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

Monoallelic mutations in MMD2 cause autosomal dominant aggressive periodontitis.

MMD2基因的单等位基因突变会导致常染色体显性遗传的侵袭性牙周炎

Iwata Tomoyuki, Mizoguchi Yoko, Yoshimoto Tetsuya, Tsumura Miyuki, Sakura Fumiaki, Johnson Jeffrey R, Matsuda Shinji, Ouhara Kazuhisa, Nagatani Yukiko, Asano Takaki, Ohnishi Hidenori, Kato Zenichiro, Mihara Keichiro, Kanegane Hirokazu, Ueda Tomoya, Sasaki Shinya, Taniguchi Yuri, Ninomiya Yurika, Ohno Yoshinori, Suzuki-Takedachi Kyoko, Sotomaru Yusuke, Sakuma Tetsushi, Yamamoto Takashi, Matsuda Yukiko, Kume Kodai, Sanui Terukazu, Nishimura Fusanori, Kajiya Mikihito, Ueki Yasuyoshi, Kurihara Hidemi, Morino Hiroyuki, Okada Satoshi, Kawakami Hideshi, Mizuno Noriyoshi

Genomic landscape of radiation-induced somatic mutations in a normal cell

正常细胞中辐射诱导体细胞突变的基因组图谱

Matsuda, Yukiko; Tanabe, Osamu

Meiotic deviations and endoreplication lead to diploid oocytes in female hybrids between bighead catfish (Clarias macrocephalus) and North African catfish (Clarias gariepinus)

减数分裂偏差和核内复制导致大头鲶鱼 (Clarias macrocephalus) 和北非鲶鱼 (Clarias gariepinus) 的雌性杂交鱼中出现二倍体卵母细胞

Dmitrij Dedukh #, Artem Lisachov #, Thitipong Panthum, Worapong Singchat, Yoichi Matsuda, Yukiko Imai, Karel Janko, Kornsorn Srikulnath

Clinical and Pathological Features of FTDP-17 with MAPT p.K298_H299insQ Mutation

MAPT p.K298_H299insQ 突变型 FTDP-17 的临床和病理特征

Morino, Hiroyuki; Kurashige, Takashi; Matsuda, Yukiko; Ono, Maiko; Sahara, Naruhiko; Miyasaka, Tomohiro; Soeda, Yoshiyuki; Shimada, Hitoshi; Yamazaki, Yu; Takahashi, Tetsuya; Izumi, Yuishin; Ito, Hidefumi; Maruyama, Hirofumi; Higuchi, Makoto; Arihiro, Koji; Suhara, Tetsuya; Takashima, Akihiko; Kawakami, Hideshi

Voltage-sensing phosphatase (Vsp) regulates endocytosis-dependent nutrient absorption in chordate enterocytes

电压感应磷酸酶(Vsp)调节脊索动物肠细胞内吞依赖性营养吸收

Adisorn Ratanayotha, Makoto Matsuda, Yukiko Kimura, Fumiko Takenaga, Tomoaki Mizuno, Md Israil Hossain, Shin-Ichi Higashijima, Takafumi Kawai, Michio Ogasawara, Yasushi Okamura

A Basic Study for Predicting Dysphagia in Panoramic X-ray Images Using Artificial Intelligence (AI)-Part 1: Determining Evaluation Factors and Cutoff Levels

利用人工智能(AI)预测全景X光片中吞咽困难的基础研究——第一部分:确定评估因素和临界值

Matsuda, Yukiko; Ito, Emi; Kuroda, Migiwa; Araki, Kazuyuki

Kv11 (ether-à-go-go-related gene) voltage-dependent K(+) channels promote resonance and oscillation of subthreshold membrane potentials

Kv11(醚-à-go-go相关基因)电压依赖性K(+)通道促进阈下膜电位的共振和振荡

Matsuoka, Toshinori; Yamasaki, Miwako; Abe, Manabu; Matsuda, Yukiko; Morino, Hiroyuki; Kawakami, Hideshi; Sakimura, Kenji; Watanabe, Masahiko; Hashimoto, Kouichi

Zonisamide can ameliorate the voltage-dependence alteration of the T-type calcium channel Ca(V)3.1 caused by a mutation responsible for spinocerebellar ataxia

唑尼沙胺可以改善由导致脊髓小脑性共济失调的突变引起的T型钙通道Ca(V)3.1的电压依赖性改变。

Hara, Naoyuki; Morino, Hiroyuki; Matsuda, Yukiko; Satoh, Kenichi; Hashimoto, Kouichi; Maruyama, Hirofumi; Kawakami, Hideshi

Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report

由纯合TWNK变异引起的中年起病型小脑共济失调:病例报告

Kume, Kodai; Morino, Hiroyuki; Miyamoto, Ryosuke; Matsuda, Yukiko; Ohsawa, Ryosuke; Kanaya, Yuhei; Tada, Yui; Kurashige, Takashi; Kawakami, Hideshi

A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia

低电压门控钙通道 CACNA1G 的突变会改变该通道的生理特性,导致脊髓小脑性共济失调。

Morino, Hiroyuki; Matsuda, Yukiko; Muguruma, Keiko; Miyamoto, Ryosuke; Ohsawa, Ryosuke; Ohtake, Toshiyuki; Otobe, Reiko; Watanabe, Masahiko; Maruyama, Hirofumi; Hashimoto, Kouichi; Kawakami, Hideshi