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Investigative Ophthalmology & Visual Science|April 26, 2003
An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5Michel Michaelides, Samantha Johnson, Alok K Tekriwal, et al.
Investigative Ophthalmology & Visual Science|August 18, 2009
A mutant connexin50 with enhanced hemichannel function leads to cell deathPeter J Minogue, Jun-Jie Tong, Anita Arora, et al.
Plos One|April 6, 2011
Dominant cone-rod dystrophy: a mouse model generated by gene targeting of the GCAP1/Guca1a genePrateek K Buch, Marija Mihelec, Phillippa Cottrill, et al.
Vision Research|January 23, 2013
X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin geneMichelle McClements, Wayne I L Davies, Michel Michaelides, et al.
Investigative Ophthalmology & Visual Science|December 23, 2008
Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficienciesRavikanth Metlapally, Michel Michaelides, Anuradha Bulusu, et al.
Gene|December 9, 2003
The rod opsin pigments from two marsupial species, the South American bare-tailed woolly opossum and the Australian fat-tailed dunnartDavid M Hunt, Catherine A Arrese, Miranda von Dornum, et al.
Molecular Ecology|February 16, 2019
Phototactic tails: Evolution and molecular basis of a novel sensory trait in sea snakesJenna M Crowe-Riddell, Bruno F Simões, Julian C Partridge, et al.
Plos One|December 20, 2012
Evolution and functional characterisation of melanopsins in a deep-sea chimaera (elephant shark, Callorhinchus milii)Wayne I L Davies, Boon-Hui Tay, Lei Zheng, et al.
The Journal of Experimental Biology|April 22, 2008
The influence of ontogeny and light environment on the expression of visual pigment opsins in the retina of the black bream, Acanthopagrus butcheriJulia Shand, Wayne L Davies, Nicole Thomas, et al.
Ophthalmic Genetics|June 22, 2017
Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalitiesValentina Cipriani, Ambreen Kalhoro, Gavin Arno, et al.
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