Simmon P. Brooks

Affiliations: 
2002-2016 School of Biosciences Cardiff University, Cardiff, Wales, United Kingdom 
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"Simmon Brooks"
Mean distance: 15.67 (cluster 6)
 
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Publications

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Muha V, Williamson R, Hills R, et al. (2019) Loss of CRMP2 O-GlcNAcylation leads to reduced novel object recognition performance in mice. Open Biology. 9: 190192
McWilliams TG, Barini E, Pohjolan-Pirhonen R, et al. (2018) Phosphorylation of Parkin at serine 65 is essential for its activation . Open Biology. 8
Dunnett SB, Brooks SP. (2018) Motor Assessment in Huntington's Disease Mice. Methods in Molecular Biology (Clifton, N.J.). 1780: 121-141
Harrison DJ, Roberton VH, Vinh NN, et al. (2018) The Effect of Tissue Preparation and Donor Age on Striatal Graft Morphology in the Mouse. Cell Transplantation. 27: 230-244
McWilliams TG, Prescott AR, Montava-Garriga L, et al. (2018) Basal Mitophagy Occurs Independently of PINK1 in Mouse Tissues of High Metabolic Demand. Cell Metabolism
Bragg RM, Coffey SR, Weston RM, et al. (2017) Corrigendum: Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.Htt(Q111/+) model of Huntington's disease. Scientific Reports. 7: 44960
Bragg RM, Coffey SR, Weston RM, et al. (2017) Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.Htt(Q111/+) model of Huntington's disease. Scientific Reports. 7: 41570
Bowles KR, Brooks SP, Hughes AC, et al. (2016) Correction: Huntingtin Subcellular Localisation Is Regulated by Kinase Signalling Activity in the StHdhQ111 Model of HD. Plos One. 11: e0165069
Yhnell E, Dunnett SB, Brooks SP. (2016) A Longitudinal Operant Assessment of Cognitive and Behavioural Changes in the HdhQ111 Mouse Model of Huntington's Disease. Plos One. 11: e0164072
Yhnell E, Dunnett SB, Brooks SP. (2016) A Longitudinal Motor Characterisation of the HdhQ111 Mouse Model of Huntington's Disease. Journal of Huntington's Disease
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