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Investigative Ophthalmology & Visual Science|July 28, 2004
Analysis of porcine optineurin and myocilin expression in trabecular meshwork cells and astrocytes from optic nerve headMinoru Obazawa, Yukihiko Mashima, Naoko Sanuki, et al.Molecular Vision|December 10, 2013
Whole-exome sequencing identifies a novel ALMS1 mutation (p.Q2051X) in two Japanese brothers with Alström syndromeSatoshi Katagiri, Kazutoshi Yoshitake, Masakazu Akahori, et al.Documenta Ophthalmologica. Advances in Ophthalmology|February 16, 2017
Differences in ocular findings in two siblings: one with complete and other with incomplete achromatopsiaShinji Ueno, Ayami Nakanishi, Akira Sayo, et al.Documenta Ophthalmologica. Advances in Ophthalmology|April 2, 2015
Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutationsKazuki Kuniyoshi, Hiroyuki Sakuramoto, Kazutoshi Yoshitake, et al.Ophthalmic Genetics|December 16, 2014
RPE65 Mutations in Two Japanese Families with Leber Congenital AmaurosisSatoshi Katagiri, Takaaki Hayashi, Mineo Kondo, et al.JCI Insight|October 6, 2017
Purinergic dysregulation causes hypertensive glaucoma-like optic neuropathyYouichi Shinozaki, Kenji Kashiwagi, Kazuhiko Namekata, et al.Genes|July 29, 2023
Functional Characteristics of Diverse PAX6 Mutations Associated with Isolated Foveal HypoplasiaItsuka Matsushita, Hiroto Izumi, Shinji Ueno, et al.Journal of Controlled Release : Official Journal of the Controlled Release Society|July 25, 2006
Improved formulations of antisense oligodeoxynucleotides using wrapped liposomesMasahiro Yamauchi, Hiroko Kusano, Etsuko Saito, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|December 12, 2012
Characterizing the phenotype and genotype of a family with occult macular dystrophyConnie J Chen, Hendrik P N Scholl, David G Birch, et al.Japanese Journal of Ophthalmology|January 4, 2019
Three cases of acute-onset bilateral photophobiaShinji Ueno, Daiki Inooka, Monika Meinert, et al.Pageof 19