于晓山东大学主页平台管理系统--中文主页

登录　 山东大学　 English　

于晓

赞

教授

性别：女

在职信息：在职

所在单位：基础医学院

入职时间：2009-11-10

学术荣誉：

访问量：

最后更新时间：..

当前位置中文主页 >> 科学研究 >> 论文成果

[101] 沈月毛 , 于晓 , 张鹏举 , 肖鹏 and 孙金鹏. Crystal structure and catalytic activity of the PPM1K N94K mutant.. Journal of Neurochemistry, 148, 550, 2019.
[102] 孙金鹏 , 王晓杰 , 王姿颖 , 张艳 , 于晓 and 易凡. β-Arrestins promote podocyte injury by inhibition of autophagy in diabetic nephropathy.. Cell death and disease., 2016 Apr 7;7:e2183., e2183, 2016.
[103] 任桂杰 , 方浩 , 肖鹏 , 于晓 and 孙金鹏. Identification of a benzo imidazole thiazole derivative as the specific irreversible inhibitor of pr. Bioorg Med Chem Lett., 2016 Oct 1;26(19):4795-8., 4795, 2016.
[104] 徐志刚 , 于晓 and 孙金鹏. Constitutive Gαi coupling activity of very large G protein-coupled receptor 1 (VLGR1) and its regul. J Biol Chem, 289, 24215, 2014.
[105] 杜吕佩 , 李敏勇 , 于晓 , 徐志刚 and 孙金鹏. FFA4 receptor (GPR120): A hot target for the development of anti-diabetic therapies.. Eur J Pharmacol., 763, 160, 2015.
[106] 杨帆 , 肖鹏 , 于晓 , 孙金鹏 and 杨照. Phosphorylation of G Protein-Coupled Receptors: From the Barcode Hypothesis to the Flute Model. Molecular Pharmacology, 92, 201, 2017.
[107] 王姿颖 , 魏欣冰 , 于晓 , 包婵婵 , 张艳 and 易凡. Novel Role of NOD2 in Mediating Ca2+ Signaling: Evidence from NOD2-regulated Podocyte TRPC6 Channels. Hypertension, 62, 506, 2013.
[108] 刘克敬 , 李景新 , 于晓 , 马雪莲 , 崔爽 and 刘传勇. Oxytocin-induced membrane hyperpolarization in pain-sensitive dorsal root ganglia neurons mediated b. neuroscience, 2015.
[109] 于晓 , 徐志刚 and 孙金鹏. The Role of G Protein-coupled Receptors in Cochlear Planar Cell Polarity.. Int J Biochem Cell Biol., 77, 220, 2016.
[110] 崔福爱 , 于晓 , 毕文祥 , 孙金鹏 and 肖鹏. The second-sphere residue T263 is important for the function and catalytic activity of PTP1B via int. The International Journal of Biochemistry& Cell Biology, 57, 84, 2014.
[111] 方浩 , 于晓 and 孙金鹏. Cadmium is a potent inhibitor of PPM phosphatases and targets the M1 binding site. scientific reports, 3, 2333, 2013.
[112] 于晓 , 徐志刚 and 孙金鹏. The very large G protein coupled receptor (Vlgr1) in hair cells. J Mol Neurosci, 2013.
[113] 崔敏 , 于晓 and 孙金鹏. Beta2- Adrenergic Receptor and Astrocyte Glucose Metabolism. J Mol Neurosci, 48, 456, 2012.
[114] 徐志刚 , 于晓 , 孙金鹏 and 王晓静. Understanding cadherin EGF LAG seven-pass G-type receptors. Journal of Neurochemistry, 131, 699, 2014.
[115] 于晓 , 孙金鹏 and 姚伟. Differences in the H2S-induced quantal release of catecholamine in adrenal chromaffin cells of neona. toxicology, 312, 12, 2013.
[116] 于晓 , 方浩 and 孙金鹏. Fast identification of novel lymphoid tyrosine phosphatase inhibitors using target-ligand interactio. J Med Chem, 57, 9309, 2014.
[117] 于晓 , 杜吕佩 and 孙金鹏. Discovery of novel FFA4 (GPR120) receptor agonists with β-arrestin2-biased characteristics.. Future Med Chem, 7, 2429, 2015.
[118] 于晓 , 孙金鹏 , 李景新 , 马雪莲 and 姚伟. H2S induces catecholamine secretion in rat adrenal chromaffin cells. toxicology, 2012.
[119] 肖鹏 , 于晓 , 孙金鹏 and 杨照. G蛋白偶联受体的信号通路多样性及药物开发. 中国科学:生命科学, 2018.
[120] 于晓 and 孙金鹏. Phospho-selective mechanisms of arrestin conformations and functions revealed by unnatural amino aci. NATURE COMMUNICATIONS, 6, 8202, 2015.

共139条 6/7

首页上页下页尾页页

版权所有 ©山东大学　地址：中国山东省济南市山大南路27号　邮编：250100　
查号台：（86）-0531-88395114
值班电话：（86）-0531-88364731　建设维护：山东大学信息化工作办公室　　