The retinoid cycle and retina disease
Retinoid cycle in the vertebrate retina: experimental approaches and mechanisms of isomerization
A2E, a byproduct of the visual cycle
Assessing structural elements that influence Schiff base stability: mutants E113Q and D190N destabilize rhodopsin through different mechanisms
Secondary binding sites of retinoids in opsin: characterization and role in regeneration
Bleaching desensitization: background and current challenges
Interphotoreceptor retinoid-binding protein––an old gene for new eyes
Visual cycle retinoid processing proteins are present in HEK293S cells
Origin of the vertebrate visual cycle: II. Visual cycle proteins are localized in whole brain including photoreceptor cells of a primitive chordate
Effect of dodecyl maltoside detergent on rhodopsin stability and function
Comparison between oleic acid and docosahexaenoic acid binding to interphotoreceptor retinoid-binding protein
Availability of 11-cis retinal and opsins without chromophore as revealed by small bleaches of rhodopsin in excised albino mouse eyes
Novel targeting strategy for generating mouse models with defects in the retinoid cycle
Recovery of the rod photoresponse in infant rats
Analysis of three genes in Leber congenital amaurosis in Indonesian patients
Inherited multifocal RPE-diseases: mechanisms for local dysfunction in global retinoid cycle gene defects