(Q40709331)

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Transgenetic investigations of prion diseases of humans and animals

scientific article published on February 1993

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Europe PubMed Central

23 September 2017

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Europe PubMed Central

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Transgenetic investigations of prion diseases of humans and animals (English)

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Europe PubMed Central

23 September 2017

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Prusiner SB

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Europe PubMed Central

PubMed ID

8097053

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23 September 2017

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English

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publication date

1 February 1993

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Europe PubMed Central

23 September 2017

Philosophical Transactions of the Royal Society B

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Europe PubMed Central

23 September 2017

339

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Europe PubMed Central

23 September 2017

239-254

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Europe PubMed Central

23 September 2017

1288

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Europe PubMed Central

23 September 2017

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

1 reference

11 October 2022

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

1 reference

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

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

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An analysis of natural scrapie in suffolk sheep

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

1 reference

11 October 2022

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Linkage of prion protein and scrapie incubation time genes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1098/RSTB.1993.0022

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1098/RSTB.1993.0022

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/10.1098/RSTB.1993.0022

Identification of a protein that purifies with the scrapie prion.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1098/RSTB.1993.0022

Purified prion proteins and scrapie infectivity copartition into liposomes

1 reference

11 October 2022

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Allele-specific sequencing confirms novel prion gene polymorphism in Creutzfeldt-Jakob disease

1 reference

11 October 2022

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Purified scrapie prions resist inactivation by UV irradiation

1 reference

11 October 2022

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

1 reference

11 October 2022

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Prion dementia without characteristic pathology

1 reference

11 October 2022

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1098/RSTB.1993.0022

N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion of PrP to the protease-resistant state

1 reference

11 October 2022

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1 reference

11 October 2022

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

1 reference

11 October 2022

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

1 reference

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Brefeldin A redistributes resident and itinerant Golgi proteins to the endoplasmic reticulum

1 reference

11 October 2022

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

1 reference

11 October 2022

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An epidemiologic critique of Creutzfeldt-Jakob disease

1 reference

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Identification of prion amyloid filaments in scrapie-infected brain.

1 reference

11 October 2022

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

1 reference

11 October 2022

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

1 reference

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Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours

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The new biology of spongiform encephalopathy: infectious amyloidoses with a genetic twist

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11 October 2022

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

1 reference

11 October 2022

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1098/RSTB.1993.0022

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

1 reference

11 October 2022

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Scrapie PrP 27-30 is a sialoglycoprotein

1 reference

11 October 2022

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A model for RNA editing in kinetoplastid mitochondria: "guide" RNA molecules transcribed from maxicircle DNA provide the edited information

1 reference

11 October 2022

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Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

1 reference

11 October 2022

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

1 reference

11 October 2022

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Predicted secondary structure and membrane topology of the scrapie prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1098/RSTB.1993.0022

Identifiers

DOI

10.1098/RSTB.1993.0022

1 reference

stated in

Europe PubMed Central

23 September 2017

1 reference

Europe PubMed Central

PubMed ID

8097053

retrieved

23 September 2017

ResearchGate publication ID

15102305

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(Q40709331)

Transgenetic investigations of prion diseases of humans and animals

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