岡本晶子

オカモトアキコ | Okamoto Akiko

所属機関・部署：
職名：研究員
競争的資金等の研究課題 (5件)：

論文 (12件)：

Pan Y, Suga A, Kimura I, Kimura C, Minegishi Y, Nakayama M, Yoshitake K, Iejima D, Minematsu N, Yamamoto M, et al. METTL23 mutation alters histone H3R17 methylation in normal-tension glaucoma. The Journal of clinical investigation. 2022
Suga A, Yoshitake K, Minematsu N, Tsunoda K, Kaoru Fujinami, Miyake Y, Kuniyoshi K, Hayashi T, Mizobuchi K, Ueno S, et al. Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing. Human mutation. 2022
Yang Pan, Daisuke Iejima, Mao Nakayama, Akiko Suga, Toru Noda, Inderjeet Kaur, Taraprasad Das, Subhabrata Chakrabarti, Robyn H. Guymer, Margaret M. DeAngelis, et al. Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro. Journal of Biological Chemistry. 2021. 296. 100456-100456
Huiping Li, Shiqin Yuan, Yuriko Minegishi, Akiko Suga, Kazutoshi Yoshitake, Xunlun Sheng, Jianping Ye, Stuart Smith, Gabor Bunkoczi, Megumi Yamamoto, et al. Novel mutations in malonyl-CoA-acyl carrier protein transacylase provoke autosomal recessive optic neuropathy. Human Molecular Genetics. 2020. 29. 3. 444-458
Akiko Suga, Megumi Yamamoto, Takeshi Iwata. Gene editing of mouse Lrrtm4, a bipolar synaptic protein, responsible for macular dystrophy in human, shows photoreceptor degeneration by light stimulation. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 2019. 60. 9

MISC (1件)：

Takeshi Iwata, Huiping Li, Yuan Shiqin, Yuriko Minegishi, Akiko Suga, Kazutoshi Yoshitake, Jianping Ye, Stuart Smith, Gabor Bunkoczi, Megumi Yamamoto, et al. Novel mutations in Malonyl-CoA-Acyl Carrier Protein Transacylase gene provoke autosomal recessive optic neuropathy. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 2020. 61. 7

学位 (1件)：

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岡本 晶子