(Q53921022)

22 May 2018

title

A novel method of generating neuronal cell lines from gene-knockout mice to study prion protein membrane orientation. (English)

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22 May 2018

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Andrea Holme

1

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22 May 2018

Maki Daniels

series ordinal

2

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22 May 2018

Judyth Sassoon

series ordinal

3

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22 May 2018

David R Brown

series ordinal

4

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22 May 2018

language of work or name

English

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publication date

1 August 2003

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22 May 2018

European Journal of Neuroscience

published in

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22 May 2018

volume

18

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22 May 2018

issue

3

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22 May 2018

page(s)

571-579

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22 May 2018

Neurons depend on astrocytes in a coculture system for protection from glutamate toxicity.

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

PrPSc-like prion protein peptide inhibits the function of cellular prion protein

21 January 2018

1 reference

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Antioxidant activity related to copper binding of native prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

The cellular prion protein binds copper in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

Role of microglia and host prion protein in neurotoxicity of a prion protein fragment.

21 January 2018

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Prion protein fragment interacts with PrP-deficient cells.

21 January 2018

1 reference

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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/10.1046%2FJ.1460-9568.2003.02780.X

Lack of prion protein expression results in a neuronal phenotype sensitive to stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

Normal prion protein has an activity like that of superoxide dismutase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

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

21 January 2018

1 reference

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Mutant prion protein-mediated aggregation of normal prion protein in the endoplasmic reticulum: implications for prion propagation and neurotoxicity

21 January 2018

1 reference

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Biogenesis and transmembrane orientation of the cellular isoform of the scrapie prion protein [published errratum appears in Mol Cell Biol 1987 May;7(5):2035]

21 January 2018

1 reference

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A transmembrane form of the prion protein in neurodegenerative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

Transmissible and genetic prion diseases share a common pathway of neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

Mutant prion proteins are partially retained in the endoplasmic reticulum

21 January 2018

1 reference

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Epithelial and endothelial expression of the green fluorescent protein reporter gene under the control of bovine prion protein (PrP) gene regulatory sequences in transgenic mice

21 January 2018

1 reference

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Functionally different GPI proteins are organized in different domains on the neuronal surface

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

21 January 2018

1 reference

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A transmembrane form of the prion protein contains an uncleaved signal peptide and is retained in the endoplasmic Reticulum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

Most pathogenic mutations do not alter the membrane topology of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.

21 January 2018

1 reference

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Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Straussler-Scheinker syndrome

21 January 2018

1 reference

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Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodents

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

Metal imbalance and compromised antioxidant function are early changes in prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

Endocytic Intermediates Involved with the Intracellular Trafficking of a Fluorescent Cellular Prion Protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

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/10.1046%2FJ.1460-9568.2003.02780.X

Functional and structural differences between the prion protein from two alleles prnp(a) and prnp(b) of mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

B lymphocytes and neuroinvasion

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1460-9568.2003.02780.X

10.1046/J.1460-9568.2003.02780.X

21 January 2018

Identifiers

DOI

1 reference

22 May 2018

PubMed ID

12911753

1 reference

22 May 2018