(Q41025440)

25 September 2017

title

Prion protein immunocytochemistry: reliable protocols for the investigation of Creutzfeldt-Jakob disease (English)

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25 September 2017

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Hayward PA

1

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25 September 2017

Bell JE

series ordinal

2

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25 September 2017

Ironside JW

series ordinal

3

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25 September 2017

publication date

1 August 1994

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Neuropathology and Applied Neurobiology

25 September 2017

published in

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25 September 2017

volume

20

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25 September 2017

issue

4

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25 September 2017

page(s)

375-383

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The mRNA encoding the scrapie agent protein is present in a variety of non-neuronal cells

25 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

A simple and effective method for inactivating virus infectivity in formalin‐fixed tissue samples from patients with Creutzfeldt‐Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

Changes in the localization of brain prion proteins during scrapie infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

Scrapie-associated prion protein accumulates in astrocytes during scrapie infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

Immunoreactivity of cerebral amyloidosis is enhanced by protein denaturation treatments

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

Localization of amyloidogenic proteins and sulfated glycosaminoglycans in nontransmissible and transmissible cerebral amyloidoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

Immunohistochemical study of kuru plaques using antibodies against synthetic prion protein peptides

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

Diffuse deposition of immunohistochemically labeled prion protein in the granular layer of the cerebellum in a patient with Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

From slow virus to prion: a review of transmissible spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

Prion protein immunocytochemistry helps to establish the true incidence of prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease). The nature and progression of spongiform change

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

Immunohistochemical localization of prion protein in spongiform encephalopathies and normal brain tissue.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

Molecular biology of prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

Molecular biology and pathology of scrapie and the prion diseases of humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.1994.TB00983.X

10.1111/J.1365-2990.1994.TB00983.X

21 January 2018

Identifiers

DOI

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25 September 2017

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