Beyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob disease (Q28472532)

25 July 2017

Beyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob disease (English)

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Beyond PrP res type 1/type 2 dichotomy in Creutzfeldt-Jakob disease (English)

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Creutzfeldt-Jakob disease

25 July 2017

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Jean-Jacques Hauw

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Emmanuelle Uro-Coste

1

Emmanuelle Uro-Coste

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Marie Bernadette Delisle

18

Marie Bernadette Delisle

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Nathalie Streichenberger

12

Nathalie Streichenberger

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James Ironside

7

James W Ironside

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author name string

Hervé Cassard

2

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25 July 2017

Stéphanie Simon

3

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25 July 2017

Séverine Lugan

4

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25 July 2017

Jean-Marc Bilheude

5

1 reference

25 July 2017

Armand Perret-Liaudet

6

1 reference

25 July 2017

Stéphane Haik

8

1 reference

25 July 2017

Christelle Basset-Leobon

9

1 reference

25 July 2017

Caroline Lacroux

10

1 reference

25 July 2017

Katell Peoch'

11

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Jan Langeveld

13

1 reference

25 July 2017

Mark W Head

14

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25 July 2017

Jacques Grassi

15

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25 July 2017

Francois Schelcher

17

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25 July 2017

Olivier Andréoletti

19

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25 July 2017

Katell Peoch

11

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25 July 2017

language of work or name

English

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publication date

14 March 2008

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1 March 2008

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25 July 2017

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4

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3

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25 July 2017

e1000029

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Creative Commons Attribution 4.0 International

25 July 2017

start time

14 March 2008

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Analysis of prion strains by PrPSc profiling 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=2279301

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

Novel proteinaceous infectious particles cause scrapie

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

Creutzfeldt-Jakob disease and blood transfusion: results of the UK Transfusion Medicine Epidemiological Review study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

Rapid and discriminatory diagnosis of scrapie and BSE in retro-pharyngeal lymph nodes of sheep

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

Screening of 145 anti-PrP monoclonal antibodies for their capacity to inhibit PrPSc replication in infected cells.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

Long-term subclinical carrier state precedes scrapie replication and adaptation in a resistant species: analogies to bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease in humans

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

Genetic influence on the structural variations of the abnormal prion protein

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

The pathology of a natural and experimental scrapie

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

Generation of monoclonal antibodies against human prion proteins in PrP0/0 mice.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

A protease-resistant protein is a structural component of the scrapie prion.

2 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1000029

Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1000029

Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1000029

Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1000029

Three reported cases of variant Creutzfeldt-Jakob disease transmission following transfusion of labile blood components

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1000029

Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1000029

Strain-specific prion-protein conformation determined by metal ions

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PPAT.1000029

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2279301

vCJD and blood transfusion in the United Kingdom

27 November 2018

1 reference

12 December 2020

Multiple prion types in the same brain: is a molecular diagnosis of CJD possible?

1 reference

12 December 2020

pH-dependent Prion Protein Conformation in Classical Creutzfeldt-Jakob Disease

1 reference

12 December 2020

Distribution of codon 129 genotype in human growth hormone-treated CJD patients in France and the UK

1 reference

12 December 2020

10.1371/JOURNAL.PPAT.1000029

Identifiers

DOI

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25 July 2017

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