 25, 2009 (v1)Journal article
TMP21 has been shown to be associated with the gamma-secretase complex and can specifically regulate gamma-cleavage without affecting epsilon-mediated proteolysis. To explore the basis of this activity, TMP21 modulation of gamma-secretase activity was investigated independent of epsilon-cleavage using an APPepsilon construct which lacks the...
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May 25, 2018 (v1)Journal article
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April 2023 (v1)Journal article
Abstract The processing of the amyloid precursor protein (APP) is one of the key events contributing to Alzheimer's disease (AD) etiology. Canonical cleavages by β- and γ-secretases lead to Aβ production which accumulate in amyloid plaques. Recently, the matrix metalloprotease MT5-MMP, referred to as η-secretase, has been identified as a novel...
Uploaded on: November 25, 2023 -
November 29, 2022 (v1)Journal article
Abstract The processing of the amyloid precursor protein (APP) is one of the key events contributing to Alzheimer's disease (AD) etiology. Canonical cleavages by β- and γ-secretases lead to Aβ production which accumulate in amyloid plaques. Recently, the matrix metalloprotease MT5-MMP, referred to as η-secretase, has been identified as a novel...
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September 1, 2007 (v1)Journal article
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May 17, 2011 (v1)Journal article
The α-secretases A Disintegrin And Metalloprotease 10 (ADAM10) and ADAM17 trigger constitutive and regulated processing of the cellular prion protein (PrPc) yielding N1 fragment. The latter depends on protein kinase C (PKC)-coupled M1/M3 muscarinic receptors activation and subsequent phosphorylation of ADAM17 on its intracytoplasmic threonine...
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September 1998 (v1)Journal article
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