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Investigative Ophthalmology & Visual Science|October 28, 2003
Transcriptional regulation and expression of the dominant drusen gene FBLN3 (EFEMP1) in mammalian retinaJames Blackburn, Emma E Tarttelin, Cheryl Y Gregory-Evans, et al.
Ophthalmic Genetics|March 5, 2026
Two novel genetic associations with sector retinitis pigmentosa: <i>USH2A</i> and <i>PRPF31</i>Shanil R Dhanji, Kirk A J Stephenson, Cheryl Y Gregory-Evans, et al.
Experimental Eye Research|May 19, 2018
Anolis carolinensis as a model to understand the molecular and cellular basis of foveal developmentNaif S Sannan, Xianghong Shan, Kevin Gregory-Evans, et al.
Ophthalmic Genetics|June 10, 2024
Asymmetric preservation of choroidal pigmentation simulating choroidal nevus in two siblings with Waardenburg syndrome type 2AKirk A J Stephenson, Katherine E Paton, Cheryl Y Gregory-Evans, et al.
Human Molecular Genetics|September 24, 2008
Translational bypass of nonsense mutations in zebrafish rep1, pax2.1 and lamb1 highlights a viable therapeutic option for untreatable genetic eye diseaseMariya Moosajee, Kevin Gregory-Evans, Charles D Ellis, et al.
Journal of Tissue Engineering and Regenerative Medicine|March 29, 2021
Photoreceptor precursor cell integration into rodent retina after treatment with novel glycopeptide PKX-001Ishaq A Viringipurampeer, Anat Yanai, Vahitha S Nizamudheen, et al.
Current Eye Research|October 21, 2010
Mesenchymal stem cells and potential applications in treating ocular diseaseAaron W Joe, Kevin Gregory-Evans
International Journal of Inflammation|March 20, 2013
Targeting inflammation in emerging therapies for genetic retinal diseaseIshaq A Viringipurampeer, Abu E Bashar, Cheryl Y Gregory-Evans, et al.
Ophthalmology|December 17, 1998
Abnormal cone synapses in human cone-rod dystrophyK Gregory-Evans, R N Fariss, D E Possin, et al.
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