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DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance among carriers and begins usually during adolescence. The reasons for such age dependence and variability remain unclear.

Developmental profile of the aberrant dopamine D2 receptor response in striatal cholinergic interneurons in DYT1 dystonia

PISANI, ANTONIO
2011-01-01

Abstract

DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance among carriers and begins usually during adolescence. The reasons for such age dependence and variability remain unclear.
2011
PLOS ONE
sì
WOS:000294686100029
2-s2.0-80052406561
Esperti anonimi
Inglese
Internazionale
STAMPA
6
9
e24261
e24261
12
21912682
Animals; Receptor; Adenosine A2A; Calcium; GTP-Binding Protein alpha Subunits; Gi-Go; Humans; Dystonia; Mice; Interneurons; Receptors; Dopamine D2; Neostriatum; Electrophysiological Processes; Acetylcholine; Molecular Chaperones; Mutation; Signal Transduction
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0024261
no
11
info:eu-repo/semantics/article
262
Sciamanna, Giuseppe; Tassone, A; Martella, Giuseppina; Mandolesi, G; Puglisi, F; Cuomo, D; Madeo, Graziella; Ponterio, G; Standaert, D; Bonsi, P; Pisa...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1353575
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