A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathies (Q48480572)

11 February 2018

title

A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathies (English)

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19 September 2022

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1

F. Tagliavini

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19 September 2022

4

M. Salmona

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19 September 2022

author name string

F. Prelli

2

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19 September 2022

M. Porro

3

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19 September 2022

O. Bugiani

5

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19 September 2022

B. Frangione

6

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19 September 2022

language of work or name

English

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publication date

1 May 1992

1 reference

11 February 2018

15 May 1992

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1375461

Biochemical and Biophysical Research Communications

19 September 2022

published in

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11 February 2018

volume

184

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11 February 2018

issue

3

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11 February 2018

page(s)

1398-1404

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11 February 2018

A cellular gene encodes scrapie PrP 27-30 protein

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Scrapie prion protein contains a phosphatidylinositol glycolipid

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Differential release of cellular and scrapie prion proteins from cellular membranes by phosphatidylinositol-specific phospholipase C.

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Differences in the Membrane Interaction of Scrapie Amyloid Precursor Proteins in Normal and Scrapie- or Creutzfeldt-Jakob Disease-Infected Brains

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7 January 2021

Identifiers

DOI

1 reference

11 February 2018

1 reference

11 February 2018