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Brain Research Bulletin|October 4, 2011
Profiles of motor and cognitive impairment in the transgenic rat model of Huntington's diseaseSteven A Fielding, Simon P Brooks, Alexander Klein, et al.Experimental Neurology|August 6, 2013
Exercise attenuates neuropathology and has greater benefit on cognitive than motor deficits in the R6/1 Huntington's disease mouse modelDavid J Harrison, Monica Busse, Rebecca Openshaw, et al.Cell Transplantation|April 12, 2018
The Effect of Tissue Preparation and Donor Age on Striatal Graft Morphology in the MouseDavid J Harrison, Victoria H Roberton, Ngoc-Nga Vinh, et al.Journal of Molecular Biology|January 7, 2014
Identification of novel alternative splicing events in the huntingtin gene and assessment of the functional consequences using structural protein homology modellingAlis C Hughes, Matthew Mort, Lyn Elliston, et al.Journal of Huntington'S Disease|September 24, 2015
In Vivo MRI Evidence that Neuropathology is Attenuated by Cognitive Enrichment in the Yac128 Huntington's Disease Mouse ModelJessica J Steventon, David J Harrison, Rebecca C Trueman, et al.Brain Research Bulletin|June 1, 2011
Selective cognitive impairment in the YAC128 Huntington's disease mouseSimon P Brooks, Nari Janghra, Gemma V Higgs, et al.Human Molecular Genetics|March 25, 2010
The Nance-Horan syndrome protein encodes a functional WAVE homology domain (WHD) and is important for co-ordinating actin remodelling and maintaining cell morphologySimon P Brooks, Margherita Coccia, Hao R Tang, et al.Stem Cell Reports|August 27, 2019
CTIP2-Regulated Reduction in PKA-Dependent DARPP32 Phosphorylation in Human Medium Spiny Neurons: Implications for Huntington DiseaseMarija Fjodorova, Morgane Louessard, Zongze Li, et al.Cell Metabolism|January 17, 2018
Basal Mitophagy Occurs Independently of PINK1 in Mouse Tissues of High Metabolic DemandThomas G McWilliams, Alan R Prescott, Lambert Montava-Garriga, et al.BMC Genomics|December 23, 2015
Similar striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntington's disease are not reflected in mutant Huntingtin inclusion prevalenceZubeyde Bayram-Weston, Timothy C Stone, Peter Giles, et al.Pageof 5