Proteasome Activity and Biological Properties of Normal Prion Protein: A Comparison between Young and Aged Cattle (Q48099715)

8 February 2018

https://api.crossref.org/works/10.1292/JVMS.10-0149

title

Proteasome Activity and Biological Properties of Normal Prion Protein: A Comparison between Young and Aged Cattle (English)

1 reference

17 June 2024

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20686352

17 June 2024

author name string

Yumi Yoshioka

1

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8 February 2018

Naotaka Ishiguro

2

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8 February 2018

Yasuo Inoshima

3

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8 February 2018

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20686352

17 June 2024

publication date

2 August 2010

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8 February 2018

Journal of Veterinary Medical Science

published in

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8 February 2018

volume

72

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8 February 2018

issue

12

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8 February 2018

page(s)

1583-1587

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8 February 2018

Distinct molecular phenotypes in bovine prion diseases

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

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Degradation of oxidized proteins by the 20S proteasome.

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Ageing and the brain

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Selective degradation of oxidized calmodulin by the 20 S proteasome

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Altered prion protein glycosylation in the aging mouse brain

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Decreased levels of proteasome activity and proteasome expression in aging spinal cord

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Antigenic characterization of an abnormal isoform of prion protein using a new diverse panel of monoclonal antibodies

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Wild-type PrP and a mutant associated with prion disease are subject to retrograde transport and proteasome degradation

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Role of cellular prion protein on LTP expression in aged mice.

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Biological and biochemical characterization of L-type-like bovine spongiform encephalopathy (BSE) detected in Japanese black beef cattle.

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Novel proteinaceous infectious particles cause scrapie

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Developmental expression of the cellular prion protein in elongating axons.

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Parkinson disease: primacy of age as a risk factor for mitochondrial dysfunction

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Ageing and exposure to oxidative stress in vivo differentially affect cellular levels of PrP in mouse cerebral microvessels and brain parenchyma

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Proteasomes and ubiquitin are involved in the turnover of the wild-type prion protein

17 June 2024

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Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains.

17 June 2024

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Identifiers

DOI

10.1292/JVMS.10-0149

1 reference

8 February 2018

1 reference

8 February 2018