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English
Prion diseases
scientific article published on 01 June 1992
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504620
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504620%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
review article
1 reference
stated in
Europe PubMed Central
title
Prion diseases
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504620
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504620%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
author name string
J Collinge
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504620
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504620%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
M S Palmer
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504620
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504620%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
publication date
1 June 1992
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504620
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504620%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
published in
Current Opinion in Genetics & Development
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504620
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504620%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
volume
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504620
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504620%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504620
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504620%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
page(s)
448-454
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504620
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504620%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
cites work
Novel proteinaceous infectious particles cause scrapie
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prions and neurodegenerative diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular biology of prion diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spontaneous neurodegeneration in transgenic mice with mutant prion protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Insertion in prion protein gene in familial Creutzfeldt-Jakob disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prion dementia without characteristic pathology
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mortality, neoplasia, and Creutzfeldt-Jakob disease in patients treated with human pituitary growth hormone in the United Kingdom
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Search for a putative scrapie genome in purified prion fractions reveals a paucity of nucleic acids
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Proteinase-resistant prion protein accumulation in Syrian hamster brain correlates with regional pathology and scrapie infectivity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Normal and scrapie-associated forms of prion protein differ in their sensitivities to phospholipase and proteases in intact neuroblastoma cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aminoacid polymorphism in human prion protein and age at death in inherited prion disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The prion's progress
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cotranslation of activated mutant p53 with wild type drives the wild-type p53 protein into the mutant conformation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distinct prion proteins in short and long scrapie incubation period mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Paradoxical shortening of scrapie incubation times by expression of prion protein transgenes derived from long incubation period mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A 'unified theory' of prion propagation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bovine spongiform encephalopathy: epidemiological studies on the origin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Naturally occurring scrapie-like spongiform encephalopathy in five domestic cats
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980156-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0959-437X(05)80156-X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504620
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504620%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
PubMed publication ID
1504620
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1504620
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1504620%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 September 2019
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