Dunnett SB - Search Results

1

Longitudinal analysis of gene expression and behaviour in the HdhQ150 mouse model of Huntington's disease.

Giles P, Elliston L, Higgs GV, Brooks SP, Dunnett SB, Jones L. Giles P, et al. Among authors: dunnett sb. Brain Res Bull. 2012 Jun 1;88(2-3):199-209. doi: 10.1016/j.brainresbull.2011.10.001. Epub 2011 Oct 6. Brain Res Bull. 2012. PMID: 22001697

2

The operant serial implicit learning task reveals early onset motor learning deficits in the Hdh knock-in mouse model of Huntington's disease.

Trueman RC, Brooks SP, Jones L, Dunnett SB. Trueman RC, et al. Among authors: dunnett sb. Eur J Neurosci. 2007 Jan;25(2):551-8. doi: 10.1111/j.1460-9568.2007.05307.x. Eur J Neurosci. 2007. PMID: 17284197

3

Striatal lesions in the mouse disrupt acquisition and retention, but not implicit learning, in the SILT procedural motor learning task.

Brooks SP, Trueman RC, Dunnett SB. Brooks SP, et al. Among authors: dunnett sb. Brain Res. 2007 Dec 14;1185:179-88. doi: 10.1016/j.brainres.2007.09.017. Epub 2007 Sep 20. Brain Res. 2007. PMID: 17964549

4

Time course of choice reaction time deficits in the Hdh(Q92) knock-in mouse model of Huntington's disease in the operant serial implicit learning task (SILT).

Trueman RC, Brooks SP, Jones L, Dunnett SB. Trueman RC, et al. Among authors: dunnett sb. Behav Brain Res. 2008 Jun 3;189(2):317-24. doi: 10.1016/j.bbr.2008.01.020. Epub 2008 Feb 12. Behav Brain Res. 2008. PMID: 18367261

5

Lesions of the premotor and supplementary motor areas fail to prevent implicit learning in the operant serial implicit learning task.

Brooks SP, Dunnett SB. Brooks SP, et al. Among authors: dunnett sb. Brain Res. 2009 Aug 11;1284:116-24. doi: 10.1016/j.brainres.2009.05.081. Epub 2009 Jun 6. Brain Res. 2009. PMID: 19501057

6

Longitudinal analysis of the behavioural phenotype in HdhQ92 Huntington's disease knock-in mice.

Brooks S, Higgs G, Jones L, Dunnett SB. Brooks S, et al. Among authors: dunnett sb. Brain Res Bull. 2012 Jun 1;88(2-3):148-55. doi: 10.1016/j.brainresbull.2010.05.003. Epub 2010 May 10. Brain Res Bull. 2012. PMID: 20457229

7

Longitudinal analysis of the behavioural phenotype in Hdh(CAG)150 Huntington's disease knock-in mice.

Brooks S, Higgs G, Jones L, Dunnett SB. Brooks S, et al. Among authors: dunnett sb. Brain Res Bull. 2012 Jun 1;88(2-3):182-8. doi: 10.1016/j.brainresbull.2010.05.004. Epub 2010 May 8. Brain Res Bull. 2012. PMID: 20457230

8

Longitudinal analysis of the behavioural phenotype in YAC128 (C57BL/6J) Huntington's disease transgenic mice.

Brooks S, Higgs G, Janghra N, Jones L, Dunnett SB. Brooks S, et al. Among authors: dunnett sb. Brain Res Bull. 2012 Jun 1;88(2-3):113-20. doi: 10.1016/j.brainresbull.2010.05.005. Epub 2010 May 10. Brain Res Bull. 2012. PMID: 20460143

9

Longitudinal analysis of the behavioural phenotype in R6/1 (C57BL/6J) Huntington's disease transgenic mice.

Brooks SP, Janghra N, Workman VL, Bayram-Weston Z, Jones L, Dunnett SB. Brooks SP, et al. Among authors: dunnett sb. Brain Res Bull. 2012 Jun 1;88(2-3):94-103. doi: 10.1016/j.brainresbull.2011.01.010. Epub 2011 Jan 25. Brain Res Bull. 2012. PMID: 21272613

10

Proteomic changes in the brains of Huntington's disease mouse models reflect pathology and implicate mitochondrial changes.

Deschepper M, Hoogendoorn B, Brooks S, Dunnett SB, Jones L. Deschepper M, et al. Among authors: dunnett sb. Brain Res Bull. 2012 Jun 1;88(2-3):210-22. doi: 10.1016/j.brainresbull.2011.01.012. Epub 2011 Jan 25. Brain Res Bull. 2012. PMID: 21272615

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