Related references
Note: Only part of the references are listed.Prions and manganese: A maddening beast
David R. Brown
METALLOMICS (2011)
The oligomerization properties of prion protein are restricted to the H2H3 domain
Nesrine Chakroun et al.
FASEB JOURNAL (2010)
Manganese chelation therapy extends survival in a mouse model of M1000 prion disease
Marcus W. Brazier et al.
JOURNAL OF NEUROCHEMISTRY (2010)
Thermodynamic and Voltammetric Characterization of the Metal Binding to the Prion Protein: Insights into pH Dependence and Redox Chemistry
Paul Davies et al.
BIOCHEMISTRY (2009)
Manganese Enhances Prion Protein Survival in Model Soils and Increases Prion Infectivity to Cells
Paul Davies et al.
PLOS ONE (2009)
The chemistry of copper binding to PrP: is there sufficient evidence to elucidate a role for copper in protein function?
Paul Davies et al.
BIOCHEMICAL JOURNAL (2008)
The stability and aggregation of ovine prion protein associated with classical and atypical scrapie correlates with the ease of unwinding of helix-2
Tim J. Fitzmaurice et al.
BIOCHEMICAL JOURNAL (2008)
Raman optical activity and circular dichroism reveal dramatic differences in the influence of divalent copper and manganese ions on prion protein folding
Fujiang Zhu et al.
BIOCHEMISTRY (2008)
Manganese binding to the prion protein
Marcus W. Brazier et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Resistance of cell lines to prion toxicity aided by phospho-ERK expression
Kay M. Uppington et al.
JOURNAL OF NEUROCHEMISTRY (2008)
Elevated manganese levels in blood and CNS in human prion disease
Shirley Hesketh et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2008)
Exposure to low dietary copper or low copper coupled with high dietary manganese for one year does not alter brain prion protein characteristics in the mature cow
L. R. Legleiter et al.
JOURNAL OF ANIMAL SCIENCE (2007)
Elevated manganese levels in blood and central nervous system occur before onset of clinical signs in scrapie and bovine spongiform encephalopathy
S. Hesketh et al.
JOURNAL OF ANIMAL SCIENCE (2007)
A newly identified type of scrapie agent can naturally infect sheep with resistant PrP genotypes
A Le Dur et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
The most infectious prion protein particles
JR Silveira et al.
NATURE (2005)
Assembly of natural and recombinant prion protein into fibrils
KW Leffers et al.
BIOLOGICAL CHEMISTRY (2005)
Copper(II) inhibits in vitro conversion of prion protein into amyloid fibrils
OV Bocharova et al.
BIOCHEMISTRY (2005)
In vitro conversion of full-length mammalian prion protein produces amyloid form with physical properties of PrPSc
OV Bocharova et al.
JOURNAL OF MOLECULAR BIOLOGY (2005)
Efficient inhibition of prion replication by PrP-Fc2 suggests that the prion is a PrPSc oligomer
J Masel et al.
JOURNAL OF MOLECULAR BIOLOGY (2005)
Prions: so many fibers, so little infectivity
BCH May et al.
TRENDS IN BIOCHEMICAL SCIENCES (2004)
Prion protein fate governed by metal binding
RN Tsenkova et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2004)
Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis
G Mallucci et al.
SCIENCE (2003)
Mapping the functional domain of the prion protein
T Cui et al.
EUROPEAN JOURNAL OF BIOCHEMISTRY (2003)
Subclinical prion disease induced by oral inoculation
AM Thackray et al.
JOURNAL OF VIROLOGY (2003)
Protease-sensitive scrapie prion protein in aggregates of heterogeneous sizes
S Tzaban et al.
BIOCHEMISTRY (2002)
Metal imbalance and compromised antioxidant function are early changes in prion disease
AM Thackray et al.
BIOCHEMICAL JOURNAL (2002)
Chronic subclinical prion disease induced by low-dose inoculum
AM Thackray et al.
JOURNAL OF VIROLOGY (2002)
Aberrant metal binding by prion protein in human prion disease
BS Wong et al.
JOURNAL OF NEUROCHEMISTRY (2001)
Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding
GP Saborio et al.
NATURE (2001)
Folding of prion protein to its native α-helical conformation is under kinetic control
IV Baskakov et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
A protease-resistant 61-residue prion peptide causes neurodegeneration in transgenic mice
S Supattapone et al.
MOLECULAR AND CELLULAR BIOLOGY (2001)
Copper refolding of prion protein
BS Wong et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2000)
Consequences of manganese replacement of copper for prion protein function and proteinase resistance
DR Brown et al.
EMBO JOURNAL (2000)