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Scientific Reports|April 26, 2025
Comprehensive identification of dysregulated extracellular matrix molecules in the corneal endothelium of patients with Fuchs endothelial corneal dystrophySoichiro Inagaki, Hanielle Vaitinadapoule, Taichi Yuasa, et al.Cornea|April 12, 2019
Association of rs613872 and Trinucleotide Repeat Expansion in the TCF4 Gene of German Patients With Fuchs Endothelial Corneal DystrophyNaoki Okumura, Ryousuke Hayashi, Masakazu Nakano, et al.Investigative Ophthalmology & Visual Science|February 28, 2019
Effect of Trinucleotide Repeat Expansion on the Expression of TCF4 mRNA in Fuchs' Endothelial Corneal DystrophyNaoki Okumura, Ryosuke Hayashi, Masakazu Nakano, et al.Ophthalmology|November 11, 2021
Association of the CYP39A1 G204E Genetic Variant with Increased Risk of Glaucoma and Blindness in Patients with Exfoliation SyndromeKatharina Bell, Mineo Ozaki, Kazuhiko Mori, et al.Nature Communications|November 14, 2025
GWAS for primary angle-closure glaucoma identifies loci related to ocular biometry and morphologyRobert N Luben, Mahantesh I Biradar, Kelsey V Stuart, et al.JAMA|February 23, 2021
Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye, Zheng Li, Zhenxun Wang, et al.Human Molecular Genetics|April 12, 2015
A common variant near TGFBR3 is associated with primary open angle glaucomaZheng Li, R Rand Allingham, Masakazu Nakano, et al.Nature Communications|August 15, 2025
Functionally deficient UBOX5 variants and primary angle-closure glaucomaZheng Li, Wee Ling Chng, Zhehao Liu, et al.Nature Genetics|February 24, 2015
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndromeTin Aung, Mineo Ozaki, Takanori Mizoguchi, et al.Nature Genetics|April 12, 2016
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucomaChiea Chuen Khor, Tan Do, Hongyan Jia, et al.Pageof 8