(Q44607260)

4 December 2017

Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and type (English)

1 reference

4 December 2017

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6

1 reference

4 December 2017

Boon-Seng Wong

5

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Pierluigi Gambetti

7

object named as

Pierluigi Gambetti

1 reference

4 December 2017

Tao Pan

1

1 reference

4 December 2017

Ruliang Li

2

1 reference

4 December 2017

Shin-Chung Kang

3

1 reference

4 December 2017

Manuela Pastore

4

1 reference

4 December 2017

Man-Sun Sy

8

1 reference

4 December 2017

language of work or name

English

0 references

publication date

1 January 2005

1 reference

Journal of Neurochemistry

4 December 2017

1 reference

4 December 2017

92

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4 December 2017

1

1 reference

4 December 2017

132-142

1 reference

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

4 December 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

Truncated forms of the human prion protein in normal brain and in prion diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

Familial and sporadic fatal insomnia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

Novel differences between two human prion strains revealed by two-dimensional gel electrophoresis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

Heterogeneity of normal prion protein in two- dimensional immunoblot: presence of various glycosylated and truncated forms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

A subtype of sporadic prion disease mimicking fatal familial insomnia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

Prion protein expression in different species: analysis with a panel of new mAbs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

The same prion strain causes vCJD and BSE

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2004.02859.X

10.1111/J.1471-4159.2004.02859.X

21 January 2018

Identifiers

DOI

1 reference

4 December 2017

1 reference