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Li Wang

Researcher at University of North Carolina at Chapel Hill

Publications -  54
Citations -  2232

Li Wang is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Reprogramming & Medicine. The author has an hindex of 22, co-authored 46 publications receiving 1562 citations. Previous affiliations of Li Wang include Chinese Academy of Sciences.

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Systematic comparison of 2A peptides for cloning multi-genes in a polycistronic vector

TL;DR: The effect of varying gene position and 2As on the expression of proteins encoded in bi-, tri-, or quad-cistronic constructs is characterized and results on protein expression ratios from different 2A constructs could serve to guide future utilization of 2A peptides in basic research and clinical applications.
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Stoichiometry of Gata4, Mef2c, and Tbx5 Influences the Efficiency and Quality of Induced Cardiac Myocyte Reprogramming

TL;DR: The results demonstrate that stoichiometry of G, M, T protein expression influences the efficiency and quality of iCM reprogramming and will provide a valuable platform for future iCM studies.
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Atorvastatin enhances the therapeutic efficacy of mesenchymal stem cells-derived exosomes in acute myocardial infarction via up-regulating long non-coding RNA H19

TL;DR: Exosomes obtained from ATV-pretreated MSCs have significantly enhanced therapeutic efficacy for treatment of AMI possibly through promoting endothelial cell function and mediates the cardioprotective roles of MSCATV-Exo in promoting angiogenesis.
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Bmi1 Is a Key Epigenetic Barrier to Direct Cardiac Reprogramming

TL;DR: Reducing levels of the polycomb complex gene Bmi1 significantly enhanced induction of beating iCMs from neonatal and adult mouse fibroblasts and acts as a critical epigenetic barrier to iCM production, potentially streamlining i CM production for therapeutic purposes.
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Single-cell transcriptomics reconstructs fate conversion from fibroblast to cardiomyocyte

TL;DR: Single-cell transcriptomics approaches enabled us to reconstruct the reprogramming trajectory and to uncover intermediate cell populations, gene pathways and regulators involved in iCM induction.