J
Jun Li
Researcher at Peking Union Medical College
Publications - 44
Citations - 949
Jun Li is an academic researcher from Peking Union Medical College. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 14, co-authored 35 publications receiving 624 citations.
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Journal ArticleDOI
Molecular machinery and interplay of apoptosis and autophagy in coronary heart disease
TL;DR: Treatment concept for CHD is provided by balancing the switch between the two responses of apoptosis and autophagy and some therapeutic drugs and pharmacologic compounds involving mTOR inhibitor and AMPK activator have been reported to regulate apoptosis.
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Isolated Coronary Artery Bypass Graft Combined With Bone Marrow Mononuclear Cells Delivered Through a Graft Vessel for Patients With Previous Myocardial Infarction and Chronic Heart Failure A Single-Center, Randomized, Double-Blind, Placebo-Controlled Clinical Trial
Shengshou Hu,Sheng Liu,Zhe Zheng,Xin Yuan,Lihuan Li,Minjie Lu,Rui Shen,Fujian Duan,Xiaoling Zhang,Jun Li,Xue-wen Liu,Yunhu Song,Wei Wang,Shihua Zhao,Zuo-Xiang He,Hao Zhang,Keming Yang,Wei Feng,Xin Wang +18 more
TL;DR: Patients with a previous myocardial infarction and chronic heart failure could potentially benefit from isolated CABG combined with autologous BMMNCs delivered through a graft vessel.
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In Vitro Effects of Pirfenidone on Cardiac Fibroblasts: Proliferation, Myofibroblast Differentiation, Migration and Cytokine Secretion
TL;DR: It is demonstrated that treatment of CFs with pirfenidone resulted in decreased proliferation, and attenuated fibroblast α-smooth muscle actin expression and collagen contractility, and point to its potential use in the treatment of adverse myocardial remodeling.
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MicroRNA-193 pro-proliferation effects for bone mesenchymal stem cells after low-level laser irradiation treatment through inhibitor of growth family, member 5.
TL;DR: It is found that the proliferation level and cell cycle-associated genes in MSCs were increased after LLLI treatment in a time-dependent manner, and miR-193 was the most highly up-regulated miRNA, and the change in it was related with the proliferationlevel.
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Aging adversely impacts biological properties of human bone marrow-derived mesenchymal stem cells: implications for tissue engineering heart valve construction.
TL;DR: BMSCs from older patients with heart valve diseases could be harvested and expanded successfully, and the phenotype and morphology were uniform as nonaged groups, however, the proliferative and differentiation properties of aged cells, as well as cytokine release and migratory abilities, are significantly impaired.