(Q41689443)

English

Genetics of prions

scientific article published on January 1997

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

1 reference

Europe PubMed Central

Genetics of prions (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

prion protein family

0 references

Stanley B. Prusiner

1

object named as

Prusiner SB

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

author name string

Scott MR

2

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

publication date

1 January 1997

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

Annual Review of Genetics

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

31

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

139-175

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

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

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Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice

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

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Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells

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

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

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

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Experimental infection of mink with bovine spongiform encephalopathy

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Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins

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Strain specific and common pathogenic events in murine models of scrapie and bovine spongiform encephalopathy

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Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein

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

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Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity

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Klinische und genealogische Beobachtungen bei einem Fall von spastischer Pseudosklerose Jakobs

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

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Circumventing tolerance to generate autologous monoclonal antibodies to the prion protein

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

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

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

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11 October 2022

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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

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

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Ψ, A cytoplasmic suppressor of super-suppressor in yeast

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Modulation of protein structure and function by asparagine-linked glycosylation

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Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein

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

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Prion protein gene variation among primates

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The risk of developing Creutzfeldt-Jakob disease in subjects with the PRNP gene codon 200 point mutation

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High prion and PrPSc levels but delayed onset of disease in scrapie-inoculated mice heterozygous for a disrupted PrP gene

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Chimeric prion protein expression in cultured cells and transgenic mice

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Frequencies of PrP gene variants in healthy cattle and cattle with BSE in Scotland

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

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

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Prion-inducing domain of yeast Ure2p and protease resistance of Ure2p in prion-containing cells

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

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Maintenance and inheritance of yeast prions.

1 reference

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Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent

1 reference

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

1 reference

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

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Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

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Three scrapie prion isolates exhibit different accumulation patterns of the prion protein scrapie isoform

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

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Deletions in the prion protein gene are not associated with CJD.

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Structure and polymorphism of the mouse prion protein gene

1 reference

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Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei

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

1 reference

11 October 2022

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Prion protein is necessary for normal synaptic function

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Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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/10.1146/ANNUREV.GENET.31.1.139

Pathogenesis of scrapie: study of the temporal development of clinical symptoms, of infectivity titres and scrapie-associated fibrils in brains of hamsters infected intraperitoneally

1 reference

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Targeting of scrapie lesions and spread of agent via the retino-tectal projection

1 reference

11 October 2022

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BSE transmission to macaques

1 reference

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Genetical control of the concentration of ME7 scrapie agent in the brain of mice

1 reference

11 October 2022

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Kuru with incubation periods exceeding two decades

1 reference

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https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Separation and properties of cellular and scrapie prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Mice devoid of PrP are resistant to scrapie

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Association between natural scrapie and PrP genotype in a flock of Suffolk sheep in Scotland

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Further purification and characterization of scrapie prions

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Identification of two biologically distinct strains of transmissible mink encephalopathy in hamsters

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Regional mapping of prion proteins in brain

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Creutzfeldt-Jakob disease in a young adult with idiopathic hypopituitarism. Possible relation to the administration of cadaveric human growth hormone

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Correspondence of yeast UAA suppressors to cloned tRNASerUCA genes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Analysis of the prion protein gene in thalamic dementia

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

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https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

The role of Hsp104 in stress tolerance and [PSI+] propagation in Saccharomyces cerevisiae

1 reference

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Developments in diagnosis for prion diseases

1 reference

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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/10.1146/ANNUREV.GENET.31.1.139

Codon 178 mutation of the human prion protein gene in a German family (Backer family): sequencing data from 72-year-old celloidin-embedded brain tissue

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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/10.1146/ANNUREV.GENET.31.1.139

Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Scrapie agent contains a hydrophobic protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Spontaneous spongiform encephalopathy in a young adult rhesus monkey.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Purification and structural studies of a major scrapie prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Introduction of a [4Fe-4S (S-cys)4]+1,+2 iron-sulfur center into a four-alpha helix protein using design parameters from the domain of the Fx cluster in the Photosystem I reaction center

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Mutation of the non-Mendelian suppressor, Psi, in yeast by hypertonic media

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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/10.1146/ANNUREV.GENET.31.1.139

Three-exon structure of the gene encoding the rat prion protein and its expression in tissues

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Monoclonal antibodies to the cellular and scrapie prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Scrapie strains retain their distinctive characteristics following passages of homogenates from different brain regions and spleen

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Glycosylation of synthetic peptides breaks helices. Phosphorylation results in distorted structure

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Predicting the CJD epidemic in humans

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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/10.1146/ANNUREV.GENET.31.1.139

Conformational transitions in peptides containing two putative alpha-helices of the prion protein.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Different allelic effects of the codons 136 and 171 of the prion protein gene in sheep with natural scrapie

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Expression of polyubiquitin and heat-shock protein 70 genes increases in the later stages of disease progression in scrapie-infected mouse brain.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

A novel progressive spongiform encephalopathy in cattle

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Amphotericin B treatment dissociates in vivo replication of the scrapie agent from PrP accumulation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Unconventional Viruses and the Origin and Disappearance of Kuru

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Different scrapie-associated fibril proteins (PrP) are encoded by lines of sheep selected for different alleles of the Sip gene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Phylogenesis of prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Linkage of prion protein and scrapie incubation time genes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Identification of candidate proteins binding to prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Identification of a protein that purifies with the scrapie prion.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Patch-clamp analysis of synaptic transmission to cerebellar purkinje cells of prion protein knockout mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Does the agent of scrapie replicate without nucleic acid?

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Creutzfeldt-Jakob Disease: Focus among Libyan Jews in Israel

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Transcriptional selectivity of viral genes in mammalian cells

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Multicopy SUP35 gene induces de-novo appearance of psi-like factors in the yeast Saccharomyces cerevisiae

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Scrapie agent reflication without the prion protein?

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

[PSI] and [URE3] as yeast prions

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Support for the prion hypothesis for inheritance of a phenotypic trait in yeast

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Bovine spongiform encephalopathy: epidemiological studies on the origin

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

The inheritance of acquired characteristics

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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/10.1146/ANNUREV.GENET.31.1.139

Role of the chaperone protein Hsp104 in propagation of the yeast prion-like factor [psi+]

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Phenotypic suppression of nonsense mutants in yeast by aminoglycoside antibiotics

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Molecular orientation and two-component nature of the crystalline fraction of spider dragline silk.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Deletion in prion protein gene in a Moroccan family

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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/10.1146/ANNUREV.GENET.31.1.139

Molecular cloning of a candidate chicken prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Human prion diseases with variant prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

French autochthonous scrapied sheep without the 136Val PrP polymorphism

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Geographical distribution of cases of Creutzfeldt-Jakob disease in England and Wales 1970-84

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Scrapie: A transmissible and hereditary disease of sheep

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Pathogenesis of Mouse Scrapie: Evidence for Spread of Infection from Central to Peripheral Nervous System

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Normal and scrapie-associated forms of prion protein differ in their sensitivities to phospholipase and proteases in intact neuroblastoma cells

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

A new variant of Creutzfeldt-Jakob disease in the UK.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Structural clues to prion replication

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Molecular biology of prion diseases

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Identification of cellular proteins binding to the scrapie prion protein.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Distinct prion proteins in short and long scrapie incubation period mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Novel proteinaceous infectious particles cause scrapie

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Scrapie prions selectively modify the stress response in neuroblastoma cells

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Creutzfeldt-Jakob disease from contaminated growth hormone extracts in France

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1146/ANNUREV.GENET.31.1.139

Identifiers

10.1146/ANNUREV.GENET.31.1.139

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 October 2017

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