Characterization of Human Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelium Cell Sheets Aiming for Clinical Application
Kamao, Hiroyuki, Mandai, Michiko, Okamoto, Satoshi, Sakai, Noriko, Suga, Akiko, Sugita, Sunao, Kiryu, Junichi, Takahashi, Masayo
Published in Stem cell reports (11.02.2014)
Published in Stem cell reports (11.02.2014)
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Journal Article
Proliferation potential of Müller glia after retinal damage varies between mouse strains
Suga, Akiko, Sadamoto, Kazuyo, Fujii, Momo, Mandai, Michiko, Takahashi, Masayo
Published in PloS one (01.04.2014)
Published in PloS one (01.04.2014)
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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
Azuma, Kunihiro, Suzuki, Takafumi, Kobayashi, Kenta, Nagahara, Masako, Imai, Hirotaka, Suga, Akiko, Iwata, Takeshi, Shiraya, Tomoyasu, Aihara, Makoto, Ueta, Takashi
Published in Cell death & disease (19.10.2024)
Published in Cell death & disease (19.10.2024)
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METTL23 mutation alters histone H3R17 methylation in normal-tension glaucoma
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
Published in The Journal of clinical investigation (01.11.2022)
Published in The Journal of clinical investigation (01.11.2022)
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Novel mutations in malonyl-CoA-acyl carrier protein transacylase provoke autosomal recessive optic neuropathy
Li, Huiping, Yuan, Shiqin, Minegishi, Yuriko, Suga, Akiko, Yoshitake, Kazutoshi, Sheng, Xunlun, Ye, Jianping, Smith, Stuart, Bunkoczi, Gabor, Yamamoto, Megumi, Iwata, Takeshi
Published in Human molecular genetics (01.02.2020)
Published in Human molecular genetics (01.02.2020)
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Optical coherence tomography findings of the peripheral retina in patients with congenital X-linked retinoschisis
Nakajima, Ayaka, Kuniyoshi, Kazuki, Iwahashi, Chiharu, Mano, Fukutaro, Hayashi, Takaaki, Kondo, Hiroyuki, Mizobuchi, Kei, Matsushita, Itsuka, Suga, Akiko, Yoshitake, Kazutoshi, Nakano, Tadashi, Iwata, Takeshi, Matsumoto, Chota, Kusaka, Shunji
Published in Frontiers in medicine (16.11.2023)
Published in Frontiers in medicine (16.11.2023)
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Cellular FLIP Inhibits β-Catenin Ubiquitylation and Enhances Wnt Signaling
Naito, Mikihiko, Katayama, Ryohei, Ishioka, Toshiyasu, Suga, Akiko, Takubo, Kohei, Nanjo, Masahiro, Hashimoto, Chizuko, Taira, Masanori, Takada, Shinji, Takada, Ritsuko, Kitagawa, Masatoshi, Matsuzawa, Shu-Ichi, Reed, John C., Tsuruo, Takashi
Published in Molecular and Cellular Biology (01.10.2004)
Published in Molecular and Cellular Biology (01.10.2004)
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Journal Article
Identification of Amino Acid Sequence in the Hinge Region of Human Vitamin D Receptor That Transfers a Cytosolic Protein to the Nucleus
Michigami, Toshimi, Suga, Akiko, Yamazaki, Miwa, Shimizu, Chika, Cai, Guiming, Okada, Shintaro, Ozono, Keiichi
Published in The Journal of biological chemistry (19.11.1999)
Published in The Journal of biological chemistry (19.11.1999)
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GENETIC ETIOLOGY AND CLINICAL FEATURES OF ACHROMATOPSIA IN JAPAN
Inooka, Taiga, Hayashi, Takaaki, Tsunoda, Kazushige, Kuniyoshi, Kazuki, Kondo, Hiroyuki, Mizobuchi, Kei, Suga, Akiko, Iwata, Takeshi, Yoshitake, Kazutoshi, Kondo, Mineo, Goto, Kensuke, Ota, Junya, Kominami, Taro, Nishiguchi, Koji M, Ueno, Shinji
Published in Retina (Philadelphia, Pa.) (01.10.2024)
Published in Retina (Philadelphia, Pa.) (01.10.2024)
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Journal Article
Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro
Pan, Yang, Iejima, Daisuke, Nakayama, Mao, Suga, Akiko, Noda, Toru, Kaur, Inderjeet, Das, Taraprasad, Chakrabarti, Subhabrata, Guymer, Robyn H., DeAngelis, Margaret M., Yamamoto, Megumi, Baird, Paul N., Iwata, Takeshi
Published in The Journal of biological chemistry (01.01.2021)
Published in The Journal of biological chemistry (01.01.2021)
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측사슬에 고리형 아민을 갖는 비타민 D 유도체
