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Publications by Eyal Banin
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
American Journal of Human Genetics
Genetics
Variable Retinal Phenotypes Caused by Mutations in the X-Linked Photopigment Gene Array
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Human Retinal Disease fromAIPL1Gene Mutations: Foveal Cone Loss With Minimal Macular Photoreceptors and Rod Function Remaining
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Exome Sequencing Identifies a Founder Frameshift Mutation in an Alternative Exon of USH1C as the Cause of Autosomal Recessive Retinitis Pigmentosa With Late-Onset Hearing Loss
PLoS ONE
Multidisciplinary
Association of Pattern Dystrophy With an HTRA1 Single-Nucleotide Polymorphism
Archives of Ophthalmology
Antioxidant or Neurotrophic Factor Treatment Preserves Function in a Mouse Model of Neovascularization-Associated Oxidative Stress
Journal of Clinical Investigation
Medicine
Retinal Incorporation and Differentiation of Neural Precursors Derived From Human Embryonic Stem Cells
Stem Cells
Medicine
Molecular Medicine
Developmental Biology
Cell Biology
Gene Delivery by Viral Vectors in Primary Cultures of Lacrimal Gland Tissue
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
