Area of research
Immunology · Surgery
Research interest
Research interests include Organ Transplantation Techniques and Outcomes, T-cell and B-cell Immunology, Immune Cell Function and Interaction, and Liver Disease and Transplantation.
Pretransplant circulating cTfh17 and donor-reactive T follicular helper responses distinguish liver transplant recipients who develop ischemia-reperfusion injury and donor-specific antibody
Reply to: Do T/B lymphocytes mask the protective effects of group 1 innate lymphoid cells against liver graft ischemia-reperfusion injury?
Effects of balance training combined with stroboscopic visual training on balance ability in college-aged male soccer players
Group 1 innate lymphoid cells protect liver transplants from ischemia-reperfusion injury via an interferon gamma–mediated pathway
Macrophage Heterogeneity in Liver Ischemia-Reperfusion Injury
Neutrophil CEACAM1 determines susceptibility to NETosis by regulating the S1PR2/S1PR3 axis in liver transplantation
T‐Cell Immunoglobulin and Mucin Domain‐Containing Protein‐4 Is Critical for Kupffer Cell Homeostatic Function in the Activation and Resolution of Liver Ischemia Reperfusion Injury
T-Cell Immunoglobulin and Mucin Domain-Containing Protein-4 Is Critical for Kupffer Cell Homeostatic Function in the Activation and Resolution of Liver Ischemia Reperfusion Injury.
Ischemia-reperfusion Injury in Allogeneic Liver Transplantation: A Role of CD4 T Cells in Early Allograft Injury
Farnesoid X Receptor Activation Protects Liver From Ischemia/Reperfusion Injury by Up-Regulating Small Heterodimer Partner in Kupffer Cells.
Glycogen synthase kinase 3β promotes liver innate immune activation by restraining AMP-activated protein kinase activation
Ag-specific CD4 T cells promote innate immune responses in liver ischemia reperfusion injury
Prolonged Ischemia Triggers Necrotic Depletion of Tissue-Resident Macrophages To Facilitate Inflammatory Immune Activation in Liver Ischemia Reperfusion Injury
Innate Immune Regulations and Liver Ischemia-Reperfusion Injury
CXCL10/CXCR3 signaling mobilized-regulatory T cells promote liver tumor recurrence after transplantation
ATF3-Mediated NRF2/HO-1 Signaling Regulates TLR4 Innate Immune Responses in Mouse Liver Ischemia/Reperfusion Injury
Myeloid PTEN Deficiency Protects Livers from Ischemia Reperfusion Injury by Facilitating M2 Macrophage Differentiation
Rapamycin Protection of Livers From Ischemia and Reperfusion Injury Is Dependent on Both Autophagy Induction and Mammalian Target of Rapamycin Complex 2-Akt Activation
Nuclear Factor Erythroid 2–Related Factor 2 Regulates Toll-Like Receptor 4 Innate Responses in Mouse Liver Ischemia-Reperfusion Injury Through Akt-Forkhead box Protein O1 Signaling Network
KEAP1-NRF2 complex in ischemia-induced hepatocellular damage of mouse liver transplants
Post-transplant endothelial progenitor cell mobilization via CXCL10/CXCR3 signaling promotes liver tumor growth
Ischaemia–reperfusion injury in liver transplantation—from bench to bedside