Behavioral testing of mouse models of Huntington's disease (HD) is a key component of preclinical assessment for potential pharmacological intervention. An open field with a force plate floor was used to quantify numerous spontaneous behaviors in a slowly progressing model of HD. CAG140 (+/+, +/−, −/−) male and female mice were compared in a longitudinal study from 6 to 65 weeks of age. Distance traveled, wall rears, wall rear duration, number of low mobility bouts, in-place movements, number of high velocity runs, and gait parameters (stride rate, stride length, and velocity) were extracted from the ground reaction forces recorded in 20-min actometer sessions. Beginning at 11 weeks, HD mice (both +/− and +/+) were consistently hypoactive t...
Motor dysfunction is a major component of the Huntington's disease (HD) phenotype, both in patients ...
Huntington\u27s disease (HD) is a neurodegenerative disease classically characterized as a movement ...
Huntington's disease is caused by a single mutation on the HTT gene which produces an expansion in t...
Behavioral testing of mouse models of Huntington's disease (HD) is a key component of preclinical as...
The R6/2 mouse is a popular model of Huntington’s disease (HD) because of its rapid progression and ...
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) presents clinically with a triad of motor, cognitive, and psychiatric symp...
BACKGROUND: Motor dysfunction is a major component of the Huntington's disease (HD) phenotype, both ...
Rationale: Huntington's disease (HD) is characterized by progressive motor dysfunction, emotional di...
Huntington's disease is caused by a single mutation resulting in an expanded polyglutamine sequence ...
Deficits in motor function are debilitating features in disorders affecting neurological, neuromuscu...
To determine the suitability of mouse models of disease for therapeutic trials, the models must be c...
Huntington's disease (HD) is characterised by motor symptoms which are often preceded by cognitive a...
In people with Huntington's disease, an expanded CAG repeat sequence on the HTT gene confers a toxic...
Motor dysfunction is a major component of the Huntington's disease (HD) phenotype, both in patients ...
Huntington\u27s disease (HD) is a neurodegenerative disease classically characterized as a movement ...
Huntington's disease is caused by a single mutation on the HTT gene which produces an expansion in t...
Behavioral testing of mouse models of Huntington's disease (HD) is a key component of preclinical as...
The R6/2 mouse is a popular model of Huntington’s disease (HD) because of its rapid progression and ...
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) presents clinically with a triad of motor, cognitive, and psychiatric symp...
BACKGROUND: Motor dysfunction is a major component of the Huntington's disease (HD) phenotype, both ...
Rationale: Huntington's disease (HD) is characterized by progressive motor dysfunction, emotional di...
Huntington's disease is caused by a single mutation resulting in an expanded polyglutamine sequence ...
Deficits in motor function are debilitating features in disorders affecting neurological, neuromuscu...
To determine the suitability of mouse models of disease for therapeutic trials, the models must be c...
Huntington's disease (HD) is characterised by motor symptoms which are often preceded by cognitive a...
In people with Huntington's disease, an expanded CAG repeat sequence on the HTT gene confers a toxic...
Motor dysfunction is a major component of the Huntington's disease (HD) phenotype, both in patients ...
Huntington\u27s disease (HD) is a neurodegenerative disease classically characterized as a movement ...
Huntington's disease is caused by a single mutation on the HTT gene which produces an expansion in t...