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Molecular Vision|December 24, 2011
Analysis of LOXL1 gene variants in Japanese patients with branch retinal vein occlusionKatsunori Hara, Masakazu Akahori, Masaki Tanito, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|February 21, 2021
A new PDE6A missense variant p.Arg544Gln in rod-cone dystrophyTakaaki Hayashi, Kei Mizobuchi, Shuhei Kameya, et al.
Clinical Ophthalmology (Auckland, N.Z.)|September 17, 2013
Two siblings with late-onset cone-rod dystrophy and no visible macular degenerationHiroyuki Sakuramoto, Kazuki Kuniyoshi, Kazushige Tsunoda, et al.
Investigative Ophthalmology & Visual Science|March 7, 2015
Association of Retinal Artery and Other Inner Retinal Structures With Distribution of Tapetal-like Reflex in Oguchi's DiseaseYu Kato, Kazushige Tsunoda, Kaoru Fujinami, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
Involvement of insulin-like growth factor-I and insulin-like growth factor binding protein-3 in corneal fibroblasts during corneal wound healingKanako Izumi, Daijiro Kurosaka, Takeshi Iwata, et al.
Progress in Retinal and Eye Research|December 29, 2022
Exploring the contribution of ARMS2 and HTRA1 genetic risk factors in age-related macular degenerationYang Pan, Yingbin Fu, Paul N Baird, et al.
Experimental Eye Research|March 22, 2008
Immunohistochemical analysis of aldehyde-modified proteins in drusen in cynomolgus monkeys (Macaca fascicularis)Sachiko Kaidzu, Masaki Tanito, Akihiro Ohira, et al.
Biochimica Et Biophysica Acta|February 21, 2006
Development of wrapped liposomes: novel liposomes comprised of polyanion drug and cationic lipid complexes wrapped with neutral lipidsMasahiro Yamauchi, Hiroko Kusano, Etsuko Saito, et al.
Journal of Human Genetics|May 16, 2018
LRRTM4-C538Y novel gene mutation is associated with hereditary macular degeneration with novel dysfunction of ON-type bipolar cellsYuichi Kawamura, Akiko Suga, Takuro Fujimaki, et al.
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