(Q36006647)

11 August 2017

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title

Pathogenesis of prion diseases (English)

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11 August 2017

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3

Herbert Budka

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author name string

Ursula Unterberger

series ordinal

1

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11 August 2017

Till Voigtländer

series ordinal

2

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11 August 2017

publication date

12 January 2005

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11 August 2017

published in

Acta Neuropathologica

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11 August 2017

volume

109

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11 August 2017

issue

1

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11 August 2017

page(s)

32-48

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https://scigraph.springernature.com/pub.10.1007/s00401-004-0953-9

11 August 2017

exact match

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cites work

Complement activation after oxidative stress: role of the lectin complement pathway

1 reference

https://api.crossref.org/works/10.1007%2FS00401-004-0953-9

Selective neuronal vulnerability in human prion diseases. Fatal familial insomnia differs from other types of prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-004-0953-9

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

https://api.crossref.org/works/10.1007%2FS00401-004-0953-9

Disease-associated prion protein in vessel walls

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-004-0953-9

Oral prion infection requires normal numbers of Peyer's patches but not of enteric lymphocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-004-0953-9

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/10.1007%2FS00401-004-0953-9

Prion protein-deficient neurons reveal lower glutathione reductase activity and increased susceptibility to hydrogen peroxide toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-004-0953-9

10.1007/S00401-004-0953-9

21 January 2018

Identifiers

DOI

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11 August 2017

1 reference