Striatal cholinergic dysfunction is a common phenotype associated with various forms of dystonia in which anti-cholinergic drugs have some therapeutic benefits. However, the underlying substrate of striatal cholinergic defects in dystonia remain poorly understood. In this study, we used a recently developed knock-in mouse model of dopamine responsive dystonia (DRD) with strong symptomatic responses to anti-cholinergic drugs, to assess changes in the prevalence and morphology of striatal cholinergic interneurons (ChIs) in a model of generalized dystonia. Unbiased stereological neuronal counts and Sholl analysis were used to address these issues. To determine the potential effect of aging on the number of ChIs, both young (3 months old) and a...
Twenty years ago, striatal cholinergic neurons were central figures in models of basal ganglia funct...
DYT1 dystonia, a common and severe primary dystonia, is caused by a 3-bp deletion in TOR1A which enc...
Striatal dysfunction is implicated in many movement disorders. However, the precise nature of defect...
Striatal cholinergic dysfunction is a common phenotype associated with various forms of dystonia in ...
Dystonia is a movement disorder of both genetic and non-genetic causes, which typically results in t...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
In early-onset generalized torsion dystonia, caused by a GAG deletion in TOR1A (DYT1), enhanced stri...
DYT1 dystonia is a severe form of inherited dystonia, characterized by involuntary twisting movement...
DYT1 dystonia is a severe form of inherited dystonia, characterized by involuntary twisting movement...
DYT1 dystonia is a severe form of inherited dystonia, characterized by involuntary twisting movement...
Interneurons comprise a minority of the striatal neuronal population of roughly 5%. However, this he...
Background: Acetylcholine-mediated transmission plays a central role in the impairment of corticostr...
Twenty years ago, striatal cholinergic neurons were central figures in models of basal ganglia funct...
DYT1 dystonia, a common and severe primary dystonia, is caused by a 3-bp deletion in TOR1A which enc...
Striatal dysfunction is implicated in many movement disorders. However, the precise nature of defect...
Striatal cholinergic dysfunction is a common phenotype associated with various forms of dystonia in ...
Dystonia is a movement disorder of both genetic and non-genetic causes, which typically results in t...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
In early-onset generalized torsion dystonia, caused by a GAG deletion in TOR1A (DYT1), enhanced stri...
DYT1 dystonia is a severe form of inherited dystonia, characterized by involuntary twisting movement...
DYT1 dystonia is a severe form of inherited dystonia, characterized by involuntary twisting movement...
DYT1 dystonia is a severe form of inherited dystonia, characterized by involuntary twisting movement...
Interneurons comprise a minority of the striatal neuronal population of roughly 5%. However, this he...
Background: Acetylcholine-mediated transmission plays a central role in the impairment of corticostr...
Twenty years ago, striatal cholinergic neurons were central figures in models of basal ganglia funct...
DYT1 dystonia, a common and severe primary dystonia, is caused by a 3-bp deletion in TOR1A which enc...
Striatal dysfunction is implicated in many movement disorders. However, the precise nature of defect...