(Q28590199)

31 January 2017

title

Cellular phenotyping of secretory and nuclear prion proteins associated with inherited prion diseases (English)

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31 January 2017

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GOA release 2020-03-11

author name string

Holger Lorenz

series ordinal

1

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31 January 2017

Otto Windl

series ordinal

2

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31 January 2017

Hans A. Kretzschmar

series ordinal

3

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31 January 2017

language of work or name

English

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publication date

8 March 2002

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Journal of Biological Chemistry

31 January 2017

published in

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31 January 2017

volume

277

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31 January 2017

issue

10

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31 January 2017

page(s)

8508–8516

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https://api.crossref.org/works/10.1074%2FJBC.M110197200

31 January 2017

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Copper binding to the N-terminal tandem repeat regions of mammalian and avian prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

The cellular prion protein binds copper in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Primary structure of the Aequorea victoria green-fluorescent protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Green fluorescent protein as a marker for gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Construction and characterization of murine neuroblastoma cell clones allowing inducible and high expression of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Structure and polymorphism of the mouse prion protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Rapid redistribution of Golgi proteins into the ER in cells treated with brefeldin A: evidence for membrane cycling from Golgi to ER

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Synthesis and trafficking of prion proteins in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Photobleaching GFP reveals protein dynamics inside live cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Molecular genetics of human prion diseases in Germany.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Prion proteins carrying pathogenic mutations are resistant to phospholipase cleavage of their glycolipid anchors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Search for a nuclear localization signal in the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Molecular cloning of a candidate chicken prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

NMR structure of the mouse prion protein domain PrP(121-231)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

ER quality control: the cytoplasmic connection

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

Cytosolic degradation of T-cell receptor alpha chains by the proteasome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

The prion protein has RNA binding and chaperoning properties characteristic of nucleocapsid protein NCP7 of HIV-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

The Metabolism and Imaging in Live Cells of the Bovine Prion Protein in Its Native Form or Carrying Single Amino Acid Substitutions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110197200

21 January 2018

Identifiers

DOI

10.1074/JBC.M110197200

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31 January 2017

1 reference