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Neurobiology of Disease|December 26, 2006
Early motor development is abnormal in complexin 1 knockout miceDervila Glynn, Rachel J Sizemore, A Jennifer MortonNeurobiology of Disease|February 18, 2011
Paradoxical function of orexin/hypocretin circuits in a mouse model of Huntington's diseaseRhîannan H Williams, A Jennifer Morton, Denis BurdakovNeurobiology of Disease|February 18, 2011
"Brain training" improves cognitive performance and survival in a transgenic mouse model of Huntington's diseaseNigel I Wood, Dervila Glynn, A Jennifer MortonHuman Molecular Genetics|August 14, 2003
Complexin II is essential for normal neurological function in miceDervila Glynn, Rachel A Bortnick, A Jennifer MortonRoyal Society Open Science|January 2, 2018
Sheep recognize familiar and unfamiliar human faces from two-dimensional imagesFranziska Knolle, Rita P Goncalves, A Jennifer MortonJournal of Neuroscience Methods|September 2, 2015
A mobile, high-throughput semi-automated system for testing cognition in large non-primate animal models of Huntington diseaseSebastian D McBride, Nicholas Perentos, A Jennifer MortonThe Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 16, 2005
Abnormalities of neurogenesis in the R6/2 mouse model of Huntington's disease are attributable to the in vivo microenvironmentWendy Phillips, A Jennifer Morton, Roger A BarkerJournal of Neuroscience Methods|July 30, 2015
A comparison of discrimination learning in touchscreen and 2-choice swim tank using an allelic series of Huntington's disease miceDervila Glynn, Elizabeth A Skillings, A Jennifer MortonNeuroreport|September 27, 2006
Limbic neurogenesis/plasticity in the R6/2 mouse model of Huntington's diseaseWendy Phillips, A Jennifer Morton, Roger A BarkerBehavioural Brain Research|May 20, 2015
Progression of behavioural despair in R6/2 and Hdh knock-in mouse models recapitulates depression in Huntington's diseaseAlessandro Ciamei, Peter J Detloff, A Jennifer MortonPageof 16