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于晓
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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
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[61] 刘春华 , 刘传勇 , 易凡 , 于晓 , 孙金鹏 , 肖鹏 , 崔福爱 and 何东方. Arrestin-biased AT1R agonism induces acute catecholamine secretion through TRPC3 coupling. NATURE COMMUNICATIONS, 8, 2017.
[62] 姚伟 , 于晓 and 马雪莲. Silicone rubber as a novel insulating material for manufacturing cylindrical glass carbon fiber elec. Materials letters, 2012.
[63] 于晓 , 姚伟 , 孙金鹏 , 刘奇迹 and 庞琦. Biochemical and functional studies of Lymphoid-specific tyrosine phosphatase (Lyp) variants S201F an. Plos one, 7, e43631, 2012.
[64] 易凡 , 于晓 , 包婵婵 , 张艳 , 王姿颖 and 魏欣冰. Novel Role of NOD2 in Mediating Ca2+ Signaling: Evidence from NOD2-regulated Podocyte TRPC6 Channels. Hypertension, 62, 506, 2013.
[65] 刘传勇 , 崔爽 , 刘克敬 , 李景新 , 于晓 and 马雪莲. Oxytocin-induced membrane hyperpolarization in pain-sensitive dorsal root ganglia neurons mediated b. neuroscience, 2015.
[66] 于晓 , 姚伟 and 孙金鹏. The catalytic region and PEST domain of PTPN18 distinctly regulate the HER2 phosphorylation and ubiq. CELL RESEARCH, 24, 1067, 2014.
[67] 于晓 , 崔敏 and 孙金鹏. A Stress response pathway in mice upregulates somatostatin level and transcription in pancreatic del. Diabetologia, 57, 1899, 2014.
[68] 孙金鹏 , 于晓 , 肖鹏 , 任桂杰 and 方浩. 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.
[69] 孙金鹏 , 崔敏 and 于晓. Beta2- Adrenergic Receptor and Astrocyte Glucose Metabolism. J Mol Neurosci, 48, 456, 2012.
[70] 易凡 , 于晓 , 王晓杰 , 王姿颖 , 张艳 and 孙金鹏. β-Arrestins promote podocyte injury by inhibition of autophagy in diabetic nephropathy.. Cell Death & Disease, 2016 Apr 7;7:e2183., e2183, 2016.
[71] 孙金鹏 , 于晓 and 徐志刚. The Role of G Protein-coupled Receptors in Cochlear Planar Cell Polarity.. Int J Biochem Cell Biol., 77, 220, 2016.
[72] 于晓 , 肖鹏 , 崔福爱 , 易凡 , 徐志刚 and 孙金鹏. Crystal Structure and Substrate Specificity of PTPN12.. Cell Reports., 15, 1345, 2016.
[73] 于晓 , 徐志刚 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.
[74] 孙金鹏 , 于晓 and 方浩. Fast identification of novel lymphoid tyrosine phosphatase inhibitors using target-ligand interactio. J Med Chem, 57, 9309, 2014.
[75] 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.
[76] 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.
[77] 杜吕佩 , 李敏勇 , 徐志刚 , 于晓 and 孙金鹏. FFA4 receptor (GPR120): A hot target for the development of anti-diabetic therapies.. Eur J Pharmacol., 763, 160, 2015.
[78] 肖鹏 , 于晓 and 孙金鹏. The catalytic role of the M2 metal ion in PP2Cα.. scientific reports, 5, 8560, 2015.
[79] 于晓. Calcium influx activates adenylyl cyclase 8 for sustained insulin secretion in rat pancreatic beta c. Diabetologia, 58, 324, 2015.
[80] 孙金鹏 and 于晓. Phospho-selective mechanisms of arrestin conformations and functions revealed by unnatural amino aci. NATURE COMMUNICATIONS, 6, 8202, 2015.
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