The utilisation of operant delayed matching and non-matching to position for probing cognitive flexibility and working memory in mouse models of Huntington's disease

Por Yhnell, Emma, Dunnett, Stephen B., Brooks, Simon P.
Publicado no J Neurosci Methods (2016)

A Longitudinal Motor Characterisation of the Hdh(Q111) Mouse Model of Huntington’s Disease

Por Yhnell, Emma, Dunnett, Stephen B., Brooks, Simon P.
Publicado no J Huntingtons Dis (2016)

A Longitudinal Operant Assessment of Cognitive and Behavioural Changes in the Hdh(Q111) Mouse Model of Huntington’s Disease

Por Yhnell, Emma, Dunnett, Stephen B., Brooks, Simon P.
Publicado no PLoS One (2016)

Huntingtin Subcellular Localisation Is Regulated by Kinase Signalling Activity in the StHdh(Q111) Model of HD

Por Bowles, Kathryn R., Brooks, Simon P., Dunnett, Stephen B., Jones, Lesley
Publicado no PLoS One (2015)

Comparison of mHTT Antibodies in Huntington’s Disease Mouse Models Reveal Specific Binding Profiles and Steady-State Ubiquitin Levels with Disease Development

Por Bayram-Weston, Zubeyde, Jones, Lesley, Dunnett, Stephen B., Brooks, Simon P.
Publicado no PLoS One (2016)

Cognitive training modifies disease symptoms in a mouse model of Huntington's disease

Por Yhnell, Emma, Lelos, Mariah J., Dunnett, Stephen B., Brooks, Simon P.
Publicado no Exp Neurol (2016)

Optimising Golgi–Cox staining for use with perfusion-fixed brain tissue validated in the zQ175 mouse model of Huntington's disease

Por Bayram-Weston, Zubeyde, Olsen, Elliott, Harrison, David J., Dunnett, Stephen B., Brooks, Simon P.
Publicado no J Neurosci Methods (2016)

Correction: Huntingtin Subcellular Localisation Is Regulated by Kinase Signalling Activity in the StHdh(Q111) Model of HD

Por Bowles, Kathryn R., Brooks, Simon P., Hughes, Alis C., Dunnett, Stephen B., Jones, Lesley
Publicado no PLoS One (2016)

Identification of three novel NHS mutations in families with Nance-Horan syndrome

Por Huang, Kristen M., Wu, Junhua, Brooks, Simon P., Hardcastle, Alison J., Lewis, Richard Alan, Stambolian, Dwight
Publicado em 2007

The Nance–Horan syndrome protein encodes a functional WAVE homology domain (WHD) and is important for co-ordinating actin remodelling and maintaining cell morphology

Por Brooks, Simon P., Coccia, Margherita, Tang, Hao R., Kanuga, Naheed, Machesky, Laura M., Bailly, Maryse, Cheetham, Michael E., Hardcastle, Alison J.
Publicado em 2010

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 prevalence...

Por Bayram-Weston, Zubeyde, Stone, Timothy C., Giles, Peter, Elliston, Linda, Janghra, Nari, Higgs, Gemma V., Holmans, Peter A., Dunnett, Stephen B., Brooks, Simon P., Jones, Lesley
Publicado no BMC Genomics (2015)

Age-Dependent Maintenance of Motor Controland Corticostriatal Innervation by Death Receptor 3

Por Twohig, Jason Peter, Roberts, Malcolm I., Gavalda, Nuria, Rees-Taylor, Emma L., Giralt, Albert, Adams, Debbie, Brooks, Simon P., Bull, Melanie J., Calder, Claudia J., Cuff, Simone, Yong, Audrey A., Alberch, Jordi, Davies, Alun, Dunnett, Stephen B., Tolkovsky, Aviva M., Wang, Eddie C. Y.
Publicado em 2010

X-linked cataract and Nance-Horan syndrome are allelic disorders

Por Coccia, Margherita, Brooks, Simon P., Webb, Tom R., Christodoulou, Katja, Wozniak, Izabella O., Murday, Victoria, Balicki, Martha, Yee, Harris A., Wangensteen, Teresia, Riise, Ruth, Saggar, Anand K., Park, Soo-Mi, Kanuga, Naheed, Francis, Peter J., Maher, Eamonn R., Moore, Anthony T., Russell-Eggitt, Isabelle M., Hardcastle, Alison J.
Publicado em 2009

Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.Htt(Q111/+) model of Huntington’s disease

Por Bragg, Robert M., Coffey, Sydney R., Weston, Rory M., Ament, Seth A., Cantle, Jeffrey P., Minnig, Shawn, Funk, Cory C., Shuttleworth, Dominic D., Woods, Emily L., Sullivan, Bonnie R., Jones, Lindsey, Glickenhaus, Anne, Anderson, John S., Anderson, Michael D., Dunnett, Stephen B., Wheeler, Vanessa C., MacDonald, Marcy E., Brooks, Simon P., Price, Nathan D., Carroll, Jeffrey B.
Publicado no Sci Rep (2017)

Corrigendum: Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.Htt(Q111/+) model of Huntington’s disease

Por Bragg, Robert M., Coffey, Sydney R., Weston, Rory M., Ament, Seth A., Cantle, Jeffrey P., Minnig, Shawn, Funk, Cory C., Shuttleworth, Dominic D., Woods, Emily L., Sullivan, Bonnie R., Jones, Lindsey, Glickenhaus, Anne, Anderson, John S., Anderson, Michael D., Dunnett, Stephen B., Wheeler, Vanessa C., MacDonald, Marcy E., Brooks, Simon P., Price, Nathan D., Carroll, Jeffrey B.
Publicado no Sci Rep (2017)