% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Hilton:272334,
author = {Hilton, Brett J and Griffin, Jarred and Fawcett, James W
and Bradke, Frank},
title = {{N}euronal maturation and axon regeneration: unfixing
circuitry to enable repair.},
journal = {Nature reviews / Neuroscience},
volume = {25},
number = {10},
issn = {1471-0048},
address = {London},
publisher = {Nature Publ. Group},
reportid = {DZNE-2024-01153},
pages = {649 - 667},
year = {2024},
abstract = {Mammalian neurons lose the ability to regenerate their
central nervous system axons as they mature during embryonic
or early postnatal development. Neuronal maturation requires
a transformation from a situation in which neuronal
components grow and assemble to one in which these
components are fixed and involved in the machinery for
effective information transmission and computation. To
regenerate after injury, neurons need to overcome this fixed
state to reactivate their growth programme. A variety of
intracellular processes involved in initiating or sustaining
neuronal maturation, including the regulation of gene
expression, cytoskeletal restructuring and shifts in
intracellular trafficking, have been shown to prevent axon
regeneration. Understanding these processes will contribute
to the identification of targets to promote repair after
injury or disease.},
subtyp = {Review Article},
keywords = {Animals / Nerve Regeneration: physiology / Axons:
physiology / Humans / Neurogenesis: physiology / Neurons:
physiology},
cin = {AG Bradke},
ddc = {570},
cid = {I:(DE-2719)1013002},
pnm = {351 - Brain Function (POF4-351)},
pid = {G:(DE-HGF)POF4-351},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:39164450},
doi = {10.1038/s41583-024-00849-3},
url = {https://pub.dzne.de/record/272334},
}