(Q33764321)

29 July 2017

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title

Prion protein interconversions and the transmissible spongiform encephalopathies (English)

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29 July 2017

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Horiuchi M

1

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29 July 2017

Caughey B

series ordinal

2

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29 July 2017

publication date

1 October 1999

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29 July 2017

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29 July 2017

volume

7

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29 July 2017

issue

10

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29 July 2017

page(s)

R231-40

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Molecular genetics of transmissible spongiform encephalopathies

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Prion protein and the transmissible spongiform encephalopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

1 reference

7 January 2021

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

NMR structure of the mouse prion protein domain PrP(121-231)

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Recombinant full-length murine prion protein, mPrP(23-231): purification and spectroscopic characterization.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Solution structure of Syrian hamster prion protein rPrP(90-231).

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Differences in the Membrane Interaction of Scrapie Amyloid Precursor Proteins in Normal and Scrapie- or Creutzfeldt-Jakob Disease-Infected Brains

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

X-ray diffraction of scrapie prion rods and PrP peptides

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Strain-dependent differences in beta-sheet conformations of abnormal prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Non-genetic propagation of strain-specific properties of scrapie prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Recombinant scrapie-like prion protein of 106 amino acids is soluble

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Biochemical typing of scrapie strains

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Molecular analysis of ovine prion protein identifies similarities between BSE and an experimental isolate of natural scrapie, CH1641.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Eight prion strains have PrP(Sc) molecules with different conformations

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Detection and discrimination of PrPSc by multi-spectral ultraviolet fluorescence.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Scrapie prion rod formation in vitro requires both detergent extraction and limited proteolysis

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Morphogenesis of amyloid plaques in 87V murine scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Aggregates of scrapie-associated prion protein induce the cell-free conversion of protease-sensitive prion protein to the protease-resistant state

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Scrapie infectivity correlates with converting activity, protease resistance, and aggregation of scrapie-associated prion protein in guanidine denaturation studies.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

A 'unified theory' of prion propagation

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Self-replication and scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Transmissible and non-transmissible amyloidoses: autocatalytic post-translational conversion of host precursor proteins to beta-pleated sheet configurations

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Seeding "one-dimensional crystallization" of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie?

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

The chemistry of scrapie infection: implications of the 'ice 9' metaphor

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

pH-dependent stability and conformation of the recombinant human prion protein PrP(90-231)

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Physical studies of conformational plasticity in a recombinant prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

A scrapie-like unfolding intermediate of the prion protein domain PrP(121-231) induced by acidic pH.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Attempts to restore scrapie prion infectivity after exposure to protein denaturants

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

The nature of the scrapie agent: the evolution of the virino

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Prionics or the kinetic basis of prion diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Quantifying the kinetic parameters of prion replication.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Prion protein and species barriers in the transmissible spongiform encephalopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Cell-free formation of protease-resistant prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Molecular assessment of the potential transmissibilities of BSE and scrapie to humans.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Protease-resistant prion protein produced in vitro lacks detectable infectivity.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Specific inhibition of in vitro formation of protease-resistant prion protein by synthetic peptides

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Inhibition of protease-resistant prion protein formation by porphyrins and phthalocyanines

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

In situ formation of protease-resistant prion protein in transmissible spongiform encephalopathy-infected brain slices.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Chaperone-supervised conversion of prion protein to its protease-resistant form

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Cell-lysate conversion of prion protein into its protease-resistant isoform suggests the participation of a cellular chaperone

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Species-independent inhibition of abnormal prion protein (PrP) formation by a peptide containing a conserved PrP sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

The importance of the disulfide bond in prion protein conversion

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Chimeric prion protein expression in cultured cells and transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Scrapie amyloid (prion) protein has the conformational characteristics of an aggregated molten globule folding intermediate

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Partial unfolding and refolding of scrapie-associated prion protein: evidence for a critical 16-kDa C-terminal domain.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Properties of the scrapie prion protein: quantitative analysis of protease resistance

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Reversibility of scrapie inactivation is enhanced by copper.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Ultrastructural studies on scrapie prion protein crystals obtained from reverse micellar solutions

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Rapid acquisition of beta-sheet structure in the prion protein prior to multimer formation

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Protease-resistant and detergent-insoluble prion protein is not necessarily associated with prion infectivity.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

A kinetic model for amyloid formation in the prion diseases: importance of seeding

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Molecular characteristics of a protease-resistant, amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Autonomous and reversible folding of a soluble amino-terminally truncated segment of the mouse prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Extremely rapid folding of the C-terminal domain of the prion protein without kinetic intermediates

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion of PrP to the protease-resistant state

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Purification and properties of the cellular and scrapie hamster prion proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Allelic origin of the abnormal prion protein isoform in familial prion diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Mutant and infectious prion proteins display common biochemical properties in cultured cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

A Mutant Prion Protein Displays an Aberrant Membrane Association When Expressed in Cultured Cells

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Effect of the D178N Mutation and the Codon 129 Polymorphism on the Metabolism of the Prion Protein

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Prion Protein Aggregation Reverted by Low Temperature in Transfected Cells Carrying a Prion Protein Gene Mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Abnormal properties of prion protein with insertional mutations in different cell types.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

A transmembrane form of the prion protein in neurodegenerative disease

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Familial mutations and the thermodynamic stability of the recombinant human prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Familial prion disease mutation alters the secondary structure of recombinant mouse prion protein: implications for the mechanism of prion formation.

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

Prion protein NMR structure and familial human spongiform encephalopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2800%2980049-0

7 January 2021

10.1016/S0969-2126(00)80049-0

Identifiers

DOI

1 reference

29 July 2017

1 reference