Qiang Shi
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Senior Staff Fellow
Also affiliated: Jiangxi University of Traditional Chinese Medicine (2025); Jiangnan University (2011–2013); Zhejiang Chinese Medical University (2008); Jiangsu University (2025); University of Science and Technology of China (2026); Dalhousie University (2018); United States Food and Drug Administration (2009–2025); Zhejiang Sci-Tech University (2023); Center for Drug Evaluation and Research (2020); North China University of Science and Technology (2022); Nanchang University (2022–2025); Johns Hopkins University (2024); Sun Yat-sen University (2016–2019); China Three Gorges University (2022); Hunan University (2002); Pfizer (United States) (2012–2014); Shanghai Jiao Tong University (2022); Capital Medical University (2017); Dalian Medical University (2012); Liaocheng University (2022); Chinese Academy of Sciences (2022–2026); Shanghai University of Electric Power (2008); Fudan University (2016–2024); Johns Hopkins Medicine (2024); China-Japan Friendship Hospital (2017); Sir Run Run Shaw Hospital (2019); Tianjin Medical University General Hospital (2015); Chinese PLA General Hospital (2023); Soochow University (2022); Inner Mongolia Electric Power (China) (2023); Shanghai Stomatological Hospital (2023); Chongqing Bureau of Geology and Minerals Exploration (2021–2024); Changchun Institute of Applied Chemistry (2022–2026); Dalian University (2012); Fudan University Shanghai Cancer Center (2023); Hefei National Center for Physical Sciences at Nanoscale (2016); Xinjiang Industry Technical College (2022); Affiliated Hospital of Taishan Medical University (2022–2025); Chongqing Maternal and Child Health Hospital (2023); Analysis and Testing Centre (2013); Shanghai Open University (2024); Xinjiang Institute of Engineering (2022); PAREXEL International (United States) (2012); Zhongshan Hospital (2016–2024); First Automotive Works (China) (2023); Changchun University of Chinese Medicine (2023); Chinese Academy of Forestry (2010–2011); Institute of Software (2009); The First Affiliated Hospital, Sun Yat-sen University (2016–2019); Jining First People's Hospital (2023); Research Institute of Wood Industry (2010–2011); First Hospital of China Medical University (2009–2011); Changchun Institute of Technology (2022); Zhejiang Pharmaceutical College (2008); Shanghai Sixth People's Hospital (2022); Obstetrics and Gynecology Hospital of Fudan University (2023); Beijing Friendship Hospital (2017); Pfizer (China) (2012–2014); Food and Drug Administration (2008–2014); State Key Laboratory of Food Science and Technology (2022–2024); State Key Laboratory of Polymer Physics and Chemistry (2022); Sichuan Research Center of New Materials (2017); South China Institute of Collaborative Innovation (2023); Center for Life Sciences (2023–2024); Shandong First Medical University (2022–2025); University of Chinese Academy of Sciences (2022); Dezhou University (2010–2013); Hebei University (2005); Northwest Normal University (2023–2024); Zhejiang University (2006–2019); Southeast University (2025); Shaanxi Normal University (2016–2018); China Medical University (2009–2011); Tsinghua University (2023–2024)
Staff Researcher
Upstream record may be merged OpenAlex, the source of these figures, lists 76 institutions in 4 countries for this author record — a pattern that usually means it combines several researchers with similar names. The totals above may include work by other people.
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Qiang Shi's research investigates molecular mechanisms underlying cellular processes, with a recent focus on ubiquitination and its role in protein regulation and disease. His work has explored the structural and mechanistic basis of deubiquitination by specific enzymes, such as USP16, and the mechanisms of ubiquitination mediated by factors like yeast Bre1-Rad6 and its human homolog RNF20/RNF40-hRAD6A. Shi has also examined the function of proteins like Synovial sarcoma X breakpoint 1 in recognizing ubiquitinated nucleosomes.
Beyond ubiquitination, his research has touched upon other cellular pathways relevant to health. This includes investigating the ferroptosis mechanism in the context of Alzheimer's disease and exploring how combinations of compounds, such as nicotinamide mononucleotide and lycopene, can prevent cognitive impairment and oxidative damage in aging models. Shi has also contributed to the study of drug-induced liver injury through co-culture systems involving primary hepatocytes and nonparenchymal liver cells in liver-chip models.
With an h-index of 35 and over 10,670 citations across more than 205 publications, Shi is recognized as a highly cited researcher. He collaborates with colleagues at the National Center for Toxicological Research, including Laura K. Schnackenberg, Katy S Papineau, and Lijun Ren.
Metrics
- h-index: 36
- Publications: 207
- Citations: 10,804
Selected Publications
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Challenges and solutions in measuring commonly used biomarkers for drug-induced liver injury in a liver-on-a-chip platform (2025)
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Toxicity of ubiquitous tire rubber antiozonant N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD) and its transformation product 6PPD-quinone (6PPD-Q) in primary human hepatocytes and liver spheroids (2025)
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Pexidartinib impairs liver mitochondrial functions causing cell death in primary human hepatocytes at clinically relevant concentrations (2025)
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Considerations from the pharmaceutical industry (IQ MPS affiliate) workshop on animal microphysiological systems and 3Rs in drug development (2025)
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New Alternative Methods in Drug Safety Assessment (2023)
Collaboration Network
Top Collaborators
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Pexidartinib impairs liver mitochondrial functions causing cell death in primary human hepatocytes at clinically relevant concentrations
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Pexidartinib impairs liver mitochondrial functions causing cell death in primary human hepatocytes at clinically relevant concentrations
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Pexidartinib impairs liver mitochondrial functions causing cell death in primary human hepatocytes at clinically relevant concentrations
- Metabolism of carcinogenic pyrrolizidine alkaloids and pyrrolizidine alkaloid<i>N</i>-oxides by rat primary hepatocytes generate the same characteristic DHP-DNA adducts
- Metabolism of carcinogenic pyrrolizidine alkaloids and pyrrolizidine alkaloid<i>N</i>-oxides by rat primary hepatocytes generate the same characteristic DHP-DNA adducts
- Metabolism of carcinogenic pyrrolizidine alkaloids and pyrrolizidine alkaloid<i>N</i>-oxides by rat primary hepatocytes generate the same characteristic DHP-DNA adducts
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Single-cell RNA-sequencing and subcellular spatial transcriptomics facilitate the translation of liver microphysiological systems for regulatory application
- Single-cell RNA-sequencing and subcellular spatial transcriptomics facilitate the translation of liver microphysiological systems for regulatory application
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