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浏览/检索结果: 共946条，第1-10条 帮助 条数/页： 5101520253035404550556065707580859095100 排序方式： 请选择题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序作者升序作者降序 Oxytocin inhibits the activity of acid-sensing ion channels through the vasopressin-1a receptor in primary sensory neurons1 期刊论文  OAI收割 出版物, 3111, 期号: 0, 页码: 1-34 作者:  Fang Qiu;  Chun-Yu Qiu;  Huilan Cai;  Ting-Ting Liu;  Zu-Wei Qu   |  收藏  |  浏览/下载：406/0  |  提交时间：2017/07/24 Oxytocin  Acid-sensing Ion Channel  Proton-gated Current  Vasopressin-1a Receptor  Dorsal Root Ganglion Neuron  Electrophysiology  Pain   Synthesis, photophysical properties and fluorescent application of novel [1,2,4]triazolo[1,5-a]pyrimidin-7(4H)-one derivatives 期刊论文  OAI收割 JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2025, 卷号: 464, 页码: 11 作者:  Gan, Suya;  Gao, Li-Xin;  Cao, Zitong;  Zhang, Chun;  Fu, Yiqiu   |  收藏  |  浏览/下载：76/0  |  提交时间：2025/04/01 [1  4]triazolo[1  5-a]pyrimidin-7(4H)-one  derivatives  Fluorescence properties  Fe 3+ions   Identification of CDKN1A as a potential key risk factor in MASLD progression 期刊论文  OAI收割 FASEB JOURNAL, 2025, 卷号: 39, 期号: 7, 页码: 15 作者:  Deng, Lijuan;  Deng, Jianxin;  Luo, Liping;  Yang, Hongjia;  Sun, Mengxue   |  收藏  |  浏览/下载：5/0  |  提交时间：2025/05/27 biomarkers  CDKN1A  liver  MASLD  RNA-seq   An efficient deep learning-based strategy to screen inhibitors for GluN1/GluN3A receptor 期刊论文  OAI收割 ACTA PHARMACOLOGICA SINICA, 2025, 页码: 9 作者:  Wang, Ze-chen;  Zeng, Yue;  Sun, Jin-yuan;  Chen, Xue-qin;  Wu, Hao-chen   |  收藏  |  浏览/下载：5/0  |  提交时间：2025/04/24 deep learning  scoring function  GluN1/GluN3A receptor  N-methyl-D-aspartate (NMDA) receptor  virtual screening  drug discovery   Activin A inhibits the migration of human lung adenocarcinoma A549 cells induced by EGF 期刊论文  OAI收割 INTERNATIONAL IMMUNOPHARMACOLOGY, 2024, 卷号: 142 作者:  Zhang, Fenglin;  Cui, Xueling;  Yang, Ke;  Guo, Rui;  Zhu, Linjing   |  收藏  |  浏览/下载：16/0  |  提交时间：2024/11/20 Lung adenocarcinoma  Cell migration  Activin A  EGF  ERK1/2 signaling  Microfluidic device   Targeting 5-Hydroxytryptamine Receptor 1A in the Portal Vein to Decrease Portal Hypertension 期刊论文  OAI收割 GASTROENTEROLOGY, 2024, 卷号: 167, 期号: 5, 页码: 993-1007 作者:  Zhu, Chang-Peng;  Liu, Shu-Qing;  Wang, Ke-Qi;  Xiong, Hai-Lin;  Aristu-Zabalza, Peio   |  收藏  |  浏览/下载：1/0  |  提交时间：2025/06/04 Portal Hypertension  Portal Vein Smooth Muscle Cells  5-Hydroxytryptamine  HTR1A  Alverine   Oroxylin A attenuates psoriasiform skin inflammation by direct targeting p62 (sequestosome 1) via suppressing M1 macrophage polarization 期刊论文  OAI收割 BRITISH JOURNAL OF PHARMACOLOGY, 2024, 页码: 23 作者:  Ma, Yuxiang;  Liu, Yunyao;  Zhong, You;  Li, Xiangzheng;  Xu, Yujiao   |  收藏  |  浏览/下载：33/0  |  提交时间：2024/10/21 autophagy  macrophage polarization  NF-kappa B  oroxylin A  sequestosome 1/p62   Discovery of pyridazinone derivatives bearing tetrahydroimidazo[1,2- a ] pyrazine scaffold as potent inhibitors of transient receptor potential canonical 5 to ameliorate hypertension-induced renal injury in rats 期刊论文  OAI收割 EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2024, 卷号: 275, 页码: 18 作者:  Xu, Yuanyuan;  Ren, Younan;  Zhang, Jie;  Niu, Bo;  Liu, Mengru   |  收藏  |  浏览/下载：14/0  |  提交时间：2024/08/22 Pyridazinone  Tetrahydroimidazo[1,2-a]pyrazine  Transient receptor potential canonical 5  Chronic kidney disease  Focal segmental glomerulosclerosis   Synthesis and biological evaluation of multimodal monoaminergic arylpiperazine derivatives with potential antidepressant profile 期刊论文  OAI收割 EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2024, 卷号: 275, 页码: 16 作者:  Zheng, Jiefang;  Zhou, Liping;  Gong, Xudong;  Yang, Feipu;  Cheng, Jiaxin   |  收藏  |  浏览/下载：15/0  |  提交时间：2024/08/22 Triple reuptake inhibitors  5-HT 1A R agonists  Antidepressants  Multimodal serotonergic compounds   INHBA promotes tumor growth and induces resistance to PD-L1 blockade by suppressing IFN-γ signaling 期刊论文  OAI收割 ACTA PHARMACOLOGICA SINICA, 2024, 页码: 14 作者:  Li, Fang-lin;  Gu, Long-hua;  Tong, Yong-liang;  Chen, Run-qiu;  Chen, Shi-yi   |  收藏  |  浏览/下载：24/0  |  提交时间：2024/10/21 cancer immunotherapy  INHBA  Activin A  IFN-gamma signaling pathway  PD-L1