(Q72356037)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8154865%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

review article

1 reference

title

Human prion diseases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8154865%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1

Prusiner SB

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8154865%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

author name string

Hsiao KK

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8154865%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

publication date

1 April 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8154865%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8154865%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

volume

35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8154865%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8154865%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

page(s)

385-395

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8154865%20AND%20SRC:MED&resulttype=core&format=json

Molecular cloning of a human prion protein cDNA

26 October 2019

cites work

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/citations/10.1089/DNA.1986.5.315

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Assignment of the human and mouse prion protein genes to homologous chromosomes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Creutzfeldt-Jakob disease prion proteins in human brains

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Fatal familial insomnia: clinical and pathologic study of five new cases

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

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

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

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

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factors

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Neurofibrillary tangles of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease share antigenic determinants with those of Alzheimer disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Neurotoxicity of a prion protein fragment

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

A dementing illness associated with a novel insertion in the prion protein gene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Straussler-Scheinker syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Creutzfeldt-Jakob disease of long duration: clinicopathological characteristics, transmissibility, and differential diagnosis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

A kinetic model for amyloid formation in the prion diseases: importance of seeding

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Prion dementia without characteristic pathology

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Immunoblotting of Creutzfeldt-Jakob disease prion proteins: host species-specific epitopes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Inherited human prion diseases

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Deletions in the prion protein gene are not associated with CJD.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Real and imagined clinicopathological limits of "prion dementia".

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

The familial occurrence of Creutzfeldt-Jakob disease and Alzheimer's disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Scrapie: A Prototype Slow Infection

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Separation and properties of cellular and scrapie prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Mice devoid of PrP are resistant to scrapie

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Clinical significance of types of cerebellar amyloid plaques in human spongiform encephalopathies

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

CNS amyloid proteins in neurodegenerative diseases.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Genetic and infectious prion diseases

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Analysis of the prion protein gene in thalamic dementia

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Chemistry and biology of prions

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Scrapie agent contains a hydrophobic protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Purification and structural studies of a major scrapie prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Counselling in general practice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Do Creutzfeldt-Jakob disease patients of Jewish Libyan origin have unique clinical features?

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Unconventional Viruses and the Origin and Disappearance of Kuru

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Linkage of prion protein and scrapie incubation time genes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Does the agent of scrapie replicate without nucleic acid?

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Creutzfeldt-Jakob Disease: Focus among Libyan Jews in Israel

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Amyloid plaques in Creutzfeldt-Jakob disease stain with prion protein antibodies

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Sträussler syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Deletion in prion protein gene in a Moroccan family

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Identical mutation in unrelated patients with Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Geographical distribution of cases of Creutzfeldt-Jakob disease in England and Wales 1970-84

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Diagnosis of Creutzfeldt-Jakob disease by Western blot identification of marker protein in human brain tissue

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

A prion protein variant in a family with the telencephalic form of Gerstmann-Straussler-Scheinker syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

PrP and the scrapie agent

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Familial myoclonic dementia masquerading as Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Aminoacid polymorphism in human prion protein and age at death in inherited prion disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Molecular biology of prion diseases

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Familial neurological disease associated with spongiform encephalopathy

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Alzheimer's disease. A family study.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Novel proteinaceous infectious particles cause scrapie

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANA.410350404

Identifiers

DOI

10.1002/ANA.410350404

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8154865%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference