(Q39409269)

11 September 2017

title

Prion protein with an E200K mutation displays properties similar to those of the cellular isoform PrP(C). (English)

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11 September 2017

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Rosenmann H

1

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11 September 2017

Talmor G

2

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11 September 2017

Halimi M

3

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11 September 2017

Yanai A

4

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11 September 2017

Gabizon R

5

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11 September 2017

Meiner Z

6

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11 September 2017

language of work or name

English

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publication date

1 March 2001

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Journal of Neurochemistry

11 September 2017

published in

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11 September 2017

volume

76

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11 September 2017

issue

6

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11 September 2017

page(s)

1654-1662

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Sorting of GPI-anchored proteins to glycolipid-enriched membrane subdomains during transport to the apical cell surface

11 September 2017

cites work

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Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

21 January 2018

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Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease

21 January 2018

1 reference

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Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease

21 January 2018

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Genetic analysis of Creutzfeldt-Jakob disease and related disorders

21 January 2018

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Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease

21 January 2018

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An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.2001.00195.X

Mutant and infectious prion proteins display common biochemical properties in cultured cells.

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1471-4159.2001.00195.X

Presence of prion protein in peripheral tissues of Libyan Jews with Creutzfeldt-Jakob disease

21 January 2018

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Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews

21 January 2018

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Separation and properties of cellular and scrapie prion proteins

21 January 2018

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Characterization of detergent-insoluble complexes containing the cellular prion protein and its scrapie isoform.

21 January 2018

1 reference

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

21 January 2018

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Molecular biology of prion diseases

21 January 2018

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21 January 2018

Inherited prion diseases

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21 January 2018

Prion Protein Biology

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Chimeric prion protein expression in cultured cells and transgenic mice

21 January 2018

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

21 January 2018

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Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform

21 January 2018

1 reference

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Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.2001.00195.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.2001.00195.X

Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.2001.00195.X

10.1046/J.1471-4159.2001.00195.X

21 January 2018

Identifiers

DOI

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11 September 2017

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