(Q48715592)

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Transgenic mice expressing bovine PrP with a four extra repeat octapeptide insert mutation show a spontaneous, non-transmissible, neurodegenerative disease and an expedited course of BSE infection.

scientific article published on 19 October 2005

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16253245%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Transgenic mice expressing bovine PrP with a four extra repeat octapeptide insert mutation show a spontaneous, non-transmissible, neurodegenerative disease and an expedited course of BSE infection (English)

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8 January 2020

neurodegeneration

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Alfonso Gutiérrez-Adán

2

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8 January 2020

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8 January 2020

Francisco J. Salguero

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8 January 2020

Juan Maria Torres

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8 January 2020

Joaquín Castilla

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8 January 2020

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8 January 2020

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B Parra

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8 January 2020

F Díaz San Segundo

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8 January 2020

M A Ramírez

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8 January 2020

A Rábano

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8 January 2020

M J Cano

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8 January 2020

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19 October 2005

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8 January 2020

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8 January 2020

579

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8 January 2020

27

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8 January 2020

6237-6246

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8 January 2020

The nature of the scrapie agent

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

The same prion strain causes vCJD and BSE

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Creutzfeldt-Jakob disease. The neuropathology of a transmission experiment

1 reference

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21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Molecular genetic studies of Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Neurological illness in transgenic mice expressing a prion protein with an insertional mutation.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Different behavior toward bovine spongiform encephalopathy infection of bovine prion protein transgenic mice with one extra repeat octapeptide insert mutation.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Subclinical bovine spongiform encephalopathy infection in transgenic mice expressing porcine prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Abnormal properties of prion protein with insertional mutations in different cell types

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

A vector for expressing foreign genes in the brains and hearts of transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Proteinase K enhanced immunoreactivity of the prion protein-specific monoclonal antibody 2A11.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Early detection of PrPres in BSE-infected bovine PrP transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Rapidly progressive dementia syndrome associated with a novel four extra repeat mutation in the prion protein gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Prion diseases: what is the neurotoxic molecule?

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Seeding "one-dimensional crystallization" of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie?

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Prion protein devoid of the octapeptide repeat region restores susceptibility to scrapie in PrP knockout mice.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

Integration of foreign genes into the mammalian germ line: genetic engineering enters a new era

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2005.09.099

21 January 2018

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