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Items Authored or Edited by Mark Hirst

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Jump to: 2011 | 2007 | 2006 | 2003 | 2001
Number of items: 8.

2011

Dallérac, G. M.; Vatsavayai, S. V.; Cummings, D. M.; Milnerwood, A. J.; Peddie, C. J.; Evans, K. A.; Walters, S. W.; Rezaie, P.; Hirst, M. C. and Murphy, K. P. S. J. (2011). Impaired long-term potentiation in the prefrontal cortex of Huntington’s disease mouse models: rescue by D1 dopamine receptor activation. Neurodegenerative Diseases, 8(4) pp. 230–239. file

2007

Cummings, Damian M.; Milnerwood, Austen J.; Dallerac, Glenn M.; Vatsavayai, Sarat C.; Hirst, Mark C. and Murphy, Kerry P. S. J. (2007). Abnormal cortical synaptic plasticity in mice transgenic for exon 1 of the human Huntington's protein. Brain Research Bulletin, 72(2-3) pp. 103–107.

Vatsavayai, Sarat C.; Dallerac, Glenn M.; Milnerwood, Austen J.; Cummings, Damian M.; Rezaie, Payam; Murphy, Kerry P.S.J. and Hirst, Mark C. (2007). Progressive CAG expansion in the brain of a novel R6/1-89Q mouse model of Huntington's disease with delayed phenotypic onset. Brain Research Bulletin, 72(2-3) pp. 98–102.

2006

Cummings, Damian M.; Milnerwood, Austen J.; Dallerac, Glenn M.; Waights, Verina; Brown, Jacki Y.; Vatsavayai, Sarat C.; Hirst, Mark C. and Murphy, Kerry P. S. J. (2006). Aberrant cortical synaptic plasticity and dopaminergic dysfunction in a mouse model of huntington's disease. Human Molecular Genetics, 15(19) pp. 2856–2868.

Milnerwood, Austen J.; Cummings, Damian M.; Dallerac, Glenn M.; Brown, Jacki Y.; Vatsavayai, Sarat C.; Hirst, Mark C.; Rezaie, Payam and Murphy, Kerry P.S.J. (2006). Early development of aberrant synaptic plasticity in a mouse model of Huntington's disease. Human Molecular Genetics, 15(10) pp. 1690–1703.

2003

Chandler, Simon P.; Kansagra, Pushpa and Hirst, Mark C. (2003). Fragile X (CGG)n repeats induce a transcriptional repression in cis upon a linked promoter: evidence for a chromatin mediated effect. BMC Molecular Biology, 4(3) file

Hirst, Mark C. and Fisch, Gene S. (2003). The Fragile X Syndrome and the Fragile X Mutation. In: Fisch, Gene S. ed. Genetics and Genomics of Neurobehavioral Disorders. Contemporary Clinical Nueroscience. USA: Humana Press, pp. 335–390.

2001

Bontekoe, C.J.M.; Bakker, C.E.; Nieuwenhuizen, I.M.; van der Linde, H.; Lans, H.; de Lange, D; Hirst, M.C. and Oostra, B.A. (2001). Instability of a (CGG)(98) repeat in the Fmr1 promoter. Human Molecular Genetics, 10(16) pp. 1693–1699.

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