Molecular genetics of inherited normal tension glaucoma von Pan, Yang, Iwata, Takeshi

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Significance of optineurin mutations in glaucoma and other diseases von Minegishi, Yuriko, Nakayama, Mao, Iejima, Daisuke, Kawase, Kazuhide, Iwata, Takeshi

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Biological Magnetic Resonance Data Bank von Hoch, Jeffrey C, Baskaran, Kumaran, Burr, Harrison, Chin, John, Eghbalnia, Hamid R, Fujiwara, Toshimichi, Gryk, Michael R, Iwata, Takeshi, Kojima, Chojiro, Kurisu, Genji, Maziuk, Dmitri, Miyanoiri, Yohei, Wedell, Jonathan R, Wilburn, Colin, Yao, Hongyang, Yokochi, Masashi

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Establishment of the Indian Chapter for Asian Eye Genetics Consortium von Iwata, Takeshi

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Protein Data Bank Japan: Celebrating our 20th anniversary during a global pandemic as the Asian hub of three dimensional macromolecular structural data von Bekker, Gert‐Jan, Yokochi, Masashi, Suzuki, Hirofumi, Ikegawa, Yasuyo, Iwata, Takeshi, Kudou, Takahiro, Yura, Kei, Fujiwara, Toshimichi, Kawabata, Takeshi, Kurisu, Genji

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Exploring the Genetic Landscape of Childhood Glaucoma von Pan, Yang, Iwata, Takeshi

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A controlled ovarian stimulation procedure suitable for cynomolgus macaques von Shimozawa, Nobuhiro, Iwata, Takeshi, Yasutomi, Yasuhiro

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Exploring the contribution of ARMS2 and HTRA1 genetic risk factors in age-related macular degeneration von Pan, Yang, Fu, Yingbin, Baird, Paul N, Guymer, Robyn H, Das, Taraprasad, Iwata, Takeshi

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Modeling retinal degeneration using patient-specific induced pluripotent stem cells von Jin, Zi-Bing, Okamoto, Satoshi, Osakada, Fumitaka, Homma, Kohei, Assawachananont, Juthaporn, Hirami, Yasuhiko, Iwata, Takeshi, Takahashi, Masayo

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New tools and functions in data‐out activities at Protein Data Bank Japan (PDBj) von Kinjo, Akira R., Bekker, Gert‐Jan, Wako, Hiroshi, Endo, Shigeru, Tsuchiya, Yuko, Sato, Hiromu, Nishi, Hafumi, Kinoshita, Kengo, Suzuki, Hirofumi, Kawabata, Takeshi, Yokochi, Masashi, Iwata, Takeshi, Kobayashi, Naohiro, Fujiwara, Toshimichi, Kurisu, Genji, Nakamura, Haruki

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Prediction of causative genes in inherited retinal disorder from fundus photography and autofluorescence imaging using deep learning techniques von Fujinami-Yokokawa, Yu, Ninomiya, Hideki, Liu, Xiao, Yang, Lizhu, Pontikos, Nikolas, Yoshitake, Kazutoshi, Iwata, Takeshi, Sato, Yasunori, Hashimoto, Takeshi, Tsunoda, Kazushige, Miyata, Hiroaki, Fujinami, Kaoru

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Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy von Khan, Kamron N., Kasilian, Melissa, Mahroo, Omar A.R., Tanna, Preena, Kalitzeos, Angelos, Robson, Anthony G., Tsunoda, Kazushige, Iwata, Takeshi, Moore, Anthony T., Fujinami, Kaoru, Michaelides, Michel

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Clinical Stages of Occult Macular Dystrophy Based on Optical Coherence Tomographic Findings von Nakamura, Natsuko, Tsunoda, Kazushige, Mizuno, Yoshinobu, Usui, Tomoaki, Hatase, Tetsuhisa, Ueno, Shinji, Kuniyoshi, Kazuki, Hayashi, Takaaki, Katagiri, Satoshi, Kondo, Mineo, Kameya, Shuhei, Yoshitake, Kazutoshi, Fujinami, Kaoru, Iwata, Takeshi, Miyake, Yozo

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BioMagResBank (BMRB) as a Resource for Structural Biology von Romero, Pedro R., Kobayashi, Naohiro, Wedell, Jonathan R., Baskaran, Kumaran, Iwata, Takeshi, Yokochi, Masashi, Maziuk, Dimitri, Yao, Hongyang, Fujiwara, Toshimichi, Kurusu, Genji, Ulrich, Eldon L., Hoch, Jeffrey C., Markley, John L.

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Retinal pigment epithelium-specific ablation of GPx4 in adult mice recapitulates key features of geographic atrophy in age-related macular degeneration von Azuma, Kunihiro, Suzuki, Takafumi, Kobayashi, Kenta, Nagahara, Masako, Imai, Hirotaka, Suga, Akiko, Iwata, Takeshi, Shiraya, Tomoyasu, Aihara, Makoto, Ueta, Takashi

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METTL23 mutation alters histone H3R17 methylation in normal-tension glaucoma von Pan, Yang, Suga, Akiko, Kimura, Itaru, Kimura, Chojiro, Minegishi, Yuriko, Nakayama, Mao, Yoshitake, Kazutoshi, Iejima, Daisuke, Minematsu, Naoko, Yamamoto, Megumi, Mabuchi, Fumihiko, Takamoto, Mitsuko, Shiga, Yukihiro, Araie, Makoto, Kashiwagi, Kenji, Aihara, Makoto, Nakazawa, Toru, Iwata, Takeshi

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Novel mutations in malonyl-CoA-acyl carrier protein transacylase provoke autosomal recessive optic neuropathy von Li, Huiping, Yuan, Shiqin, Minegishi, Yuriko, Suga, Akiko, Yoshitake, Kazutoshi, Sheng, Xunlun, Ye, Jianping, Smith, Stuart, Bunkoczi, Gabor, Yamamoto, Megumi, Iwata, Takeshi

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Editorial: Personalized medicine-Where do we stand regarding bench to bedside translation? von Raghavendran, Hanumantha Rao Balaji, Kumaramanickavel, Govindasamy, Iwata, Takeshi

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Dominant Mutations in RP1L1 Are Responsible for Occult Macular Dystrophy von Akahori, Masakazu, Tsunoda, Kazushige, Miyake, Yozo, Fukuda, Yoko, Ishiura, Hiroyuki, Tsuji, Shoji, Usui, Tomoaki, Hatase, Tetsuhisa, Nakamura, Makoto, Ohde, Hisao, Itabashi, Takeshi, Okamoto, Haru, Takada, Yuichiro, Iwata, Takeshi

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Compound heterozygous mutations in a mouse model of Leber congenital amaurosis reveal the role of CCT2 in photoreceptor maintenance von Suga, Akiko, Minegishi, Yuriko, Yamamoto, Megumi, Ueda, Koji, Iwata, Takeshi

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