Dr Vanessa Davies

2012

• Wells, T. et al. 2012. Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome. Human Molecular Genetics 21 (22), pp.4836-4844. (10.1093/hmg/dds315)

2009

• White, K. E. et al., 2009. OPA1 deficiency associated with increased autophagy in retinal ganglion cells in a murine model of dominant optic atrophy. Investigative Ophthalmology & Visual Science 50 (6), pp.2567-2571. (10.1167/iovs.08-2913)
• Yu-Wai-Man, P. et al., 2009. Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophy. Investigative Ophthalmology & Visual Science 50 (10), pp.4561-4566. (10.1167/iovs.09-3634)

2008

• Davies, V. J. et al. 2008. A missense mutation in the murine Opa3 gene models human Costeff syndrome. Brain 131 (2), pp.368-380. (10.1093/brain/awm333)

2007

• Davies, V. J. et al. 2007. Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function. Human Molecular Genetics 16 (11), pp.1307-1318. (10.1093/hmg/ddm079)
• Jones, P. M. et al. 2007. Impaired processing of local geometric features during navigation in a water maze following hippocampal lesions in rats. Behavioral Neuroscience 121 (6), pp.1258-1271. (10.1037/0735-7044.121.6.1258)
• Kanade, R. et al. 2007. Re-amputation occurrence in the diabetic population in South Wales, UK. International Wound Journal 4 (4), pp.344-352. (10.1111/j.1742-481X.2007.00313.x)

2006

• Davies, V. J. and Votruba, M. 2006. Focus on molecules: the OPA1 protein. Experimental Eye Research 83 (5), pp.1003-1004. (10.1016/j.exer.2005.11.021)