(Q40537021)

21 September 2017

1 reference

title

Inherited prion diseases and transmission to rodents (English)

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21 September 2017

0 references

Tateishi J

1

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21 September 2017

Kitamoto T

series ordinal

2

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21 September 2017

language of work or name

1 reference

1 January 1995

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21 September 2017

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21 September 2017

volume

5

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21 September 2017

issue

1

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21 September 2017

page(s)

53-59

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Novel proteinaceous infectious particles cause scrapie

21 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.X

Molecular biology of prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.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.1750-3639.1995.TB00577.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.1750-3639.1995.TB00577.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.1750-3639.1995.TB00577.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.1750-3639.1995.TB00577.X

Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.X

Immunoreactivity of cerebral amyloidosis is enhanced by protein denaturation treatments

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.X

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.X

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.X

Creutzfeldt-Jakob disease in Japan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.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.1750-3639.1995.TB00577.X

An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.X

Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.X

Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00577.X

10.1111/J.1750-3639.1995.TB00577.X

21 January 2018

Identifiers

DOI

1 reference

21 September 2017

1 reference