(Q40618333)

22 September 2017

1 reference

title

The neurochemistry of prion diseases (English)

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22 September 2017

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2

Prusiner SB

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22 September 2017

1

DeArmond SJ

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PubMed ID

7901326

22 September 2017

language of work or name

English

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publication date

1 November 1993

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Journal of Neurochemistry

22 September 2017

13

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based on heuristic

inferred from page(s)

published in

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22 September 2017

61

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22 September 2017

5

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22 September 2017

1589-1601

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Does the agent of scrapie replicate without nucleic acid?

22 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Purified scrapie prions resist inactivation by procedures that hydrolyze, modify, or shear nucleic acids.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Carbohydrate ligands of the LEC cell adhesion molecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Identification of prion amyloid filaments in scrapie-infected brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Changes in the localization of brain prion proteins during scrapie infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Scrapie infectivity, fibrils and low molecular weight protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Neurite outgrowth in response to transfected N-CAM and N-cadherin reveals fundamental differences in neuronal responsiveness to CAMs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Argyrophilic plaques in mice inoculated with scrapie from particular sources.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

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/10.1111%2FJ.1471-4159.1993.TB09792.X

Purified prion proteins and scrapie infectivity copartition into liposomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Immunoaffinity purification and neutralization of scrapie prion infectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Experimental transmission of a Kuru-like syndrome to chimpanzees

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

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/10.1111%2FJ.1471-4159.1993.TB09792.X

Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Inherited human prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

A prion protein variant in a family with the telencephalic form of Gerstmann-Straussler-Scheinker syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Proteinase-resistant prion protein accumulation in Syrian hamster brain correlates with regional pathology and scrapie infectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Delineation of olfactory pathways in the frog nervous system by unique glycoconjugates and N-CAM glycoforms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Fatal familial insomnia: clinical and pathologic study of five new cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Separation and properties of cellular and scrapie prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

A cellular gene encodes scrapie PrP 27-30 protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Insertions in the prion protein gene in atypical dementias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Molecular properties, partial purification, and assay by incubation period measurements of the hamster scrapie agent.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Further purification and characterization of scrapie prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Scrapie prions aggregate to form amyloid-like birefringent rods

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Assignment of the human and mouse prion protein genes to homologous chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Regional mapping of prion proteins in brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

Synthesis and trafficking of prion proteins in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

A 'unified theory' of prion propagation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.1993.TB09792.X

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/10.1111/J.1471-4159.1993.TB09792.X

Resistance of the scrapie agent to inactivation by psoralens.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Temporary and permanent modifications to a single strain of mouse scrapie on transmission to rats and hamsters

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease). The nature and progression of spongiform change

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the Chimpanzee

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Identification of a protein that purifies with the scrapie prion.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Pathogenesis of scrapie (strain 263K) in hamsters infected intracerebrally, intraperitoneally or intraocularly.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Purified scrapie prions resist inactivation by UV irradiation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

The Scrapie Agent: Evidence Against its Dependence for Replication on Intrinsic Nucleic Acid

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Scrapie in the central nervous system: neuroanatomical spread of infection and Sinc control of pathogenesis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Search for a putative scrapie genome in purified prion fractions reveals a paucity of nucleic acids

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

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/10.1111/J.1471-4159.1993.TB09792.X

Structures and functional roles of the sugar chains of human erythropoietins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Scrapie produced experimentally in goats with special reference to the clinical syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Scrapie PrP 27-30 is a sialoglycoprotein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Molecular biology of prion diseases

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

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/10.1111/J.1471-4159.1993.TB09792.X

Novel proteinaceous infectious particles cause scrapie

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1471-4159.1993.TB09792.X

Identifiers

DOI

10.1111/J.1471-4159.1993.TB09792.X

1 reference

22 September 2017

1 reference

PubMed ID

7901326