SAITOH HIROSHI, SUGA AKIKO, KAIBARA YUYA, HORIE KYOHEI, MASHIKO TOSHIYA
Year of Publication 14.04.2023
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Year of Publication 14.04.2023
Patent
Identification of Novel Mutations in the LRR-Cap Domain of C21orf2 in Japanese Patients With Retinitis Pigmentosa and Cone-Rod Dystrophy
Suga, Akiko, Mizota, Atsushi, Kato, Mitsuhiro, Kuniyoshi, Kazuki, Yoshitake, Kazutoshi, Sultan, William, Yamazaki, Masashi, Shimomura, Yoshikazu, Ikeo, Kazuho, Tsunoda, Kazushige, Iwata, Takeshi
Published in Investigative ophthalmology & visual science (01.08.2016)
Published in Investigative ophthalmology & visual science (01.08.2016)
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Journal Article
Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole‐exome sequencing
Suga, Akiko, Yoshitake, Kazutoshi, Minematsu, Naoko, Tsunoda, Kazushige, Fujinami, Kaoru, Miyake, Yozo, Kuniyoshi, Kazuki, Hayashi, Takaaki, Mizobuchi, Kei, Ueno, Shinji, Terasaki, Hiroko, Kominami, Taro, Nao‐I, Nobuhisa, Mawatari, Go, Mizota, Atsushi, Shinoda, Kei, Kondo, Mineo, Kato, Kumiko, Sekiryu, Tetsuju, Nakamura, Makoto, Kusuhara, Sentaro, Yamamoto, Hiroyuki, Yamamoto, Shuji, Mochizuki, Kiyofumi, Kondo, Hiroyuki, Matsushita, Itsuka, Kameya, Shuhei, Fukuchi, Takeo, Hatase, Tetsuhisa, Horiguchi, Masayuki, Shimada, Yoshiaki, Tanikawa, Atsuhiro, Yamamoto, Shuichi, Miura, Gen, Ito, Nana, Murakami, Akira, Fujimaki, Takuro, Hotta, Yoshihiro, Tanaka, Koji, Iwata, Takeshi
Published in Human mutation (01.12.2022)
Published in Human mutation (01.12.2022)
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VITAMIN D DERIVATIVE HAVING CYCLIC AMINE IN SIDE CHAIN
HORIE, Kyohei, MASHIKO, Toshiya, KAIBARA, Yuya, SUGA, Akiko, SAITOH, Hiroshi
Year of Publication 24.03.2022
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Year of Publication 24.03.2022
Patent
LRRTM4-C538Y novel gene mutation is associated with hereditary macular degeneration with novel dysfunction of ON-type bipolar cells
Kawamura, Yuichi, Suga, Akiko, Fujimaki, Takuro, Yoshitake, Kazutoshi, Tsunoda, Kazushige, Murakami, Akira, Iwata, Takeshi
Published in Journal of human genetics (01.08.2018)
Published in Journal of human genetics (01.08.2018)
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Journal Article
Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency
Yang, Lizhu, Fujinami, Kaoru, Ueno, Shinji, Kuniyoshi, Kazuki, Hayashi, Takaaki, Kondo, Mineo, Mizota, Atsushi, Naoi, Nobuhisa, Shinoda, Kei, Kameya, Shuhei, Fujinami-Yokokawa, Yu, Liu, Xiao, Arno, Gavin, Pontikos, Nikolas, Kominami, Taro, Terasaki, Hiroko, Sakuramoto, Hiroyuki, Katagiri, Satoshi, Mizobuchi, Kei, Nakamura, Natsuko, Mawatari, Go, Kurihara, Toshihide, Tsubota, Kazuo, Miyake, Yozo, Yoshitake, Kazutoshi, Iwata, Takeshi, Tsunoda, Kazushige
Published in Scientific reports (26.03.2020)
Published in Scientific reports (26.03.2020)
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Journal Article
Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association
Fujinami-Yokokawa, Yu, Fujinami, Kaoru, Kuniyoshi, Kazuki, Hayashi, Takaaki, Ueno, Shinji, Mizota, Atsushi, Shinoda, Kei, Arno, Gavin, Pontikos, Nikolas, Yang, Lizhu, Liu, Xiao, Sakuramoto, Hiroyuki, Katagiri, Satoshi, Mizobuchi, Kei, Kominami, Taro, Terasaki, Hiroko, Nakamura, Natsuko, Kameya, Shuhei, Yoshitake, Kazutoshi, Miyake, Yozo, Kurihara, Toshihide, Tsubota, Kazuo, Miyata, Hiroaki, Iwata, Takeshi, Tsunoda, Kazushige
Published in Scientific reports (12.06.2020)
Published in Scientific reports (12.06.2020)
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Journal Article
Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance
Kameya, Shuhei, Fujinami, Kaoru, Ueno, Shinji, Hayashi, Takaaki, Kuniyoshi, Kazuki, Ideta, Ryuichi, Kikuchi, Sachiko, Kubota, Daiki, Yoshitake, Kazutoshi, Katagiri, Satoshi, Sakuramoto, Hiroyuki, Kominami, Taro, Terasaki, Hiroko, Yang, Lizhu, Fujinami-Yokokawa, Yu, Liu, Xiao, Arno, Gavin, Pontikos, Nikolas, Miyake, Yozo, Iwata, Takeshi, Tsunoda, Kazushige
Published in Investigative ophthalmology & visual science (01.08.2019)
Published in Investigative ophthalmology & visual science (01.08.2019)
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