(Q48539668)

English

Changes in the glycosylation pattern of prion protein in murine scrapie. Implications for the mechanism of neurodegeneration in prion diseases.

scientific article published on 18 July 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

Changes in the glycosylation pattern of prion protein in murine scrapie. Implications for the mechanism of neurodegeneration in prion diseases. (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

prion protein family

0 references

1 reference

based on heuristic

inferred from title

neurodegeneration

1 reference

based on heuristic

inferred from title

author name string

Milene Russelakis-Carneiro

1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

Gabriela P Saborio

2

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

Laurence Anderes

3

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

Claudio Soto

4

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

language of work or name

0 references

publication date

18 July 2002

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

Journal of Biological Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

277

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

39

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

36872-36877

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

Novel proteinaceous infectious particles cause scrapie

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Nearly ubiquitous tissue distribution of the scrapie agent precursor protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

The acute inflammatory response in CNS following injection of prion brain homogenate or normal brain homogenate.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Neuronal apoptosis in Creutzfeldt-Jakob disease.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Dendritic and synaptic alterations of hippocampal pyramidal neurones in scrapie-infected mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Normal host prion protein necessary for scrapie-induced neurotoxicity.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Neuronal spread of scrapie agent and targeting of lesions within the retino-tectal pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Massive retinotectal projection in rats.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Glycosylation differences between the normal and pathogenic prion protein isoforms

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Prion glycoprotein: structure, dynamics, and roles for the sugars

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

PrPc glycoform heterogeneity as a function of brain region: implications for selective targeting of neurons by prion strains

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Acquisition of protease resistance by prion proteins in scrapie-infected cells does not require asparagine-linked glycosylation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

De novo generation of a PrPSc-like conformation in living cells.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Wild-type PrP and a mutant associated with prion disease are subject to retrograde transport and proteasome degradation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Selective neuronal targeting in prion disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Cellular and subcellular morphological localization of normal prion protein in rodent cerebellum

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M202229200

21 January 2018

Identifiers

10.1074/JBC.M202229200

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/12130636

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