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

Discovery of MK-8768, a Potent and Selective mGluR2 Negative Allosteric Modulator

发现MK-8768,一种强效且选择性的mGluR2负变构调节剂

Rudd, Michael T; Manley, Peter J; Hanney, Barbara; Meng, Zhaoyang; Shu, Youheng; de Leon, Pablo; Frie, Jessica L; Han, Yongxin; Wai, Jenny Miu-Chun; Yang, Zhi-Qiang; Perkins, James J; Hurzy, Danielle M; Manikowski, Jesse J; Zhu, Hong; Bungard, Christopher J; Converso, Antonella; Meissner, Robert S; Cosden, Mali L; Hayashi, Ikuo; Ma, Lei; O'Brien, Julie; Uebele, Victor N; Schachter, Joel B; Bhandari, Neetesh; Ward, Gwendolyn J; Fillgrove, Kerry L; Lu, Bing; Liang, Yuexia; Dubost, David C; Puri, Vanita; Eddins, Donnie M; Vardigan, Joshua D; Drolet, Robert E; Kern, Jonathan T; Uslaner, Jason M

Familial Gastrointestinal Stromal Tumor Associated with Zebra-like Pigmentation

与斑马样色素沉着相关的家族性胃肠道间质瘤

Takuma Hayashi, Ikuo Konishi

Anti-pruritic effect of isothiocyanates: Potential involvement of toll-like receptor 3 signaling

异硫氰酸酯的止痒作用:可能与 Toll 样受体 3 信号通路有关

Moriyama, Masaki; Konno, Mitsuhiro; Serizawa, Kanako; Yuzawa, Natsumi; Majima, Yuki; Hayashi, Ikuo; Suzuki, Tomohiko; Kainoh, Mie

Exploratory clinical characterization of experimentally-induced ulcerative colitis nonhuman primates

对实验诱导的非人灵长类动物溃疡性结肠炎进行探索性临床特征分析

Takahashi, Nobuyuki; Kitazawa, Chinatsu; Itani, Yoshitaka; Awaga, Yuji; Hama, Aldric; Hayashi, Ikuo; Takamatsu, Hiroyuki

Gaps in Understanding Mechanism and Lack of Treatments: Potential Use of a Nonhuman Primate Model of Oxaliplatin-Induced Neuropathic Pain

对机制理解的不足和治疗手段的缺乏:非人灵长类动物模型在奥沙利铂诱导神经性疼痛研究中的潜在应用

Hama, Aldric; Natsume, Takahiro; Ogawa, Shin'ya; Higo, Noriyuki; Hayashi, Ikuo; Takamatsu, Hiroyuki

Gain-of-function enhancement of IP3 receptor modal gating by familial Alzheimer's disease-linked presenilin mutants in human cells and mouse neurons

家族性阿尔茨海默病相关早老素突变体在人类细胞和小鼠神经元中增强IP3受体模式门控的功能

Cheung, King-Ho; Mei, Lijuan; Mak, Don-On Daniel; Hayashi, Ikuo; Iwatsubo, Takeshi; Kang, David E; Foskett, J Kevin

Single chain variable fragment against nicastrin inhibits the gamma-secretase activity.

针对尼卡斯特林的单链可变片段可抑制γ-分泌酶活性

Hayashi Ikuo, Takatori Sho, Urano Yasuomi, Iwanari Hiroko, Isoo Noriko, Osawa Satoko, Fukuda Maiko A, Kodama Tatsuhiko, Hamakubo Takao, Li Tong, Wong Philip C, Tomita Taisuke, Iwatsubo Takeshi