High titers of transmissible spongiform encephalopathy infectivity associated with extremely low levels of PrPSc in vivo. (Q34699610)

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8 January 2020

title

High titers of transmissible spongiform encephalopathy infectivity associated with extremely low levels of PrPSc in vivo (English)

1 reference

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transmissible spongiform encephalopathy

8 January 2020

main subject

0 references

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1

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8 January 2020

Declan King

3

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8 January 2020

Karen Chapman

5

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8 January 2020

Jean C Manson

7

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8 January 2020

author name string

Susan L Campbell

2

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8 January 2020

Anne Bellon

4

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8 January 2020

R Anthony Williamson

6

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8 January 2020

language of work or name

English

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publication date

8 October 2007

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Journal of Biological Chemistry

8 January 2020

published in

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8 January 2020

volume

282

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8 January 2020

issue

49

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8 January 2020

page(s)

35878-35886

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Molecular biology and pathogenesis of prion diseases

8 January 2020

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Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein

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A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy

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Changing a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers

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Eight prion strains have PrP(Sc) molecules with different conformations

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Mutant PrPSc conformers induced by a synthetic peptide and several prion strains

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Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice

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Identification of a gene which controls the incubation period of some strains of scrapie agent in mice

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Motif-grafted antibodies containing the replicative interface of cellular PrP are specific for PrPSc

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Toward molecular dissection of PrPC-PrPSc interactions

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Transmissible and genetic prion diseases share a common pathway of neurodegeneration

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Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol

21 January 2018

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Conversion of PrP to a self-perpetuating PrPSc-like conformation in the cytosol

21 January 2018

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

21 January 2018

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

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M704329200

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17923484%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference