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

Third Liver Resection for Re-recurrent Hepatocellular Carcinoma: Assessment of the Prognostic Factors of Long-term Survival

第三次肝切除术治疗复发性肝细胞癌:长期生存预后因素评估

Kori, Mayuko; Shimada, Kei; Hashimoto, Takuya

Endogenous aldehyde-induced DNA-protein crosslinks are resolved by transcription-coupled repair

内源性醛诱导的DNA-蛋白质交联通过转录偶联修复解决

Yasuyoshi Oka, Yuka Nakazawa, Mayuko Shimada, Tomoo Ogi

ALS-linked mutant TDP-43 in oligodendrocytes induces oligodendrocyte damage and exacerbates motor dysfunction in mice

少突胶质细胞中的 ALS 相关突变 TDP-43 会诱发少突胶质细胞损伤并加剧小鼠的运动功能障碍

Mai Horiuchi #, Seiji Watanabe #, Okiru Komine, Eiki Takahashi, Kumi Kaneko, Shigeyoshi Itohara, Mayuko Shimada, Tomoo Ogi, Koji Yamanaka2

Genetic background variation impacts microglial heterogeneity and disease progression in amyotrophic lateral sclerosis model mice

遗传背景变异影响肌萎缩侧索硬化症模型小鼠的小胶质细胞异质性和疾病进展。

Okiru Komine,Syuhei Ohnuma,Kunihiko Hinohara,Yuichiro Hara,Mayuko Shimada,Tomohiro Akashi,Seiji Watanabe,Akira Sobue,Noe Kawade,Tomoo Ogi,Koji Yamanaka

Inducing multiple nicks promotes interhomolog homologous recombination to correct heterozygous mutations in somatic cells

诱导多个缺口促进同源重组以纠正体细胞中的杂合突变

Akiko Tomita, Hiroyuki Sasanuma, Tomoo Owa, Yuka Nakazawa, Mayuko Shimada, Takahiro Fukuoka, Tomoo Ogi, Shinichiro Nakada

Aicardi-Goutières syndrome with SAMHD1 deficiency can be diagnosed by unscheduled DNA synthesis test

患有 SAMHD1 缺乏症的 Aicardi-Goutières 综合征可通过非常规 DNA 合成测试进行诊断

Chikako Senju, Yuka Nakazawa, Mayuko Shimada, Dai Iwata, Michiko Matsuse, Katsumi Tanaka, Yasushi Miyazaki, Shinichi Moriwaki, Norisato Mitsutake, Tomoo Ogi

Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled Repair

DNA损伤停滞的RNAPII泛素化促进转录偶联修复

Yuka Nakazawa, Yuichiro Hara, Yasuyoshi Oka, Okiru Komine, Diana van den Heuvel, Chaowan Guo, Yasukazu Daigaku, Mayu Isono, Yuxi He, Mayuko Shimada, Kana Kato, Nan Jia, Satoru Hashimoto, Yuko Kotani, Yuka Miyoshi, Miyako Tanaka, Akira Sobue, Norisato Mitsutake, Takayoshi Suganami, Akio Masuda, Kinji

Digenic mutations in ALDH2 and ADH5 impair formaldehyde clearance and cause a multisystem disorder, AMeD syndrome

ALDH2 和 ADH5 的双基因突变会损害甲醛清除,并导致一种多系统疾病——AMeD 综合征。

Yasuyoshi Oka ,Motoharu Hamada ,Yuka Nakazawa ,Hideki Muramatsu ,Yusuke Okuno ,Koichiro Higasa ,Mayuko Shimada ,Honoka Takeshima ,Katsuhiro Hanada ,Taichi Hirano ,Toshiro Kawakita ,Hirotoshi Sakaguchi ,Takuya Ichimura ,Shuichi Ozono ,Kotaro Yuge ,Yoriko Watanabe ,Yuko Kotani ,Mutsumi Yamane ,Yumiko Kasugai ,Miyako Tanaka ,Takayoshi Suganami ,Shinichiro Nakada ,Norisato Mitsutake ,Yuichiro Hara ,Kohji Kato ,Seiji Mizuno ,Noriko Miyake ,Yosuke Kawai ,Katsushi Tokunaga ,Masao Nagasaki ,Seiji Kito ,Keiichi Isoyama ,Masafumi Onodera ,Hideo Kaneko ,Naomichi Matsumoto ,Fumihiko Matsuda ,Keitaro Matsuo ,Yoshiyuki Takahashi ,Tomoji Mashimo ,Seiji Kojima ,Tomoo Ogi

XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency

人类受试者的 XRCC4 缺陷会导致明显的神经系统表型,但不会导致明显的免疫缺陷

Chaowan Guo, Yuka Nakazawa, Lisa Woodbine, Andrea Björkman, Mayuko Shimada, Heather Fawcett, Nan Jia, Kaname Ohyama, Tao-Sheng Li, Yuji Nagayama, Norisato Mitsutake, Qiang Pan-Hammarström, Andrew R Gennery, Alan R Lehmann, Penny A Jeggo, Tomoo Ogi

PRKDC mutations in a SCID patient with profound neurological abnormalities

患有严重神经系统异常的重症联合免疫缺陷症患者的PRKDC基因突变

Lisa Woodbine,Jessica A Neal, Nanda-Kumar Sasi, Mayuko Shimada, Karen Deem, Helen Coleman, William B Dobyns, Tomoo Ogi, Katheryn Meek, E Graham Davies, Penny A Jeggo