Prion protein isoforms, a convergence of biological and structural investigations. (Q40464138)

20 September 2017

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title

Prion protein isoforms, a convergence of biological and structural investigations. (English)

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20 September 2017

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3

Prusiner SB

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20 September 2017

2

Cohen FE

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20 September 2017

Baldwin MA

1

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PubMed ID

7642588

20 September 2017

language of work or name

English

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publication date

1 August 1995

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Journal of Biological Chemistry

20 September 2017

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20 September 2017

270

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20 September 2017

19197-19200

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20 September 2017

33

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Molecular biology of prion diseases

20 September 2017

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https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Does the agent of scrapie replicate without nucleic acid?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Novel proteinaceous infectious particles cause scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Encephalopathy in mice produced by inoculation with scrapie brain material.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Comparison of scrapie and transmissible mink encephalopathy in hamsters. II. Clinical signs, pathology, and pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

The possible nature of the transmissible agent of scrapie.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Self-replication and scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Unconventional Viruses and the Origin and Disappearance of Kuru

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Further purification and characterization of scrapie prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Identification of a protein that purifies with the scrapie prion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Measurement of the scrapie agent using an incubation time interval assay

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Scrapie prions aggregate to form amyloid-like birefringent rods

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Purification and structural studies of a major scrapie prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Identification of scrapie prion protein-specific mRNA in scrapie-infected and uninfected brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

A cellular gene encodes scrapie PrP 27-30 protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Separation and properties of cellular and scrapie prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Purification and properties of the cellular and scrapie hamster prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Isolation and structural studies of the intact scrapie agent protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Scrapie prion protein contains a phosphatidylinositol glycolipid

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Glycosylinositol phospholipid anchors of the scrapie and cellular prion proteins contain sialic acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Asparagine-linked glycosylation of the scrapie and cellular prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Attempts to restore scrapie prion infectivity after exposure to protein denaturants

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Cell-free formation of protease-resistant prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Identification of a gene which controls the incubation period of some strains of scrapie agent in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Scrapie in mice. Agent-strain differences in the distribution and intensity of grey matter vacuolation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Transmission of bovine spongiform encephalopathy and scrapie to mice: strain variation and the species barrier

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Perturbation of the secondary structure of the scrapie prion protein under conditions that alter infectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Thermal stability and conformational transitions of scrapie amyloid (prion) protein correlate with infectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Developments in diagnosis for prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

A prion-like protein from chicken brain copurifies with an acetylcholine receptor-inducing activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Molecular cloning of a candidate chicken prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Proposed three-dimensional structure for the cellular prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Neurotoxicity of a prion protein fragment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Amyloid fibril formation requires a chemically discriminating nucleation event: studies of an amyloidogenic sequence from the bacterial protein OsmB

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Immunoaffinity purification and neutralization of scrapie prion infectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Scrapie prion liposomes and rods exhibit target sizes of 55,000 Da.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Prion protein gene variation among primates

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Mice devoid of PrP are resistant to scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Prion protein peptides induce alpha-helix to beta-sheet conformational transitions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Transmissible mink encephalopathy species barrier effect between ferret and mink: PrP gene and protein analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Alzheimer disease and the prion disorders amyloid beta-protein and prion protein amyloidoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

[URE3] as an altered URE2 protein: evidence for a prion analog in Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Measurement of the β-sheet-forming propensities of amino acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.33.19197

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

21 January 2018

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1074/JBC.270.33.19197

A new (two-repeat) octapeptide coding insert mutation in Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1074/JBC.270.33.19197

Diversity of oligosaccharide structures linked to asparagines of the scrapie prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1074/JBC.270.33.19197

Further analysis of nucleic acids in purified scrapie prion preparations by improved return refocusing gel electrophoresis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1074/JBC.270.33.19197

Identifiers

DOI

10.1074/JBC.270.33.19197

1 reference

20 September 2017

1 reference

PubMed ID

7642588