Prion disease--the propagation of infectious protein topologies (Q34094859)

31 July 2017

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title

Prion disease--the propagation of infectious protein topologies (English)

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31 July 2017

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G S Jackson

1

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31 July 2017

J Collinge

series ordinal

2

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31 July 2017

publication date

1 October 2000

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31 July 2017

published in

Microbes and Infection

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31 July 2017

volume

2

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31 July 2017

issue

12

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31 July 2017

page(s)

1445-1449

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

31 July 2017

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7 January 2021

Scrapie prion protein contains a phosphatidylinositol glycolipid

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Molecular biology of prion diseases

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing.

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Scrapie strain variation and mutation

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Mice devoid of PrP are resistant to scrapie

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Mutations and polymorphisms in the prion protein gene

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Quantifying the kinetic parameters of prion replication.

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Cell-free formation of protease-resistant prion protein.

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Structural mobility of the human prion protein probed by backbone hydrogen exchange

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Proteins can adopt totally different folded conformations

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Multiple folding pathways for heterologously expressed human prion protein

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Neurotoxicity of a prion protein fragment

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

The cellular prion protein (PrP) selectively binds to Bcl-2 in the yeast two-hybrid system

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Analysis of interaction sites in homo- and heteromeric complexes containing Bcl-2 family members and the cellular prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

PrP deposition, microglial activation, and neuronal apoptosis in murine scrapie

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Normal host prion protein necessary for scrapie-induced neurotoxicity.

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

Strain-specific prion-protein conformation determined by metal ions

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https://api.crossref.org/works/10.1016%2FS1286-4579%2800%2901299-5

7 January 2021

10.1016/S1286-4579(00)01299-5

Identifiers

DOI

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release_lg666k45yncqbngswllauajpwm

31 July 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/lg666k45yncqbngswllauajpwm

24 November 2022

mapped directly with Wikidata item

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