Huntington's disease (HD) presents clinically with a triad of motor, cognitive, and psychiatric symptoms. Cognitive symptoms often occur early within the disease progression, prior to the onset of motor symptoms, and they are significantly burdensome to people who are affected by HD. In order to determine the suitability of mouse models of HD in recapitulating the human condition, these models must be behaviorally tested and characterized. Operant behavioral testing offers an automated and objective method of behaviorally profiling motor, cognitive, and psychiatric dysfunction in HD mice. Furthermore, operant testing can also be employed to determine any behavioral changes observed after any associated interventions or experimental therapeu...
Huntington’s disease (HD) is characterised by motor symptoms which are often preceded by cognitive a...
Behavioral testing of mouse models of Huntington's disease (HD) is a key component of preclinical as...
Huntington’s disease (HD) is a fatal autosomal dominant neurodegenerative disease caused by a polygl...
Huntington’s disease (HD) presents clinically with a triad of motor, cognitive, and psychiatric symp...
Huntington’s disease (HD) presents clinically with a triad of motor, cognitive, and psychiatric sym...
Huntington's disease (HD) is characterised by motor symptoms which are often preceded by cognitive a...
Huntington's disease is the result of an expanded CAG repeat in the gene that codes for the protein ...
Rationale: Huntington's disease (HD) is characterized by progressive motor dysfunction, emotional di...
In this review, we explore the similarities and differences in the behavioural neurobiology found in...
Huntington\u27s disease (HD) is a neurodegenerative disease classically characterized as a movement ...
Huntington s disease (HD) is a devastating neurodegenerative disorder caused by a genetic mutation t...
Huntington Disease (HD) is a neurodegenerative disorder that is caused by a CAG trinucleotide repeat...
In people with Huntington's disease, an expanded CAG repeat sequence on the HTT gene confers a toxic...
Huntington’s disease (HD) is characterised by motor symptoms which are often preceded by cognitive a...
Behavioral testing of mouse models of Huntington's disease (HD) is a key component of preclinical as...
Huntington’s disease (HD) is a fatal autosomal dominant neurodegenerative disease caused by a polygl...
Huntington’s disease (HD) presents clinically with a triad of motor, cognitive, and psychiatric symp...
Huntington’s disease (HD) presents clinically with a triad of motor, cognitive, and psychiatric sym...
Huntington's disease (HD) is characterised by motor symptoms which are often preceded by cognitive a...
Huntington's disease is the result of an expanded CAG repeat in the gene that codes for the protein ...
Rationale: Huntington's disease (HD) is characterized by progressive motor dysfunction, emotional di...
In this review, we explore the similarities and differences in the behavioural neurobiology found in...
Huntington\u27s disease (HD) is a neurodegenerative disease classically characterized as a movement ...
Huntington s disease (HD) is a devastating neurodegenerative disorder caused by a genetic mutation t...
Huntington Disease (HD) is a neurodegenerative disorder that is caused by a CAG trinucleotide repeat...
In people with Huntington's disease, an expanded CAG repeat sequence on the HTT gene confers a toxic...
Huntington’s disease (HD) is characterised by motor symptoms which are often preceded by cognitive a...
Behavioral testing of mouse models of Huntington's disease (HD) is a key component of preclinical as...
Huntington’s disease (HD) is a fatal autosomal dominant neurodegenerative disease caused by a polygl...