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Documenta Ophthalmologica. Advances in Ophthalmology|July 10, 2019
Late-onset night blindness with peripheral flecks accompanied by progressive trickle-like macular degenerationKazushige Tsunoda, Kaoru Fujinami, Kazutoshi Yoshitake, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|September 5, 2006
Discovery of potential sorbitol dehydrogenase inhibitors from virtual screeningConnie Darmanin, Takeshi Iwata, Deborah A Carper, et al.
HGG Advances|June 1, 2025
Clinical features and molecular mechanisms of RP1L1 variants causing occult macular dystrophyYang Pan, Daisuke Iejima, Kazutoshi Yoshitake, et al.
Ophthalmic Genetics|June 26, 2025
A novel NR2F1-associated microdeletion underlying Bosch-Boonstra-Schaaf optic atrophy syndromeTakaaki Hayashi, Kei Mizobuchi, Akiko Suga, et al.
Advances in Experimental Medicine and Biology|August 17, 2010
Suppression of drusen formation by compstatin, a peptide inhibitor of complement C3 activation, on cynomolgus monkey with early-onset macular degenerationZai-Long Chi, Tsunehiko Yoshida, John D Lambris, et al.
Progress in Retinal and Eye Research|October 4, 2016
Significance of optineurin mutations in glaucoma and other diseasesYuriko Minegishi, Mao Nakayama, Daisuke Iejima, et al.
Vascular Pharmacology|June 15, 2005
Alteration in endothelial function and modulation by treatment with pioglitazone in rabbit renal artery from short-term hypercholesterolemiaJun Taniguchi, Hideo Honda, Yoichi Shibusawa, et al.
Communications Biology|June 3, 2024
Compound heterozygous mutations in a mouse model of Leber congenital amaurosis reveal the role of CCT2 in photoreceptor maintenanceAkiko Suga, Yuriko Minegishi, Megumi Yamamoto, et al.
Investigative Ophthalmology & Visual Science|September 11, 2014
Overexpression of HtrA1 and exposure to mainstream cigarette smoke leads to choroidal neovascularization and subretinal deposits in aged miceMao Nakayama, Daisuke Iejima, Masakazu Akahori, et al.
Ophthalmic Genetics|April 10, 2018
Autosomal dominant retinitis pigmentosa with macular involvement associated with a disease haplotype that included a novel PRPH2 variant (p.Cys250Gly)Satoshi Katagiri, Takaaki Hayashi, Kei Mizobuchi, et al.
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