Molecular biology and pathology of scrapie and the prion diseases of humans (Q36477026)

14 August 2017

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title

Molecular biology and pathology of scrapie and the prion diseases of humans (English)

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14 August 2017

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1

Prusiner SB

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14 August 2017

2

DeArmond SJ

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14 August 2017

1 July 1991

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14 August 2017

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14 August 2017

1

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14 August 2017

4

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14 August 2017

297-310

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Novel proteinaceous infectious particles cause scrapie

14 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Unconventional Viruses and the Origin and Disappearance of Kuru

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Experimental transmission of a Kuru-like syndrome to chimpanzees

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

The familial occurrence of Creutzfeldt-Jakob disease and Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Fibrils from brains of cows with new cattle disease contain scrapie-associated protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Bovine spongiform encephalopathy: detection and quantitation of fibrils, fibril protein (PrP) and vacuolation in brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Encephalopathy in mice produced by inoculation with scrapie brain material.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Nature of the Scrapie Agent

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Self-replication and scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

An experimental examination of the scrapie agent in cell membrane mixtures. II. The association of scrapie activity with membrane fractions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Measurement of the scrapie agent using an incubation time interval assay

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Scrapie agent contains a hydrophobic protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Further studies of the infectivity and stability of extracts and homogenates derived from scrapie affected mouse brains.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Purified prion proteins and scrapie infectivity copartition into liposomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Identification of a protein that purifies with the scrapie prion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Further purification and characterization of scrapie prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

A protease-resistant protein is a structural component of the scrapie prion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Purification and structural studies of a major scrapie prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

A cellular gene encodes scrapie PrP 27-30 protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Molecular cloning and complete sequence of prion protein cDNA from mouse brain infected with the scrapie agent

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Molecular cloning of a human prion protein cDNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Purification and properties of the cellular and scrapie hamster prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Molecular mass, biochemical composition, and physicochemical behavior of the infectious form of the scrapie precursor protein monomer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Scrapie prion protein contains a phosphatidylinositol glycolipid

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Differential release of cellular and scrapie prion proteins from cellular membranes by phosphatidylinositol-specific phospholipase C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Identification of glycoinositol phospholipid linked and truncated forms of the scrapie prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Permethylation and tandem mass spectrometry of oligosaccharides having free hexosamine: analysis of the glycoinositol phospholipid anchor glycan from the scrapie prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Subcellular distribution and physicochemical properties of scrapie-associated precursor protein and relationship with scrapie agent

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Specific proteins associated with Creutzfeldt-Jakob disease and scrapie share antigenic and carbohydrate determinants

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Asparagine-linked glycosylation of the scrapie and cellular prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Intracellular accumulation of the cellular prion protein after mutagenesis of its Asn-linked glycosylation sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Nuclease treatment results in high specific purification of Creutzfeldt-Jakob disease infectivity with a density characteristic of nucleic acid-protein complexes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Nuclease-resistant polyadenylated RNAs of significant size are detected by PCR in highly purified Creutzfeldt-Jakob disease preparations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

The molecular pathogenesis of astrogliosis in scrapie and Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Isolation of cDNAs of scrapie-modulated RNAs by subtractive hybridization of a cDNA library

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Scrapie prions aggregate to form amyloid-like birefringent rods

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Antibodies to a scrapie prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Identification of prion amyloid filaments in scrapie-infected brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Amyloid plaques in Creutzfeldt-Jakob disease stain with prion protein antibodies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

CNS amyloid proteins in neurodegenerative diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Infection-specific particle from the unconventional slow virus diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Abnormal fibrils from scrapie-infected brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Ultrastructural morphology of amyloid fibrils from neuritic and amyloid plaques.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Scrapie infectivity, fibrils and low molecular weight protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Immunoaffinity purification and neutralization of scrapie prion infectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Distinct prion proteins in short and long scrapie incubation period mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Two alleles of a neural protein gene linked to scrapie in sheep

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Three hamster species with different scrapie incubation times and neuropathological features encode distinct prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Human prion protein cDNA: molecular cloning, chromosomal mapping, and biological implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Isolation of a cDNA clone encoding the leader peptide of prion protein and expression of the homologous gene in various tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Nerve growth factor increases mRNA levels for the prion protein and the beta-amyloid protein precursor in developing hamster brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Acquisition of protease resistance by prion proteins in scrapie-infected cells does not require asparagine-linked glycosylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Biogenesis and transmembrane orientation of the cellular isoform of the scrapie prion protein [published errratum appears in Mol Cell Biol 1987 May;7(5):2035]

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Evidence for a secretory form of the cellular prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Predicted secondary structure and membrane topology of the scrapie prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Non-hydrophobic extracytoplasmic determinant of stop transfer in the prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Unusual topogenic sequence directs prion protein biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Partial purification and evidence for multiple molecular forms of the scrapie agent

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Genetics and polymorphism of the mouse prion gene complex: control of scrapie incubation time

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

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/10.1111%2FJ.1750-3639.1991.TB00673.X

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Identical mutation in unrelated patients with Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Inherited human prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Straussler-Scheinker syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Prion dementia without characteristic pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Deletion in prion protein gene in a Moroccan family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Creutzfeldt-Jakob Disease: Focus among Libyan Jews in Israel

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Homozygotes for Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Gerstmann-Sträussler-Scheinker disease. I. Extending the clinical spectrum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Neurofibrillary tangles of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease share antigenic determinants with those of Alzheimer disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Comparison of Experimental Binding Data and Theoretical Models in Proteins Containing Subunits*

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

The allosteric transition of glycogen phosphorylase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Structural basis of the allosteric behaviour of phosphofructokinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

A mutant T4 lysozyme displays five different crystal conformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Demonstration by NMR of folding domains in lysozyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

Genetic analysis of the folding pathway for the tail spike protein of phage P22

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

CYTOPLASMIC INHERITANCE OF THE ORGANIZATION OF THE CELL CORTEX IN PARAMECIUM AURELIA

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

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/10.1111%2FJ.1750-3639.1991.TB00673.X

Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Linkage of the gene for the scrapie-associated fibril protein (PrP) to the Sip gene in Cheviot sheep

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Requirement of a protein component for scrapie infectivity.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Replication of the scrapie agent in hamsters infected intracerebrally confirms the pathogenesis of an amyloid-inducing virosis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

A novel progressive spongiform encephalopathy in cattle.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

An analysis of natural scrapie in suffolk sheep

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Linkage of prion protein and scrapie incubation time genes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Prions and neurodegenerative diseases

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Presence of mitochondrial D-loop DNA in scrapie-infected brain preparations enriched for the prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Analysis of linkage between scrapie incubation period and the prion protein gene in mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Different forms of the bovine PrP gene have five or six copies of a short, G-C-rich element within the protein-coding exon

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Immunoblotting of Creutzfeldt-Jakob disease prion proteins: host species-specific epitopes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

ON THE NATURE OF ALLOSTERIC TRANSITIONS: A PLAUSIBLE MODEL

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Linkage of the scrapie-associated fibril protein (PrP) gene and Sinc using congenic mice and restriction fragment length polymorphism analysis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Paradoxical shortening of scrapie incubation times by expression of prion protein transgenes derived from long incubation period mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Scrapie PrP 27-30 is a sialoglycoprotein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.X

Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1111/J.1750-3639.1991.TB00673.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.1750-3639.1991.TB00673.X

Identifiers

DOI

10.1111/J.1750-3639.1991.TB00673.X

1 reference

14 August 2017

1 reference

PubMed ID

1669719