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Number of items: 6.

Williams, Pete A., Piechota, Malgorzata, Von Ruhland, Christopher John, Taylor, Elaine, Morgan, James Edwards and Votruba, Marcela 2012. Opa1 is essential for retinal ganglion cell synaptic architecture and connectivity. Brain 135 (2) , pp. 493-505. 10.1093/brain/awr330

Yu-Wai-Man, Patrick, Davies, Vanessa J., Piechota, Malgorzata, Cree, Lynsey M., Votruba, Marcela and Chinnery, Patrick 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
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White, Kathryn E., Davies, Vanessa J., Hogan, Vanessa E., Piechota, Malgorzata, Nichols, Philip P., Turnbull, Douglas M. and Votruba, Marcela 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
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Piechota, Malgorzata 2009. Characterisation of a novel model of optic atrophy. PhD Thesis, Cardiff University.
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Davies, Vanessa J., Powell, Kathryn A., White, Kathryn E., Yip, Wan Fen, Hogan, Vanessa, Hollins, Andrew John, Davies, Jennifer Rhian, Piechota, Malgorzata, Brownstein, David G., Moat, Stuart James, Nichols, Philip P., Wride, Michael A., Boulton, Michael Edwin and Votruba, Marcela 2008. A missense mutation in the murine Opa3 gene models human Costeff syndrome. Brain 131 (2) , pp. 368-380. 10.1093/brain/awm333

Davies, Vanessa J., Hollins, Andrew John, Piechota, Malgorzata, Yip, Wan Fen, Davies, Jennifer Rhian, White, Kathryn, Nicols, Phillip, Boulton, Michael Edwin and Votruba, Marcela 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

This list was generated on Sun Dec 8 08:32:34 2019 GMT.