ORCA
Online Research @ CardiffÂ
Browse by All Cardiff Authors
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Williams, Pete A., Piechota, Malgorzata, Von Ruhland, Christopher John, Taylor, Elaine, Morgan, James Edwards  ORCID: https://orcid.org/0000-0002-8920-1065 and Votruba, Marcela ORCID: https://orcid.org/0000-0002-7680-9135
2012.
Opa1 is essential for retinal ganglion cell synaptic architecture and connectivity.
Brain
135
(2)
, pp. 493-505.
10.1093/brain/awr330
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Yu-Wai-Man, Patrick, Davies, Vanessa J., Piechota, Malgorzata, Cree, Lynsey M., Votruba, Marcela ORCID: https://orcid.org/0000-0002-7680-9135 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 ORCID: https://orcid.org/0000-0002-7680-9135
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 ORCID: https://orcid.org/0000-0002-0324-9376, Davies, Jennifer Rhian, Piechota, Malgorzata, Brownstein, David G., Moat, Stuart James, Nichols, Philip P., Wride, Michael A., Boulton, Michael Edwin and Votruba, Marcela ORCID: https://orcid.org/0000-0002-7680-9135
2008.
A missense mutation in the murine Opa3 gene models human Costeff syndrome.
Brain
131
(2)
, pp. 368-380.
10.1093/brain/awm333
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Davies, Vanessa J., Hollins, Andrew John ORCID: https://orcid.org/0000-0002-0324-9376, Piechota, Malgorzata, Yip, Wan Fen, Davies, Jennifer Rhian, White, Kathryn, Nicols, Phillip, Boulton, Michael Edwin and Votruba, Marcela ORCID: https://orcid.org/0000-0002-7680-9135
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
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