日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Clinical features and molecular mechanisms of RP1L1 variants causing occult macular dystrophy

RP1L1变异引起隐匿性黄斑营养不良的临床特征和分子机制

Yang Pan,Daisuke Iejima,Kazutoshi Yoshitake,Kazushige Tsunoda,Takeshi Iwata

METTL23 mutation alters histone H3R17 methylation in normal-tension glaucoma

METTL23 突变改变正常眼压性青光眼的组蛋白 H3R17 甲基化

Yang Pan, Akiko Suga, Itaru Kimura, Chojiro Kimura, Yuriko Minegishi, Mao Nakayama, Kazutoshi Yoshitake, Daisuke Iejima, Naoko Minematsu, Megumi Yamamoto, Fumihiko Mabuchi, Mitsuko Takamoto, Yukihiro Shiga, Makoto Araie, Kenji Kashiwagi, Makoto Aihara, Toru Nakazawa, Takeshi Iwata

Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro

Gtf2i-β/δ 转录因子与 ARMS2 基因结合可导致 AMD 患者体内和体外循环中 HTRA1 增加

Yang Pan, Daisuke Iejima, Mao Nakayama, Akiko Suga, Toru Noda, Inderjeet Kaur, Taraprasad Das, Subhabrata Chakrabarti, Robyn H Guymer, Margaret M DeAngelis, Megumi Yamamoto, Paul N Baird, Takeshi Iwata

HTRA1 (high temperature requirement A serine peptidase 1) gene is transcriptionally regulated by insertion/deletion nucleotides located at the 3' end of the ARMS2 (age-related maculopathy susceptibility 2) gene in patients with age-related macular degeneration

在患有年龄相关性黄斑变性的患者中,HTRA1(高温要求丝氨酸肽酶 1)基因受位于 ARMS2(年龄相关性黄斑病变易感性 2)基因 3' 端的插入/缺失核苷酸的转录调控

Daisuke Iejima, Takeshi Itabashi, Yuich Kawamura, Toru Noda, Shinsuke Yuasa, Keiichi Fukuda, Chio Oka, Takeshi Iwata

Enhanced optineurin E50K-TBK1 interaction evokes protein insolubility and initiates familial primary open-angle glaucoma

增强的视神经素 E50K-TBK1 相互作用引起蛋白质不溶性并引发家族性原发性开角型青光眼

Yuriko Minegishi, Daisuke Iejima, Hiroaki Kobayashi, Zai-Long Chi, Kazuhide Kawase, Tetsuya Yamamoto, Tomohisa Seki, Shinsuke Yuasa, Keiichi Fukuda, Takeshi Iwata