Dysfunctional Dopaminergic Neurones in Mouse Models of Huntington's Disease: A Role for SK3 Channels

Glenn M. Dallérac,Grégoire Levasseur,Sarat C. Vatsavayai,Austen J. Milnerwood,Damian M. Cummings,Igor Kraev,Chloé Huetz,Karen A. Evans,Steve W. Walters,Payam Rezaie,Yoon Cho,Mark C. Hirst,Kerry P.S.J. Murphy

Dysfunctional Dopaminergic Neurones in Mouse Models of Huntington's Disease: A Role for SK3 Channels

2015

Glenn M. Dallérac
Grégoire Levasseur
Sarat C. Vatsavayai
Austen J. Milnerwood
Damian M. Cummings
Igor Kraev
Chloé Huetz
Karen A. Evans
Steve W. Walters
Payam Rezaie
Yoon Cho
Mark C. Hirst
Kerry P.S.J. Murphy

Background: Huntington's disease (HD) is a late-onset fatal neurodegenerative disorder caused by a CAG trinucleotide repeat expansion in the gene coding for the p

Keywords:

Huntington's disease
Neurodegeneration
Huntingtin
Pathology
Dopamine
Neuroscience
Trinucleotide repeat expansion
Cancer research
SK3
Substantia nigra
Biology
Dopaminergic
Pars compacta
Huntingtin Protein
Dopamine receptor

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