(Q47596163)

4 February 2018

title

Spongiform encephalopathies. Breech-birth prions (English)

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4 February 2018

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Hope J

1

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4 February 2018

language of work or name

English

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publication date

1 December 1999

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4 February 2018

published in

Nature

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4 February 2018

volume

402

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4 February 2018

issue

6763

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4 February 2018

page(s)

737, 739

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4 February 2018

https://scigraph.springernature.com/pub.10.1038/45413

exact match

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cites work

A transmembrane form of the prion protein in neurodegenerative disease

1 reference

Transmissible and genetic prion diseases share a common pathway of neurodegeneration

21 January 2018

1 reference

Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein

21 January 2018

1 reference

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

21 January 2018

1 reference

A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy

21 January 2018

1 reference

Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions.

21 January 2018

1 reference

Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel

21 January 2018

1 reference

The cellular prion protein binds copper in vivo

21 January 2018

1 reference

The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells

21 January 2018

1 reference

Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein

21 January 2018

1 reference

B lymphocytes and neuroinvasion

21 January 2018

1 reference

The cellular prion protein binds copper in vivo

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/45413

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4 February 2018

Dimensions Publication ID

1025191755

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1 reference

4 February 2018