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The Journal of Biological Chemistry|September 1, 2004
Rhodopsin signaling and organization in heterozygote rhodopsin knockout miceYan Liang, Dimitrios Fotiadis, Tadao Maeda, et al.
Vision Research|May 22, 2007
Novel RDH12 mutations associated with Leber congenital amaurosis and cone-rod dystrophy: biochemical and clinical evaluationsWenyu Sun, Christina Gerth, Akiko Maeda, et al.
The European Journal of Neuroscience|February 28, 2002
Characterization of retinal guanylate cyclase-activating protein 3 (GCAP3) from zebrafish to manYoshikazu Imanishi, Ning Li, Izabela Sokal, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 15, 2009
Phenotypic variability due to a novel Glu292Lys variation in exon 8 of the BEST1 gene causing best macular dystrophyElliott H Sohn, Peter J Francis, Jacque L Duncan, et al.
Ophthalmology|September 8, 2004
Photodynamic therapy with verteporfin in ocular histoplasmosis: uncontrolled, open-label 2-year studyPhilip J Rosenfeld, David A Saperstein, Neil M Bressler, et al.
Ophthalmology|August 3, 2002
Photodynamic therapy of subfoveal choroidal neovascularization with verteporfin in the ocular histoplasmosis syndrome: one-year results of an uncontrolled, prospective case seriesDavid A Saperstein, Philip J Rosenfeld, Neil M Bressler, et al.
The Journal of Biological Chemistry|March 10, 2005
Role of photoreceptor-specific retinol dehydrogenase in the retinoid cycle in vivoAkiko Maeda, Tadao Maeda, Yoshikazu Imanishi, et al.
Human Gene Therapy|February 4, 2006
Adenoviral vector-delivered pigment epithelium-derived factor for neovascular age-related macular degeneration: results of a phase I clinical trialPeter A Campochiaro, Quan Dong Nguyen, Syed Mahmood Shah, et al.
Ophthalmology. Retina|April 10, 2025
Phenotypic Spectrum of Benign Lobular Inner Nuclear Layer Proliferations: A Multicenter Analysis and Review of the LiteratureMichael Javaheri, Christian J Sanfilippo, Sundeep K Kasi, et al.
Lancet (London, England)|July 18, 2014
Oral 9-cis retinoid for childhood blindness due to Leber congenital amaurosis caused by RPE65 or LRAT mutations: an open-label phase 1b trialRobert K Koenekoop, Ruifang Sui, Juliana Sallum, et al.
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