(Q44881216)

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The residue 129 polymorphism in human prion protein does not confer susceptibility to Creutzfeldt-Jakob disease by altering the structure or global stability of PrPC.

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28 December 2019

The residue 129 polymorphism in human prion protein does not confer susceptibility to Creutzfeldt-Jakob disease by altering the structure or global stability of PrPC (English)

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28 December 2019

prion protein family

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protein structure

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Creutzfeldt-Jakob disease

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based on heuristic

inferred from title

Graham S Jackson

2

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28 December 2019

Jonathan Waltho

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28 December 2019

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John Collinge

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28 December 2019

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Laszlo L P Hosszu

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28 December 2019

Clare R Trevitt

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28 December 2019

Samantha Jones

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28 December 2019

Mark Batchelor

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28 December 2019

Daljit Bhelt

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28 December 2019

Kanella Prodromidou

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28 December 2019

Anthony R Clarke

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28 December 2019

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27 April 2004

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28 December 2019

Journal of Biological Chemistry

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28 December 2019

279

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28 December 2019

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28 December 2019

28515-28521

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28 December 2019

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Prion diseases of humans and animals: their causes and molecular basis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Self-replication and scrapie

1 reference

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21 January 2018

Novel proteinaceous infectious particles cause scrapie

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Cell-free formation of protease-resistant prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

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/10.1074%2FJBC.M313762200

21 January 2018

Unaltered susceptibility to BSE in transgenic mice expressing human prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Molecular classification of sporadic Creutzfeldt-Jakob disease.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Thermodynamic beta-sheet propensities measured using a zinc-finger host peptide.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

An efficient 3D NMR technique for correlating the proton and 15N backbone amide resonances with the alpha-carbon of the preceding residue in uniformly 15N/13C enriched proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

A 15n-filtered 2D 1H TOCSY experiment for assignment of aromatic ring resonances and selective identification of tyrosine ring resonances in proteins: Description and application to Photoactive Yellow Protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Protein backbone angle restraints from searching a database for chemical shift and sequence homology

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination

1 reference

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21 January 2018

Primary structure effects on peptide group hydrogen exchange

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

An integrated kinetic analysis of intermediates and transition states in protein folding reactions.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Location and properties of metal-binding sites on the human prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

NMR structure of the bovine prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

The crystal structure of the globular domain of sheep prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Solution structure of the E200K variant of human prion protein. Implications for the mechanism of pathogenesis in familial prion diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

NMR solution structure of the human prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313762200

21 January 2018

Crystal structure of the human prion protein reveals a mechanism for oligomerization

1 reference

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21 January 2018

Prion protein NMR structure and familial human spongiform encephalopathies

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Chemical shifts in denatured proteins: resonance assignments for denatured ubiquitin and comparisons with other denatured proteins

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Relationship between nuclear magnetic resonance chemical shift and protein secondary structure

1 reference

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21 January 2018

PROCHECK: a program to check the stereochemical quality of protein structures

1 reference

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21 January 2018

The same prion strain causes vCJD and BSE

1 reference

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21 January 2018

Strain-specific prion-protein conformation determined by metal ions

1 reference

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21 January 2018

Multiple folding pathways for heterologously expressed human prion protein

1 reference

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21 January 2018

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1 reference

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Identifiers

10.1074/JBC.M313762200

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15123682%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15123682%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

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