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Human Molecular Genetics|April 16, 2011
The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65Vanda S Lopes, Daniel Gibbs, Richard T Libby, et al.
Plos One|November 24, 2011
Characterisation of a C1qtnf5 Ser163Arg knock-in mouse model of late-onset retinal macular degenerationXinhua Shu, Ulrich F O Luhmann, Tomas S Aleman, et al.
Human Molecular Genetics|January 8, 2004
Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequenceArtur V Cideciyan, Tomas S Aleman, Malgorzata Swider, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosaJames W Kijas, Artur V Cideciyan, Tomas S Aleman, et al.
Ophthalmology|March 8, 2003
Clinicopathologic effects of mutant GUCY2D in Leber congenital amaurosisAnn H Milam, Mark R Barakat, Nisha Gupta, et al.
Clinical Ophthalmology (Auckland, N.Z.)|March 10, 2021
A Virtual Reality Orientation and Mobility Test for Inherited Retinal Degenerations: Testing a Proof-of-Concept After Gene TherapyTomas S Aleman, Alexander J Miller, Katherine H Maguire, et al.
Human Molecular Genetics|April 18, 2003
Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal laminationSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|October 3, 2009
Normal central retinal function and structure preserved in retinitis pigmentosaSamuel G Jacobson, Alejandro J Roman, Tomas S Aleman, et al.
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