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IEEE Transactions on Magnetics|July 1, 2014
Influence of Iron Oxide Nanoparticles on Innate and Genetically Modified Secretion Profiles of Mesenchymal Stem CellsAbu Emran Bashar, Andrew Metcalfe, Anat Yanai, et al.Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|September 6, 2025
The effect of oral belzutifan on retinal hemangioblastomas in von Hippel-Lindau syndromeKirk A J Stephenson, Jennifer Y M Ling, Olubayo Kolawole, et al.Cell Transplantation|March 13, 2012
Focused magnetic stem cell targeting to the retina using superparamagnetic iron oxide nanoparticlesAnat Yanai, Urs O Häfeli, Andrew L Metcalfe, et al.Investigative Ophthalmology & Visual Science|June 27, 2006
Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunctionMichel Michaelides, Sharon A Jenkins, Milam A Brantley, et al.Human Molecular Genetics|June 7, 2013
RD3 gene delivery restores guanylate cyclase localization and rescues photoreceptors in the Rd3 mouse model of Leber congenital amaurosis 12Laurie L Molday, Hidayat Djajadi, Paul Yan, et al.Experimental Eye Research|February 8, 2003
Expression of opsin genes early in ocular development of humans and miceEmma E Tarttelin, James Bellingham, Lindsay C Bibb, et al.Human Molecular Genetics|July 28, 2007
SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular colobomaCheryl Y Gregory-Evans, Mariya Moosajee, Matthew D Hodges, et al.Investigative Ophthalmology & Visual Science|July 3, 2025
Quantitative Choroidal Analysis of Molecularly Characterized Retinitis PigmentosaKirk A J Stephenson, Tiffany Tse, Jiwon Hwang, et al.Current Biology : CB|December 18, 2007
Short-wavelength light sensitivity of circadian, pupillary, and visual awareness in humans lacking an outer retinaFarhan H Zaidi, Joseph T Hull, Stuart N Peirson, et al.American Journal of Human Genetics|March 17, 2004
Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11qCarmel Toomes, Helen M Bottomley, Richard M Jackson, et al.Pageof 7