Expression of unglycosylated mutated prion protein facilitates PrP(Sc) formation in neuroblastoma cells infected with different prion strains (Q40854367)

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scientific article published on October 2000

Language	Label	Description	Also known as
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

Statements

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

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Cultured cell sublines highly susceptible to prion infection

1 reference

11 October 2022

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

1 reference

11 October 2022

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

1 reference

11 October 2022

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

1 reference

11 October 2022

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

1 reference

11 October 2022

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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

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

1 reference

11 October 2022

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Biological evidence that scrapie agent has an independent genome

1 reference

11 October 2022

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

1 reference

11 October 2022

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Chimeric prion protein expression in cultured cells and transgenic mice

1 reference

11 October 2022

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

1 reference

11 October 2022

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

1 reference

11 October 2022

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Typing prion isoforms.

1 reference

11 October 2022

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Characterization of scrapie infection in mouse neuroblastoma cells

1 reference

11 October 2022

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

1 reference

11 October 2022

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

1 reference

11 October 2022

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Encephalopathy in mice produced by inoculation with scrapie brain material

1 reference

11 October 2022

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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

Identifiers

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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