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

Pharmacological inhibition of histamine N-methyltransferase extends wakefulness and suppresses cataplexy in a mouse model of narcolepsy

在嗜睡症小鼠模型中,组胺N-甲基转移酶的药理学抑制可延长清醒时间并抑制猝倒。

Naganuma, Fumito; Girgin, Birkan; Agu, Anne Bernadette S; Hirano, Kyosuke; Nakamura, Tadaho; Yanai, Kazuhiko; Vetrivelan, Ramalingam; Mochizuki, Takatoshi; Yanagisawa, Masashi; Yoshikawa, Takeo

Regulation of wakefulness by neurotensin neurons in the lateral hypothalamus.

下丘脑外侧区神经降压素神经元对觉醒的调节

Naganuma Fumito, Khanday Mudasir, Bandaru Sathyajit Sai, Hasan Whidul, Hirano Kyosuke, Yoshikawa Takeo, Vetrivelan Ramalingam

Gene Expression Profiling in the Cortex of Fabp4 Knockout Mice

Fabp4基因敲除小鼠皮层基因表达谱分析

Kirikae, Hinako; He, Xiaofeng; Ohnishi, Tetsuo; Miyazaki, Hirofumi; Yoshikawa, Takeo; Owada, Yuji; Maekawa, Motoko

Genetic and functional analyses of SPTLC1 in juvenile amyotrophic lateral sclerosis

青少年肌萎缩侧索硬化症中SPTLC1的遗传和功能分析

Okubo, So; Naruse, Hiroya; Ishiura, Hiroyuki; Sudo, Atsushi; Esaki, Kayoko; Mitsui, Jun; Matsukawa, Takashi; Satake, Wataru; Greimel, Peter; Shingai, Nanoka; Oya, Yasushi; Yoshikawa, Takeo; Tsuji, Shoji; Toda, Tatsushi

SPTLC2 variants are associated with early-onset ALS and FTD due to aberrant sphingolipid synthesis

SPTLC2 变异体与早发性肌萎缩侧索硬化症 (ALS) 和额颞叶痴呆 (FTD) 相关,这是由于鞘脂合成异常所致。

Naruse, Hiroya; Ishiura, Hiroyuki; Esaki, Kayoko; Mitsui, Jun; Satake, Wataru; Greimel, Peter; Shingai, Nanoka; Machino, Yuka; Kokubo, Yasumasa; Hamaguchi, Hirotoshi; Oda, Tetsuya; Ikkaku, Tomoko; Yokota, Ichiro; Takahashi, Yuji; Suzuki, Yuta; Matsukawa, Takashi; Goto, Jun; Koh, Kishin; Takiyama, Yoshihisa; Morishita, Shinichi; Yoshikawa, Takeo; Tsuji, Shoji; Toda, Tatsushi

De Novo Variants Found in Three Distinct Schizophrenia Populations Hit a Common Core Gene Network Related to Microtubule and Actin Cytoskeleton Gene Ontology Classes

在三个不同的精神分裂症人群中发现的新生变异体,均与微管和肌动蛋白细胞骨架基因本体论类别相关的共同核心基因网络有关。

Loe-Mie, Yann; Plançon, Christine; Dubertret, Caroline; Yoshikawa, Takeo; Yalcin, Binnaz; Collins, Stephan C; Boland, Anne; Deleuze, Jean-François; Gorwood, Philip; Benmessaoud, Dalila; Simonneau, Michel; Lepagnol-Bestel, Aude-Marie

Impairment of serine transport across the blood-brain barrier by deletion of Slc38a5 causes developmental delay and motor dysfunction

Slc38a5基因缺失导致血脑屏障丝氨酸转运受损,进而引起发育迟缓和运动功能障碍。

Radzishevsky, Inna; Odeh, Maali; Bodner, Oded; Zubedat, Salman; Shaulov, Lihi; Litvak, Maxim; Esaki, Kayoko; Yoshikawa, Takeo; Agranovich, Bella; Li, Wen-Hong; Radzishevsky, Alex; Gottlieb, Eyal; Avital, Avi; Wolosker, Herman

Antitumor Activity of an Anti-EGFR/HER2 Bispecific Antibody in a Mouse Xenograft Model of Canine Osteosarcoma

抗EGFR/HER2双特异性抗体在犬骨肉瘤小鼠异种移植模型中的抗肿瘤活性

Tateyama, Nami; Suzuki, Hiroyuki; Ohishi, Tomokazu; Asano, Teizo; Tanaka, Tomohiro; Mizuno, Takuya; Yoshikawa, Takeo; Kawada, Manabu; Kaneko, Mika K; Kato, Yukinari

Epitope Mapping of Anti-Mouse CCR3 Monoclonal Antibodies Using Flow Cytometry

利用流式细胞术对小鼠CCR3单克隆抗体进行表位定位

Tateyama, Nami; Asano, Teizo; Suzuki, Hiroyuki; Li, Guanjie; Yoshikawa, Takeo; Tanaka, Tomohiro; Kaneko, Mika K; Kato, Yukinari

Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia

非典型钙黏蛋白基因 CDH23 在前脉冲抑制中的作用及其与精神分裂症的关系

Balan, Shabeesh; Ohnishi, Tetsuo; Watanabe, Akiko; Ohba, Hisako; Iwayama, Yoshimi; Toyoshima, Manabu; Hara, Tomonori; Hisano, Yasuko; Miyasaka, Yuki; Toyota, Tomoko; Shimamoto-Mitsuyama, Chie; Maekawa, Motoko; Numata, Shusuke; Ohmori, Tetsuro; Shimogori, Tomomi; Kikkawa, Yoshiaki; Hayashi, Takeshi; Yoshikawa, Takeo