Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Browse by All Cardiff Authors

Number of items: 5.

Wells, Timothy ORCID: https://orcid.org/0000-0003-3618-0595, Davies, Jennifer Rhian, Guschina, Irina, Ball, Daniel, Davies, Jeffrey Stephens, Davies, Vanessa J., Evans, Bronwen Alice James ORCID: https://orcid.org/0000-0002-3082-1008 and Votruba, Marcela ORCID: https://orcid.org/0000-0002-7680-9135 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

Powell, Kathryn Ann, Davies, Jennifer Rhian, Taylor, Elaine, Wride, Michael A. and Votruba, Marcela ORCID: https://orcid.org/0000-0002-7680-9135 2011. Mitochondrial localization and ocular expression of mutant Opa3 in a mouse model of 3-methylglutaconicaciduria type III. Investigative Ophthalmology & Visual Science 52 (7) , pp. 4369-4380. 10.1167/iovs.10-6406
file

Davies, Jennifer Rhian 2011. Neuro-ophthalmological syndrome 3-methylglutaconic aciduria: a molecular and functional study of the B6; C3-Opa3L122P mouse model. PhD Thesis, Cardiff University.
file

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

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

This list was generated on Sat Apr 27 12:12:10 2024 BST.