Showing results (11-20 of 129) with videos related to
Sort By:
Pageof 13
Ophthalmic Research|June 22, 2011
Pharmacological enhancement of ex vivo gene therapy neuroprotection in a rodent model of retinal degenerationKevin Gregory-Evans, Kelvin Po, Francis Chang, et al.Precision Clinical Medicine|June 13, 2022
RNA-based therapies in animal models of Leber congenital amaurosis causing blindnessXia Wang, Xianghong Shan, Kevin Gregory-Evans, et al.Genomics|November 1, 2002
Characterization of the genomic and transcriptional structure of the CRX gene: substantial differences between human and mouseMatthew D Hodges, Helena Vieira, Kevin Gregory-Evans, et al.Journal of Medical Genetics|December 14, 2004
Ocular coloboma: a reassessment in the age of molecular neuroscienceC Y Gregory-Evans, M J Williams, S Halford, et al.Molecular Vision|May 23, 2009
Ex vivo gene therapy using intravitreal injection of GDNF-secreting mouse embryonic stem cells in a rat model of retinal degenerationKevin Gregory-Evans, Francis Chang, Matthew D Hodges, et al.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.Pageof 13