Professor | Rong Qi | Asia Growth Partners

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Name	Rong Qi
Contact Information	ronaqi@bjmu.edu.cn
Language ability	Chinese, English
Province	Beijing

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Name

Rong Qi

Contact Information

ronaqi@bjmu.edu.cn

Language ability

Chinese, English

Province

Beijing

University/Lab Affiliation and Title	Peking University
Faculty	Basic Medical Sciences
Academic Background & Achievements	2004 - PhD in Science from China Pharmaceutical University Postdoctoral Research Fellow at University of Michigan Ann Arbor, School of Medicine (2008-2010) Visiting Professor at National Taiwan University Oasis Scholar at Shihezi University
Work Experience	Current - Professor and Doctoral Supervisor at Peking University, Department of Pharmacology PI at the Ministry of Education Key Laboratory of Molecular Cardiovascular Science, Peking University PI at the Key Laboratory of Vascular Medicine of the Ministry of Health
Awards	Excellent SCI Paper Citation Award from the Medical Department of Peking University Excellent SCI Paper Award from the Basic Medical College

University/Lab Affiliation and Title

Peking University

Faculty

Basic Medical Sciences

Academic Background & Achievements

2004 - PhD in Science from China Pharmaceutical University
Postdoctoral Research Fellow at University of Michigan Ann Arbor, School of Medicine (2008-2010)
Visiting Professor at National Taiwan University
Oasis Scholar at Shihezi University

Work Experience

Current - Professor and Doctoral Supervisor at Peking University, Department of Pharmacology
PI at the Ministry of Education Key Laboratory of Molecular Cardiovascular Science, Peking University
PI at the Key Laboratory of Vascular Medicine of the Ministry of Health

Awards

Excellent SCI Paper Citation Award from the Medical Department of Peking University
Excellent SCI Paper Award from the Basic Medical College

Areas of Focus	Prevention and treatment of cardiovascular diseases and new drug discovery
Publications	Formulation and Intestinal Absorption of Naringenin Loaded Nanostructured Lipid Carrier and Its Inhibitory Effects on Nonalcoholic Fatty Liver Disease, Hu R, Liu S, Anwaier G, Wang QY, Shen WL, Shen Q, Qi R, 2021 Naringenin attenuates nonalcoholic fatty liver disease by downregulating NLRP3/NF-κB pathway in mice, Wang QY, Ou YJ, Hu GM, Wen C, Yue SS, Chen C, Xu L, Xie J, Dai H, Xiao H, Zhang YY, Qi R, 2020 Inhibitory effects and mechanism of probucol on elastase-induced abdominal aortic aneurysm in mice, Chen C, Wang YX, Cao YN, Wang QY, Anwaier G, Zhang Q, Qi R, 2020 Inhibitory Effects of Cycloastragenol on Abdominal Aortic Aneurysm and its Related Mechanisms, Wang YX, Chen C, Wang QY, Cao YN, Xu L, Qi R, 2019 Thermosensitive Hydrogel Containing Doxycycline Exerts Inhibitory Effects on Abdominal Aortic Aneurysm Induced By Pancreatic Elastase in Mice, Yu MM, Dong AJ, Chen C, Xu S, Cao YN, Liu S, Zhang Q, Qi R, 2017 Preventive effects of simvastatin nanoliposome on isoproterenol-induced cardiac remodeling in mice, Tuerdi N, Xu L, Zhu BL, Chen C, Cao YN, Wang YX, Zhang Q, Li ZJ, Qi R, 2016 G5-PEG PAMAM dendrimer incorporating nanostructured lipid carriers enhance oral bioavailability and plasma lipid-lowering effect of probucol, Qi R, Li YZ, Chen C, Cao YN, Yu MM, Xu L, He B, Jie X, Shen WW, Wang YN, van Dongen MA, Liu GQ, Banaszak Holl MM, Zhang Q, Ke X, 2015 Efficient in vitro siRNA delivery and potent gene silencing in vivo using PEG-modified PAMAM dendrimers, Tang Y, Li YB, Wang B, Lin RY, van Dongen M, Zurcher DM, Gu XY, Banaszak Holl MM, Liu GQ, Qi R, 2012 PEG-conjugated PAMAM dendrimers mediate efficient intramuscular gene expression, Qi R, Gao Y, Tang Y, He RR, Liu TL, He Y, Sun S, Li BY, Li YB, Liu G, 2009 Spontaneous Atherosclerosis in Aged Lipoprotein Lipase–Deficient Mice With Severe Hypertriglyceridemia on a Normal Chow Diet, Zhang XH, Qi R, Xian XD, Yang F, Blackstein M, Deng X, Fan JL, Ross C, Karasinska J, Hayden MR, Liu GQ, 2008

