Jianhui Chang
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Also affiliated: Australian National University (2022); National Institutes of Health (2005); IBM (United States) (1988); Guangdong University of Technology (2024); Central South University (2020–2025); Chinese Academy of Medical Sciences & Peking Union Medical College (2011–2012); Hong Kong University of Science and Technology (2024); Peking University (2005–2024); Inner Mongolia University (2024); University of Michigan (2005); Southern University of Science and Technology (2020–2022); National Institute of Dental and Craniofacial Research (2005); Nanjing Drum Tower Hospital (2025); IBM Research - Thomas J. Watson Research Center (1988); China Telecom (China) (2025–2026); Peng Cheng Laboratory (2021); China Telecom (2024–2026); State Key Laboratory of Pharmaceutical Biotechnology (2025); China University of Mining and Technology - Beijing (2018–2019); The Hong Kong University of Science and Technology (Guangzhou) (2024); Shanghai Ocean University (2024); Xiangtan University (2018); Kanagawa Dental University (2005); Nanjing University (2025)
Research Areas
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Biography and Research Information
OverviewAI-generated summary
Jianhui Chang's research focuses on cellular senescence, aging, and the impact of various interventions on stem cell function and tissue injury. Chang has investigated the role of cellular senescence in promoting adverse effects of chemotherapy and contributing to cancer relapse. Studies have explored methods to clear senescent cells, such as using ABT263, to rejuvenate aged hematopoietic stem cells in mice. Additionally, Chang has examined the potential of proteolysis-targeting chimera technology to mitigate drug toxicity and enhance senolytic activity.
Further research has involved evaluating natural compounds, like resveratrol and piperlongumine, for their ability to ameliorate long-term hematopoietic stem cell injury induced by ionizing irradiation and for their potential as senolytic agents. Chang's work also touches upon the molecular mechanisms underlying age-related changes, such as the decrease in osteoprogenitors with age due to DNA damage and senescence. The researcher's publication record includes work on diverse topics, such as information-flow security and flexible perovskite solar cells.
Metrics
- h-index: 32
- Publications: 103
- Citations: 6,547
Selected Publications
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Targeting cellular senescence alleviates bone marrow aging (2026)
Collaboration Network
Top Collaborators
- Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
- Cellular Senescence Promotes Adverse Effects of Chemotherapy and Cancer Relapse
- Discovery of piperlongumine as a potential novel lead for the development of senolytic agents
- Using proteolysis-targeting chimera technology to reduce navitoclax platelet toxicity and improve its senolytic activity
- Resveratrol ameliorates ionizing irradiation-induced long-term hematopoietic stem cell injury in mice
Showing 5 of 25 shared publications
- Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
- Cellular Senescence Promotes Adverse Effects of Chemotherapy and Cancer Relapse
- DNA damage and senescence in osteoprogenitors expressing Osx1 may cause their decrease with age
- Hematopoietic stem cell senescence and cancer therapy-induced long-term bone marrow injury.
- Exposure to Low-Dose 56Fe-Ion Radiation Induces Long-Term Epigenetic Alterations in Mouse Bone Marrow Hematopoietic Progenitor and Stem Cells
Showing 5 of 13 shared publications
- Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
- M1 and M2 macrophages differentially regulate hematopoietic stem cell self-renewal and ex vivo expansion
- Total Body Irradiation in the “Hematopoietic” Dose Range Induces Substantial Intestinal Injury in Non-Human Primates
- C/EBPδ Deficiency Sensitizes Mice to Ionizing Radiation-Induced Hematopoietic and Intestinal Injury
- Inter-Strain Differences in LINE-1 DNA Methylation in the Mouse Hematopoietic System in Response to Exposure to Ionizing Radiation
Showing 5 of 11 shared publications
- Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
- Cellular Senescence Promotes Adverse Effects of Chemotherapy and Cancer Relapse
- Using proteolysis-targeting chimera technology to reduce navitoclax platelet toxicity and improve its senolytic activity
- Systemic clearance of p16 INK4a ‐positive senescent cells mitigates age‐associated intervertebral disc degeneration
- Oxidation resistance 1 is a novel senolytic target
Showing 5 of 8 shared publications
- Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
- Exposure to Low-Dose 56Fe-Ion Radiation Induces Long-Term Epigenetic Alterations in Mouse Bone Marrow Hematopoietic Progenitor and Stem Cells
