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@ARTICLE{Zocher:271346,
author = {Zocher, Sara},
title = {{T}argeting neuronal epigenomes for brain rejuvenation.},
journal = {The EMBO journal},
volume = {43},
number = {16},
issn = {0261-4189},
address = {Hoboken, NJ [u.a.]},
publisher = {Wiley},
reportid = {DZNE-2024-01047},
pages = {3312 - 3326},
year = {2024},
abstract = {Aging is associated with a progressive decline of brain
function, and the underlying causes and possible
interventions to prevent this cognitive decline have been
the focus of intense investigation. The maintenance of
neuronal function over the lifespan requires proper
epigenetic regulation, and accumulating evidence suggests
that the deterioration of the neuronal epigenetic landscape
contributes to brain dysfunction during aging. Epigenetic
aging of neurons may, however, be malleable. Recent reports
have shown age-related epigenetic changes in neurons to be
reversible and targetable by rejuvenation strategies that
can restore brain function during aging. This review
discusses the current evidence that identifies neuronal
epigenetic aging as a driver of cognitive decline and a
promising target of brain rejuvenation strategies, and it
highlights potential approaches for the specific
manipulation of the aging neuronal epigenome to restore a
youthful epigenetic state in the brain.},
subtyp = {Review Article},
keywords = {Humans / Brain: metabolism / Epigenesis, Genetic / Animals
/ Neurons: metabolism / Aging: genetics / Epigenome /
Rejuvenation: physiology / Cognitive Dysfunction: genetics /
Cognitive Dysfunction: metabolism / Cognitive Decline
(Other) / Epigenetic Rejuvenation (Other) / Epigenome
Editing (Other) / Neuron Aging (Other) / Neuronal Epigenome
(Other)},
cin = {AG Toda ; AG Toda},
ddc = {570},
cid = {I:(DE-2719)1710014},
pnm = {352 - Disease Mechanisms (POF4-352)},
pid = {G:(DE-HGF)POF4-352},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:39009672},
pmc = {pmc:PMC11329789},
doi = {10.1038/s44318-024-00148-8},
url = {https://pub.dzne.de/record/271346},
}