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Inherited prion diseases
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8197105
retrieved
7 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Inherited prion diseases.
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8197105
retrieved
7 August 2017
main subject
prion protein family
0 references
author
Stanley B. Prusiner
series ordinal
1
object named as
Prusiner SB
1 reference
stated in
Europe PubMed Central
PubMed ID
8197105
retrieved
7 August 2017
language of work or name
English
0 references
publication date
1 May 1994
1 reference
stated in
Europe PubMed Central
PubMed ID
8197105
retrieved
7 August 2017
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
Europe PubMed Central
PubMed ID
8197105
retrieved
7 August 2017
volume
91
1 reference
stated in
Europe PubMed Central
PubMed ID
8197105
retrieved
7 August 2017
issue
11
1 reference
stated in
Europe PubMed Central
PubMed ID
8197105
retrieved
7 August 2017
page(s)
4611-4614
1 reference
stated in
Europe PubMed Central
PubMed ID
8197105
retrieved
7 August 2017
cites work
Mutations and polymorphisms in the prion protein gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Genetic and infectious prion diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
The familial occurrence of Creutzfeldt-Jakob disease and Alzheimer's disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the Chimpanzee
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Creutzfeldt-Jakob Disease: Focus among Libyan Jews in Israel
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Creutzfeldt-Jakob disease prion proteins in human brains
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Distinct prion proteins in short and long scrapie incubation period mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Insertion in prion protein gene in familial Creutzfeldt-Jakob disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
The search for scrapie agent nucleic acid
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Deletion in prion protein gene in a Moroccan family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Do Creutzfeldt-Jakob disease patients of Jewish Libyan origin have unique clinical features?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Fatal familial insomnia: clinical and pathologic study of five new cases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Molecular biology of prion diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Aminoacid polymorphism in human prion protein and age at death in inherited prion disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Analysis of the prion protein gene in thalamic dementia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
A dementing illness associated with a novel insertion in the prion protein gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Identification of heterogeneous PrP gene deletions in controls by detection of allele-specific heteroduplexes (DASH)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Familial neurological disease associated with spongiform encephalopathy.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
27 July 2018
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
26 September 2018
[18F]FDG PET in fatal familial insomnia: the functional effects of thalamic lesions.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
26 September 2018
Deletions in the prion protein gene are not associated with CJD.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
26 September 2018
Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
26 September 2018
Spontaneous neurodegeneration in transgenic mice with mutant prion protein
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
26 September 2018
Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43836
retrieved
26 September 2018
New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8197105
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8197105
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
[The hereditary form of Creutzfeldt-Jakob disease (the Backer family)]
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8197105
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8197105
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
PrP and the scrapie agent
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8197105
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8197105
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Linkage of prion protein and scrapie incubation time genes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8197105
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Precise targeting of the pathology of the sialoglycoprotein, PrP, and vacuolar degeneration in mouse scrapie
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8197105
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.91.11.4611
1 reference
stated in
Europe PubMed Central
PubMed ID
8197105
retrieved
7 August 2017
ADS bibcode
1994PNAS...91.4611P
0 references
PMCID
43836
1 reference
stated in
Europe PubMed Central
PubMed ID
8197105
retrieved
7 August 2017
PubMed ID
8197105
1 reference
stated in
Europe PubMed Central
PubMed ID
8197105
retrieved
7 August 2017
ResearchGate publication ID
15002371
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