- M1 and M2 macrophages differentially regulate hematopoietic stem cell self-renewal and ex vivo expansion
- The Wave2 scaffold Hem-1 is required for transition of fetal liver hematopoiesis to bone marrow
- Hematopoietic stem cells from Ts65Dn mouse bone marrow are deficient in the repair of DNA double-strand breaks
Showing 5 of 7 shared publications
- Inter-Strain Differences in LINE-1 DNA Methylation in the Mouse Hematopoietic System in Response to Exposure to Ionizing Radiation
- Low Doses of Oxygen Ion Irradiation Cause Acute Damage to Hematopoietic Cells in Mice
- BMS-345541 Sensitizes MCF-7 Breast Cancer Cells to Ionizing Radiation by Selective Inhibition of Homologous Recombinational Repair of DNA Double-Strand Breaks
- Low doses of oxygen ion irradiation cause long-term damage to bone marrow hematopoietic progenitor and stem cells in mice
- 28Si total body irradiation injures bone marrow hematopoietic stem cells via induction of cellular apoptosis
Showing 5 of 6 shared publications
- C/EBPδ Deficiency Sensitizes Mice to Ionizing Radiation-Induced Hematopoietic and Intestinal Injury
- Inter-Strain Differences in LINE-1 DNA Methylation in the Mouse Hematopoietic System in Response to Exposure to Ionizing Radiation
- Low Doses of Oxygen Ion Irradiation Cause Acute Damage to Hematopoietic Cells in Mice
- Low doses of oxygen ion irradiation cause long-term damage to bone marrow hematopoietic progenitor and stem cells in mice
- Whole body proton irradiation causes acute damage to bone marrow hematopoietic progenitor and stem cells in mice
- Oxidation resistance 1 is a novel senolytic target
- Low Doses of Oxygen Ion Irradiation Cause Acute Damage to Hematopoietic Cells in Mice
- Low doses of oxygen ion irradiation cause long-term damage to bone marrow hematopoietic progenitor and stem cells in mice
- 28Si total body irradiation injures bone marrow hematopoietic stem cells via induction of cellular apoptosis
- Whole body proton irradiation causes acute damage to bone marrow hematopoietic progenitor and stem cells in mice
- Using proteolysis-targeting chimera technology to reduce navitoclax platelet toxicity and improve its senolytic activity
- DNA damage and senescence in osteoprogenitors expressing Osx1 may cause their decrease with age
- Elimination of senescent osteoclast progenitors has no effect on the age‐associated loss of bone mass in mice
- Long-Term Clearance of Senescent Cells Prevents the Hematopoietic Stem Cell Aging in Naturally Aged Mice
- Targeting cellular senescence alleviates bone marrow aging
- Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
- Hematopoietic stem cell senescence and cancer therapy-induced long-term bone marrow injury.
- M1 and M2 macrophages differentially regulate hematopoietic stem cell self-renewal and ex vivo expansion
- Hematopoietic stem cells from Ts65Dn mouse bone marrow are deficient in the repair of DNA double-strand breaks
- Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
- Resveratrol ameliorates ionizing irradiation-induced long-term hematopoietic stem cell injury in mice
- Hematopoietic stem cell senescence and cancer therapy-induced long-term bone marrow injury.
- Hematopoietic stem cells from Ts65Dn mouse bone marrow are deficient in the repair of DNA double-strand breaks
- C/EBPδ Deficiency Sensitizes Mice to Ionizing Radiation-Induced Hematopoietic and Intestinal Injury
- Low Doses of Oxygen Ion Irradiation Cause Acute Damage to Hematopoietic Cells in Mice
- Low doses of oxygen ion irradiation cause long-term damage to bone marrow hematopoietic progenitor and stem cells in mice
- Whole body proton irradiation causes acute damage to bone marrow hematopoietic progenitor and stem cells in mice
- Using proteolysis-targeting chimera technology to reduce navitoclax platelet toxicity and improve its senolytic activity
- DNA damage and senescence in osteoprogenitors expressing Osx1 may cause their decrease with age
- Elimination of senescent osteoclast progenitors has no effect on the age‐associated loss of bone mass in mice
- Long-Term Clearance of Senescent Cells Prevents the Hematopoietic Stem Cell Aging in Naturally Aged Mice
- Exposure to Low-Dose 56Fe-Ion Radiation Induces Long-Term Epigenetic Alterations in Mouse Bone Marrow Hematopoietic Progenitor and Stem Cells
- Long-term epigenetic effects of exposure to low doses of 56Fe in the mouse lung
- Inter-Strain Differences in LINE-1 DNA Methylation in the Mouse Hematopoietic System in Response to Exposure to Ionizing Radiation
- Exposure to Low-Dose 56Fe-Ion Radiation Induces Long-Term Epigenetic Alterations in Mouse Bone Marrow Hematopoietic Progenitor and Stem Cells
- Long-term epigenetic effects of exposure to low doses of 56Fe in the mouse lung
- 28Si total body irradiation injures bone marrow hematopoietic stem cells via induction of cellular apoptosis
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