(Q48106612)

8 February 2018

title

PrP-deficient mice are resistant to scrapie. (English)

1 reference

8 February 2018

author

Adriano Aguzzi

5

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8 February 2018

author name string

Weissmann C

1

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8 February 2018

Büeler H

2

1 reference

8 February 2018

Fischer M

3

1 reference

8 February 2018

Sailer A

4

1 reference

8 February 2018

Aguet M

6

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8 February 2018

language of work or name

English

0 references

publication date

1 June 1994

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8 February 2018

Annals of the New York Academy of Sciences

published in

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8 February 2018

volume

724

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8 February 2018

page(s)

235-240

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8 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1994.TB38913.X

Molecular biology of prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1994.TB38913.X

Mice devoid of PrP are resistant to scrapie

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1994.TB38913.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.1749-6632.1994.TB38913.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.1749-6632.1994.TB38913.X

Natural and experimental prion diseases of humans and animals

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1994.TB38913.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1994.TB38913.X

10.1111/J.1749-6632.1994.TB38913.X

21 January 2018

Identifiers

DOI

1 reference

8 February 2018

PubMed ID

8030944

1 reference

8 February 2018