Areas of Focus

Prevention and treatment of cardiovascular diseases and new drug discovery

Publications

Formulation and Intestinal Absorption of Naringenin Loaded Nanostructured Lipid Carrier and Its Inhibitory Effects on Nonalcoholic Fatty Liver Disease, Hu R, Liu S, Anwaier G, Wang QY, Shen WL, Shen Q, Qi R, 2021
Naringenin attenuates nonalcoholic fatty liver disease by downregulating NLRP3/NF-κB pathway in mice, Wang QY, Ou YJ, Hu GM, Wen C, Yue SS, Chen C, Xu L, Xie J, Dai H, Xiao H, Zhang YY, Qi R, 2020
Inhibitory effects and mechanism of probucol on elastase-induced abdominal aortic aneurysm in mice, Chen C, Wang YX, Cao YN, Wang QY, Anwaier G, Zhang Q, Qi R, 2020
Inhibitory Effects of Cycloastragenol on Abdominal Aortic Aneurysm and its Related Mechanisms, Wang YX, Chen C, Wang QY, Cao YN, Xu L, Qi R, 2019
Thermosensitive Hydrogel Containing Doxycycline Exerts Inhibitory Effects on Abdominal Aortic Aneurysm Induced By Pancreatic Elastase in Mice, Yu MM, Dong AJ, Chen C, Xu S, Cao YN, Liu S, Zhang Q, Qi R, 2017
Preventive effects of simvastatin nanoliposome on isoproterenol-induced cardiac remodeling in mice, Tuerdi N, Xu L, Zhu BL, Chen C, Cao YN, Wang YX, Zhang Q, Li ZJ, Qi R, 2016
G5-PEG PAMAM dendrimer incorporating nanostructured lipid carriers enhance oral bioavailability and plasma lipid-lowering effect of probucol, Qi R, Li YZ, Chen C, Cao YN, Yu MM, Xu L, He B, Jie X, Shen WW, Wang YN, van Dongen MA, Liu GQ, Banaszak Holl MM, Zhang Q, Ke X, 2015
Efficient in vitro siRNA delivery and potent gene silencing in vivo using PEG-modified PAMAM dendrimers, Tang Y, Li YB, Wang B, Lin RY, van Dongen M, Zurcher DM, Gu XY, Banaszak Holl MM, Liu GQ, Qi R, 2012
PEG-conjugated PAMAM dendrimers mediate efficient intramuscular gene expression, Qi R, Gao Y, Tang Y, He RR, Liu TL, He Y, Sun S, Li BY, Li YB, Liu G, 2009
Spontaneous Atherosclerosis in Aged Lipoprotein Lipase–Deficient Mice With Severe Hypertriglyceridemia on a Normal Chow Diet, Zhang XH, Qi R, Xian XD, Yang F, Blackstein M, Deng X, Fan JL, Ross C, Karasinska J, Hayden MR, Liu GQ, 2008

Cardiovascular Disease Prevention Treatment Drug Discovery Molecular Compounds Mechanism Of Action Drug Targets Drug Delivery Biological Efficacy

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