GPCRS

作品数:70被引量:111H指数:6
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相关领域:医药卫生生物学更多>>
相关作者:陈京金艳燕黄思罗白波徐志卿更多>>
相关机构:济宁医学院华中科技大学南京邮电大学首都医科大学更多>>
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相关基金:国家自然科学基金中国博士后科学基金国家重点基础研究发展计划湖南省自然科学基金更多>>
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Systematical identification of regulatory GPCRs by single-cell trajectory inference reveals the role of ADGRD1 and GPR39 in adipogenesis
《Science China(Life Sciences)》2025年第4期1057-1072,共16页Chuan Ye Xuemei Wang Jun Lin Chenyang Wu Yuhua Gao Chenghao Guo Yunxi Liao Ziyan Rao Shaodong Huang Weixuan Chen Ying Huang Jinpeng Sun Dongyu Zhao Changtao Jiang 
supported by the National Natural Science Foundation of China(32270603,31925021,82130022,92357305,82341226,32271232);the National Key Research and Development Program of China(2021YFF1201100,2018YFA0800701);the Fundamental Research Funds for the Central Universities(BMU2021YJ057)。
Adipogenesis is the healthy expansion of white adipose tissue(WAT),serving as a compensatory response to maintain metabolic homeostasis in the presence of excess energy in the body.Therefore,the identification of nove...
关键词:ADIPOGENESIS GPCRS trajectory inference 
Molecular and cellular mechanisms of itch sensation and the anti-itch drug targets被引量:1
《Acta Pharmacologica Sinica》2025年第3期539-553,共15页Meng Sun Zhen-ru Chen Hui-juan Ding Jing Feng 
supported by grants from the National Natural Science Foundation of China(grant no.82171214 and 32241003);the Shanghai Municipal Natural Science Foundation(grant no.23ZR1474500);the State Key Laboratory of Chemical Biology,Shanghai Institute of Materia Medica,Chinese Academy of Sciences.
Itch is an uncomfortable feeling that evokes a desire to scratch.This protective reflex can effectively eliminate parasites that invade the skin.When itchy skin becomes severe or lasts for more than six weeks,it has d...
关键词:ITCH GPCRS Mrgprs TRP channels CYTOKINES NEUROIMMUNE 
GPR34 senses demyelination to promote neuroinflammation and pathologies被引量:1
《Cellular & Molecular Immunology》2024年第10期1131-1144,共14页Bolong Lin Yubo Zhou Zonghui Huang Ming Ma Minghui Qi Zhongjun Jiang Guoyang Li Yueli Xu Jiaxian Yan Di Wang Xiaqiong Wang Wei Jiang Rongbin Zhou 
supported by the National Key Research and Development Program of China(grant number 2020YFA0509101);the National Natural Science Foundation of China(grant numbers 81821001,82130107,U20A20359);the CAS Project for Young Scientists in Basic Research(YSBR-074).
Sterile neuroinflammation is a major driver of multiple neurological diseases.Myelin debris can act as an inflammatory stimulus to promote inflammation and pathologies,but the mechanism is poorly understood.Here,we sh...
关键词:NEUROINFLAMMATION GPCRS MICROGLIA 
趋化素受体的研究进展
《生物化工》2024年第4期194-200,共7页常晓华 汤语萱 罗天煜 吴蓓丽 何茂洲 
浙江省自然科学基金(LQ24C050004)。
趋化素受体是G蛋白偶联受体(G Protein-Coupled Receptors,GPCRs)家族的重要成员,广泛分布于人体各组织器官中,参与炎症反应、血管生成、脂质和葡萄糖代谢等多种生理过程,与炎症性疾病、癌症、代谢综合征等多种疾病的发生发展密切相关...
关键词:G蛋白偶联受体(GPCRs) 趋化素 趋化素受体 药物研发 
GPCRs involved in metabolic diseases:pharmacotherapeutic development updates被引量:1
《Acta Pharmacologica Sinica》2024年第7期1321-1336,共16页Cheng Jin Hui Chen Li Xie Yuan Zhou Li-li Liu Jian Wu 
supported partially by the National Natural Science Foundation of China (NSFC#82370625,82170624,81871997,81572356);the National Key R&D Program of China (#2016YFE0107400)to J.W.
