Area of research
Sensory Systems · Neurology
Research interest
Research interests include Hearing, Cochlea, Tinnitus, Genetics, Vestibular and auditory disorders, Hearing Loss and Rehabilitation, and Ear Surgery and Otitis Media.
Gene Therapy vs Cochlear Implantation in Restoring Hearing Function and Speech Perception for Individuals With Congenital Deafness
Audiological characteristics following gene therapy in patients with autosomal recessive deafness 9
A Qualitative Study of Migraine Headache Experience in Patients with Patent Foramen Ovale Based on the Symptom Management Theory
The role of audiological features and horizontal semicircular canal function at various frequencies in vestibular migraine and Menière’s disease
AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial
AAV‐Mediated Gene Therapy Restores Hearing in Patients with DFNB9 Deafness
Hair cell-specific Myo15 promoter-mediated gene therapy rescues hearing in DFNB9 mouse model
A base editor for the long-term restoration of auditory function in mice with recessive profound deafness
Clinical practice guidelines for gene therapy to treat hereditary hearing loss
Varying mechanical forces drive sensory epithelium formation
Prognosis of vestibular dysfunction in idiopathic sudden sensorineural hearing loss with vertigo: a prospective cohort study
P2X7 receptor is required for the ototoxicity caused by aminoglycoside in developing cochlear hair cells
The fudan tinnitus relieving system application for tinnitus management
Rescue of autosomal dominant hearing loss by in vivo delivery of mini dCas13X-derived RNA base editor
Identification of a prognostic index system and tumor immune infiltration characterization for lung adenocarcinoma based on mRNA molecular of pyroptosis
Bioinformatic Identification of Key Genes Leading to Increased Mitochondrial Mass in Cochlear Hair Cells
Inhibiting DNA methylation alleviates cisplatin-induced hearing loss by decreasing oxidative stress-induced mitochondria-dependent apoptosis via the LRP1–PI3K/AKT pathway
The crosstalk between the Notch, Wnt, and SHH signaling pathways in regulating the proliferation and regeneration of sensory progenitor cells in the mouse cochlea
Tinnitus Is Associated With Extended High-frequency Hearing Loss and Hidden High-frequency Damage in Young Patients
Laminin-Coated Electrospun Regenerated Silk Fibroin Mats Promote Neural Progenitor Cell Proliferation, Differentiation, and Survival in vitro
Association of Vertigo With Hearing Outcomes in Patients With Sudden Sensorineural Hearing Loss
The Role of Autoimmunity in the Pathogenesis of Sudden Sensorineural Hearing Loss
Novel compounds protect auditory hair cells against gentamycin-induced apoptosis by maintaining the expression level of H3K4me2
Vestibular Dysfunctions in Sudden Sensorineural Hearing Loss: A Systematic Review and Meta-analysis
Characterization of Wnt and Notch-Responsive Lgr5+ Hair Cell Progenitors in the Striolar Region of the Neonatal Mouse Utricle
MiR-182-5p protects inner ear hair cells from cisplatin-induced apoptosis by inhibiting FOXO3a
Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange‐Nielsen deafness syndrome
Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment
In vivo overexpression of X-linked inhibitor of apoptosis protein protects against neomycin-induced hair cell loss in the apical turn of the cochlea during the ototoxic-sensitive period
Inhibition of the Activation and Recruitment of Microglia-Like Cells Protects Against Neomycin-Induced Ototoxicity