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Dr Vanessa Davies
Research Institute Manager
- daviesvj@caerdydd.ac.uk
- +44 29206 88340
- Adeilad Hadyn Ellis, Ystafell 3.34A, Heol Maendy, Caerdydd, CF24 4HQ
Cyhoeddiad
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
- Yu-Wai-Man, P., Davies, V. J., Piechota, M., Cree, L. M., Votruba, M. and Chinnery, P. F. 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)
- White, K. E., Davies, V. J., Hogan, V. E., Piechota, M., Nichols, P. P., Turnbull, D. M. and Votruba, M. 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)
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
- Jones, P. M., Pearce, J. M., Davies, V. J., Good, M. A. and McGregor, A. 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)
- 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)
- Kanade, R., Van Deursen, R. W. M., Burton, J., Davies, V. J., Harding, K. G. and Price, P. E. 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)
Articles
- 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)
- Yu-Wai-Man, P., Davies, V. J., Piechota, M., Cree, L. M., Votruba, M. and Chinnery, P. F. 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)
- White, K. E., Davies, V. J., Hogan, V. E., Piechota, M., Nichols, P. P., Turnbull, D. M. and Votruba, M. 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)
- 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)
- Jones, P. M., Pearce, J. M., Davies, V. J., Good, M. A. and McGregor, A. 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)
- 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)
- Kanade, R., Van Deursen, R. W. M., Burton, J., Davies, V. J., Harding, K. G. and Price, P. E. 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)
- 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)