G protein-coupled receptors(GPCRs)are expressed in a variety of cell types and tissues,and activation of GPCRs is involved in enormous metabolic pathways,including nutrient synthesis,transportation,storage or insulin ...
关键词:G protein-coupled receptor ANTAGONIST AGONIST diabetes metabolic syndrome nonalcoholic steatohepatitis 
红芪多糖经SCFAs-GPCRs改善脾气虚型DGP大鼠小肠动力的机制研究
《中华中医药杂志》2024年第7期3436-3441,共6页魏昭晖 李荣科 张磊 刘苗 万生芳 
国家自然科学基金项目(No.82060914);中医学一流学科“岐黄英才”导师专项基金;甘肃省优秀博士生项目(No.23JRRA1225);甘肃中医药大学研究生创新项目(No.2022-07)。
目的:观察红芪多糖(HPS)对脾气虚型糖尿病胃轻瘫(DGP)大鼠短链脂肪酸(SCFAs)-G蛋白偶联受体(GPCRs)的影响,探讨HPS改善脾气虚型DGP大鼠小肠动力的可能机制。方法:72只SPF级Wistar雄性大鼠随机分为空白组(10只)和造模组(62只),造模组采...
关键词:糖尿病胃轻瘫 红芪多糖 G蛋白偶联受体 短链脂肪酸 肠动力 机制 动物模型 
Exploring structure-based drug discovery of GPCRs beyond the orthosteric binding site
《hLife》2024年第5期211-226,共16页Zhao Chen Xintong Ren Yu Zhou Niu Huang 
This work is supported by Beijing Municipal Science&Technology Commission(Z201100005320012 to N.H.)and Tsinghua University.
G-protein coupled receptors(GPCRs)are the largest family of druggable targets.In recent years,GPCR structural biology has made great advances,revealing the three-dimensional structures of many GPCRs and their interact...
关键词:G-protein coupled receptor(GPCR) allosteric pocket structure-based virtual screening(SBVS) negative allosteric modulator(NAM) positive allosteric modulator(PAM) artificial intelligence(AI) 
G protein-coupled receptors(GPCRs):advances in structures,mechanisms,and drug discovery被引量:1
《Signal Transduction and Targeted Therapy》2024年第5期1938-1980,共43页Mingyang Zhang Ting Chen Xun Lu Xiaobing Lan Ziqiang Chen Shaoyong Lu 
This study was supported by grants from the National Key R&D Program of the Ministry of Science and Technology(No.2023YFC3404700);the National Natural Science Foundation of China(No.22077082);the Shanghai Frontiers Science Center of Cellular Homeostasis and the Human Diseases,and the Innovative Research Team of High-Level Local Universities in Shanghai.
G protein-coupled receptors(GPCRs),the largest family of human membrane proteins and an important class of drug targets,play a role in maintaining numerous physiological processes.Agonist or antagonist,orthosteric eff...
关键词:STERIC DESIGNING MECHANISMS 
GPCRs andβ-arrestins—an on-off relationship
《Cell Research》2023年第11期819-820,共2页Alex R.B.Thomsen 
Traditionally,G protein-coupled receptor(GPCR)-mediated G protein signaling has been thought to be terminated by receptor phosphorylation followed by recruitment ofβ-arrestins,which uncouples G protein from the recep...
关键词:al. terminated INSIGHT 
A promising small molecule binding pocket in class B GPCRs: expanding potential for drug development被引量:1
《Signal Transduction and Targeted Therapy》2023年第9期3888-3889,共2页Huan Xiao Qian Sun Qiu Sun 
This work was supported by Natural Science Foundation of Sichuan Province(Grants 2023NSFSC1839,2023NSFSC1154).
Recently,Xu et al.1 have published in Nature,solved the high-resolution structure of a small molecule agonist PCO371 and Gs bound human parathyroid hormone receptor 1(PTH1R)by cryo-electron microscopy.This study revea...
关键词:EXPANDING INSIGHT CLASS 
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