(Q46249938)

20 December 2017

title

Spontaneous neurodegeneration in transgenic mice with mutant prion protein (English)

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20 December 2017

0 references

1 reference

6

Prusiner SB

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20 December 2017

5

DeArmond SJ

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20 December 2017

Hsiao KK

1

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20 December 2017

Scott M

series ordinal

2

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20 December 2017

Foster D

series ordinal

3

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20 December 2017

Groth DF

series ordinal

4

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20 December 2017

language of work or name

English

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publication date

1 December 1990

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20 December 2017

published in

Science

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20 December 2017

volume

250

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20 December 2017

issue

4987

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20 December 2017

page(s)

1587-1590

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20 December 2017

Epigenetic control of transgene expression and imprinting by genotype-specific modifiers

cites work

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Identification of a protein that purifies with the scrapie prion

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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/10.1126/SCIENCE.1980379

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Introns increase transcriptional efficiency in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Encephalopathy in mice produced by inoculation with scrapie brain material

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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/10.1126/SCIENCE.1980379

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Proposed genetic basis of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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/10.1126/SCIENCE.1980379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Separation and properties of cellular and scrapie prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

A cellular gene encodes scrapie PrP 27-30 protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Further purification and characterization of scrapie prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Anticipation in Huntington's disease is inherited through the male line but may originate in the female

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Localization of a human gene homologous to the PrP gene on the p arm of chromosome 20 and detection of PrP-related antigens in normal human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Prions. Sheep disease in human clothing

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

Distinct prion proteins in short and long scrapie incubation period mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.1980379

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

21 January 2018

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1126/SCIENCE.1980379

Linkage of prion protein and scrapie incubation time genes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1126/SCIENCE.1980379

Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodents

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1126/SCIENCE.1980379

Experimental transmission of an autosomal dominant spongiform encephalopathy: does the infectious agent originate in the human genome?

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1126/SCIENCE.1980379

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/10.1126/SCIENCE.1980379

A comparison of some biological characteristics of the mouse-passaged scrapie agents, 22A and ME7

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1126/SCIENCE.1980379

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/10.1126/SCIENCE.1980379

Identifiers

DOI

10.1126/SCIENCE.1980379

1 reference

20 December 2017

release_d5zb5yg64fgpteeglvqhwswj4i

ADS bibcode

1990Sci...250.1587H

0 references

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/d5zb5yg64fgpteeglvqhwswj4i

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

20 December 2017