(Q41237869)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8576163%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

title

Mutant and infectious prion proteins display common biochemical properties in cultured cells (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8576163%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8576163%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

S Lehmann

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8576163%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

language of work or name

English

0 references

publication date

1 January 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8576163%20AND%20SRC:MED&resulttype=core&format=json

Journal of Biological Chemistry

14 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8576163%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

volume

271

1 reference

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14 October 2019

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8576163%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

page(s)

1633-1637

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8576163%20AND%20SRC:MED&resulttype=core&format=json

Prion diseases and neurodegeneration

14 October 2019

cites work

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A cellular gene encodes scrapie PrP 27-30 protein

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Scrapie strain infection in vitro induces changes in neuronal cells

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Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

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

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A Mutant Prion Protein Displays an Aberrant Membrane Association When Expressed in Cultured Cells

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Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies

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Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

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

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Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families

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Distinct prion proteins in short and long scrapie incubation period mice

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A chemical modification that makes glycoinositol phospholipids resistant to phospholipase C cleavage: fatty acid acylation of inositol

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

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism

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Identification of a gene which controls the incubation period of some strains of scrapie agent in mice

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Evidence that the Transmission of One Source of Scrapie Agent to Hamsters Involves Separation of Agent Strains from a Mixture

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THE INTRACELLULAR LOCATION OF THE AGENT OF MOUSE SCRAPIE.

21 January 2018

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Nature of the Scrapie Agent

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Partial purification and evidence for multiple molecular forms of the scrapie agent

21 January 2018

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Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells

21 January 2018

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Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients

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