(Q34410655)

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The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob disease

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

prion protein family

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1 reference

based on heuristic

inferred from title

Marcelo A Barria

object named as

Marcelo A Barria

4

0 references

object named as

Mark W Head

7

0 references

object named as

James W Ironside

6

0 references

Diane L Ritchie

5

object named as

Diane L Ritchie

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Alexander Howard Peden

1

object named as

Alexander H Peden

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

author name string

Deep P Sarode

2

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Carl R Mulholland

3

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

publication date

21 October 2014

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Acta Neuropathologica Communications

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

152

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

copyright license

Creative Commons Attribution 4.0 International

21 October 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

https://scigraph.springernature.com/pub.10.1186/s40478-014-0152-4

0 references

Molecular barriers to zoonotic transmission of prions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Small ruminant nor98 prions share biochemical features with human gerstmann-sträussler-scheinker disease and variably protease-sensitive prionopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Variably protease-sensitive prionopathy in the UK: a retrospective review 1991-2008.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Glycoform-selective prion formation in sporadic and familial forms of prion disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt-Jakob disease: a case report.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Sensitive and specific detection of sporadic Creutzfeldt-Jakob disease brain prion protein using real-time quaking-induced conversion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Distinct stability states of disease-associated human prion protein identified by conformation-dependent immunoassay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

A novel human disease with abnormal prion protein sensitive to protease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Diagnosis of human prion disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4210614

6 July 2018

Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0152-4

21 January 2018

A case of protease sensitive prionopathy in a patient in the UK.

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0152-4

21 January 2018

The first case of protease-sensitive prionopathy (PSPr) in The Netherlands: a patient with an unusual GSS-like clinical phenotype

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0152-4

21 January 2018

Heparin enhances the cell-protein misfolding cyclic amplification efficiency of variant Creutzfeldt-Jakob disease.

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0152-4

21 January 2018

Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002.

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0152-4

21 January 2018

Comparison of the level, distribution and form of disease-associated prion protein in variant and sporadic Creutzfeldt-Jakob diseased brain using conformation-dependent immunoassay and Western blot

1 reference

https://pubmed.ncbi.nlm.nih.gov/25331173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variably protease-sensitive prionopathy in a PRNP codon 129 heterozygous UK patient with co-existing tau, α synuclein and Aβ pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/25331173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monitoring plasma processing steps with a sensitive Western blot assay for the detection of the prion protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/25331173

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/S40478-014-0152-4

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

ResearchGate publication ID

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