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Cited by 325

The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.

The Mechanistic Links Between Proteasome Activity, Aging and Agerelated Diseases

Open access
Saez, Isabel, Vilchez, David·2014·Current Genomics

Abstract

Damaged and misfolded proteins accumulate during the aging process, impairing cell function and tissue homeostasis. These perturbations to protein homeostasis (proteostasis) are hallmarks of age-related neurodegenerative disorders such as Alzheimer's, Parkinson's or Huntington's disease. Damaged proteins are degraded by cellular clearance mechanisms such as the proteasome, a key component of the proteostasis network. Proteasome activity declines during aging, and proteasomal dysfunction is associated with late-onset disorders. Modulation of proteasome activity extends lifespan and protects organisms from symptoms associated with proteostasis disorders. Here we review the links between proteasome activity, aging and neurodegeneration. Additionally, strategies to modulate proteasome activity and delay the onset of diseases associated to proteasomal dysfunction are discussed herein.

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Metadata

Authors
Saez, I., & Vilchez, D.
Venue
Current Genomics
Published
2014-03-31
Volume
15
Issue
1
Pages
38-51
ISSN
1389-2029 (ISSN-L)
OpenAlex
W2062834833
Cited by
325
References
43
FWCI
6.33
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: The Mechanistic Links Between Proteasome Activity, Aging and Agerelated Diseases. https://app.cochat.ai/papers/10.2174/138920291501140306113344
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Saez, I., & Vilchez, D. (2014). The Mechanistic Links Between Proteasome Activity, Aging and Agerelated Diseases. Current Genomics. https://doi.org/10.2174/138920291501140306113344

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

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.