% 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{Blaess:266094,
author = {Blaess, Sandra and Krabbe, Sabine},
title = {{C}ell type specificity for circuit output in the midbrain
dopaminergic system},
journal = {Current opinion in neurobiology},
volume = {83},
issn = {0959-4388},
address = {Philadelphia, Pa.},
publisher = {Current Biology},
reportid = {DZNE-2023-01095},
pages = {102811},
year = {2023},
abstract = {Midbrain dopaminergic neurons are a relatively small group
of neurons in the mammalian brain controlling a wide range
of behaviors. In recent years, increasingly sophisticated
tracing, imaging, transcriptomic, and machine learning
approaches have provided substantial insights into the
anatomical, molecular, and functional heterogeneity of
dopaminergic neurons. Despite this wealth of new knowledge,
it remains unclear whether and how the diverse features
defining dopaminergic subclasses converge to delineate
functional ensembles within the dopaminergic system. Here,
we review recent studies investigating various aspects of
dopaminergic heterogeneity and discuss how development,
behavior, and disease influence subtype characteristics. We
then outline what further approaches could be pursued to
gain a more inclusive picture of dopaminergic diversity,
which could be crucial to understanding the functional
architecture of this system.},
subtyp = {Review Article},
keywords = {Animals / Mesencephalon: metabolism / Brain / Dopaminergic
Neurons: physiology / Mammals},
cin = {AG Krabbe},
ddc = {610},
cid = {I:(DE-2719)5000059},
pnm = {351 - Brain Function (POF4-351)},
pid = {G:(DE-HGF)POF4-351},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:37972537},
doi = {10.1016/j.conb.2023.102811},
url = {https://pub.dzne.de/record/266094},
}