(Q34448005)

2 August 2017

The origin of bovine spongiform encephalopathy: the human prion disease hypothesis (English)

1 reference

2 August 2017

0 references

Alan C F Colchester

1

1 reference

PubMed ID

16139661

2 August 2017

Nancy T H Colchester

series ordinal

2

1 reference

PubMed ID

16139661

2 August 2017

language of work or name

English

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publication date

1 September 2005

1 reference

2 August 2017

1 reference

2 August 2017

366

1 reference

2 August 2017

856-861

1 reference

2 August 2017

9488

1 reference

When did bovine spongiform encephalopathy (BSE) start? Implications on the prediction of a new variant of Creutzfeldt-Jakob disease (nvCJD) epidemic

2 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Bovine spongiform encephalopathy (BSE) and its epidemiology

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Identification of possible animal origins of prion disease in human beings.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Biomedicine. A fresh look at BSE

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Rendering practices and inactivation of transmissible spongiform encephalopathy agents

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Molecular analysis of ovine prion protein identifies similarities between BSE and an experimental isolate of natural scrapie, CH1641.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Intracerebral transmission of scrapie to cattle.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Mad cows and monkey business: the end of vCJD?

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Preventing accidental transmission of human transmissible spongifom encephalopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Survival of scrapie virus after 3 years' interment

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Sporadic and familial CJD: classification and characterisation.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

Human prion diseases: epidemiology and integrated risk assessment.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2967218-2

7 January 2021

10.1016/S0140-6736(05)67218-2

Identifiers

DOI

1 reference

2 August 2017

1 reference

PubMed ID

16139661