(Q40854367)

English

Expression of unglycosylated mutated prion protein facilitates PrP(Sc) formation in neuroblastoma cells infected with different prion strains

scientific article published on October 2000

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Expression of unglycosylated mutated prion protein facilitates PrP(Sc) formation in neuroblastoma cells infected with different prion strains (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

prion protein family

0 references

1 reference

based on heuristic

inferred from title

Stanley B. Prusiner

3

object named as

Prusiner SB

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

author name string

Korth C

1

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Kaneko K

2

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

language of work or name

0 references

publication date

1 October 2000

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Journal of General Virology

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

81

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Pt 10

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

2555-2563

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Glycosylation differences between the normal and pathogenic prion protein isoforms

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Cultured cell sublines highly susceptible to prion infection

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Molecular cloning and complete sequence of prion protein cDNA from mouse brain infected with the scrapie agent

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Scrapie-Infected Spleens: Analysis of Infectivity, Scrapie-Associated Fibrils, and Protease-Resistant Proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Protease-resistant PrP deposition in brain and non-central nervous system tissues of a murine model of bovine spongiform encephalopathy

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Dominant-negative inhibition of prion formation diminished by deletion mutagenesis of the prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Biological evidence that scrapie agent has an independent genome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Chimeric prion protein expression in cultured cells and transgenic mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

A comparison of some biological characteristics of the mouse-passaged scrapie agents, 22A and ME7

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Typing prion isoforms.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Characterization of scrapie infection in mouse neuroblastoma cells

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Encephalopathy in mice produced by inoculation with scrapie brain material.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Prion protein conformation in a patient with sporadic fatal insomnia

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Diversity of oligosaccharide structures linked to asparagines of the scrapie prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

A subtype of sporadic prion disease mimicking fatal familial insomnia.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Selective neuronal targeting in prion disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Scrapie produced experimentally in goats with special reference to the clinical syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Intracellular accumulation of the cellular prion protein after mutagenesis of its Asn-linked glycosylation sites

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Host and transmissible spongiform encephalopathy agent strain control glycosylation of PrP.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Precise targeting of the pathology of the sialoglycoprotein, PrP, and vacuolar degeneration in mouse scrapie

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Blockade of glycosylation promotes acquisition of scrapie-like properties by the prion protein in cultured cells

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Nucleic acids in prion preparations: unspecific background or essential component?

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Eight prion strains have PrP(Sc) molecules with different conformations

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

Propagation of prion strains through specific conformers of the prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1099/0022-1317-81-10-2555

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10.1099/0022-1317-81-10-2555

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

ResearchGate publication ID

0 references

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