KO mice. Neuroimaging studies of DYT11 M-D patients show reduced dopamine D2 receptor (D2R) availability, although the possibility of increased endogenous dopamine, and consequently, competitive D2R occupancy cannot be ruled out. KO mice also exhibited a significant increase of dopamine release after amphetamine injection in comparison to wild-type (WT) littermates. KO mice. The results suggest that reduction of striatal D2R and enhanced striatal dopamine release may contribute to the pathophysiology of DYT11 M-D patients
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
Dystonia is a movement disorder of both genetic and non-genetic causes, which typically results in t...
Striatal cholinergic dysfunction is a common phenotype associated with various forms of dystonia in ...
KO mice. Neuroimaging studies of DYT11 M-D patients show reduced dopamine D2 receptor (D2R) availab...
Purpose To study striatal dopamine D-2 receptor availability in DYT11 mutation carriers of the autos...
DYT1 dystonia is an inherited disease linked to mutation in the TOR1A gene encoding for the protein ...
Dystonia pathophysiology has been partly linked to downregulation and dysfunction of dopamine D2 rec...
Striatal dysfunction is implicated in many movement disorders. However, the precise nature of defect...
In early-onset generalized torsion dystonia, caused by a GAG deletion in TOR1A (DYT1), enhanced stri...
Dopamine D2 receptors (D2Rs) are of crucial importance in the striatal processing of motor informati...
International audienceDopamine D2 receptor signaling is central for striatal function and movement, ...
Of the five known dopamine receptors, D-1A and D-2 represent the major subtypes expressed in the str...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
Dystonia is a movement disorder of both genetic and non-genetic causes, which typically results in t...
Striatal cholinergic dysfunction is a common phenotype associated with various forms of dystonia in ...
KO mice. Neuroimaging studies of DYT11 M-D patients show reduced dopamine D2 receptor (D2R) availab...
Purpose To study striatal dopamine D-2 receptor availability in DYT11 mutation carriers of the autos...
DYT1 dystonia is an inherited disease linked to mutation in the TOR1A gene encoding for the protein ...
Dystonia pathophysiology has been partly linked to downregulation and dysfunction of dopamine D2 rec...
Striatal dysfunction is implicated in many movement disorders. However, the precise nature of defect...
In early-onset generalized torsion dystonia, caused by a GAG deletion in TOR1A (DYT1), enhanced stri...
Dopamine D2 receptors (D2Rs) are of crucial importance in the striatal processing of motor informati...
International audienceDopamine D2 receptor signaling is central for striatal function and movement, ...
Of the five known dopamine receptors, D-1A and D-2 represent the major subtypes expressed in the str...
DYT1 dystonia, a severe form of genetically determined human dystonia, exhibits reduced penetrance a...
Dystonia is a movement disorder of both genetic and non-genetic causes, which typically results in t...
Striatal cholinergic dysfunction is a common phenotype associated with various forms of dystonia in ...