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Documenta Ophthalmologica. Advances in Ophthalmology|March 17, 2019
Novel biallelic loss-of-function KCNV2 variants in cone dystrophy with supernormal rod responsesTomoko Kutsuma, Satoshi Katagiri, Takaaki Hayashi, et al.
The Journal of Biological Chemistry|February 26, 2021
Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitroYang Pan, Daisuke Iejima, Mao Nakayama, et al.
Scientific Reports|September 21, 2016
CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex InstabilityYuriko Minegishi, XunLun Sheng, Kazutoshi Yoshitake, et al.
Investigative Ophthalmology & Visual Science|May 31, 2018
Effect of Timolol on Optineurin Aggregation in Transformed Induced Pluripotent Stem Cells Derived From Patient With Familial GlaucomaSatoshi Inagaki, Kazuhide Kawase, Michinori Funato, et al.
The Journal of Clinical Investigation|September 13, 2022
METTL23 mutation alters histone H3R17 methylation in normal-tension glaucomaYang Pan, Akiko Suga, Itaru Kimura, et al.
Human Genome Variation|January 18, 2019
Novel mutations in the <i>RS1</i> gene in Japanese patients with X-linked congenital retinoschisisHiroyuki Kondo, Kazuma Oku, Satoshi Katagiri, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 19, 2021
The membrane-linked adaptor FRS2β fashions a cytokine-rich inflammatory microenvironment that promotes breast cancer carcinogenesisYasuto Takeuchi, Natsuko Kimura, Takahiko Murayama, et al.
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