(Q33604068)

28 July 2017

1 reference

title

Agents that cause transmissible subacute spongiform encephalopathies (English)

1 reference

28 July 2017

Dormont D

1

1 reference

28 July 2017

publication date

1 January 1999

1 reference

Biomedicine and Pharmacotherapy

28 July 2017

published in

1 reference

28 July 2017

volume

53

1 reference

28 July 2017

issue

1

1 reference

28 July 2017

page(s)

3-8

1 reference

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

28 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Degenerative disease of the central nervous system in New Guinea; the endemic occurrence of kuru in the native population

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

A novel progressive spongiform encephalopathy in cattle

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Novel proteinaceous infectious particles cause scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Resistance of Scrapie Agent to Decontamination

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Inactivation of the scrapie agent by near monochromatic ultraviolet light

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Autoclaving does not decontaminate formol-fixed scrapie tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

The effect of beta-propiolactone on the scrapie agent

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Comparative analysis of scrapie agent inactivation methods

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Scrapie prions aggregate to form amyloid-like birefringent rods

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Pathogenesis of mouse scrapie: Effect of route of inoculation on infectivity titres and dose-response curves

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Molecular properties, partial purification, and assay by incubation period measurements of the hamster scrapie agent.

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Newer data on the inactivation of scrapie virus or Creutzfeldt-Jakob disease virus in brain tissue

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Resistance of the scrapie agent to inactivation by psoralens.

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

On the biology of prions

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Prion Protein Genes: Evolutionary and Functional Aspects

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Immunologic and molecular biologic studies of prion proteins in bovine spongiform encephalopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Abnormal fibrils from scrapie-infected brain

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

NMR structure of the mouse prion protein domain PrP(121-231)

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

A Mutant Prion Protein Displays an Aberrant Membrane Association When Expressed in Cultured Cells

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Mutant and infectious prion proteins display common biochemical properties in cultured cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Prion protein is necessary for normal synaptic function

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Transgenetic investigations of prion diseases of humans and animals

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Inherited prion disease

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

1 reference

7 January 2021

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Valine homozygous 129 PrP genotype in a French growth-hormone-related Creutzfeldt-Jakob disease patient

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Mice devoid of PrP are resistant to scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Normal host prion protein necessary for scrapie-induced neurotoxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Pathogenesis of mouse scrapie: Dynamics of agent replication in spleen, spinal cord and brain after infection by different routes

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

A crucial role for B cells in neuroinvasive scrapie.

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Structural clues to prion replication

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Cell-free formation of protease-resistant prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Are prions misfolded molecular chaperones?

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples.

1 reference

https://api.crossref.org/works/10.1016%2FS0753-3322%2899%2980053-5

7 January 2021

10.1016/S0753-3322(99)80053-5

Identifiers

DOI

1 reference

28 July 2017

1 reference