(Q30871448)

27 June 2017

Overexpressed protein disulfide isomerase in brains of patients with sporadic Creutzfeldt-Jakob disease (English)

1 reference

sporadic Creutzfeldt-Jakob disease

27 June 2017

1 reference

1 reference

Gert Lubec

6

1 reference

ORCID Public Data File 2021

author name string

Byong Chul Yoo

1

1 reference

27 June 2017

Kurt Krapfenbauer

2

1 reference

27 June 2017

Nigel Cairns

3

1 reference

27 June 2017

Girma Belay

4

1 reference

27 June 2017

Michal Bajo

5

1 reference

27 June 2017

language of work or name

English

0 references

publication date

1 December 2002

1 reference

27 June 2017

1 reference

27 June 2017

334

1 reference

27 June 2017

3

1 reference

27 June 2017

196-200

1 reference

The spatial patterns of prion protein deposits in Creutzfeldt-Jakob disease: comparison with beta-amyloid deposits in Alzheimer's disease.

27 June 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases).

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Prion protein glycosylation is sensitive to redox change

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Binding of disease-associated prion protein to plasminogen.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Identification of proteins by matrix-assisted laser desorption ionization-mass spectrometry following in-gel digestion in low-salt, nonvolatile buffer and simplified peptide recovery

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Protein disulfide-isomerase

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Effect of protein application mode and acrylamide concentration on the resolution of protein spots separated by two-dimensional gel electrophoresis.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

High-level expression and characterization of a purified 142-residue polypeptide of the prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

1 reference

7 January 2021

Thioredoxin converts the Syrian hamster (29-231) recombinant prion protein to an insoluble form

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Drebrin, a dendritic spine protein, is manifold decreased in brains of patients with Alzheimer's disease and Down syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

A role for intermolecular disulfide bonds in prion diseases?

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Neurobiology: p25 protein in neurodegeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Physical studies of conformational plasticity in a recombinant prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

10.1016/S0304-3940(02)01071-6

Identifiers

DOI

1 reference

27 June 2017

1 reference