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

Whole-genome 3D architectural screen reveals modulators of brain DNA structure

全基因组三维结构筛选揭示大脑DNA结构的调节因子

Parasar, Bibudha; Venkatesh, Achuthan Raja; Perera, Jonathan; Sosnick, Lucas; Moghadami, Siavash; Seo, Yunji; Shi, Jenny; Chan, Lynette; Takenawa, Satoshi; Akiyama, Tetsuya; Sianto, Odilia; Uenaka, Takeshi; Hadjipanayis, Angela; Wernig, Marius; Gitler, Aaron D; Tan, Longzhi

TDP-43 nuclear loss in FTD/ALS causes widespread alternative polyadenylation changes

在额颞叶痴呆/肌萎缩侧索硬化症中,TDP-43 核丢失会导致广泛的替代性多聚腺苷酸化改变。

Zeng, Yi; Lovchykova, Anastasiia; Akiyama, Tetsuya; Rayner, Stephanie L; Maheswari Jawahar, Vidhya; Liu, Chang; Sianto, Odilia; Guo, Caiwei; Calliari, Anna; Prudencio, Mercedes; Dickson, Dennis W; Petrucelli, Leonard; Gitler, Aaron D

Cryptic splicing in synaptic and membrane excitability genes links TDP-43 loss to neuronal dysfunction.

突触和膜兴奋性基因中的隐蔽剪接将 TDP-43 的缺失与神经元功能障碍联系起来

Guo Caiwei, Chen Kuchuan, Vatsavayai Sarat C, Akiyama Tetsuya, Zeng Yi, Liu Chang, Sianto Odilia, Yang Edith, Bombosch Juliane, Powell Rasheen, Zhen Shannon, Mekhoubad Shila, Morrie Ryan D, Miller Georgiana, Green Eric M, Petrucelli Leonard, Seeley William W, Gitler Aaron D

KIF5A downregulation in spinal muscular atrophy links axonal regeneration defects with ALS.

脊髓性肌萎缩症中 KIF5A 的下调将轴突再生缺陷与 ALS 联系起来

Akiyama Tetsuya, Zeng Yi, Guo Caiwei, Gautier Olivia, Koepke Lauren, Bombosch Juliane, Sianto Odilia, Ross Jay P, Hoang Phuong Thi, Zhao Luke Yuchen, Spencer Cole, Monje Michelle, Day John W, Gitler Aaron D

Nonsense-mediated decay masks cryptic splicing events caused by TDP-43 loss.

无义介导衰变掩盖了由 TDP-43 缺失引起的隐蔽剪接事件

Zeng Yi, Sianto Odilia, Lovchykova Anastasiia, Liu Chang, Akiyama Tetsuya, Petrucelli Leonard, Gitler Aaron D

Updated Genetic Analysis of Japanese Familial ALS Patients Carrying SOD1 Variants Revealed Phenotypic Differences for Common Variants

对携带SOD1变异的日本家族性ALS患者进行的最新基因分析揭示了常见变异的表型差异

Nishiyama, Ayumi; Niihori, Tetsuya; Suzuki, Naoki; Izumi, Rumiko; Akiyama, Tetsuya; Kato, Masaaki; Funayama, Ryo; Nakayama, Keiko; Warita, Hitoshi; Aoki, Yoko; Aoki, Masashi

Cracking the cryptic code in amyotrophic lateral sclerosis and frontotemporal dementia: Towards therapeutic targets and biomarkers

破解肌萎缩侧索硬化症和额颞叶痴呆的神秘密码:探索治疗靶点和生物标志物

Akiyama, Tetsuya; Koike, Yuka; Petrucelli, Leonard; Gitler, Aaron D

Reduced PHOX2B stability causes axonal growth impairment in motor neurons with TARDBP mutations

PHOX2B稳定性降低会导致TARDBP突变运动神经元的轴突生长受损。

Mitsuzawa, Shio; Suzuki, Naoki; Akiyama, Tetsuya; Ishikawa, Mitsuru; Sone, Takefumi; Kawada, Jiro; Funayama, Ryo; Shirota, Matsuyuki; Mitsuhashi, Hiroaki; Morimoto, Satoru; Ikeda, Kensuke; Shijo, Tomomi; Ohno, Akiyuki; Nakamura, Naoko; Ono, Hiroya; Ono, Risako; Osana, Shion; Nakagawa, Tadashi; Nishiyama, Ayumi; Izumi, Rumiko; Kaneda, Shohei; Ikeuchi, Yoshiho; Nakayama, Keiko; Fujii, Teruo; Warita, Hitoshi; Okano, Hideyuki; Aoki, Masashi

Omics Approach to Axonal Dysfunction of Motor Neurons in Amyotrophic Lateral Sclerosis (ALS)

肌萎缩侧索硬化症(ALS)运动神经元轴突功能障碍的组学研究

Suzuki, Naoki; Akiyama, Tetsuya; Warita, Hitoshi; Aoki, Masashi

Establishment of In Vitro FUS-Associated Familial Amyotrophic Lateral Sclerosis Model Using Human Induced Pluripotent Stem Cells.

利用人类诱导多能干细胞建立体外FUS相关家族性肌萎缩侧索硬化症模型

Ichiyanagi Naoki, Fujimori Koki, Yano Masato, Ishihara-Fujisaki Chikako, Sone Takefumi, Akiyama Tetsuya, Okada Yohei, Akamatsu Wado, Matsumoto Takuya, Ishikawa Mitsuru, Nishimoto Yoshinori, Ishihara Yasuharu, Sakuma Tetsushi, Yamamoto Takashi, Tsuiji Hitomi, Suzuki Naoki, Warita Hitoshi, Aoki Masashi, Okano Hideyuki