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Aspinall-O'Dea, M., Pierce, A., Pellicano, F., Williamson, A. J., Scott, M. T. , Walker, M. J., Holyoake, T. L. and Whetton, A. D. (2015) Antibody-based detection of protein phosphorylation status to track the efficacy of novel therapies using nanogram protein quantities from stem cells and cell lines. Nature Protocols, 10(1), pp. 149-168. (doi: 10.1038/nprot.2015.007) (PMID:25521791)

Robinson, L., Plano, A., Cobb, S. and Riedel, G. (2013) Long-term home cage activity scans reveal lowered exploratory behaviour in symptomatic female Rett mice. Behavioural Brain Research, 250, pp. 148-156. (doi: 10.1016/j.bbr.2013.04.041)

McLeod, F., Ganley, R., Williams, L., Selfridge, J., Bird, A. and Cobb, S.R. (2013) Reduced seizure threshold and altered network oscillatory properties in a mouse model of Rett syndrome. Neuroscience, 231, pp. 195-205. (doi: 10.1016/j.neuroscience.2012.11.058) (PMID:23238573)

Gadalla, K.K.E. et al. (2013) Improved survival and reduced phenotypic severity following AAV9/MECP2 gene transfer to neonatal and juvenile male Mecp2 knockout mice. Molecular Therapy, 21(1), pp. 18-30. (doi: 10.1038/mt.2012.200) (PMID:23011033) (PMCID:PMC3536818)

Robinson, L. et al. (2012) Morphological and functional reversal of phenotypes in a mouse model of Rett syndrome. Brain, 135(9), pp. 2699-2710. (doi: 10.1093/brain/aws096) (PMID:22525157) (PMCID:PMC3437019)

Weng, S.-M., Bailey, M. E.S. and Cobb, S. R. (2011) Rett syndrome: from bed to bench. Pediatrics and Neonatology, 52(6), pp. 309-316. (doi: 10.1016/j.pedneo.2011.08.002)

Weng, S.-M., McLeod, F., Bailey, M.E.S. and Cobb, S.R. (2011) Synaptic plasticity deficits in an experimental model of Rett Syndrome: LTP saturation and its pharmacological reversal. Neuroscience, 180, pp. 314-321. (doi: 10.1016/j.neuroscience.2011.01.061)

Cobb, S., Guy, J. and Bird, A. (2010) Reversibility of functional deficits in experimental models of Rett syndrome. Biochemical Society Transactions, 38(2), pp. 498-506. (doi: 10.1042/BST0380498)

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