NIA workshop on senescence in brain aging and Alzheimer's disease and its related dementias
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There is no universally accepted definition or biomarkers of cellular senescence.
“One of the major challenges to our trial and related studies as this field moves forward is the lack of a universally accepted definition and biomarkers of cellular senescence (57).”
From Senolytic Therapy to Modulate the Progression of Alzheimer's Disease (SToMP-AD): A Pilot Clinical Trial (2022) · cites this paper as [57]
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Novel cell markers with altered expression in brain aging and Alzheimer's disease: A review
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- Authors
- DiBattista, A. M., Sierra, F., & Masliah, E.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- DiBattista, Amanda M.
- Venue
- GeroScience
- Published
- 2020-01-13
- Volume
- 42
- Issue
- 2
- Pages
- 389-396
- ISSN
- 2152-4041 (ISSN-L)
- 2509-2715
- 2509-2723
- PMC
- PMC7206469
- OpenAlex
- W2999033920
- Cited by
- 16
- References
- 7
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 4 · 2023: 1 · 2022: 2 · 2021: 5 · 2020: 1
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- GeroScience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- cellular senescence, brain aging, Alzheimer's disease, Alzheimer's disease and related dementias, senescence-associated secretory phenotype, neurodegeneration, inflammation, cell cycle arrest, apoptosis resistance
- MeSH terms
- Aging, Alzheimer Disease, Brain, Humans
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