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Biochimica Et Biophysica Acta|June 24, 2003
Gene structure and tissue expression of human selenoprotein W, SEPW1, and identification of a retroprocessed pseudogene, SEPW1PJames Bellingham, Kevin Gregory-Evans, Margaret F Fox, et al.
Human Mutation|May 18, 2026
Expanding the Genotypic Landscape of Congenital Stationary Night Blindness in an Ethnically Diverse Canadian PopulationJennifer Ling, Mustansir Pindwarawala, Cheryl Y Gregory-Evans, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|July 23, 2024
Novel Variants in ABCA4-Related Retinopathies with Structural Re-Assessment of Variants of Uncertain SignificanceKevin Gregory-Evans, Olubayo U Kolawole, Robert S Molday, et al.
Plos One|October 25, 2011
Foxf2: a novel locus for anterior segment dysgenesis adjacent to the Foxc1 geneRichard McKeone, Helena Vieira, Kevin Gregory-Evans, et al.
Ophthalmic Genetics|November 25, 2025
Identification of novel pathogenic variants in the <i>PHYH</i> gene and extending the phenotypic range in Refsum diseaseCheryl Y Gregory-Evans, Anna Lehman, Andre Mattman, et al.
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.
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