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Cited by 265

The DOI matches its Crossref record; 146 of the 146 references it cites were found in a registry or an index.

The biological function of the cellular prion protein: an update

Open access
Wulf, Marie-Angela, Senatore, Assunta, Aguzzi, Adriano·2017·BMC Biology

Abstract

The misfolding of the cellular prion protein (PrP C ) causes fatal neurodegenerative diseases. Yet PrP C is highly conserved in mammals, suggesting that it exerts beneficial functions preventing its evolutionary elimination. Ablation of PrP C in mice results in well-defined structural and functional alterations in the peripheral nervous system. Many additional phenotypes were ascribed to the lack of PrP C , but some of these were found to arise from genetic artifacts of the underlying mouse models. Here, we revisit the proposed physiological roles of PrP C in the central and peripheral nervous systems and highlight the need for their critical reassessment using new, rigorously controlled animal models.

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Metadata

Authors
Wulf, M.-A., Senatore, A., & Aguzzi, A.
Venue
BMC Biology
Published
2017-05-02
Volume
15
Issue
1
Pages
34-34
ISSN
1741-7007 (ISSN-L)
OpenAlex
W2611707378
Cited by
265
References
146
FWCI
11.16
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: The biological function of the cellular prion protein: an update. https://app.cochat.ai/papers/10.1186/s12915-017-0375-5
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Wulf, M.-A., Senatore, A., & Aguzzi, A. (2017). The biological function of the cellular prion protein: an update. BMC Biology. https://doi.org/10.1186/s12915-017-0375-5

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.