Area of research
Otorhinolaryngology · Physiology
Research interest
Research interests include Sinusitis and nasal conditions, Asthma and respiratory diseases, Cancer Immunotherapy and Biomarkers, and Advanced Sensor and Energy Harvesting Materials.
Human apical-out nasal organoids reveal an essential role of matrix metalloproteinases in airway epithelial differentiation
Squalene-epoxidase-catalyzed 24(S),25-epoxycholesterol synthesis promotes trained-immunity-mediated antitumor activity
Ultrasensitive, Fast-Response, and Stretchable Temperature Microsensor Based on a Stable Encapsulated Organohydrogel Film for Wearable Applications
Flame‐retardant, flexible, and breathable smart humidity sensing fabrics based on hydrogels for respiratory monitoring and non‐contact sensing
High‐Performance Strain Sensors Based on Organohydrogel Microsphere Film for Wearable Human–Computer Interfacing
T cell-intrinsic STING signaling promotes regulatory T cell induction and immunosuppression by upregulating FOXP3 transcription in cervical cancer
Suppression of ACE2 SUMOylation protects against SARS-CoV-2 infection through TOLLIP-mediated selective autophagy
Global burden of oropharyngeal cancer attributable to human papillomavirus by anatomical subsite and geographic region
Fe-doped Mo2C for boosting electrocatalytic N2 reduction
Perfluoroalkyl substance pollutants activate the innate immune system through the AIM2 inflammasome
DUSP16 promotes cancer chemoresistance through regulation of mitochondria-mediated cell death
Tetrahydrocurcumin alleviates allergic airway inflammation in asthmatic mice by modulating the gut microbiota
Predictive biomarkers and mechanisms underlying resistance to PD1/PD-L1 blockade cancer immunotherapy
Perfluorooctanesulfonate and perfluorooctanoate exacerbate airway inflammation in asthmatic mice and in vitro
In Vitro Model of Fully Differentiated Human Nasal Epithelial Cells Infected With Rhinovirus Reveals Epithelium-Initiated Immune Responses
Human nasal epithelial cells derived from multiple subjects exhibit differential responses to H3N2 influenza virus infection in vitro