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

Dual regulation of mitochondrial fusion by Parkin-PINK1 and OMA1.

Parkin-PINK1 和 OMA1 对线粒体融合的双重调控

Yamada Tatsuya, Ikeda Arisa, Murata Daisuke, Wang Hu, Zhang Cissy, Khare Pratik, Adachi Yoshihiro, Ito Fumiya, Quirós Pedro M, Blackshaw Seth, López-Otín Carlos, Langer Thomas, Chan David C, Le Anne, Dawson Valina L, Dawson Ted M, Iijima Miho, Sesaki Hiromi

Impact of atopic dermatitis on renal dysfunction: insights from patient data and animal models.

特应性皮炎对肾功能障碍的影响:来自患者数据和动物模型的启示

Ikeda Arisa, Peng Ge, Zhao Wanchen, Abudouwanli Alafate, Ikeda Shigaku, Niyonsaba François, Suzuki Yusuke

AMP-IBP5: A Multifunctional Antimicrobial Peptide for Advanced Wound Healing and Inflammatory Skin Disorders

AMP-IBP5:一种用于高级伤口愈合和炎症性皮肤疾病的多功能抗菌肽

Abudouwanli, Alafate; Peng, Ge; Yang, Mengyao; Zhao, Wanchen; Sun, Quan; Wang, Shan; Tan, Yi; Ikeda, Arisa; Ogawa, Hideoki; Okumura, Ko; Niyonsaba, François

Conditional diffusion model for inverse prediction of process parameters and dendritic microstructures from mechanical properties

基于力学性能的工艺参数和树枝状微观结构反向预测的条件扩散模型

Ikeda, Arisa; Higuchi, Ryo; Yokozeki, Tomohiro; Endo, Katsuhiro; Kojima, Yuta; Suzuki, Misato; Muramatsu, Mayu

A Case of Atypical Hemolytic Uremic Syndrome With a Complement Factor I Mutation Triggered by a Femoral Neck Fracture

一例由股骨颈骨折诱发的补体因子 I 突变引起的非典型溶血性尿毒综合征

Kano, Toshiki; Io, Hiroaki; Sasaki, Yu; Muto, Masahiro; Muto, Sayaka; Ogiwara, Kei; Ikeda, Arisa; Iwasaki, Hiroyuki; Suzuki, Yusuke

A nucleotide diphosphate kinase mediates tethering between mitochondria prior to fusion

核苷二磷酸激酶介导线粒体融合前的系链连接。

Ikeda, Arisa; Iijima, Miho; Sesaki, Hiromi

Correction: Atypical histological abnormalities in an adult patient with nephronophthisis harboring NPHP1 deletion: a case report

更正:一例伴有NPHP1基因缺失的成人肾痨患者的非典型组织学异常:病例报告

Akira, Maiko; Suzuki, Hitoshi; Ikeda, Arisa; Iwasaki, Masako; Honda, Daisuke; Takahara, Hisatsugu; Rinno, Hisaki; Tomita, Shigeki; Suzuki, Yusuke

Atypical histological abnormalities in an adult patient with nephronophthisis harboring NPHP1 deletion: a case report

一例伴有NPHP1基因缺失的肾痨成人患者的非典型组织学异常:病例报告

Akira, Maiko; Suzuki, Hitoshi; Ikeda, Arisa; Iwasaki, Masako; Honda, Daisuke; Takahara, Hisatsugu; Rinno, Hisaki; Tomita, Shigeki; Suzuki, Yusuke

High-fidelity endonuclease variant HypaCas9 facilitates accurate allele-specific gene modification in mouse zygotes

高保真核酸内切酶变体HypaCas9可促进小鼠合子中精确的等位基因特异性基因修饰

Ikeda, Arisa; Fujii, Wataru; Sugiura, Koji; Naito, Kunihiko

Generation of genetically modified mice using SpCas9-NG engineered nuclease.

利用SpCas9-NG工程核酸酶生成转基因小鼠

Fujii Wataru, Ito Haruka, Kanke Takuya, Ikeda Arisa, Sugiura Koji, Naito Kunihiko