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Journal of Huntington'S Disease|February 27, 2018
Early Neurodegeneration in R6/2 Mice Carrying the Huntington's Disease Mutation with a Super-Expanded CAG Repeat, Despite Normal LifespanCatherine Kielar, A Jennifer MortonExperimental Brain Research|September 30, 2018
Indices of comparative cognition: assessing animal models of human brain functionSebastian D McBride, A Jennifer MortonJournal of Huntington'S Disease|September 4, 2015
Social Behaviour is Impaired in the R6/2 Mouse Model of Huntington’s DiseaseNigel I Wood, A Jennifer MortonBrain Research|May 20, 2009
Management of sleep/wake cycles improves cognitive function in a transgenic mouse model of Huntington's diseasePatrick N Pallier, A Jennifer MortonBrain Research Bulletin|May 24, 2006
Calcineurin inhibitors cause an acceleration of the neurological phenotype in a mouse transgenic for the human Huntington's disease mutationDavid Hernández-Espinosa, A Jennifer MortonJournal of Huntington'S Disease|April 1, 2016
Delayed Onset and Reduced Cognitive Deficits through Pre-Conditioning with 3-Nitropropionic Acid is Dependent on Sex and CAG Repeat Length in the R6/2 Mouse Model of Huntington's DiseaseElizabeth A Skillings, A Jennifer MortonBrain Research Bulletin|August 12, 2003
Chronic lithium chloride treatment has variable effects on motor behaviour and survival of mice transgenic for the Huntington's disease mutationNigel I Wood, A Jennifer MortonThe European Journal of Neuroscience|January 1, 1992
Accelerated Differentiation in Response to Retinoic Acid After Retrovirally Mediated Gene Transfer of GAP-43 into Mouse Neuroblastoma CellsA. Jennifer Morton, Timothy N. BussNeuroimage|May 6, 2015
The Cambridge MRI database for animal models of Huntington diseaseStephen J Sawiak, A Jennifer MortonExperimental Brain Research|July 22, 2005
Atypical diabetes associated with inclusion formation in the R6/2 mouse model of Huntington's disease is not improved by treatment with hypoglycaemic agentsMark J Hunt, A Jennifer MortonPageof 16