(Q34536351)

2 August 2017

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title

Small is not beautiful: antagonizing functions for the prion protein PrP(C) and its homologue Dpl. (English)

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2 August 2017

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Axel Behrens

1

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Adriano Aguzzi

object named as

Adriano Aguzzi

series ordinal

2

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publication date

1 March 2002

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2 August 2017

published in

Trends in Neurosciences

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2 August 2017

volume

25

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2 August 2017

issue

3

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2 August 2017

page(s)

150-154

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Prions: health scare and biological challenge.

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Novel proteinaceous infectious particles cause scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

The PrP-like protein Doppel gene in sheep and cattle: cDNA sequence and expression

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Genomic organization, comparative analysis, and genetic polymorphisms of the bovine and ovine prion Doppel genes (PRND)

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Expression and structural characterization of the recombinant human doppel protein

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Physiological expression of the gene for PrP-like protein, PrPLP/Dpl, by brain endothelial cells and its ectopic expression in neurons of PrP-deficient mice ataxic due to Purkinje cell degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Antioxidant activity related to copper binding of native prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

B lymphocytes and neuroinvasion

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Strain-specific prion-protein conformation determined by metal ions

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Brain copper content and cuproenzyme activity do not vary with prion protein expression level

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Prion protein is necessary for normal synaptic function

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Altered circadian activity rhythms and sleep in mice devoid of prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Normal neurogenesis and scrapie pathogenesis in neural grafts lacking the prion protein homologue Doppel

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Mice devoid of PrP are resistant to scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Prion Protein Biology

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Prion protein devoid of the octapeptide repeat region restores susceptibility to scrapie in PrP knockout mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Developmental expression of the prion protein gene in glial cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Prion protein expression and superoxide dismutase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Normal cellular prion protein is preferentially expressed on subpopulations of murine hemopoietic cells

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

NEUROBIOLOGY:PrP's Double Causes Trouble

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Prions prevent neuronal cell-line death.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Prion and prejudice: normal protein and the synapse

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

In vivo transfer of GPI-linked complement restriction factors from erythrocytes to the endothelium

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

A transmembrane form of the prion protein in neurodegenerative disease

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

BCL-2 family: regulators of cell death

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2800%2902089-0

7 January 2021

10.1016/S0166-2236(00)02089-0

Identifiers

DOI

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release_aju2266b7fbofbdx7ezb2g4dkm

2 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/aju2266b7fbofbdx7ezb2g4dkm

24 November 2022

mapped directly with Wikidata item

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