Novel GUCY2D Variant (E843Q) at Mutation Hotspot Associated with Macular Dystrophy in a Japanese Patient von Takeda, Yukito, Kubota, Daiki, Oishi, Noriko, Maruyama, Kaori, Gocho, Kiyoko, Yamaki, Kunihiko, Igarashi, Tsutomu, Takahashi, Hiroshi, Kameya, Shuhei

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Tyrosinase Family Proteins Are Antigens Specific to Vogt-Koyanagi-Harada Disease von Yamaki, Kunihiko, Gocho, Kiyoko, Hayakawa, Koichi, Kondo, Isao, Sakuragi, Shozo

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Epidemiological survey of intraocular inflammation in Japan von Goto, Hiroshi, Mochizuki, Manabu, Yamaki, Kunihiko, Kotake, Satoshi, Usui, Masahiko, Ohno, Shigeaki

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Multimodal imaging of a case of peripheral cone dystrophy von Ito, Naoko, Kameya, Shuhei, Gocho, Kiyoko, Hayashi, Takaaki, Kikuchi, Sachiko, Katagiri, Satoshi, Gekka, Tamaki, Yamaki, Kunihiko, Takahashi, Hiroshi, Tsuneoka, Hiroshi

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Reactive gliosis of astrocytes and Müller glial cells in retina of POMGnT1-deficient mice von Takahashi, Hisatomo, Kanesaki, Hironori, Igarashi, Tsutomu, Kameya, Shuhei, Yamaki, Kunihiko, Mizota, Atsushi, Kudo, Akira, Miyagoe-Suzuki, Yuko, Takeda, Shin'ichi, Takahashi, Hiroshi

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Detailed Morphological Changes of Foveoschisis in Patient with X-Linked Retinoschisis Detected by SD-OCT and Adaptive Optics Fundus Camera von Yamaki, Kunihiko, Kubota, Daiki, Gocho, Kiyoko, Kameya, Shuhei, Akeo, Keiichiro, Takahashi, Hiroshi

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Novel RP1L1 Variants and Genotype-Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy von Fujinami, Kaoru, Kameya, Shuhei, Kikuchi, Sachiko, Ueno, Shinji, Kondo, Mineo, Hayashi, Takaaki, Shinoda, Kei, Machida, Shigeki, Kuniyoshi, Kazuki, Kawamura, Yuichi, Akahori, Masakazu, Yoshitake, Kazutoshi, Katagiri, Satoshi, Nakanishi, Ayami, Sakuramoto, Hiroyuki, Ozawa, Yoko, Tsubota, Kazuo, Yamaki, Kunihiko, Mizota, Atsushi, Terasaki, Hiroko, Miyake, Yozo, Iwata, Takeshi, Tsunoda, Kazushige

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A driver role for GABA metabolism in controlling stem and proliferative cell state through GHB production in glioma von El-Habr, Elias A., Dubois, Luiz G., Burel-Vandenbos, Fanny, Bogeas, Alexandra, Lipecka, Joanna, Turchi, Laurent, Lejeune, François-Xavier, Coehlo, Paulo Lucas Cerqueira, Yamaki, Tomohiro, Wittmann, Bryan M., Fareh, Mohamed, Mahfoudhi, Emna, Janin, Maxime, Narayanan, Ashwin, Morvan-Dubois, Ghislaine, Schmitt, Charlotte, Verreault, Maité, Oliver, Lisa, Sharif, Ariane, Pallud, Johan, Devaux, Bertrand, Puget, Stéphanie, Korkolopoulou, Penelope, Varlet, Pascale, Ottolenghi, Chris, Plo, Isabelle, Moura-Neto, Vivaldo, Virolle, Thierry, Chneiweiss, Hervé, Junier, Marie-Pierre

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Ultrastructural changes in rat eyes with experimental Vogt-Koyanagi-Harada disease von Hayakawa, Koichi, Ishikawa, Makoto, Yamaki, Kunihiko

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Wistar Rat Palpebral Conjunctiva Contains More Slow-cycling Stem Cells That Have Larger Proliferative Capacity: Implication for Conjunctival Epithelial Homeostasis von Chen, Wensheng, Ishikawa, Makoto, Yamaki, Kunihiko, Sakuragi, Shozo

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Novel GUCY2D variant (E843Q) at mutation hotspot associated with macular dystrophy in Japanese patient von Takeda, Yukito, Kubota, Daiki, Oishi, Noriko, Maruyama, Kaori, Gocho, Kiyoko, Yamaki, Kunihiko, Igarashi, Tsutomu, Takahashi, Hiroshi, Kameya, Shuhei

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Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation von Kubota, Daiki, Gocho, Kiyoko, Akeo, Keiichiro, Kikuchi, Sachiko, Sugahara, Michitaka, Matsumoto, Celso Soiti, Shinoda, Kei, Mizota, Atsushi, Yamaki, Kunihiko, Takahashi, Hiroshi, Kameya, Shuhei

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Identification of Autoreactive T Cells in Vogt-Koyanagi-Harada Disease von Gocho, Kiyoko, Kondo, Isao, Yamaki, Kunihiko

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A new mutation in the RP1L1 gene in a patient with occult macular dystrophy associated with a depolarizing pattern of focal macular electroretinograms von Kabuto, Takenori, Takahashi, Hisatomo, Goto-Fukuura, Yoko, Igarashi, Tsutomu, Akahori, Masakazu, Kameya, Shuhei, Iwata, Takeshi, Mizota, Atsushi, Yamaki, Kunihiko, Miyake, Yozo, Takahashi, Hiroshi

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Intraocular Inflammation and Antigen Presentation von Yamaki, Kunihiko

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Research Article Cone Dystrophy in Patient with Homozygous RP1L1 Mutation von Kikuchi, Sachiko, Kameya, Shuhei, Gocho, Kiyoko, El Shamieh, Said, Akeo, Keiichiro, Sugawara, Yuko, Yamaki, Kunihiko, Zeitz, Christina, Audo, Isabelle, Takahashi, Hiroshi

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Animal Models of Vogt-Koyanagi-Harada Disease (Sympathetic Ophthalmia) von Yamaki, Kunihiko, Ohono, Shigeaki

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Experimentally induced Vogt–Koyanagi–Harada disease in two Akita dogs von Yamaki, Kunihiko, Takiyama, Naoaki, Itho, Norihiko, Mizuki, Nobuhisa, Seiya, Maehara, Sinsuke, Wakaiki, Hayakawa, Kouichi, Kotani, Tadao

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Intraocular Inflammation and Antigen Presentation von Yamaki, Kunihiko

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Experimental Autoimmune Uveitis Induced by Immunization with Retinal Pigment Epithelium-Specific 65-kDa Protein Peptides von Nakamura, Hideo, Yamaki, Kunihiko, Kondo, Isao, Sakuragi, Shozo

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