Dallérac, GM;
Levasseur, G;
Vatsavayai, SC;
Milnerwood, AJ;
Cummings, DM;
Kraev, I;
Huetz, C;
... Murphy, KP; + view all
(2015)
Dysfunctional Dopaminergic Neurones in Mouse Models of Huntington's Disease: A Role for SK3 Channels.
Neurodegenerative Diseases
, 15
(2)
93 - 108.
10.1159/000375126.
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Abstract
Huntington's disease (HD) is a late-onset fatal neurodegenerative disorder caused by a CAG trinucleotide repeat expansion in the gene coding for the protein huntingtin and is characterised by progressive motor, psychiatric and cognitive decline. We previously demonstrated that normal synaptic function in HD could be restored by application of dopamine receptor agonists, suggesting that changes in the release or bioavailability of dopamine may be a contributing factor to the disease process.
Type: | Article |
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Title: | Dysfunctional Dopaminergic Neurones in Mouse Models of Huntington's Disease: A Role for SK3 Channels |
Location: | Switzerland |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1159/000375126 |
Publisher version: | http://dx.doi.org/10.1159/000375126 |
Language: | English |
Additional information: | © 2015 S. Karger AG, Basel |
UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences > Neuro, Physiology and Pharmacology |
URI: | https://discovery.ucl.ac.uk/id/eprint/1466863 |
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