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

Hyaloklossia Labbé, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites.

蛙类中的 Hyaloklossia Labbé, 1896 (Alveolata: Apicomplexa):对一种新物种的描述,并提出一个新的亚科来容纳这些神秘的寄生虫

Tokiwa Toshihiro, Chou Shyun, Tochigi Yuki, Katayama Kentaro, Duszynski Donald W

Cellular Expression and Subcellular Localization of Wwox Protein During Testicular Development and Spermatogenesis in Rats

大鼠睾丸发育和精子发生过程中Wwox蛋白的细胞表达和亚细胞定位

Mahmud, Md Abdullah Al; Noguchi, Maki; Domon, Ayaka; Tochigi, Yuki; Katayama, Kentaro; Suzuki, Hiroetsu

Characterization of Novel Nonobese Type 2 Diabetes Rat Model with Enlarged Kidneys

新型非肥胖型2型糖尿病大鼠肾脏增大模型的特征分析

Domon, Ayaka; Katayama, Kentaro; Tochigi, Yuki; Suzuki, Hiroetsu

Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon

利用 piggyBac 转座子生成非病毒、无转基因的类肝细胞

Hokahiro Katayama, Kentaro Yasuchika, Yuya Miyauchi, Hidenobu Kojima, Ryoya Yamaoka, Takayuki Kawai, Elena Yukie Yoshitoshi, Satoshi Ogiso, Sadahiko Kita, Katsutaro Yasuda, Naoya Sasaki, Ken Fukumitsu, Junji Komori, Takamichi Ishii, Shinji Uemoto

Characterization of the skeletal fusion with sterility (sks) mouse showing axial skeleton abnormalities caused by defects of embryonic skeletal development

对骨骼融合伴不育(sks)小鼠进行表征,该小鼠表现出由胚胎骨骼发育缺陷引起的轴骨骼异常。

Akiyama, Kouyou; Katayama, Kentaro; Tsuji, Takehito; Kunieda, Tetsuo

A mutation in the nuclear pore complex gene Tmem48 causes gametogenesis defects in skeletal fusions with sterility (sks) mice

核孔复合体基因Tmem48的突变会导致骨骼融合不育(sks)小鼠的配子发生缺陷。

Akiyama, Kouyou; Noguchi, Junko; Hirose, Michiko; Kajita, Shimpei; Katayama, Kentaro; Khalaj, Maryam; Tsuji, Takehito; Fairfield, Heather; Byers, Candice; Reinholdt, Laura; Ogura, Atsuo; Kunieda, Tetsuo

A novel feedback mechanism by Ephrin-B1/B2 in T-cell activation involves a concentration-dependent switch from costimulation to inhibition

Ephrin-B1/B2 在 T 细胞活化过程中的一种新反馈机制涉及从共刺激到抑制的浓度依赖性转变

Hiroki Kawano, Yoshio Katayama, Kentaro Minagawa, Manabu Shimoyama, Mark Henkemeyer, Toshimitsu Matsui

Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalities

对小鼠 Koa 突变相关的染色体倒位进行表征,揭示了骨骼异常的原因。

Katayama, Kentaro; Miyamoto, Sayaka; Furuno, Aki; Akiyama, Kouyou; Takahashi, Sakino; Suzuki, Hiroetsu; Tsuji, Takehito; Kunieda, Tetsuo

Renal Modulation: The Renin-Angiotensin-Aldosterone System (RAAS)

肾脏调节:肾素-血管紧张素-醛固酮系统(RAAS)

Domon, Ayaka; Katayama, Kentaro; Yamada, Takashi; Tochigi, Yuki; Suzuki, Hiroetsu; Natarajan, Aruna; Jose, Pedro A