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

MITOL deletion in the brain impairs mitochondrial structure and ER tethering leading to oxidative stress

脑内MITOL基因缺失会损害线粒体结构和内质网连接,从而导致氧化应激。

Nagashima, Shun; Takeda, Keisuke; Ohno, Nobuhiko; Ishido, Satoshi; Aoki, Motohide; Saitoh, Yurika; Takada, Takumi; Tokuyama, Takeshi; Sugiura, Ayumu; Fukuda, Toshifumi; Matsushita, Nobuko; Inatome, Ryoko; Yanagi, Shigeru

CAMDI interacts with the human memory-associated protein KIBRA and regulates AMPAR cell surface expression and cognition

CAMDI 与人类记忆相关蛋白 KIBRA 相互作用,并调节 AMPAR 细胞表面表达和认知功能。

Fukuda, Toshifumi; Nagashima, Shun; Inatome, Ryoko; Yanagi, Shigeru

Psychiatric behaviors associated with cytoskeletal defects in radial neuronal migration

与放射状神经元迁移中细胞骨架缺陷相关的精神行为

Fukuda, Toshifumi; Yanagi, Shigeru

Rescue of CAMDI deletion-induced delayed radial migration and psychiatric behaviors by HDAC6 inhibitor

HDAC6抑制剂可挽救CAMDI缺失引起的延迟放射状迁移和精神行为。

Fukuda, Toshifumi; Nagashima, Shun; Abe, Takaya; Kiyonari, Hiroshi; Inatome, Ryoko; Yanagi, Shigeru

CAMDI, a novel disrupted in schizophrenia 1 (DISC1)-binding protein, is required for radial migration.

CAMDI 是一种新型的精神分裂症紊乱 1 (DISC1) 结合蛋白,是放射状迁移所必需的

Fukuda Toshifumi, Sugita Satoko, Inatome Ryoko, Yanagi Shigeru

Protocadherin-alpha family is required for serotonergic projections to appropriately innervate target brain areas

原钙粘蛋白-α家族是血清素投射适当地支配目标大脑区域所必需的

Shota Katori, Shun Hamada, Yukiko Noguchi, Emi Fukuda, Toshifumi Yamamoto, Hideko Yamamoto, Sonoko Hasegawa, Takeshi Yagi

Mitochondrial ubiquitin ligase MITOL ubiquitinates mutant SOD1 and attenuates mutant SOD1-induced reactive oxygen species generation

线粒体泛素连接酶MITOL泛素化突变型SOD1,并减弱突变型SOD1诱导的活性氧生成。

Yonashiro, Ryo; Sugiura, Ayumu; Miyachi, Misako; Fukuda, Toshifumi; Matsushita, Nobuko; Inatome, Ryoko; Ogata, Yoshinobu; Suzuki, Takehiro; Dohmae, Naoshi; Yanagi, Shigeru

A novel mitochondrial ubiquitin ligase plays a critical role in mitochondrial dynamics

一种新型线粒体泛素连接酶在线粒体动力学中发挥关键作用

Yonashiro, Ryo; Ishido, Satoshi; Kyo, Shinkou; Fukuda, Toshifumi; Goto, Eiji; Matsuki, Yohei; Ohmura-Hoshino, Mari; Sada, Kiyonao; Hotta, Hak; Yamamura, Hirohei; Inatome, Ryoko; Yanagi, Shigeru

A targeting mutation of tyrosine 1062 in Ret causes a marked decrease of enteric neurons and renal hypoplasia

靶向突变Ret蛋白中的酪氨酸1062会导致肠神经元显著减少和肾发育不全。

Jijiwa, Mayumi; Fukuda, Toshifumi; Kawai, Kumi; Nakamura, Akari; Kurokawa, Kei; Murakumo, Yoshiki; Ichihara, Masatoshi; Takahashi, Masahide