Ashley I. Bush

Prof. Dr. Ashley I. Bush

Melbourne Dementia Research Centre, The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC 3052, Australia
orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2017 in Cell
Verified
Journal Article
Closed access
BSBrent R. Stockwell
Brent R. Stockwell
JAJosé Pedro Friedmann Angeli
José Pedro Friedmann Angeli
HBHülya Bayir
Hülya Bayir
Ashley I. BushAshley I. Bush
Ashley I. Bush
MCMarcus Conrad
Marcus Conrad
DZDonna D. Zhang
Donna D. Zhang

1 March 2004 in Nature Reviews Drug Discovery
Verified
Journal Article
Closed access
PDF file
KBKevin J. Barnham
Kevin J. Barnham
CMColin L. Masters
Colin L. Masters
Ashley I. BushAshley I. Bush
Ashley I. Bush

13 May 2005 in Nature Reviews Neuroscience
Verified
Journal Article
Closed access
PDF file
CFChristopher J. Frederickson
Christopher J. Frederickson
JKJae-Young Koh
Jae-Young Koh
Ashley I. BushAshley I. Bush
Ashley I. Bush

11 November 2021 in Nature Reviews Cancer
Verified
Journal Article
Closed access
PDF file
EGEva J. Ge
Eva J. Ge
Ashley I. BushAshley I. Bush
Ashley I. Bush
ACAngela Casini
Angela Casini
PCPaul A. Cobine
Paul A. Cobine
JCJustin R. Cross
Justin R. Cross
CCChristopher J. Chang
Christopher J. Chang

2 September 1994 in Science
Verified
Journal Article
Closed access
PDF file
Ashley I. BushAshley I. Bush
Ashley I. Bush
WPW. Pettingell
W. Pettingell
GMG Multhaup
G Multhaup
MPM D Paradis
M D Paradis
JVJ. Vonsattel
J. Vonsattel
RTR. Tanzi
R. Tanzi
A beta 1-40, a major component of Alzheimer's disease cerebral amyloid, is present in the cerebrospinal fluid and remains relatively soluble at high concentrations (less than or equal to 3.7 mM). Thus, physiological factors which induce A beta amyloid formation could provide clues to the pathogenesis of the disease. It has been shown that human A beta specifically and saturably binds zinc. Here, concentrations of zinc above 300 nM rapidly destabilized human A beta 1-40 solutions, inducing tinctorial amyloid formation. However, rat A beta 1-40 binds zinc less avidly and is immune to these effects, perhaps explaining the scarcity with which these animals form cerebral A beta amyloid. These data suggest a role for cerebral zinc metabolism in the neuropathogenesis of Alzheimer's disease.

1 May 2001 in Neuron
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Journal Article
Closed access
RCRobert A Cherny
Robert A Cherny
CACraig S Atwood
Craig S Atwood
MXMichel E Xilinas
Michel E Xilinas
DGDanielle N Gray
Danielle N Gray
WJWalton D Jones
Walton D Jones
Ashley I. BushAshley I. Bush
Ashley I. Bush