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Wei Tuo
weituo@ioz.ac.cn
English, Chinese, French
Beijing
Chinese Academy of Sciences
Institute of Zoology
  • PhD: University of Chinese Academy of Sciences/National Center for Nanoscience and Technology and Aix-Marseille University
  • Published over 40 academic papers in international journals
  • Cited over 5800 times, H-index of 31
  • Applied for 13 domestic and international patents (9 granted)
  • 2015-2021 - Harvard Medical School, Boston Children's Hospital, MIT, University of Texas Southwestern Medical Center - Postdoctoral Research
  • 2021-Present - Institute of Zoology, Chinese Academy of Sciences - Researcher
Development of organ or cell-targeted lipid nanoparticle delivery systems
Development of novel gene editing delivery systems and gene editing therapy
Targeted gene therapy research for major diseases (e.g., tumors, metabolic diseases, genetic diseases)
  • Surface Engineering of Lipid Nanoparticles: Targeted Nucleic Acid Delivery and Beyond, Lin Y, Cheng Q*, Wei T*, 2023
  • Lung SORT LNPs enable precise homology-directed repair mediated CRISPR/Cas genome correction in cystic fibrosis models, Wei T#, Sun Y#, Cheng Q#, Chatterjee S, Traylor Z, Johnson LT, Coquelin ML, Wang J, Torres MJ, Lian X, Wang X, Xiao Y, Hodges CA, Siegwart DJ, 2023
  • Lipid Nanoparticle (LNP) Enables mRNA Delivery for Cancer Therapy, Zong Y, Lin Y, Wei T*, Cheng Q*, 2023
  • Lipid nanoparticles for mRNA therapy: recent advances in targeted delivery, Wei T*, Tao W*, Cheng Q*, 2022
  • Systemic nanoparticle delivery of CRISPR/Cas9 ribonucleoproteins for effective tissue-specific genome editing, Wei T#, Cheng Q#, Min YL, Olson EN, Siegwart DJ*, 2020
  • Selective ORgan Targeting (SORT) nanoparticles for tissue specific mRNA delivery and CRISPR/Cas gene editing, Cheng Q#, Wei T#, Farbiak L, Johnson LT, Dilliard SA, Siegwart DJ*, 2020
  • Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for in Vivo CRISPR/Cas-Based Genome Editing, Wei T, Cheng Q, Farbiak L, Anderson DG*, Langer R*, Siegwart DJ*, 2020
  • Multifunctional aptamer-based nanoparticles for targeted drug delivery to circumvent cancer resistance, Liu J#, Wei T#, Zhao J, Huang Y, Deng H, Kumar A, Wang C, Liang Z, Ma X*, Liang X-J*, 2016
  • Anticancer drug nanomicelles formed by self-assembling amphiphilic dendrimer to combat cancer drug resistance, Wei T, Chen C, Liu J, Liu C, Posocco P, Liu X, Cheng Q, Huo S, Liang Z, Fermeglia M, Pricl S, Liang X-J*, Rocchi P, Peng L*, 2015
  • Functionalized Nanoscale Micelles Improve Drug Delivery for Cancer Therapy in Vitro and in Vivo, Wei T#, Liu J#, Ma H, Cheng Q, Huang Y, Zhao J, Huo S, Xue X, Liang Z, Liang X-J*, 2013
Nanoparticles Lipid Gene Therapy Crispr Cancer Genetic Diseases Drug Delivery Biomedicine Targeted Therapy Nanotechnology

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